Thermodynamic Properties of Organic Compounds and Their Mixtures, Hong, Hall, 1997 PDF

Survey of volume IV/8
Thermodynamic Properties of Organic Compounds

and their Mixtures
1. Enthalpies of Fusion and Transition of Organic Compounds Subvolume A
2. Densities of Aliphatic Hydrocarbons: Alkanes Subvolume B
3. Densities of Aliphatic Hydrocarbons: Alkenes, Alkadienes,

Alkynes, and Miscellaneous Compounds Subvolume C
4. Densities of Monocyclic Hydrocarbons Subvolume D
5. Vapor Pressure of Aliphatic Halohydrocarbons
6. Densities of Aliphatic Halohydrocarbons
7. Densities of Aromatic Hydrocarbons

Thermodynamic Properties
of Organic Compounds
and their Mixtures
Subvolume D
Densities of Monocyclic Hydrocarbons
R. C. Wilhoit, X. Hong, M. Frenkel, K. R. Hall
Edited by K. R. Hall and K. N. Marsh
Thermodynamics Research Center

The Texas A&M University System
College Station, Texas 77843-3111, USA
Editors
K.R. Hall
TheTexas A&M University System
K.N. Marsh
former
now
University of Christchurch
New Zealand
Authors
R.C. Wilhoit
X. Hong
M. Frenkel
K.R. Hall
Preface
Critically evaluated experimental data covering the densities of organic compounds is essential for both
scientific and industrial applications. Knowledge of densities is important in many areas, including custody
transfer of materials, product specification, development of various predictive methods, and for
characterizing compounds and estimating their purity.
Various compilations of densities for organic compounds have been published. The early Landolt-
Brnstein compilation [23-ano] contained recommended values at specific temperatures. International
Critical Tables [28-ano-1] provided recommended densities at 0 C and values of constants for either a
second or third order polynomial equation to represent densities as a function of temperature. This
compilation also gave the range of validity of the equation and the limits of uncertainty, references used in
the evaluation and those not considered. This compilation is one of the most comprehensive ever published.
Timmermans [50-tim, 65-tim], Dreisbach [55-dre, 59-dre, 61-dre] and Landolt-Brnstein [71-ano] published
additional compilations, primarily of experimental data. These compilations contained experimental data
along with reference sources but no estimates of uncertainty for the data nor recommended values.
The Thermodynamics Research Center has published recommended values for the densities of organic
compounds since 1942 in its two loose leaf publications: TRC Thermodynamic Tables - Hydrocarbons and
Non-Hydrocarbons. These compilations are updated with four supplements per year. References to the
literature values used in the selection and those not used in the selection appear in the references for each
table. The accuracy of the values ia apparent from the number of significant figures provided. More
recently, the Design Institute of Physical Property Data, Project 801 has assembled a set of recommended
equations for the densities of over 1500 compounds [89-dau/dan, 91-dau/dan, 92-dau/dan, 93-dau/dan, 94-
dau/dan, 95-dau/dan]. Densities are represented by an equation fit to selected values from the freezing
temperature to the critical temperature. References to sources of data used in the evaluation and those not
used are given along with a quality assessment. In many cases, the equation does not fit density values at
intermediate temperatures, especially at 293.15 K and 298.15 K, within the experimental uncertainty. Thus,
the equation is not useful for purity comparisons, custody transfer, or product specification when the highest
accuracy is required. Smith and Srivastava [86-smi/sri, 86-smi/sri-1] recently have published a compilation
(in two volumes) which contains recommended values in tabular form as well as equations with statistical
information regarding the fit. However, this compilation contains no indication of data quality or
uncertainties.
The present volume contains densities for monocyclic, non-aromatic hydrocarbons including
alkylcycloalkanes, alkylcycloalkenes, alkenylcycloalkanes, alkylcyclodienes, alkenylcycloalkenes,
alkadienylcycloalkanes, alkynylcycloalkanes, alkylcyclotrienes, alkenylcyclodienes, alkylcyclotetraenes,
dialkenylcycloalkenes, trialkenylcycloalkanes and other related compounds which have been collected from
the literature published from 1870 to early 1996. The various compilations listed above also have been
consulted for sources of original data. This volume continues our effort in evaluation of the densities of
organic compounds (see volume IV/8B [96-wil/mar] for the densities of alkanes and volume IV/8C [96-
wil/mar-1] for the densities of alkenes, alkynes and alkadienes). All experimental density values have been
evaluated critically and assigned numerical uncertainties individually. These assessments have been used to
derive an equation to fit the data and to obtain recommended values with uncertainties. Detailed evaluation
procedures appear in Chapter 1. Algorithms for the automatic selection of data used in the fit and for the
selection of the type of equation and order of polynomial have been developed. The algorithms depend upon
the assigned uncertainties, the distribution of density values over the experimental temperature range, and
the magnitude and distribution of differences between observed and smoothed values. These algorithms can
fit any kind of data to a function of independent variables. We have collected data for 820 compounds,
consisting of 2672 data sets (total of 3903 data points) drawn from 1250 sources of which 1216 sets have
been used in the evaluation. The other data sets have been rejected, but references to them are given.
The volume contains six chapters; a list of references, and two indexes (Chemical Abstracts Service
Registry Number Index and Chemical Name Index). Chapter 1 contains: a short introduction; a description
of the tables; a detailed description of the methods used in the evaluation, selection and smoothing process;
a glossary of symbols and a description of the nomenclature used. Chapter 2 covers the alkylcycloalkanes,
Chapter 3 contains the alkylcycloalkenes and alkenylcycloalkanes, Chapter 4 has the monocyclic
hydrocarbons of general formula CnH2n-4, Chapter 5 provides the monocyclic hydrocarbons of general
formula CnH2n-6, and Chapter 6 presents the monocyclic hydrocarbons of general formula CnH2n-8. Section
1.7.2 describes the method used to determine the sequence of the compounds. The tables contain the
original literature data along with their estimated uncertainties and the evaluated data in both numerical form
and as coefficients to equations with selected statistical information. When data cover a sufficient
temperature range, graphical plots of the deviations of the experimental data from the recommended
equation are given. The chemical name index contains the IUPAC names for the compounds, as well as
alternate names that often appear in practice.
This volume should be useful to a wide community of researchers, data specialists, and engineers
working in the field of physical and organic chemistry, chemical engineering, material science,
environmental chemistry, chemical aspects of energy technology, and those engaged in the development of
new predictive procedures. The book should also be of use to students and faculty in Chemistry and
Chemical Engineering departments at universities as a reference book of evaluated thermophysical
properties.
Acknowledgments
The authors wish to express their sincere appreciation to staff members of the Thermodynamics Research
Center (TRC), part of the Chemical Engineering Division of the Texas Engineering Experiment Station in
The Texas A&M University System. Our special thanks to Steve Conroy who supervised the preparation of
the camera-ready copy of the manuscript. Also we thank Mark Sutton, Stephanie Hale and Yong Lee for
their assistance in formatting the text and preparing the graphs.
College Station, August 1997 R. C. Wilhoit, X. Hong, M. Frenkel, K. R. Hall

References
23-ano Landolt-Brnstein Physikalisch-Chemische Tabellen, Hauptwerk, Vol. 1, Roth, W.A., Scheel,
K. (eds.), Springer-Verlag: Berlin (1923).
28-ano-1 International Critical Tables of Numerical Data, Physics, Chemistry and Technology
Vol. III, Washburn, E. W. (ed.), McGraw-Hill: New York (1928).
50-tim Timmermans, J.; Physico-Chemical Constants of Pure Organic Compounds, Vol. 1, Elsevier:
New York (1950).
55-dre Dreisbach, R. R.; Physical Properties of Chemical Compounds, Advances in Chemistry Series
No. 15, Am. Chem. Soc.: Washington, D. C. (1955).
59-dre Dreisbach, R. R.; Physical Properties of Chemical Compounds - II, Advances in Chemistry
Series No. 22, Am. Chem. Soc., Washington, D. C. (1959).
61-dre Dreisbach, R. R.; Physical Properties of Chemical Compounds, Advances in Chemistry Series
No. 29, Am. Chem. Soc.: Washington, D.C. (1961).
65-tim Timmermans, J.; Physico-Chemical Constants of Pure Organic Compounds, Vol. II, Elsevier:
New York (1965).
71-ano Landolt-Brnstein Sechste Auflage, II Band, Eigenschaften der Materie in ihren

Aggregatzustanden, 1 Teil, Mechanisch-thermische Zustandsgrssen. Springer-Verlag:
Berlin (1971).
86-smi/sri Smith, B. D.; Srivastava, R.; Thermodynamic Data for Pure Compounds, Part B. Halogenated
Hydrocarbons and Alcohols, Elsevier: New York (1986).
86-smi/sri-1 Smith, B. D.; Srivastava, R.; Thermodynamic Data for Pure Compounds, Part A.
Hydrocarbons and Ketones, Elsevier: New York (1986).
89-dau/dan Daubert, T. E.; Danner, R. P.; Physical and Thermodynamic Properties of Pure Chemicals:
Data Compilation. Taylor & Francis: London (1989).
Data Compilation, Supplement 1. Taylor & Francis: London (1991).
96-wil/mar Wilhoit, R. C.; Marsh, K. N.; Hong, X.; Gadalla, N.; Frenkel, M.; Densities of Aliphatic
Hydrocarbons: Alkanes.
Landolt-Brnstein, New Series, Vol. IV/8B, Springer: Berlin (1996)
96-wil/mar-1 Wilhoit, R. C.; Marsh, K. N.; Hong, X.; Gadalla, N.; Frenkel, M.; Densities of Aliphatic
Hydrocarbons: Alkenes, Alkadienes, Alkynes and Miscellaneous Compounds.
Landolt-Brnstein, New Series, Vol. IV/8C, Springer: Berlin (1996)
1.1 Basic Concepts 1
1 Introduction
1.1 Basic Concepts

The mass density of a substance is an intensive quantity defined by:
= m/v (1.1)
where m is the mass and v is the volume of the sample. Both these quantities are extensive quantities.
Other densities often referred to in the literature are the relative density and the molar density. Relative
density, also called specific gravity, is:
r = / 0 (1.2)
where 0 is the density of a standard substance. It is necessary to specify the conditions of temperature and
pressure for the standard substance. The most common reference material is water often at the temperature
of its maximum density, 4 C, at atmospheric pressure. The molar density is defined as
m = 1/V (1.3)
where V is the volume occupied by one mole of the substance. The only densities reported in this volume
are the mass densities; relative and molar densities have been converted to mass densities, and all densities
have been reported in SI units. The API specific gravity is: (API) = 141.5/r 131.5, in which r is
(288.68 K)/(288.68 K), and the standard substance is water at 288.68 K (60 F).
The density of a material is a function of temperature and pressure but its value at some standard
condition (for example, 293.15 K or 298.15 K at either atmospheric pressure or at the vapor pressure of
the compound) often is used to characterize a compound and to ascertain its purity. Accurate density
measurements as a function of temperature are important for custody transfer of materials when the
volume of the material transferred at a specific temperature is known but contracts specify the mass of
material transferred. Engineering applications utilize the density of a substance widely, frequently for the
efficient design and safe operation of chemical plants and equipment. The density and the vapor pressure
are the most often-quoted properties of a substance, and the properties most often required for prediction
of other properties of the substance. In this volume, we do not report the density of gases, but rather the
densities of solids as a function of temperature at atmospheric pressure and the densities of liquids either
at atmospheric pressure or along the saturation line up to the critical temperature.
The purpose of this compilation is to tabulate the densities of compounds, hence only minimal
description of experimental methods used to measure the density of liquids or solids appears. Detailed
descriptions of methods for density determination of solids, liquids and gases, along with appropriate
density reference standards, appear in a chapter by Davis and Koch in Physical Methods of Chemistry,
Volume VI, Determination of Thermodynamic Properties [86-ros/bae].
The two principal experimental apparatus used to determine the density of a liquid are: the pycnometer
and the vibrating tube densimeter. The pycnometer method involves measuring the mass of a liquid in a
vessel of known volume. The volume of the pycnometer, either at the temperature of measurement or at
some reference temperature, is determined using a density standard, usually water or mercury. Using
considerable care and a precision analytical balance accurate to 10-5 g, it is possible to achieve densities
accurate to a few parts in 106 with a pycnometer having a volume of 25 cm3 to 50 cm3.
Landolt-Brnstein
New Series IV/8D
2 1.2 Scope of the Compilation
It is common to achieve accuracies of 1 part in 105 and routine measurements can achieve 1 part in 104
with pycnometers having volumes as small as 5 cm3
The vibrating tube densimeter relies upon the fact that the frequency f of vibration for a U or V shaped
tube depends upon the mass of material in the tube:
= A/ f 2 + B (1.4)
Calibration of the apparatus is necessary; usually water and air or nitrogen are the reference materials.
Vibrating tube densimeters designed to operate close to atmospheric pressure can achieve repeatability of
parts in 106. If the reciprocal of the frequency is linear in density, accuracies of 1 part in 105 are readily
achievable.
The principal experimental method used to measure the density of a solid is determination of the mass
of liquid displaced by a known mass of solid. It is essential that the solid have no appreciable solubility in
the liquid, that all occluded air be removed from the solid and that the density of the displacement fluid be
less than that of the solid lest the solid float. Densities of crystalline solids also can be determined from
the dimensions of the unit cell. Davis and Koch discuss other methods for measuring the density of liquids
and solids such as: hydrostatic weighing of a buoy and flotation methods.
1.2 Scope of the Compilation

Volume IV/8D presents observed values for the densities of monocyclic hydrocarbons, the majority of
which are important industrial compounds. These values represent a compilation and evaluation of data
from the scientific literature covering approximately the past 100 years. The values presented come from
the TRC Source Database. The Thermodynamics Research Center has assembled these data over a period
of years and has used them to provide the evaluated density values listed in the TRC Thermodynamic
Tables - Hydrocarbons. An additional literature search has been performed immediately before producing
this compilation to locate new or missing data and to bring the collection up-to-date. This compilation
should include at least 90% of the pertinent data reported in the literature. The usual experimental
conditions are in contact with air at one atmosphere below the normal boiling point of the hydrocarbon,
and in equilibrium with the vapor phase above the normal boiling point. In the summary tables,
temperatures reported on the Kelvin scale have been obtained by adding 273.15 to temperatures originally
given on the Celsius scale.
Densities have units of kilograms per cubic meter (kgm-3). Values reported in units of grams per
milliliter, where the liter is the volume of one kilogram of water at its temperature of maximum density
convert to kgm-3 when multiplied by 0.999972 (as defined by the 12th General Conference of the
International Committee on Weights and Measure, 1964). Values of specific gravity relative to water at a
stated reference temperature become density upon multiplication by the accepted density of water at the
reference temperature. Most reported densities for liquids below the boiling point apply to the air-
saturated liquid.
Compounds are identified by an IUPAC approved name, the empirical molecular formula, and the
Chemical Abstracts Service Registry Number. A summary table is available for each compound which
includes the reported temperature and density values, an assigned uncertainty for the density, the
difference between the observed and smoothed density values and an index key to the source of the data.
A complete list of references, identified by the index keys, appears at the end of the volume.
Where appropriate, tables of smoothed, recommended values are given at integral multiples of 10 K
over the experimental range of temperatures. Values at 293.15 K and 298.15 K are included when they are
in the range of the original data set. The recommended values also have assigned uncertainties.
Landolt-Brnstein
New Series IV/8D
3 1.4 Evaluation, Selection, and Smoothing of Data
1.3 Description of Data Tables

Data for a particular compound are selected, evaluated and smoothed in one of four ways, depending
upon the number and accuracy of the reported values and upon their distribution over the temperature
range.
Case 1. When the data set consists of at least four acceptable, effectively distinct values (see
section 1.5.3), the densities in selected subsets are fit to a function of temperature using the least
squares criterion. A summary table for the selected set gives the densities, their estimated
uncertainties, the deviations between observed and calculated values, an index key to the list of
references and a plotting symbol. If sufficient space remains, some data outside the selected set
also are included in the summary table along with reference keys to any remaining data. A plot of
the deviations between observed and calculated values is shown for the selected subset. Error bars
indicate the size of the estimated uncertainties for the data. Distinct plotting symbols identify the
five data sources that have the smallest average estimated uncertainties. A single symbol represents
all remaining data in the selected set. A table consisting of smoothed, recommended values
(calculated from the fitted functions) also is given. Estimated uncertainties are given for the
recommended values which also appear as a continuous line on the deviation plot. Densities of
crystal phases are in a separate section of the table. In most cases, these densities have not been fit
as a function of temperature. Values of parameters, statistical measures of the fit, and references to
sources of critical constants appear at the beginning of these sections.
Case 2. For data sets that do not meet the criteria of Case 1, but contain acceptable values over a
temperature range of at least two degrees, the results are smoothed using a linear function of
temperature with an estimated coefficient of thermal expansion. A table of smoothed recommended
values is presented.
Case 3. For data sets that do not meet the criteria of either Case 1 or 2 but contain two or more
values at a single temperature, a recommended value is given for this temperature by taking a
weighted average of the observed values.
Case 4. For data sets that contain only single values at one or two temperatures, the reported values are
given rather than recommended values.
1.4 Evaluation, Selection and Smoothing of Data

1.4.1 Assignment of Uncertainties
The Thermodynamics Research Center staff have assigned an uncertainty value to each observed and
recommended density value listed in the tables. The true value of the property has a 95% probability of
being in the range covered by + or - the uncertainty about the reported value. Assignment of uncertainty is
a subjective evaluation based upon what is known about the measurement when the value is entered into
the database, and includes the effects of all sources of experimental error. The errors have been
propagated to the listed density at the reported temperature. Uncertainties reported by the investigators are
considered but not necessarily adopted. Often, investigators report repeatability, but they usually do not
provide uncertainty.
Errors in density result from errors in temperature measurement or control; calibration of instruments;
transfer, handling and weighing of samples; and impurities in the samples. At temperatures well below the
critical temperature and near room temperature, standard techniques easily achieve accuracies of 0.05%.
For the compounds in this compilation, that level corresponds to about 0.4 kgm-3. Under these
conditions, errors in temperature are not very significant. This level of accuracy only requires
temperatures to be known within 0.5 K. At temperatures approaching the critical temperature,
Landolt-Brnstein
New Series IV/8D
measurements become more demanding because of the rapid increase in the coefficient of thermal
expansion. Greater accuracy, in general, requires careful attention to calibration, mass determination and
sample handling techniques. It is assumed that values obtained by pycnometers have been corrected for
buoyancy of air, unless the author specifically says otherwise. This correction increases the apparent
density by 0.05 - 0.1%. When this correction has not been made, the estimated uncertainty is greater.
Most measurements of densities of liquids below their normal boiling points are made in the presence
of air. Densities reported here refer to liquids in equilibrium with a gas phase consisting of a mixture or air
and vapor at a total pressure of one atmosphere below the normal boiling point and of vapor at the
equilibrium vapor pressure above the boiling point. Thus air is not regarded as an impurity. The effect of
dissolved air and other gases on the densities of liquid hydrocarbons has been reported by Ashcroft and
Ben Isa (97-ash/ben). The differences they observed between the density of a liquid saturated with air at 1
atm and 298.15 K and the air-free liquid are shown in Table 1.
Table 1. Difference between densities of liquids saturated with air at 1 atm and 298.15 K and air free
liquids at the same temperature
Compound (air sat.) - (air free) Compound (air sat.) - (air free)
kgm-3 kgm-3
Heptane -0.089 Tetradecane -0.054
Octane -0.081 Hexadecane -0.047
Nonane -0.072 Cyclohexane -0.068
Decane -0.067 Methylcyclohexane -0.077
Dodecane -0.059 Toluene -0.062
A major source of error in most measurements is the presence of impurities in the sample. The effect
of an impurity depends upon its amount in the sample and upon the difference between its density and the
density of the principal constituent. Even when the sample purity is provided quantitatively, the impurities
often are not identified individually. Nevertheless, a report of sample purity reduces the estimated
uncertainty because it can be taken as evidence that the investigator has considered sample purity. The
most ubiquitous impurity in liquids is water, and, because its density differs significantly from those of
hydrocarbons, it is a common source of error. Exclusion of water requires that the sample be protected
from the atmosphere during transfer, and that special precautions be taken to remove the sample from
containers.
The principal source of high purity samples from 1952 to 1960 was the American Petroleum Institute
Research Project 6 at Carnegie-Mellon University. These samples were distributed to researchers through
the API Project 44 from Carnegie-Mellon University and Texas A&M University. Phillips Petroleum Co.
also supplied high purity samples, but they ceased doing so. Samples for 300 compounds from API
Project 42 are available from the Thermodynamics Research Center, along with limited supplies of
samples for compounds from API Project 6.
1.4.2 Quantitative Effect of Impurity on Density of Liquids

The molar volume of a mixture of components, V, in terms of the mole fractions xi and partial molar
volumes of the components Vi is:
c
V = xiVi (1.5)
i =1
Landolt-Brnstein
New Series IV/8D
1.4 Evaluation, Selection, and Smoothing of Data 5
For an ideal solution, the partial molal volumes equal the molar volumes of the pure liquid components.
Denoting component the main components as 1 and the impurities as > 1, the volume becomes:
c
V = x1V1 + xiVi . (1.6)
i=2
Then using,
= M /V (1.7)
and the molar mass of the mixture:

c
M = xi M i (1.8)
i =1
and assuming that the xi are small for i > 1, then
1 c

= 1 1 wi vi (1.9)
w1 i=2
where vi = Vi /Mi are partial specific volumes of the impurities and wi is the mass fraction of component i.
Finally, the density of the mixture is related to the density of the main component and the impurities i by:
1 c
w
= 1 1 i (1.10)
w1 i =2 i
The observed value of the density of a sample is sometimes presented as evidence of its purity.
Assuming the sample contains a single impurity, equation (1.10) can be solved for - 1:
1 = 1 (1 w1 1 w2 / 2 ) / w1 (1.11)
If water is the single impurity, with 2 = 1000 kgm-3 and 1 = 800 kgm-3, equation (1.10) gives the values
summarized in Table 2.
Table 2. Effect of water as an impurity on density

of a sample.
100 w2 ( 1)/ kgm-3
0.02 0.032
0.05 0.080
0.10 0.16
0.2 0.32
If we replace - 1 by its uncertainty u in equation (1.11) then w2 is the minimum value of the mass
fraction of the impurity that could be reliably detected. The uncertainty in - 1 includes the uncertainty
in the measurement of but also the uncertainty in 1 , the density of the pure sample. The value of 1
must be determined for a sample whose purity is known, by some independent means, with an accuracy
considerably greater than the one being tested. An example using equation (1.11) and Table 3 is the
determination of a small impurity of cis-1,2-dimethylcyclopentane in trans-1,2-dimethylcyclopentane.
Table 3 contains numerical solutions of equation (1.11) at various densities and uncertainties.
The selected densities of trans- and cis-1,2-dimethylcylopentane are (746.83 0.15)kgm-3 and
(768.09 0.18)kgm-3 respectively at 298.15 K. Assuming the density of the sample with the impurity is
accurate to within 0.4 kgm-3, the total uncertainty is {(0.4)2 + (0.15)2}1/2 = 0.43 kgm-3.
Because 1/2 = 0.972, |1 -2| / u = 49.4.
Landolt-Brnstein
New Series IV/8D
Interpolation with these values from Table 3 indicates that the minimum mass fraction of cis-1,2-
dimethylcyclopentane that can be detected by density measurement is 0.020. This corresponds to a purity
of 98.0 mass %. The minimum detectable mass fraction of 1,1-dimethylcyclopentane is 0.130 for the same
assumptions. Hence density measurement is not a sensitive method to determine purity when the density
of the impurity is close to that of the compound under consideration.
Table 3. Minimum mass fraction of impurity detectable by density measurement for a mixture.
1 /2
2 1 / u
0.8 0.9 0.95 1.0 1.05 1.1 1.2
500 0.0025 0.0022 0.0021 0.0020 0.0019 0.0018 0.0017
200 0.0062 0.0055 0.0052 0.0050 0.0047 0.0045 0.0041
100 0.0123 0.0110 0.0104 0.0099 0.0094 0.0090 0.0083
50 0.024 0.022 0.021 0.020 0.019 0.018 0.016
20 0.059 0.053 0.050 0.048 0.046 0.044 0.040
10 0.111 0.100 0.095 0.091 0.087 0.083 0.077
5 0.200 0.182 0.174 0.167 0.160 0.154 0.143
2 0.385 0.357 0.345 0.333 0.323 0.312 0.294
1 0.556 0.526 0.513 0.500 0.488 0.476 0.454
1.4.3 Procedure for Selection and Smoothing of Density Values - Case 1

A selected subset of the reported densities is fit to functions of temperature using the least squares
criterion. Up to a boundary temperature Tb (approximately 0.8Tc), the calculated density is represented x
by a polynomial in temperature with coefficients a of order p,

k
p
x = ak T k . (1.12)
k =0
Above Tb the smoothed values are given by a modification of the Guggenheim equation [67-gug]
( )[
x = 1 + 1.75 + 0.75 3 c + b1 ( Tc T ) + b2 ( Tc T ) + b3 (Tc T ) + b4 ( Tc T )
2 3 4
] (1.13)
where Tc is the critical temperature and = (1-T/Tc)1/3. Selected values of critical constants are constant.
Continuity with equation (1.12) results from forcing the two functions and their first derivatives with
respect to temperature to be equal at the boundary. When no values are available above this temperature,
only the polynomial is used.
The following steps, implemented by a computer program written in C, generate the smoothed,
recommended values. Input to the program consists of the set of observed density values, temperatures,
estimated uncertainties, critical constants and values of certain parameters used by the program.
Step 1. Separate the initial data into two sets, corresponding to temperatures above and below Tb .
Step 2. Make an initial selection from the low temperature set by rejecting all points with zero
uncertainty and all points with uncertainties above a limit determined by the data selection
algorithm described in section 1.5.2. Zero uncertainties are assigned to values that are not
experimental and are included for comparison only (these are most often values recommended in
other compilations).
Step 3. Determine the effective number of data values, ne, as described in 1.5.3. If the effective
number of values is less than four, terminate the calculation. If the total number of values is more
than eight and the effective number is greater than or equal to four but less than eight, make
another initial data selection with relaxed selection criteria.
Landolt-Brnstein
New Series IV/8D
1.4 Evaluation, Selection, and Smoothing of Data 7
Step 4. For the j-th value in the set calculate normalized values, and T and weighting factors,
n,j n,j,
w j = 1 / u 2j where uj is the uncertainty assigned to the j-th observed density and n , j = j

where is the mean value of the observed density in the set. and Tn , j = T k T k where T k is the
mean value of the T jk value in the set..
Step 5. Using = a1T , fit the data subject to least squares with points weighted by w .
n n j
Step 6. Calculate the standard deviation for this fit. Eliminate any points from this set for which
| | > 3.5, where j = j x , j .
j
Step 7. Fit the remaining normalized values to a series of polynomials, n = a k T k , starting

with order 1 and increasing in order. Use wj as weighting factors and stop increasing the order
when satisfying one of the following conditions:
1. A value of p given as an input parameter to the program is reached, or
2. 2k < 11
. [1 + 1 / (n k )]2 2k 1 (see glossary of symbols) and the deviations pass the random
deviation test (see 1.5.4).
Step 8. If any points have | | > 2.2 for the final polynomial, eliminate these points and repeat
j
step 7.
Step 9. Calculate parameter a0 .
Step 10. Apply the initial data selection described in step 2 to the high temperature data set.
Step 11. Fit the selected high temperature data with the modified Guggenheim equation using least
squares with weighting factors w . j
Step 12. The following procedure provides continuity at the boundary. Set equation (1.13) and its
first derivative at Tb equal to the corresponding values from equation (1.12) at Tb. Eliminate
parameters b3 and b4 from these two simultaneous equations to obtain a function containing
parameters b1 and b2 which can be evaluated for the high temperature range using least squares. Do
not use densities at temperatures within 2 K of the critical temperature.
Step 13. Generate the output table of temperature, observed densities, estimated uncertainties, and
difference between observed and calculated densities and arrange it in order of year of publication
with authors. For data from a particular source, arrange in order of temperature.
Step 14. Calculate the table of smoothed and recommended values with their corresponding
estimated uncertainties.
Coefficients A, B, C, D and E listed in the heading of Table 1 for each compound correspond to a0, a1,
a2, a3 and a4 in equation (1.12) for temperatures below Tb. is the weighted standard deviation for
O
individual points in this region (see the glossary). If the data set includes values above Tb, the coefficients
A, B, C and D correspond to b1, b2, b3 and b4 in equation (1.13) for this range. The weighted standard
deviation, c,w, and the unweighted standard deviation for the fit, c,uw, include both ranges. If the data set
covers only values below Tb then c,w and c,uw represent that range only.
The uncertainty in the smoothed values depends upon the uncertainties in the original observed values
and upon the magnitude of deviations between observed and calculated values. To approximate the
contribution of these two effects at the temperature T, the uncertainties u (T) for the low temperature range
x
are calculated from:

1/ 2

u x (T ) = u(T ) 2 + Ckl (T k T k )(T l T l ) (1.14)
k l
In this equation, u(T) represents the uncertainty of the observed data in the vicinity of T and is
Landolt-Brnstein
New Series IV/8D
8 1.5 Calculation Procedures
approximated by fitting a polynomial of order 1-3 to the estimated uncertainties as a function of

temperature (other symbols appear in the glossary). Uncertainties in the smoothed data for the high
temperature range are calculated using:
[
u x ( T ) = u x (Tb ) + h( T ) ]
1/ 2
2 2
(1.15)
where u (Tb) is the uncertainty calculated using equation (1.14) for the low temperature range at the
x
boundary temperature Tb and h(T) is a polynomial in temperature fit to the reciprocals of the estimated
uncertainties in the high temperature region.

When the data set for a particular compound satisfies the criteria for Case 2, it is smoothed by a linear
function of temperature,
x = a 0 + a1T (1.16)
The coefficient a1 is either calculated from two densities of sufficient accuracy reported at different
temperatures, preferably by the same investigator, or estimated by examination of the coefficient of
expansion of similar compounds obtained from a least squares calculation. The constant term then results
from equation (1.17) after eliminating values with large uncertainties
( )
a 0 = w j j a1Tj / w j (1.17)
The uncertainties for the smoothed values are:
ux (T ) = [ 20 + 12 (T T ) 2 ]2 (1.18)
where T is the weighted mean temperature for the accepted set, 20 = ( w j 2j ) / w j and 1 is the
estimated standard deviation of a1 .

The recommended density at a particular temperature is the weighted mean observed density for that
temperature. The corresponding uncertainty is the standard deviation from the mean for each value.
1.5 Calculation Procedures

1.5.1 Least Squares Calculation
Parameters of all the smoothing functions are adjusted to minimize the function
2 = w j 2j (1.19)
by the singular value decomposition of the matrix of independent variables of the function. The
parameters are calculated by functions svdcmp and svbksb described in [88-pre/fla] modified to accept
weighting factors. The covariance matrix used in equation (1.14) is calculated by the function covar from
the same book.
Landolt-Brnstein
New Series IV/8D
1.5 Calculation Procedures 9
1.5.2 Selection of Data Based upon Estimated Uncertainties

The selection procedure is:
Step 1. Obtain T, the range of temperatures covered by the data set.
Step 2. For each density value, , in the set, calculate,
j
(
x jl = exp q Tj Tl ) (1.20)
z1 = x jl (1.21)
l j
z2 = ul x jl (1.22)
l j
y = u j z11.5 z21 (1.23)
Accept point j if y d; reject it otherwise

Step 3. Repeat steps 1 and 2 with points accepted in the first pass.
The accepted points are those that remain from Step 3. The constants q and d are:
[
q = 2.628 g1 1 + ( T / 30)
2
] / T
d = g 2 / log 10 (1 + n)
The number z2 / z1 is a weighted mean of all points in the set other than the j-th point. The weighting factor
decreases exponentially with the difference in temperature of the l-th point from the j-th point. The
parameter g1 determines the rate of decrease. This procedure compares the uncertainty of the j-th point to
the weighted mean of other points. The parameter g2 determines the rejection level from this comparison
for the j-th point. Larger values of g2 are less selective. Values for g1 and g2 are supplied to the algorithm.
For all cases g1 is in the range of 1 to 2 (usually 1.8). The value of g2 is in the range of 2 to 3 (kgm-3)
(usually 2.5).
1.5.3 Count of the Effective Number of Density Values in a Set

The number of degrees of freedom in a least squares fit is the number of distinct data values minus the
number of adjustable parameters. To obtain a meaningful smoothing of data, the order of the polynomial
function is limited to values which gives three or more degrees of freedom. However, if two or more
density values in the set are at the same (or nearly the same) temperature, they should count as only one
point in calculating the degrees of freedom. In general, the effective number of density values minus the
number of fitting parameters is used as the degrees of freedom. Effective data values are those that are
separated by at least 1.2 K.
1.5.4 Testing a Set of Deviations between Observed and Calculated Density Values
for a Random Distribution
One of the criteria for acceptance of the order of a polynomial least squares fit is that the deviations
between calculated and random values be distributed randomly over the range of conditions covered by
the data. The concept of randomness for this purpose probably cannot be defined rigorously. However, the
following test for randomness is used whenever the original data set contains seven or more values.
Landolt-Brnstein
New Series IV/8D
10 1.6 Glossary of Symbols
Step 1. Sort the values in order of increasing temperature

Step 2. Separate the total range of temperature, T, into s subranges each of size T/s. Form s
subsets of data corresponding to these temperature subranges.
Step 3. Make the following comparison for each subset j which has at least four members.
j j
0.01 < and 0.2 <
ns j
If both comparisons are true for any subset, the test for randomness fails.
Step 4. Apply steps 2 and 3 to the data for s from 2 to an upper limit. The upper limit is
determined by the number of values in the original set according to the following table.
n, number of values in original maximum number of

set subsets
7 to 10 2
11 to 20 3
21 to 33 4
> 33 5
1.6 Glossary of Symbols

ak parameters in the polynomial function for densities at temperatures Tb
bk k-th parameter in modified Guggenheim equation for density at temperatures >Tb
g 1, g 2 parameters used in the data selection algorithm
n number of accepted values of density in a set
ne effective number of accepted values of density in a set
ns number of density values in subset s
p order of the polynomial for density values at temperatures Tb
s number of subsets in the random deviation algorithm
uj uncertainty assigned to the j-th observed density value in a set
w j weighting factor for the j-th density value in a set
C k,l Element k,l of the variance-covariance matrix for the polynomial parameters
T absolute temperature
Tb boundary temperature
Tc critical temperature
T j temperature for the j-th observed density
Tk mean value of the T jk values in a set
T n,j T jk - T k , normalized value of the j-th temperature raised to the k power
j -
j x,j
j (1 - T /Tc)1/3
j
density
(API) API specific gravity
mean value of observed densities in a set
o density of a standard substance
c critical density
Landolt-Brnstein
New Series IV/8D
11 1.7 Compound Nomenclature
j observed value of j-th density in a data set

m molar density
n,j - , normalized density for the j-th value
j
r relative density
x,j calculated value of the j-th density in a data set
(2/n)1/2, standard deviation for density values in a set
2k 2j for all values in a set fit to a polynomial of order k
T T - T1, range of temperatures for data in a set
n
The following symbols refer to components in a mixture at a fixed temperature
c number of components in the mixture

i component number
vi partial specific volume of component i in the mixture
wi mass fraction of component i in the mixture
xi mole fraction of component i in the mixture
Mi molar mass (molecular weight) of component i
V molar volume of a mixture
Vi partial molal volume of component i in the mixture
density of a mixture of components
i density of pure component i
Symbols used in the tables:
A, B, C, D, E coefficients in function for density (see section 1.4.3)

calc calculated density, x
exp observed value of j-th density in a data set, j
O
( w j 2j / w j )1/ 2 , for low temperature range only
c,w ( w j 2j / w j )1/ 2 , for low and high temperature range combined
c,uw [ 2j / n(n p 2)]1 / 2 , for low and high temperature range combined
2est estimated uncertainty, u j
1.7 Compound Nomenclature

1.7.1 Names of Compounds Used in the Tables
Compound names follow the style: <side chains> <ring name>, where <ring name> is the name of the
cyclic group. Saturated rings are cycloalkanes, such as: cyclobutane, cyclohexane. Unsaturated rings are
cycloalkenes, cycloalkynes, cycloalkadienes, etc.
Side chains, which are attached to the ring, are called radicals in the accepted style for alkanes, alkenes,
alkynes, alkadienes, etc. Thus, names such as butyl, pentyl, hexyl refer to saturated, straight chain, alkyl
radicals. Names such as ethenyl, 1-propenyl, 2-butenyl indicate normal radicals with a double bond at the
position indicated by the number. Prefixes such as di, tri, tetra specify 2, 3, 4 radical groups.
Landolt-Brnstein
New Series IV/8D
The names of branched side chains are enclosed in parenthesis with the position of the side chain shown
by the preceding number. Examples are: (1-methylethyl), (same as isopropyl), (2-ethyl-3-methyl-butyl).
Branched unsaturated side chains are named similarly with a number preceding the base chain to specify
the position of the double or triple bond. Thus (1,3-dimethyl-2-butenyl) indicates:
Names such as ethylidene, propylidene indicate that the double bond is attached directly to the ring, for
example: (1-methylethylidene)cyclohexane
Side chain names are ordered alphabetically within a compound name: butyl, diethyl, dimethyl, ethyl,
methyl, methylene, (1-methylethyl), propyl, tetramethyl. Each side chain name is preceded by its position
number on the ring. The starting point for numbering positions on saturated rings is arbitrary. The first
side chain in the name is number 1. Thus, 1-ethyl-4-methyl-2-propylcyclohexane is:
For unsaturated rings the multiple bond (or one of the multiple bonds if more than one exists) is position
1. Thus, 3-butyl-1-methylcyclopentene is:
The prefixes cis- and trans- identify geometrical isomers of compounds that contain two side chains on
a ring where cis means that the two groups are on the same side of the ring and trans means they are on
opposite sides. Thus cis-1,3-dimethylcyclohexane and trans-1,3-dimethylcyclohexane are:
cis trans
Geometrical isomers of compounds that contain more than two side chains on a ring are identified by
prefixes r-, c-, and t- preceding the positional number for each group. The r- prefix precedes the number
of the first side chain. This is the reference group that determines the relative orientation of the other
groups. The c- designation means the group is on the same side as the reference group while the t-
means the group is on the side opposite the reference group. For example, r-1-ethyl, c-2-methyl, t-3-
propylcyclopentane means that the methyl group is on the same side as the ethyl group, and the propyl
group is on the opposite side. Prefixes (Z)- and (E)- identify geometrical isomers that differ in the relative
orientation of groups on either side of a double bond in a side chain. The IUPAC rules (93-ano-1) apply,
thus (Z)-(1-methyl-2-propenyl)cyclohexane is:
Landolt-Brnstein
New Series IV/8D
1.7 Compound Nomenclature 13
Rings with double bonds that contain eight or more carbon atoms can also exist in two or more
geometrical forms. These are identified by the (Z)- and (E)- prefixes.
In some cases, the orientation of the side chains is not reported or known at the time the original source
is published. In most of these cases, the samples used for the density measurements are mixtures of
geometrical isomers. When only data on such mixtures are available, they are used as the basis for the
selected and recommended values. The estimated uncertainties reflect the possible differences between the
densities of such mixtures and the pure isomers. In some cases, values of such undefined mixtures and of
specific geometrical isomers are available then both sets of data are shown, but the recommended values
are derived from data on the specific isomers. In cases for which the values for the undefined mixtures
cover a wider temperature range than those of the pure isomers, recommended values are given for both
sets of data.
Compounds that contain an asymmetric substitutions on a carbon atoms exist in enantiomorphic forms.
These differ only in the direction of rotation of polarized light. When the absolute configuration has been
identified in the original report, these compounds are identified by (R)- and (S)- prefixes. Sometimes
prefixes such as d-, l-, (+)-, and (-)-, which are given in the original report have been used. Very often no
identification of the optical isomer is given even when the compound contains an asymmetric carbon
atom. Then it is assumed that the samples are racemic mixtures. However, none of these distinctions affect
the densities of liquids, therefore all the isomers of this type are combined to determined the
recommended values. If a compound contains more than one asymmetric compound diastereomers can
exist. In principle, these might have different densities, but no examples have been found.
Names of compounds in the name index include all those shown in the tables. In addition, other
IUPAC systematic names, Chemical Abstracts indexing names and certain trivial or obsolete names are
also included.
1.7.2 Order of Compounds in the Tables
Compounds in the tables are sorted in the following order:

1. By formula type CnH2n-x , where x = 0, 2, 4, 6, 8
2. Within each formula type by carbon number, n
3. Within each carbon number by ring size from 3 to the maximum
4. Within each ring size alphabetically by the names of the
side chains (omitting positional numbers), as described above
5. Finally by positional numbers of the side chains.
References
67-gug Guggenheim, E. A.; Thermodynamics, 5th edition, North-Holland Publishing
Company: Amsterdam (1957).
86-ros/bae Rossiter, B. W.; Baetzold, R. C.; Physical Methods of Chemistry, 2nd edition, Vol.
VI, Determination of Thermodynamic Properties, John Wiley & Sons: New York
(1986).
Landolt-Brnstein
New Series IV/8D
88-pre/fla Press, W. H.; Flannery, B. P.; Teukolsky, S. A.; Vetterling, W. T.; Numerical
Recipes in C, Cambridge Univ. Press: New York (1988).
93-ano-1 Panico, R.; Powell, W. H.; Richer, J. C.; A Guide to IUPAC Nomenclature of
Organic Compounds: Recommendation 1993, Blackwell Scientific Publications:
Oxford (1993).
97-ash/ben Ashcroft, S. J.; Ben Isa, M.; J. Chem. Eng. Data, (in press), (1997)
Landolt-Brnstein
New Series IV/8D
2. Tabulated Data on Density - Alkylcycloalkanes (CnH2n)
2.1 Alkylcycloalkanes (CnH2n), C3 to C5 17
2.1 Alkylcycloalkanes (CnH2n), C3 to C5
Cyclopropane [75-19-4] C3H6 MW = 42.0806 1
Tc = 398.00 K [96-dau]
c = 259.00 kgm-3 [96-dau]
Table 1. Coefficients for the polynomial expansion equations. Standard deviations (see introduction):
= 1.3761 (low temperature range), c,w = (1.2305 combined temperature ranges, weighted),
O
c,uw = 2.7685 10-1 (combined temperature ranges, unweighted).

T = 193.15 to 335.00 K T = 335.00 to 398.00 K
Coefficient = A + BT + CT 2 + DT 3 + = [1 + 1.75(1 - T/Tc)1/3 + 0.75(1 - T/Tc)]
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
A 1.65474 103 4.82099 10-1
B -9.97937 -5.47531 10-3
-2
C 3.66243 10 -8.09668 10-5
-5
D -4.96798 10 1.32545 10-6
Table 2. Experimental values with uncertainties and deviation from calculated values.
T exp 2 est exp calc Ref. (Symbol T exp 2 est exp calc Ref. (Symbol
K kg m 3
kg m3 in Fig. 1) K kg m 3
kg m3 in Fig. 1)
crystal 318.15 586.40 0.39 -0.66 70-lin/sil()

94.00 913.0 30.00 88-nij/vos 323.15 577.60 0.40 -0.38 70-lin/sil()
liquid 328.15 568.70 0.41 0.38 70-lin/sil()
193.15 735.20 1.50 -0.38 38-gro/wak() 333.15 559.20 0.42 1.15 70-lin/sil()
233.15 688.60 1.00 -0.68 38-gro/wak() 338.15 549.50 0.43 2.10 70-lin/sil()
240.40 680.70 1.00 -1.39 38-gro/wak() 343.15 539.50 0.44 2.34 70-lin/sil()
193.15 735.20 0.70 -0.38 39-gro/lin( ){ 348.15 528.70 0.45 1.69 70-lin/sil()
203.15 723.50 0.60 1.10 39-gro/lin( ){ 353.15 517.50 0.46 0.96 70-lin/sil()
213.15 711.90 0.60 1.41 39-gro/lin( ){ 358.15 505.50 0.47 0.09 70-lin/sil()
223.15 700.20 0.60 0.65 39-gro/lin( ){ 363.15 492.70 0.48 -0.57 70-lin/sil()
233.15 688.60 0.50 -0.68 39-gro/lin( ){ 368.15 478.70 0.49 -1.10 70-lin/sil()
240.45 680.70 0.50 -1.34 39-gro/lin( ){ 373.15 463.60 0.50 -1.03 70-lin/sil()
243.15 676.90 0.50 -2.49 39-gro/lin( ){ 378.15 446.90 0.55 -0.37 70-lin/sil()
235.10 688.90 0.40 1.57 62-has/sno( ) 383.15 428.30 0.62 1.32 70-lin/sil()
238.00 685.60 0.40 1.15 62-has/sno( ) 388.15 403.30 0.80 1.06 70-lin/sil()
293.15 626.80 0.34 1.68 70-lin/sil() 393.15 370.70 1.00 1.92 70-lin/sil()
298.15 619.10 0.35 0.74 70-lin/sil() 397.15 322.50 1.50 4.22 70-lin/sil()
303.15 611.20 0.36 -0.02 70-lin/sil() 397.35 318.10 2.50 5.03 70-lin/sil()
308.15 603.00 0.37 -0.64 70-lin/sil() 397.55 313.40 3.00 6.71 70-lin/sil1)
313.15 594.80 0.38 -0.80 70-lin/sil()
1) Not included in Fig. 1.
Further references: [1889-hof, 00-gus, 17-jae, 20-mou/bou, 22-tra/win-1].
cont.
Landolt-Brnstein
New Series IV/8D
18 2.1 Alkylcycloalkanes (CnH2n), C3 to C5
Cyclopropane (cont.)
Fig. 1. The symbols show the deviation of the calculated from the experimental values from Table 2. The curves
above and below the zero line indicate the calculated error region of the recommended values given in Table 3. The
error bars represent the experimental errors. (Error bars smaller than the symbols are omitted for clarity of the figure.)
Table 3. Recommended values (fit to the reliable experimental values according to the equations
= A + BT + CT 2 + DT 3 + or = [1 + 1.75(1 - T/Tc)1/3 + 0.75(1 - T/Tc)][c + A(Tc -T )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
K kg m3 K kg m3 K kg m3
190.00 740.04 1.12 260.00 662.74 0.70 330.00 564.60 0.90
200.00 726.40 0.94 270.00 652.38 0.72 340.00 543.58 1.00
210.00 714.12 0.81 280.00 641.29 0.72 350.00 523.19 1.08
220.00 702.91 0.71 290.00 629.19 0.72 360.00 501.05 1.15
230.00 692.46 0.64 300.00 615.77 0.72 370.00 474.41 1.22
240.00 682.48 0.65 310.00 600.72 0.76 380.00 440.16 1.30
250.00 672.67 0.68 320.00 583.77 0.78 390.00 391.32 1.36
Landolt-Brnstein
New Series IV/8D
Methylcyclopropane [594-11-6] C4H8 MW = 56.11 2
Table 1. Coefficients of the polynomial expansion

equation. Standard deviations (see introduction):
c,w = 2.9179 10-1 (combined temperature ranges,
weighted), c,uw = 7.3304 10-2 (combined
temperature ranges, unweighted).
T = 253.15 to 298.15 K
Coefficient = A + BT + CT 2 + DT 3 +
A 1.01482 103
B -1.27805
K kg m
3
kg m3 in Fig. 1)
253.15 691.30 3.00 0.02 1895-dem() 293.15 640.00 1.00 -0.16 56-ano( ){
265.15 676.00 3.00 0.06 1895-dem() 298.15 634.00 1.00 0.23 71-goo-1()
293.15 640.00 1.00 -0.16
52-ano-4( )
cont.
Landolt-Brnstein
New Series IV/8D
Methylcyclopropane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
250.00 695.30 2.96 280.00 656.96 1.83 298.15 633.77 1.19
260.00 682.52 3.25 290.00 644.18 1.16 300.00 631.40 1.28
270.00 669.74 2.72 293.15 640.16 1.10 310.00 618.62 2.47
Cyclobutane [287-23-0] C4H8 MW = 56.1075 3

c,w = 1.0556 101 (combined temperature ranges,
weighted), c,uw = 4.8517 (combined
T = 194.65 to 293.15 K
A 9.61715 102
B -9.14896 10-1
K kg m 3
kg m3 in Fig. 1)
crystal II 194.65 802.00 5.00 18.37 42-ben()

117.00 948.00 30.00 92-ste/leh 206.15 788.00 5.00 14.89 42-ben()
crystal I 227.15 761.00 5.00 7.10 42-ben()
173.00 840.00 50.00 53-car/tem 236.15 731.00 5.00 -14.66 42-ben()
liquid 247.15 715.00 5.00 -20.60 42-ben()
268.15 718.50 1.00 2.11 07-wil/bru( ){ 273.15 698.00 5.00 -13.81 42-ben1)
273.15 703.80 1.00 -8.01 07-wil/bru( ){ 293.15 694.31 0.40 0.80 52-kaa/coo( )
cont.
Landolt-Brnstein
New Series IV/8D
Cyclobutane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
190.00 787.89 15.00 240.00 742.14 13.00 290.00 696.40 1.50
200.00 778.74 13.00 250.00 732.99 15.00 293.15 693.51 0.80
210.00 769.59 11.00 260.00 723.84 13.00 298.15 688.94 2.00
220.00 760.44 10.00 270.00 714.69 10.00 300.00 687.25 2.50
230.00 751.29 11.00 280.00 705.54 8.00
Landolt-Brnstein
New Series IV/8D
Ethylcyclopropane [1191-96-4] C5H10 MW = 70.13 4
Table 1. Fit with estimated B coefficient for 13

accepted points. Deviation w = 1.162.
Coefficient = A + BT
A 976.90
B -1.000
T exp 2 est exp calc Ref. T exp 2 est exp calc Ref.
K kg m3 kg m3 K kg m3 kg m3
293.15 678.4 4.00 -5.35 13-zel/sch1) 293.15 677.0 2.00 -6.75 37-gro
273.15 697.5 4.00 -6.25 13-zel/sch 1) 293.15 684.0 0.60 0.25 42-van/mee
273.15 705.5 3.00 1.75 16-phi 293.15 683.9 0.40 0.15 47-ano-1
291.40 686.6 3.00 1.10 16-phi 293.15 683.9 0.50 0.15 49-van/gre
293.15 683.2 3.00 -0.55 16-ros-1 293.15 684.0 0.40 0.25 54-pom/foo-1
293.15 678.2 3.00 -5.55 22-cha 293.15 684.3 0.60 0.55 55-gra/gre
273.15 697.5 3.00 -6.25 22-cha 293.15 683.5 0.60 -0.25 69-par/kho
293.15 676.4 2.00 -7.35 30-les-1
1)
Not included in calculation of linear coefficients.
Table 3. Recommended values.

T exp 2 est T exp 2 est T exp 2 est
K kg m 3
K kg m 3
K kg m3
270.00 706.9 4.7 290.00 686.9 1.3 298.15 678.8 1.6
280.00 696.9 2.8 293.15 683.8 1.2 300.00 676.9 1.8
1,1-Dimethylcyclopropane [1630-94-0] C5H10 MW = 70.13 5

A 953.17
B -1.000
K kg m 3
kg m3 K kg m 3
kg m3
293.15 660.4 0.50 0.38 1898-gus/pop 283.15 669.75 0.30 -0.27 44-boo/per
290.15 661.9 1.00 -1.12 00-gus 283.15 669.7 1.00 -0.32 44-gre-1
287.55 668.1 1.00 2.48 39-whi/pop 293.15 658.9 0.50 -1.12 48-sho/cra
293.15 660.4 0.50 0.38 41-whi/pop 293.15 661.8 1.50 1.78 53-slo/gri
287.55 668.1 1.00 2.48 41-whi/pop 293.15 667.1 4.00 7.08 57-lev/kos 1)
1)
cont.
Landolt-Brnstein
New Series IV/8D
1,1-Dimethylcyclopropane (cont.)

3 3
K kg m K kg m K kg m3
280.00 673.2 1.9 293.15 660.0 1.3 300.00 653.2 2.5
290.00 663.2 1.0 298.15 655.0 2.2
cis-1,2-Dimethylcyclopropane [930-18-7] C5H10 MW = 70.13 6

A 975.31
B -0.960
K kg m3
kg m3 K kg m 3
kg m3
293.15 692.8 1.00 -1.09 29-bau-1 293.15 693.9 0.20 0.01 53-ano-1
273.15 713.2 2.00 0.14 29-bau-1 293.15 693.9 0.20 0.01 53-ano-11
293.15 694.1 0.40 0.21 49-ano-2 293.15 694.1 1.00 0.21 55-kel/gre
293.15 693.7 0.40 -0.19 51-ano-5

T exp 2 est T exp 2est T exp 2 est
K kg m 3
K kg m3 K kg m3
270.00 716.1 0.9 290.00 696.9 0.2 298.15 689.1 0.3
280.00 706.5 0.5 293.15 693.9 0.2 300.00 687.3 0.4
trans-1,2-Dimethylcyclopropane [2402-06-4] C5H10 MW = 70.13 7

A 948.29
B -0.950
K kg m3
kg m3 K kg m 3
kg m3
295.15 675.4 4.00 7.51 12-ost 1) 293.15 669.8 0.20 0.01 49-ano-2
293.15 676.9 5.00 7.11 29-bau-11) 293.15 669.7 0.40 -0.09 53-ano-1
273.15 698.5 5.00 9.71 29-bau-1 293.15 669.8 1.00 0.01 55-kel/gre
1)
cont.
Landolt-Brnstein
New Series IV/8D
trans-1,2-Dimethylcyclopropane (cont.)

3 3
270.00 691.8 1.0 290.00 672.8 0.4 298.15 665.0 0.4
280.00 682.3 0.6 293.15 669.8 0.3 300.00 663.6 0.5
Methylcyclobutane [598-61-8] C5H10 MW = 70.134 8

T = 273.15 to 293.15 K
A 1.20341 103
B -2.60011
C 2.93226 10-3
K kg m3 kg m3 in Fig. 1) K kg m3 kg m3 in Fig. 1)
273.15 713.50 1.50 1.53 13-dem/doj1) 273.15 711.80 1.50 -0.17 16-phi-1( )
288.15 697.60 0.60 -0.06
13-dem/doj( ) 291.15 695.00 1.50 0.05 16-phi-1( )
291.15 695.00 0.60 0.05
13-dem/doj( ) 273.15 711.80 1.00 -0.17 16-phi()
293.15 693.10 0.60 -0.08
13-dem/doj( ) 291.15 695.00 1.00 0.05 16-phi()
273.15 711.80 1.50 -0.17 14-phi-3( ) 293.15 693.30 0.80 0.12 29-ros( ) {
273.15 712.20 1.50 0.23 14-phi-3( ) 273.15 712.00 1.00 0.03 37-gro/ipa()
291.15 695.00 1.50 0.05 14-phi-3( ) 293.15 693.00 1.00 -0.18 38-ipa/pin-2()
273.15 712.20 1.50 0.23 16-phi-1( )
Further references: [12-zel/sch, 54-luk/ovo].
cont.
Landolt-Brnstein
New Series IV/8D
Methylcyclobutane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 715.14 1.59 290.00 695.98 1.08 298.15 688.85 0.85
280.00 705.27 1.38 293.15 693.18 0.99 300.00 687.28 0.80
Landolt-Brnstein
New Series IV/8D
Cyclopentane [287-92-3] C5H10 MW = 70.134 9
Tc = 511.70 K [96-dau]
c = 270.00 kgm-3 [96-dau]
= 1.8036 (low temperature range), c,w = (8.7880 10-1 combined temperature ranges, weighted),
O

T = 188.63 to 420.00 K T = 420.00 to 511.70 K
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
2
A 9.13652 10 4.38621
B -1.01827 10-5 -1.94738 10-1
C -1.81801 10-3 2.87479 10-3
-6
D -2.88017 10 -1.34859 10-5
-9
E 8.10380 10
K kg m 3
kg m3 in Fig. 1)
273.15 764.96 0.10 0.54 37-tim/hen( ) 483.15 503.00 3.00 -0.65 62-kha-1( )
288.15 750.31 0.10 0.65 37-tim/hen( ) 493.15 478.00 5.00 -5.69 62-kha-1( )
303.15 735.69 0.10 0.91 37-tim/hen( ) 503.15 449.00 6.00 18.34 62-kha-1( )
275.43 762.76 0.20 0.57 44-gar( ) 508.15 429.00 8.00 49.75 62-kha-11)
282.62 755.70 0.20 0.58 44-gar( ) 298.15 740.35 0.10 0.61 70-ewi/lev()
283.24 755.11 0.20 0.60 44-gar( ) 298.15 740.36 0.10 0.62 70-mar-1( )
289.39 749.11 0.20 0.68 44-gar1) 313.15 725.13 0.30 0.28 80-sid/goe( )
289.84 748.66 0.20 0.67 44-gar1) 293.15 743.94 0.04 -0.76 86-hol/got6( )
293.15 745.34 0.20 0.64 44-gar1) 293.15 743.94 0.05 -0.76 86-hol/got7( ) {
293.15 745.30 0.20 0.60 44-gar1) 298.15 737.36 0.10 -2.38 86-tar/dia( )
298.02 740.62 0.20 0.75 44-gar1) 298.15 740.22 0.08 0.48 87-luo/ham()
293.15 745.36 0.05 0.66 46-for/gla() 298.15 739.92 0.10 0.18 87-luo/ham()
298.15 740.43 0.05 0.69 46-for/gla() 188.63 840.21 0.42 0.32 92-gar/cac1( )
353.15 683.32 0.60 -2.79 47-kay( ) 2) 192.79 836.70 0.42 0.06 92-gar/cac1( )
393.15 635.99 0.80 -15.24 47-kay1) 2) 198.85 831.58 0.42 -0.21 92-gar/cac1( )
433.15 579.35 1.50 -21.67 47-kay( ) 2) 208.10 823.73 0.41 -0.43 92-gar/cac1( )
473.15 503.49 2.00 -7.54 47-kay( ) 2) 216.70 816.08 0.41 -0.76 92-gar/cac1( )
508.15 365.03 3.00 -14.22 47-kay( ) 2) 219.65 813.84 0.41 -0.44 92-gar/cac1( )
373.15 668.00 2.00 0.02 62-kha-1( ) 222.41 811.46 0.41 -0.40 92-gar/cac1( )
393.15 644.00 2.00 -7.23 62-kha-11) 225.90 808.02 0.40 -0.76 92-gar/cac1( )
413.15 617.00 2.00 -19.32 62-kha-11) 229.82 804.93 0.40 -0.34 92-gar/cac1( )
433.15 589.00 2.20 -12.02 62-kha-1( ) 234.38 800.79 0.40 -0.36 92-gar/cac1( )
453.15 558.00 2.40 20.42 62-kha-1( ) 240.35 795.82 0.40 0.14 92-gar/cac1( )
473.15 523.00 2.60 11.97 62-kha-1( ) 244.61 791.96 0.40 0.23 92-gar/cac1( )
2) Calculated from equation given by author.
cont.
Landolt-Brnstein
New Series IV/8D
Cyclopentane (cont.)
Table 2. (cont.)
K 3
kg m kg m3 in Fig. 1) K kg m 3
kg m3 in Fig. 1)
246.59 790.06 0.39 0.18 92-gar/cac1( ) 278.79 759.56 0.38 0.67 92-gar/cac-11)
248.74 787.96 0.39 0.10 92-gar/cac1( ) 280.57 757.73 0.38 0.59 92-gar/cac-11)
251.48 785.36 0.39 0.08 92-gar/cac1( ) 282.57 755.84 0.38 0.67 92-gar/cac-11)
254.25 782.84 0.39 0.19 92-gar/cac1( ) 284.83 753.59 0.38 0.65 92-gar/cac-11)
257.45 779.82 0.39 0.22 92-gar/cac1( ) 286.36 752.05 0.38 0.62 92-gar/cac-11)
260.47 777.02 0.39 0.31 92-gar/cac1( ) 290.18 748.47 0.37 0.82 92-gar/cac-11)
263.77 773.93 0.39 0.40 92-gar/cac1( ) 292.49 746.16 0.37 0.80 92-gar/cac-11)
266.47 771.34 0.39 0.42 92-gar/cac1( ) 294.35 744.27 0.37 0.76 92-gar/cac-11)
268.02 769.80 0.39 0.38 92-gar/cac1( ) 295.90 742.65 0.37 0.67 92-gar/cac-11)
272.85 765.31 0.38 0.60 92-gar/cac-11) 297.45 741.04 0.37 0.60 92-gar/cac-11)
274.52 763.69 0.38 0.61 92-gar/cac-11) 299.02 739.36 0.37 0.48 92-gar/cac-11)
276.78 761.52 0.38 0.65 92-gar/cac-11) 293.15 744.60 0.60 -0.10 93-jan/xie1)
278.21 760.12 0.38 0.66 92-gar/cac-11)
Further references: [1893-wis/hen, 03-eyk, 15-ros, 19-cha/sim-1, 19-cha/sim-2, 19-eyk, 19-eyk-1, 22-
cha, 22-cha/van, 30-god/cau, 30-ruz/sto, 32-gar/eva, 33-hof/lan, 33-zel/kaz, 34-god, 38-eva, 38-vog, 39-
wib/hoo, 41-ano-1, 41-ben-1, 43-ano, 43-ano-2, 43-too, 44-can, 46-ano, 46-baz/ste, 46-gei/can, 46-kay-1,
46-ser/spu, 47-huc/har, 47-kay, 47-spi/huf, 49-den/fid, 49-foe/fen, 49-wei, 56-ano, 61-shi/hil, 62-kha-1,
65-wat/mcl, 69-bou/lam, 69-bra/fre, 69-rod/hsu, 70-pol/mur-2, 72-jon/wee, 73-lev, 79-for/dar, 80-sid/goe,
81-kiy/ben, 82-gri/phi, 84-tan/tak, 86-hne/cib].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
180.00 846.46 0.34 293.15 744.70 0.11 400.00 645.89 3.92
190.00 838.83 0.38 298.15 739.74 0.11 410.00 638.53 4.93
200.00 830.85 0.45 300.00 737.90 0.11 420.00 631.73 6.09
210.00 822.56 0.50 310.00 727.98 0.14 430.00 611.18 6.35
220.00 813.97 0.51 320.00 718.08 0.23 440.00 577.23 6.37
230.00 805.11 0.48 330.00 708.27 0.37 450.00 545.61 6.41
240.00 796.00 0.44 340.00 698.58 0.58 460.00 524.08 6.47
250.00 786.68 0.37 350.00 689.06 0.87 470.00 513.11 6.55
260.00 777.16 0.30 360.00 679.77 1.26 480.00 506.56 6.69
270.00 767.49 0.23 370.00 670.75 1.74 490.00 492.40 6.93
280.00 757.70 0.16 380.00 662.06 2.34 500.00 452.66 7.42
290.00 747.83 0.12 390.00 653.76 3.06 510.00 349.91 8.62
cont.
Landolt-Brnstein
New Series IV/8D
28 2.1 Alkylcycloalkanes (CnH2n), C3 to C5 - 2.2 Alkylcycloalkanes (CnH2n), C6
Cyclopentane (cont.)
2.2 Alkylcycloalkanes (CnH2n), C6

2.2.1 Cyclopropanes
1-Ethyl-1-methylcyclopropane [53778-43-1] C6H12 MW = 84.16 10
Table 1. Experimental and recommended values with uncertainties.

T exp 2 est Ref. T exp 2 est Ref.
K kg m3 K kg m3
293.15 701.8 0.20 48-ano-3 293.15 701.3 0.60 53-slo/gri-1
293.15 701.5 0.40 49-der/gre 293.15 701.7 0.20 Recommended
Landolt-Brnstein
New Series IV/8D
2.2 Alkylcycloalkanes (CnH2n), C6 29
1-Ethyl-2-methylcyclopropane [19217-47-1] C6H12 MW = 84.16 11
Table 1. Experimental values with uncertainties.

T exp 2 est Ref.
3
K kg m
293.15 695.0 1.50 32-les/wak -0
294.15 696.1 1.50 32-les/wak -0
cis-1-Ethyl-2-methylcyclopropane [19781-68-1] C6H12 MW = 84.16 12
Table 1. Experimental value with uncertainty.

T exp 2 est Ref.
K kg m3
293.15 714.6 0.40 55-kel/gre
trans-1-Ethyl-2-methylcyclopropane [19781-69-2] C6H12 MW = 84.16 13
Table 1. Experimental and recommended

values with uncertainties.
T exp 2 est Ref.
K kg m3
293.15 693.5 0.40 55-kel/gre
293.15 693.3 1.00 69-par/kho
293.15 693.5 0.40 Recommended
(1-Methylethyl)cyclopropane [3638-35-5] C6H12 MW = 84.16 14

K kg m3 K kg m3
293.15 688.9 4.00 48-ano-61) 293.15 698.6 0.40 54-ano-10
293.15 698.3 0.20 49-sla/wis 293.15 698.1 1.00 61-luk/zot1)
293.15 688.9 2.00 49-van/gre1) 293.15 698.1 0.80 69-par/kho
293.15 698.6 0.20 52-sla/wis-1 293.15 698.4 0.20 Recommended
1)
Not included in calculation of recommended value.
Propylcyclopropane [2415-72-7] C6H12 MW = 84.16 15

T exp 2 est Ref.
3
K kg m
289.85 712.1 2.00 37-boe/tak
293.15 711.2 0.60 55-gra/gre
Landolt-Brnstein
New Series IV/8D
30 2.2 Alkylcycloalkanes (CnH2n), C6
1,1,2-Trimethylcyclopropane [4127-45-1] C6H12 MW = 84.16 16

3 3
K kg m K kg m
680.3 8.00 694.7 0.30
1)
293.65 01-zel/zel 293.15 48-boo/gre
293.15 694.8 0.60 12-kis 293.15 686.1 2.00 48-lev
288.45 688.8 6.00 12-ost1) 293.15 692.7 2.00 50-pet
293.15 681.0 6.00 22-cha1) 293.15 694.7 0.50 52-kel/gre
288.45 688.8 6.00 22-cha1) 293.15 686.1 0.70 52-lev/gla
293.15 696.7 2.00 41-whi/car 293.15 694.8 0.60 54-kaz/luk-1
293.15 694.1 0.60 41-whi/car 293.15 694.8 0.70 56-gra/kos
293.15 685.3 4.00 46-bar/bur1) 293.15 694.8 0.80 69-par/kho
293.15 694.7 0.30 47-boo/gre 293.15 694.2 0.30 Recommended
1)
1,2,3-Trimethylcyclopropane [42984-19-0] C6H12 MW = 84.16 17

T exp 2 est Ref.
3
K kg m
291.15 694.6 10.00 01-zel/zel
r-1, c-2, t-3-Trimethylcyclopropane [4806-59-1] C6H12 MW = 84.16 18

T exp 2 est Ref.
3
K kg m
293.15 697.9 0.60 55-kel/gre
2.2.2 Cyclobutanes
Ethylcyclobutane [4806-61-5] C 6H12 MW = 84.16 19

A 1021.05
B -1.000
cont.
Landolt-Brnstein
New Series IV/8D
Ethylcyclobutane (cont.)
K kg m3
kg m3 K kg m 3
kg m3
293.15 745.0 8.00 17.10 08-zel/gut1) 293.15 727.9 0.30 -0.00 46-boo/gre
283.15 754.0 8.00 16.10 08-zel/gut1) 293.15 727.9 0.30 -0.00 46-gre-1
293.15 728.3 0.60 0.40 13-kis-3 293.15 727.9 0.20 -0.00 48-boo/gre
273.15 746.1 0.60 -1.80 13-kis-3 293.15 728.0 0.20 0.10 48-boo/gre
293.15 727.9 0.30 -0.05 39-wib/hoo 293.15 726.9 1.00 -1.00 48-tur/luk
298.15 723.2 0.30 0.30 39-wib/hoo 293.15 728.0 0.50 0.10 49-der/gre
293.15 727.9 0.30 -0.05 42-van/mee
1)

3 3
270.00 751.1 4.6 290.00 731.1 0.7 298.15 722.9 1.0
280.00 741.1 2.6 293.15 727.9 0.3 300.0 721.0 1.2
trans-1,2-Dimethylcyclobutane [15679-02-4] C6H12 MW = 84.16 20

T exp 2 est Ref.
3
K kg m
293.15 712.2 2.00 32-zel/tur-1
293.15 702.9 0.50 54-kaz/luk-3
293.15 703.4 0.7 Recommended
cis-1,3-Dimethylcyclobutane [2398-09-6] C6H12 MW = 84.16 21

T exp 2 est Ref.
3
K kg m
293.15 710.6 0.60 49-kaz/luk
trans-1,3-Dimethylcyclobutane [2398-10-9] C6H12 MW = 84.16 22

T exp 2 est Ref.
K kg m3
293.15 701.6 0.60 49-kaz/luk
Landolt-Brnstein
New Series IV/8D
2.2.3 Cyclopentanes - Cyclohexane
Methylcyclopentane [96-37-7] C6H12 MW = 84.16 23
Tc = 532.70 K [96-dau]
c = 264.00 kgm-3 [96-dau]
= 1.0472 10-1 (low temperature range), c,w = (9.6285 10-2 combined temperature ranges, weighted),
O

T = 273.15 to 430.00 K T = 430.00 to 532.70 K
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
A 1.20619 103 6.60080 10-1
B -2.81171 -1.26408 10-2
-3
C 6.40249 10 1.12855 10-4
-6
D -7.28464 10 -3.73278 10-7
K kg m 3
kg m3 in Fig. 1)
273.15 767.35 0.10 -0.06 37-tim/hen( {) 313.15 729.90 0.50 0.05 47-kay1) 2)
288.15 753.41 0.10 0.10 37-tim/hen( {) 333.15 710.70 0.60 -0.02 47-kay() 2)
303.15 739.46 0.10 0.20 37-tim/hen( {) 353.15 690.76 0.70 -0.12 47-kay() 2)
276.43 764.42 0.20 0.11 44-gar() 373.15 669.85 0.80 -0.15 47-kay() 2)
276.57 764.29 0.20 0.11 44-gar() 393.15 647.61 0.90 -0.10 47-kay() 2)
284.43 756.92 0.20 0.12 44-gar() 413.15 623.66 1.10 -0.01 47-kay() 2)
285.15 756.26 0.20 0.14 44-gar() 433.15 597.47 1.30 -0.03 47-kay() 2)
291.42 750.44 0.20 0.19 44-gar1) 453.15 568.29 1.50 0.27 47-kay() 2)
291.93 749.97 0.20 0.20 44-gar1) 473.15 534.85 1.70 -0.08 47-kay() 2)
300.51 741.97 0.20 0.23 44-gar1) 493.15 494.85 2.00 -0.24 47-kay() 2)
300.76 741.73 0.20 0.23 44-gar1) 508.15 456.03 3.00 0.44 47-kay() 2)
307.43 735.45 0.20 0.21 44-gar() 293.15 748.45 0.30 -0.18 80-sid/goe1)
293.15 748.58 0.05 -0.05 46-for/gla( ) 313.15 729.42 0.30 -0.43 80-sid/goe()
298.15 743.91 0.05 -0.04 46-for/gla( )
Further references: [1897-mar-2, 1897-zel-1, 1899-mar-3, 02-zel/mos, 10-eng/hal, 11-zel, 19-cha/sim-1,
19-cha/sim-2, 22-cha, 22-cha/bec, 22-cha/van, 27-bra/hun, 27-cha/bec, 30-cha/mil, 30-god/cau, 31-hic,
32-gar/eva, 33-hof/lan, 34-god, 34-zel/kaz, 35-zel/kaz, 38-eva, 38-vog, 39-gro/wac, 39-wib/hoo, 40-
moo/ren, 41-ano-1, 42-van/mee, 43-ano, 43-gri/lud, 44-can, 45-cra/boo, 45-gre/vog, 45-zel/arb, 46-ano,
46-baz/ste, 46-gei/can, 46-kay-1, 49-den/fid, 49-foe/fen, 51-ano, 52-cla/har, 54-seu, 54-smi/otv, 59-
ehr/web, 61-bel/web, 62-kae/web, 62-sus/lyz, 68-kem/buc, 69-rod/hsu, 80-fen/khu, 87-hol/goe, 90-
com/fra].
cont.
Landolt-Brnstein
New Series IV/8D
Methylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 770.39 0.20 350.00 694.07 0.67 450.00 572.88 2.27
280.00 760.96 0.15 360.00 683.87 0.77 460.00 557.16 2.33
290.00 751.58 0.14 370.00 673.37 0.86 470.00 540.46 2.41
293.15 748.63 0.15 380.00 662.54 0.92 480.00 522.35 2.51
298.15 743.95 0.17 390.00 651.33 0.98 490.00 502.09 2.66
300.00 742.22 0.18 400.00 639.69 1.06 500.00 478.52 2.91
310.00 732.82 0.24 410.00 627.58 1.19 510.00 449.73 3.37
320.00 723.36 0.34 420.00 614.97 1.41 520.00 411.68 4.45
330.00 713.77 0.45 430.00 601.80 1.77 530.00 346.57 8.47
340.00 704.02 0.56 440.00 587.79 2.22
Landolt-Brnstein
New Series IV/8D
Cyclohexane [110-82-7] C6H12 MW = 84.16 24
Tc = 553.80 K [96-dau]
c = 273.00 kgm-3 [96-dau]
O

T = 280.15 to 445.00 K T = 445.00 to 553.80 K
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
A 9.70258 102 6.11512 10-1
-5
B -1.88689 10 -1.34197 10-2
-3
C -4.23488 10 1.32162 10-4
-6
D 9.37240 10 -4.65394 10-7
-9
E -8.64854 10
303.10 768.17 0.39 -1.01 1899-you/for1) 547.10 390.52 0.60 0.38 1899-you/for( )
313.10 759.07 0.38 -0.59 1899-you/for1) 550.10 364.03 0.85 -3.10 1899-you/for1)
323.10 749.57 0.38 -0.46 1899-you/for1) 552.10 339.33 0.00 -4.99 1899-you/for1)
333.10 740.03 0.38 -0.26 1899-you/for1) 273.15 796.73 0.30 -0.42 10-you-11)
343.10 730.57 0.38 0.14 1899-you/for1) 283.15 787.40 0.30 -0.50 10-you-11)
353.10 720.56 0.38 0.14 1899-you/for1) 293.15 777.90 0.30 -0.66 10-you-11)
363.10 710.58 0.39 0.32 1899-you/for( ) 303.15 768.50 0.30 -0.63 10-you-11)
373.10 700.33 0.39 0.41 1899-you/for( ) 310.15 759.10 0.30 -3.38 10-you-11)
383.10 689.51 0.39 0.11 1899-you/for( ) 323.15 749.60 0.30 -0.38 10-you-11)
393.10 678.70 0.40 0.05 1899-you/for( ) 333.15 740.00 0.30 -0.24 10-you-11)
403.10 668.00 0.40 0.33 1899-you/for( ) 343.15 730.60 0.30 0.22 10-you-11)
413.10 656.51 0.40 0.09 1899-you/for( ) 353.15 720.60 0.32 0.23 10-you-11)
423.10 644.87 0.40 -0.00 1899-you/for( ) 363.15 710.60 0.32 0.39 10-you-1( )
433.10 632.47 0.42 -0.53 1899-you/for( ) 288.15 783.13 0.20 -0.11 36-mas1)
443.10 619.92 0.42 -0.85 1899-you/for1) 306.30 766.14 0.20 -0.01 36-mas1)
453.10 606.76 0.42 -0.94 1899-you/for( ) 318.50 754.52 0.20 0.05 36-mas1)
463.10 591.37 0.44 -1.90 1899-you/for( ) 337.20 736.59 0.20 0.33 36-mas1)
473.10 578.03 0.44 0.09 1899-you/for( ) 352.35 721.58 0.20 0.40 36-mas( )
483.10 561.64 0.44 -0.27 1899-you/for( ) 372.35 700.78 0.20 0.07 36-mas( )
493.10 546.45 0.45 1.42 1899-you/for( ) 298.15 773.84 0.03 -0.02 67-cru/cut( )
503.10 527.15 0.45 0.29 1899-you/for( ) 301.15 771.10 0.20 0.07 67-pre/fel1)
513.10 506.33 0.46 -0.24 1899-you/for( ) 313.15 759.44 0.20 -0.17 67-pre/fel1)
523.10 482.04 0.47 -0.77 1899-you/for( ) 323.15 749.70 0.20 -0.28 67-pre/fel1)
533.10 452.84 0.48 -0.45 1899-you/for( ) 333.15 740.23 0.20 -0.01 67-pre/fel1)
538.10 435.92 0.49 0.91 1899-you/for( ) 333.15 740.23 0.20 -0.01 67-pre/fel1)
543.10 412.54 0.50 -0.27 1899-you/for( ) 343.15 730.18 0.20 -0.20 67-pre/fel()
cont.
Landolt-Brnstein
New Series IV/8D
Cyclohexane (cont.)
Table 2. (Cont.)
K 3
kg m3 in Fig. 1)
298.15 773.92 0.10 0.06 81-aic/tar1) 280.15 790.65 0.05 -0.03 92-ano-3()
308.15 764.43 0.10 0.04 81-aic/tar1) 280.16 790.65 0.05 -0.02 92-ano-3()
318.15 754.71 0.10 -0.10 81-aic/tar1) 283.15 787.88 0.05 -0.02 92-ano-3()
333.15 740.11 0.10 -0.13 81-aic/tar() 283.15 787.87 0.05 -0.03 92-ano-3()
283.15 787.90 0.30 0.00 81-dym/you1) 288.15 783.22 0.05 -0.02 92-ano-31)
288.15 783.20 0.30 -0.04 81-dym/you1) 288.16 783.22 0.05 -0.01 92-ano-31)
298.19 773.80 0.30 -0.02 81-dym/you1) 293.15 778.55 0.05 -0.01 92-ano-31)
313.23 759.50 0.40 -0.03 81-dym/you1) 298.11 773.89 0.05 -0.01 92-ano-31)
333.36 739.90 0.50 -0.14 81-dym/you1) 303.14 769.13 0.05 -0.01 92-ano-31)
353.29 719.70 0.50 -0.53 81-dym/you1) 308.15 764.36 0.05 -0.03 92-ano-31)
373.28 699.30 0.50 -0.44 81-dym/you1) 313.13 759.60 0.05 -0.03 92-ano-31)
393.20 678.30 0.60 -0.24 81-dym/you( ) 318.07 754.84 0.05 -0.05 92-ano-3()
308.15 763.51 0.21 -0.88 81-mal/rae1) 323.15 749.91 0.05 -0.07 92-ano-3()
308.22 763.51 0.21 -0.81 81-mal/rae1) 323.15 749.92 0.05 -0.06 92-ano-3()
318.15 753.80 0.20 -1.01 81-mal/rae1) 298.15 773.90 0.30 0.04 93-beg/tuk1)
328.27 744.20 0.21 -0.81 81-mal/rae1) 303.15 769.10 0.30 -0.03 93-beg/tuk1)
348.31 725.84 0.21 0.61 81-mal/rae( ) 313.15 759.50 0.30 -0.11 93-beg/tuk1)
293.15 778.58 0.03 0.02 87-mar-1( ){ 333.15 740.40 0.30 0.16 93-beg/tuk1)
298.15 773.90 0.03 0.04 87-mar-1( ){ 353.15 720.10 0.30 -0.27 93-beg/tuk1)
303.15 769.17 0.03 0.04 87-mar-1( ){ 373.15 699.20 0.40 -0.67 93-beg/tuk( )
308.15 764.41 0.03 0.02 87-mar-1( ){ 393.15 677.80 0.50 -0.80 93-beg/tuk( )
313.15 759.62 0.03 0.01 87-mar-1( ){ 433.15 631.40 0.65 -1.54 93-beg/tuk1)
318.15 754.80 0.04 -0.01 87-mar-1( ){ 453.15 605.50 0.80 -2.13 93-beg/tuk( )
323.15 749.96 0.04 -0.02 87-mar-1( ){ 473.15 576.80 1.00 -1.06 93-beg/tuk( )
Further references: [1825-far, 1894-bru-2, 1897-zel-1, 1898-for, 1898-mar, 00-you/for-1, 01-sab/sen,
01-zel-1, 03-sab/mai, 11-dra, 11-ski/rit, 15-von/hin, 16-ric/shi, 19-cha/sim-2, 19-ric/shi, 22-cha/van, 25-
eis/gor, 26-des, 26-mat, 26-pav, 26-tim/mar-1, 27-bou, 27-bra/hun, 28-ada/mar, 29-smy/sto, 29-str-1, 30-
god/cau, 30-tau/sta, 31-bru/hic-1, 31-kag, 32-gar/eva, 32-vor/fis, 32-zel/tur-1, 33-azi/bha, 34-car/jon, 34-
god, 34-rot/nag, 34-was/spe, 35-ear/gla, 35-wel, 36-bro/dur, 36-roz, 37-loz/dya, 38-eva, 38-pau/nik, 38-
vog, 39-phi-1, 39-wat/lee-2, 39-wib/hoo, 40-ano, 40-moo/ren, 42-gei, 43-ano, 44-can, 44-fri/har-1, 44-gar,
44-huc, 45-gre/vog, 46-boo/gre, 46-for/gla, 46-gei/can, 46-vog, 47-huc/har, 47-spi/huf, 49-ano-4, 49-
den/fid, 49-foe/fen, 49-wei, 50-bro/ewa, 51-ano, 51-shu/min, 53-par/cha, 54-dix/sch, 54-smi/otv, 54-
wec/hun, 55-cut/jon, 55-ham/sto, 55-kus, 56-moo/sty, 57-hol, 58-rea/sag, 59-wu /how, 61-del, 61-gom/liu,
61-shi/hil, 62-nag-2, 62-rat/rao, 62-sus/lyz, 63-jef, 63-plu/dow, 63-pod, 64-moe/tho, 64-sca/sat, 65-
for/moo, 65-wat/mcl, 66-bat, 66-bat/all, 66-ber/rea, 66-kat/cha, 66-lut/kov, 66-sab/bel, 67-fin/ken, 67-
loi/mer, 67-mur/sri, 67-nat/rao, 67-rid/but, 68-bar/sat, 68-kem/buc, 68-pow/swi, 68-ver, 69-bru/gub, 69-
cho/nai, 69-rod/hsu, 69-smi/kur, 70-fin, 70-kon/lya, 70-sto/lev, 70-str/svo, 71-len/hay, 71-nag/oht, 71-
san/fel, 72-jon/wee, 72-kon, 72-let, 72-let-1, 72-mar/mur, 73-che/cha, 73-lev, 73-li /lu , 73-nag/oht, 73-
min/rue, 73-paz, 73-paz-1, 73-paz-2, 73-paz-3, 73-san/hut, 73-svo/ves, 74-jai/nor, 74-kon/ani, 74-mye/cle,
74-pur/pol, 75-hsu/cle, 76-for/ben, 76-ha /mor, 76-tri/kri, 77-bou/lu, 77-hwa/rob, 77-rad/tas, 78-kiy/hal,
78-nat/yad, 79-for/dar, 79-goa/ott, 79-hoe/hoe, 79-mah/sur, 79-maj/svo, 79-mal/pat, 79-mur, 80-aic/tar,
80-aic/tar-1, 80-fen/khu, 80-jon/has, 80-mar/sym, 80-mar/you, 80-oht/nag]
cont.
Landolt-Brnstein
New Series IV/8D
Cyclohexane (cont.)
Further references: (cont.)

[80-sid/goe, 80-sur, 81-aic/tar-2, 81-kiy/ben, 81-nai/nai, 81-mal/rae, 81-tas/djo, 82-ami/pat, 82-bha/tre,
82-bha/tre-1, 82-bha/tre-2, 82-bha/tre-3, 82-bha/tre-4, 82-chy/str, 82-dig/jad, 82-gri/goa, 82-gri/phi, 82-
gro/ing, 83-nat/tri, 83-wec, 83-wec/byl, 84-bau/mee, 84-cre/com, 84-gar/rey, 84-sin/nig, 85-hra/gik, 85-
mar/bha, 85-osw/rao, 85-sae/com, 85-sin/mah, 85-sin/sha, 85-tam/mur, 85-tan/nak, 86-aww/sal, 86-
hol/got-8, 86-sae/com, 86-san/sha, 86-tar/dia, 86-tar/dia-1, 87-ami, 87-lin, 87-luo/ham, 87-man/ami, 87-
nag/rob, 87-yad/yad, 88-cha/sur, 88-gar/cob-1, 88-jun/tar, 88-nag-1, 88-nag-2, 88-man/ami, 88-sai/tan,
88-sun/sch-1, 89-bec/ric, 89-der/poi, 89-lai/rod, 89-mat/gon, 89-rai/shu, 89-ram/sur, 90-all/bee, 90-
che/pet, 90-jos/ami, 90-jos/ami-2, 90-sin/mal, 91-kna/skj, 91-kri/vis, 91-pap/eva, 91-pap/zio, 91-ric/lau,
91-she/wan, 91-tre-9, 91-tre, 91-tre-1, 92-acr/ten-4, 92-acr/ten-8, 92-pit/mar, 92-qin/hof, 92-qin/hof-2, 92-
wei/wil, 92-yos/kat, 94-del/fer, 94-kri/vis, 94-toj/ram, 95-art/mun-3, 95-gaw/dor, 95-org/igl, 95-osw/pat,
95-pet/gas].
cont.
Landolt-Brnstein
New Series IV/8D
2.2 Alkylcycloalkanes (CnH2n), C6 - 2.3 Alkylcycloalkanes (CnH2n), C7 37
Cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 790.82 0.06 360.00 713.43 0.27 460.00 597.85 0.88
290.00 781.51 0.05 370.00 703.15 0.30 470.00 582.77 0.88
293.15 778.56 0.05 380.00 692.68 0.34 480.00 566.95 0.86
298.15 773.86 0.05 390.00 682.01 0.37 490.00 550.37 0.84
300.00 772.11 0.05 400.00 671.10 0.41 500.00 532.67 0.82
310.00 762.62 0.08 410.00 659.93 0.45 510.00 513.15 0.80
320.00 753.03 0.12 420.00 648.48 0.49 520.00 490.66 0.80
330.00 743.32 0.16 430.00 636.72 0.55 530.00 463.27 0.82
340.00 733.50 0.19 440.00 624.60 0.64 540.00 427.15 0.88
350.00 723.54 0.23 450.00 611.92 0.85 550.00 368.05 1.15

2.3.1 Cyclopropanes
Butylcyclopropane [930-57-4] C7H14 MW = 98.19 25

T exp 2 est Ref.
3
K kg m
293.15 728.5 0.40 55-gra/gre
293.15 728.3 0.40 55-gra/gre
293.15 728.4 0.4 Recommended
1,1-Diethylcyclopropane [1003-19-6] C7H14 MW = 98.19 26

K kg m 3
K kg m3
293.15 713.8 0.50 44-boo 293.15 713.7 0.40 45-gre/waa
293.15 713.5+ 0.40 44-boo/per 293.15 713.8 0.50 48-sho/cra
293.15 713.7+ 0.50 45-boo/gre 293.15 713.7 0.4 Recommended
Landolt-Brnstein
New Series IV/8D
1-Ethyl-2,2-dimethylcyclopropane [41845-47-0] C7H14 MW = 98.19 27

T exp 2 est Ref.
3
K kg m
293.15 710.5 0.40 60-kac/tog
cis-1-Ethyl-2,3-dimethylcyclopropane [500004-95-5] C7H14 MW = 98.19 28

T exp 2 est Ref.
K kg m3
293.15 746.0 2.00 55-kel/gre
trans-1-Ethyl-2,3-dimethylcyclopropane [500004-94-4] C7H14 MW = 98.19 29

T exp 2 est Ref.
K kg m3
293.15 722.2 2.00 55-kel/gre
1-Methyl-1-(1-methylethyl)cyclopropane [13150-79-3] C7H14 MW = 98.19 30

T exp 2 est Ref.
K kg m3
293.15 722.7 0.50 46-ano-2
293.15 721.5 1.00 53-slo/gri-1
293.15 722.5 0.7 Recommended
1-Methyl-2-(1-methylethyl)cyclopropane [78757-65-0] C7H14 MW = 98.19 31

T exp 2 est Ref.
3
K kg m
293.15 710.2 2.00 13-kis-3
293.15 710.2 2.00 13-kis-4
293.15 710.1 2.00 13-kis/amo
(1-Methylpropyl)cyclopropane [5750-02-7] C7H14 MW = 98.19 32

T exp 2 est Ref.
3
K kg m
293.15 728.3 0.30 52-sla/wis-1
Landolt-Brnstein
New Series IV/8D
1-Methyl-2-propylcyclopropane [19217-48-2] C7H14 MW = 98.19 33

T exp 2 est Ref.
3
K kg m
291.15 720.6 2.00 32-les/wak
cis-1-Methyl-2-propylcyclopropane [500004-93-3] C7H14 MW = 98.19 34

T exp 2 est Ref.
K kg m3
293.15 729.5 2.00 55-kel/gre
trans-1-Methyl-2-propylcyclopropane [500004-92-2] C7H14 MW = 98.19 35

T exp 2 est Ref.
K kg m3
293.15 715.3 0.40 55-kel/gre
1,1,2,2-Tetramethylcyclopropane [4127-47-3] C7H14 MW = 98.19 36

K kg m3 K kg m3
293.15 717.0 0.40 48-ano-4 293.15 718.6 0.40 51-ano-3
293.15 718.8 0.70 49-lev/gla 293.15 718.6 2.00 55-kel/gre
293.15 718.4 0.30 50-boo/gre 293.15 718.3 0.3 Recommended
293.15 718.4 0.40 50-boo/gre
2.3.2 Cyclobutanes
cis-1-Ethyl-3-methylcyclobutane [500025-74-1] C7H14 MW = 98.19 37

T exp 2 est Ref.
3
K kg m
293.15 731.6 0.70 52-kaz/luk
trans-1-Ethyl-3-methylcyclobutane [500025-75-2] C7H14 MW = 98.19 38

T exp 2 est Ref.
3
K kg m
293.15 722.4 0.70 52-kaz/luk
Landolt-Brnstein
New Series IV/8D
(1-Methylethyl)cyclobutane [872-56-0] C7H14 MW = 98.19 39

accepted points. Deviation w= 0.969.
A 1016.46
B -0.950
Table 2. Experimental values with uncertainties and

deviation from calculated values.
T exp 2 est exp calc Ref.
K 3
kg m kg m3
287.65 746.4 1.50 3.21 36-kaz

293.15 737.6 0.50 -0.37 49-der/gre
293.15 738.0 1.00 0.03 55-kaz/luk

T exp 2 est
K kg m3
280.00 750.5 1.5
290.00 741.0 1.0
293.15 738.0 1.0
298.15 733.2 1.2
Propylcyclobutane [4806-62-6] C7H14 MW = 98.19 40

T exp 2 est Ref.
3
K kg m
292.15 744.0 1.50 27-zel/kaz
2.3.3 Cyclopentanes
Ethylcyclopentane [1640-89-7] C 7H14 MW = 98.19 41

Tc = 569.50 K [96-dau]
c = 262.00 kgm-3 [96-dau]
O

T = 275.28 to 440.00 K T = 440.00 to 569.50 K
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
A 9.40285 102 3.14583 10-1
-1
B -3.16123 10 -3.84557 10-3
-4
C -9.43225 10 2.88798 10-5
D -8.76556 10-8
cont.
Landolt-Brnstein
New Series IV/8D
Ethylcyclopentane (cont.)
K 3
kg m3 in Fig. 1)
293.15 766.60 0.20 0.04 43-ano() 333.15 729.65 0.60 -0.63 47-kay( ) 2)
273.15 782.70 0.40 -0.86 44-can1) 353.15 710.59 0.70 -0.42 47-kay( ) 2)
293.15 766.30 0.40 -0.26 44-can1) 373.15 690.97 0.80 -0.02 47-kay( ) 2)
313.15 748.60 0.40 -0.20 44-can() 393.15 670.58 0.90 0.37 47-kay( ) 2)
275.28 781.90 0.20 0.11 44-gar( ){ 413.15 649.19 1.00 0.51 47-kay( ) 2)
275.62 781.61 0.20 0.11 44-gar( ){ 433.15 626.51 1.40 0.12 47-kay( ) 2)
284.95 773.55 0.20 -0.07 44-gar( ){ 453.15 602.16 2.00 -0.53 47-kay( ) 2)
285.15 773.39 0.20 -0.06 44-gar( ){ 473.15 575.62 2.40 -0.21 47-kay( ) 2)
292.68 766.99 0.20 0.03 44-gar( ){ 493.15 546.10 3.00 0.18 47-kay( ) 2)
293.03 766.59 0.20 -0.07 44-gar( ){ 513.15 512.26 4.00 0.29 47-kay( ) 2)
302.73 758.33 0.20 0.19 44-gar( ){ 533.15 471.16 5.00 0.12 47-kay( ) 2)
303.15 757.97 0.20 0.20 44-gar( ){ 553.15 413.83 6.00 -0.80 47-kay( ) 2)
310.05 752.00 0.20 0.40 44-gar( ){ 568.15 316.05 0.00 -8.07 47-kay1) 2)
293.15 766.56 0.20 0.00 46-ano() 293.15 766.45 0.10 -0.11
49-for/ros( )
293.15 766.66 0.30 0.10 47-kay1) 2) 298.15 762.15 0.10 -0.04
49-for/ros( )
313.15 748.30 0.50 -0.50 47-kay( ) 2) 303.15 757.78 0.10 0.01
49-for/ros( )
2)
Calculated from equation given by author.
Further references: [05-zel-1, 25-eis/gor, 27-cha/bec, 32-gar/eva, 34-zel/kaz, 35-zel/kaz, 38-eva, 39-
gro/wac, 39-pin/ipa, 39-pin/ipa-1, 39-tur/mak, 40-moo/ren, 45-boo/gre, 45-cra/boo, 45-gre, 46-baz/ste,
46-boo/gre, 46-gei/can, 46-kay-1, 47-gla/wil, 49-boo/hen, 49-den/fid, 49-foe/fen, 50-pla/sha, 51-zel, 62-
ano-3].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 786.17 0.16 360.00 704.24 0.67 470.00 580.25 2.76
280.00 777.82 0.16 370.00 694.19 0.75 480.00 565.95 2.99
290.00 769.28 0.19 380.00 683.96 0.83 490.00 550.85 3.23
293.15 766.56 0.21 390.00 673.53 0.92 500.00 534.84 3.51
298.15 762.19 0.24 400.00 662.92 1.01 510.00 517.67 3.81
300.00 760.56 0.25 410.00 652.12 1.11 520.00 498.97 4.19
310.00 751.64 0.31 420.00 641.13 1.22 530.00 478.17 4.67
320.00 742.54 0.38 430.00 629.95 1.33 540.00 454.27 5.34
330.00 733.25 0.45 440.00 618.58 1.45 550.00 425.38 6.41
340.00 723.77 0.52 450.00 606.64 2.37 560.00 386.32 8.40
350.00 714.10 0.59 460.00 593.83 2.56
cont.
Landolt-Brnstein
New Series IV/8D
Ethylcyclopentane (cont.)
1,1-Dimethylcyclopentane [1638-26-2] C7H14 MW = 98.19 42

c,w = 1.3502 (combined temperature ranges,
T = 288.15 to 303.15 K
A 1.01086 103
B -8.75856 10-1
cont.
Landolt-Brnstein
New Series IV/8D
1,1-Dimethylcyclopentane (cont.)
K 3
kg m3 in Fig. 1)
293.15 754.60 0.60 0.50 08-kis-3( ) 293.15 754.80 0.60 0.70 49-baz/ukh( )
288.15 759.00 1.00 0.52 31-cha/mil( ) 293.15 754.40 0.30 0.30 49-den/fid( ){
293.15 755.10 1.00 1.00 31-cha/mil1) 293.15 754.46 0.10 0.36 49-for/ros( )
293.15 750.00 0.50 -4.10 33-bru/hic( ) 298.15 749.89 0.10 0.17 49-for/ros( )
293.15 754.50 0.40 0.40 43-ano() 303.15 745.30 0.10 -0.04 49-for/ros( )
293.15 754.60 0.60 0.50 46-ano( ) 293.15 754.30 0.30 0.20 50-boo/gre()
293.15 752.30 2.00 -1.80 49-baz/ukh1) 293.15 754.60 0.50 0.50 51-tur/ada()
Further references: [05-kis-2, 13-kis, 13-kis-3].
cont.
Landolt-Brnstein
New Series IV/8D
1,1-Dimethylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 765.62 2.54 293.15 754.10 0.15 300.00 748.10 0.15
290.00 756.86 0.35 298.15 749.72 0.13 310.00 739.34 0.51

T exp 2 est Ref.
K kg m3
293.15 762.8 8.00 08-kis-3
291.65 758.1 8.00 08-kis-3
293.15 764.0 6.00 28-cha/dev
cis-1,2-Dimethylcyclopentane [1192-18-3] C7H14 MW = 98.19 44

T = 273.15 to 303.15 K
A 1.03467 103
B -8.94116 10-1
K kg m 3
kg m3 in Fig. 1)
288.15 776.40 1.00 -0.63 30-cha( ) 303.15 763.72 0.40 0.10 44-chi()
293.15 771.80 1.00 -0.76 30-cha1) 293.15 772.70 0.40 0.14 45-ano-8()
293.15 772.64 0.40 0.08 35-chi( ) 293.15 772.60 0.70 0.04 49-den/fid( )
288.15 777.10 0.40 0.07 38-chi-1( ) 293.15 772.60 0.10 0.04 49-for/ros( )
293.15 772.70 0.40 0.14 38-chi-1( ) 298.15 768.05 0.10 -0.04 49-for/ros( )
293.15 772.30 0.40 -0.26 43-ano() 303.15 763.62 0.10 0.00 49-for/ros( )
273.15 790.36 0.40 -0.08 44-chi() 293.15 772.80 0.40 0.24 57-ano-4( )
288.15 777.07 0.40 0.04 44-chi() 293.15 772.60 0.40 0.04 63-lib/bra( ){
293.15 772.64 0.40 0.08 44-chi()
Further references: [41-tur/vse].
cont.
Landolt-Brnstein
New Series IV/8D
cis-1,2-Dimethylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 793.26 0.18 293.15 772.56 0.45 300.00 766.44 0.20
280.00 784.32 0.81 298.15 768.09 0.18 310.00 757.49 0.83
290.00 775.38 0.53
trans-1,2-Dimethylcyclopentane [822-50-4] C7H14 MW = 98.19 45

T = 273.15 to 303.15 K
A 1.01239 103
B -8.90688 10-1
cont.
Landolt-Brnstein
New Series IV/8D
trans-1,2-Dimethylcyclopentane (cont.)
293.15 751.35 0.40 0.07 35-chi( ) 303.15 742.40 0.40 0.02 44-chi()
288.15 755.81 0.40 0.07 38-chi-1( ){ 293.15 751.30 0.40 0.02 45-ano-8( )
293.15 751.35 0.40 0.07 38-chi-1( ){ 293.15 751.42 0.10 0.14 49-for/ros( )
293.15 750.60 0.80 -0.68 40-gla1) 298.15 746.84 0.10 0.01 49-for/ros( )
298.15 746.00 0.80 -0.83 40-gla( ) 303.15 742.39 0.10 0.01 49-for/ros( )
293.15 750.70 0.60 -0.58 43-ano( ) 293.15 751.50 0.60 0.22 54-pin/hof( )
273.15 769.18 0.40 0.08 44-chi() 293.15 751.50 0.50 0.22 54-pin/hof1( )
288.15 755.81 0.40 0.07 44-chi() 293.15 751.50 0.40 0.22 57-ano-4()
293.15 751.35 0.40 0.07 44-chi() 293.15 751.40 0.40 0.12 63-lib/bra()
Further references: [30-cha].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 771.90 0.58 293.15 751.28 0.15 300.00 745.18 0.15
280.00 762.99 0.32 298.15 746.83 0.15 310.00 736.27 0.25
290.00 754.09 0.28

K kg m
3
K kg m3
293.15 754.1 4.00 1897-zel-1 293.15 746.0 2.00 49-boo/hen
291.15 749.7 4.00 02-zel-1 293.15 746.4 2.00 50-boo/gre
297.15 741.0 4.00 02-zel-1 293.15 745.4 4.00 50-kop/noz
293.15 756.1 8.00 05-kis-1 293.15 747.0 4.00 55-ano-8
293.15 746.0 2.00 46-baz/ste
cis-1,3-Dimethylcyclopentane [2532-58-3] C7H14 MW = 98.19 47

T = 288.15 to 303.15 K
A 1.02400 103
B -9.51237 10-1
K kg m
3
kg m3 in Fig. 1)
288.15 749.80 1.00 -0.10 26-cha( ) 298.15 740.23 0.10 -0.16

49-for/ros( )
292.85 745.60 1.00 0.17 26-cha( ) 303.15 735.71 0.10 0.08
49-for/ros( )
288.15 749.80 0.50 -0.10 30-cha/mil() 293.15 744.50 0.40 -0.64 {
51-ano( )
288.15 750.40 1.50 0.50 38-eva( ) 293.15 744.90 0.40 -0.24 51-ano-3()
293.15 746.30 1.50 1.16 38-eva1) 293.15 745.00 0.60 -0.14 53-bir/dea( )
293.15 745.70 0.70 0.56 48-boo/gre( ) 293.15 745.60 0.60 0.46 54-bir/dea()
293.15 744.77 0.10 -0.37
49-for/ros( )
Further references: [40-gla].
cont.
Landolt-Brnstein
New Series IV/8D
cis-1,3-Dimethylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 757.65 0.50 293.15 745.14 0.35 300.00 738.62 0.20
290.00 748.14 0.65 298.15 740.39 0.20 310.00 729.12 0.35
Landolt-Brnstein
New Series IV/8D
trans-1,3-Dimethylcyclopentane [1759-58-6] C7H14 MW = 98.19 48

T = 293.15 to 303.15 K
A 1.00288 103
B -8.67855 10-1
K kg m
3
kg m3 in Fig. 1)
293.15 748.80 0.40 0.34 48-ano-3( ) { 303.15 739.83 0.10 0.04 49-for/ros( )
293.15 748.70 0.70 0.24 48-boo/gre() 293.15 748.10 1.00 -0.36 53-bir/dea()
293.15 748.00 1.50 -0.46 48-boo/gre() 293.15 748.50 1.00 0.04 53-bir/dea()
293.15 748.78 0.10 0.32 49-for/ros( ) 298.15 743.70 1.00 -0.42 53-bir/dea()
298.15 744.33 0.10 0.21 49-for/ros( ) 298.15 744.20 1.00 0.08 53-bir/dea()
Further references: [32-gar/eva, 49-den/fid].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 751.20 0.57 298.15 744.13 0.20 310.00 733.84 0.35
293.15 748.46 0.30 300.00 742.52 0.20
2.3.4 Cyclohexanes and Cycloheptane
Methylcyclohexane [108-87-2] C7H14 MW = 98.19 49
Tc = 572.10 K [96-dau]
c = 266.00 kgm-3 [96-dau]
O

T = 178.05 to 460.00 K T = 460.00 to 572.10 K
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
A 9.66739 102 7.40338 10-1
-5
B -2.48282 10 -1.51277 10-2
-3
C -4.97048 10 1.34708 10-4
-5
D 1.26438 10 -4.29882 10-7
-8
E -1.20215 10
K kg m3
kg m3 in Fig. 1)
273.15 786.38 0.20 -0.26 22-tim/van( ) 372.65 698.23 0.30 -0.74 36-mas( )
273.15 786.40 0.20 -0.24 23-tim/van() 293.15 770.00 0.50 0.67 39-gro/wac1)
178.05 868.91 0.30 0.46 36-mas( ) 353.15 717.00 0.40 0.27 39-gro/wac( )
209.65 841.42 0.30 -0.13 36-mas( ) 285.60 775.30 0.30 -0.57 44-fri/har-11)
227.95 825.59 0.30 -0.17 36-mas( ) 323.45 742.50 0.30 -0.50 44-fri/har-1( )
250.25 806.36 0.30 -0.10 36-mas( ) 339.95 728.30 0.30 -0.19 44-fri/har-1( )
273.15 786.48 0.20 -0.16 36-mas( ) 357.15 713.10 0.30 -0.03 44-fri/har-1( )
288.15 773.38 0.20 -0.28 36-mas1) 370.65 701.30 0.30 0.48 44-fri/har-1( )
303.10 760.44 0.20 -0.27 36-mas1) 274.71 785.31 0.20 0.02 44-gar()
318.35 747.00 0.20 -0.45 36-mas( ) 275.28 784.80 0.20 0.00 44-gar()
333.85 733.58 0.30 -0.30 36-mas( ) 284.60 776.77 0.20 0.04 44-gar()
353.10 716.58 0.30 -0.19 36-mas( ) 291.66 770.66 0.20 0.04 44-gar1)
cont.
Landolt-Brnstein
New Series IV/8D
Methylcyclohexane (cont.)
Table 2. (cont.)
K 3
kg m3 in Fig. 1)
770.12 0.20 576.80 1.00

1)
292.31 0.06 44-gar 483.15 0.55 57-fra( )
293.15 769.32 0.20 -0.01 44-gar1) 493.15 561.80 1.00 0.12 57-fra( )
293.15 769.33 0.20 -0.00 44-gar1) 503.15 546.80 1.00 0.30 57-fra( )
302.09 761.69 0.20 0.10 44-gar1) 513.15 530.00 1.00 -0.37 57-fra( )
309.59 755.19 0.20 0.11 44-gar() 523.15 511.30 1.00 -1.35 57-fra( )
293.15 769.34 0.05 0.01
46-for/gla( ) 533.15 490.60 1.00 -1.76 57-fra( )
298.15 764.99 0.05 -0.01
46-for/gla( ) 543.15 469.00 1.00 0.97 57-fra( )
293.15 769.40 0.30 0.07 47-kay1) 2) 553.15 437.50 1.00 0.39 57-fra( )
313.15 752.31 0.40 0.33 47-kay1) 2) 558.15 422.50 1.00 4.85 57-fra1)
333.15 735.01 0.40 0.52 47-kay( ) 2) 563.15 406.20 1.00 12.67 57-fra1)
353.15 717.33 0.45 0.60 47-kay( ) 2) 298.15 764.59 0.38 -0.41 76-chr/lau1)
373.15 699.09 0.50 0.58 47-kay( ) 2) 298.15 764.50 0.25 -0.50 76-chr/lau1)
393.15 680.12 0.55 0.53 47-kay( ) 2) 303.15 760.29 0.40 -0.38 76-chr/lau1)
413.15 660.17 0.60 0.46 47-kay( ) 2) 308.15 756.02 0.41 -0.31 76-chr/lau1)
433.15 638.96 0.65 0.43 47-kay( ) 2) 313.15 751.67 0.42 -0.31 76-chr/lau1)
453.15 616.10 0.70 0.41 47-kay( ) 2) 318.15 747.39 0.43 -0.24 76-chr/lau1)
473.15 591.11 0.80 0.86 47-kay( ) 2) 323.15 742.97 0.44 -0.29 76-chr/lau1)
493.15 563.20 0.90 1.52 47-kay( ) 2) 328.15 738.60 0.45 -0.28 76-chr/lau( )
513.15 531.10 1.10 0.73 47-kay( ) 2) 333.15 734.27 0.46 -0.22 76-chr/lau( )
533.15 492.11 2.60 -0.25 47-kay( ) 2) 338.15 730.07 0.47 -0.01 76-chr/lau( )
553.15 436.56 0.40 -0.55 47-kay( ) 2) 343.15 725.62 0.48 -0.04 76-chr/lau( )
553.15 438.56 2.50 1.45 47-kay1) 2) 348.15 721.21 0.50 0.00 76-chr/lau( )
568.15 353.30 3.00 -6.33 47-kay1) 2) 353.15 716.76 0.51 0.03 76-chr/lau1)
353.15 716.20 0.50 -0.53 57-fra1) 203.00 846.80 0.34 -0.46 79-jon/has( )
363.15 707.60 0.50 -0.09 57-fra( ) 223.00 830.00 0.35 -0.04 79-jon/has( )
373.15 698.40 0.60 -0.11 57-fra( ) 253.00 804.10 0.35 0.02 79-jon/has( )
383.15 689.50 1.00 0.35 57-fra( ) 203.00 846.80 0.34 -0.46 79-jon/has( )
393.15 679.80 1.00 0.21 57-fra( ) 223.00 830.00 0.35 -0.04 79-jon/has( )
403.15 670.30 1.00 0.51 57-fra( ) 253.00 804.10 0.35 0.02 79-jon/has( )
413.15 659.80 1.00 0.09 57-fra( ) 298.00 765.00 0.36 -0.13 79-jon/has1)
423.15 649.30 1.00 -0.00 57-fra( ) 298.15 765.14 0.10 0.14 79-mur-1()
433.15 638.60 1.00 0.07 57-fra( ) 293.15 769.44 0.05 0.11 85-tam/mur( ){
443.15 626.30 1.00 -1.04 57-fra( ) 298.15 765.14 0.10 0.14 79-mur-1()
453.15 615.10 1.00 -0.59 57-fra( ) 293.15 769.44 0.05 0.11 85-tam/mur( ){
463.15 603.40 1.00 -0.08 57-fra( ) 298.15 764.97 0.05 -0.03 85-tam/mur( ){
473.15 590.90 1.00 0.65 57-fra( ) 303.15 760.65 0.05 -0.02 85-tam/mur( ){
cont.
Landolt-Brnstein
New Series IV/8D
Further references: [1892-ber, 1897-kno-1, 1897-zel, 1899-kur-1, 01-sab/sen, 03-mar-2, 05-sab/sen-1,

06-eyk-1, 08-kis-3, 11-kis-4, 13-von/eis, 19-cha/sim-1, 19-cha/sim-2, 19-eyk, 22-cha/van, 26-des, 26-mat,
26-tim/mar, 26-tim/mar-1, 26-wei/hen, 27-bra/hun, 28-ada/mar, 30-god/cau, 30-tau/sta, 32-gar/eva, 32-
hic/bru, 32-ton/fen, 33-bro/qui, 33-sig/cra, 34-god, 35-mam, 36-bro/dur, 37-loz/dya, 38-eva, 38-vog, 38-
wil/lan, 39-cow/jef, 39-tur/mak, 39-wib/hoo, 40-ano, 40-moo/ren, 42-gei, 43-ano, 44-huc, 45-fid, 45-
gre/vog, 46-baz/ste, 46-gei/can, 49-den/fid, 49-gel/mar, 54-chi/maq, 55-bal/tur, 55-gar/hal, 55-roc/sie, 55-
roe/sie, 55-web, 56-ano-5, 59-yen/ree, 61-shi/hil, 61-shu/tul, 63-raj/ran, 66-rob/edm, 69-bra/fre, 69-
rod/hsu, 72-let-1, 73-chi/hou, 73-nag/oht, 74-mye/cle, 74-rao/nai, 74-rao/nai-1, 75-hol/zie, 75-hsu/cle, 75-
mus/ver, 79-maj/svo, 80-dia/cre, 80-fen/khu, 80-sid/goe, 80-sur, 82-gri/phi, 83-gri/phi, 84-tan/tak, 86-
hol/got, 86-tar/dia-1, 88-cha/sur, 88-gar/cob-1, 89-ram/sur, 90-che/pet, 91-aiz/kat, 91-ric/lau, 92-yos/kat,
94-del/fer, 95-pet/gas].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
170.00 875.17 0.64 300.00 763.40 0.22 440.00 630.92 0.94
180.00 866.81 0.53 310.00 754.72 0.25 450.00 619.42 1.00
190.00 858.36 0.44 320.00 746.01 0.29 460.00 607.41 1.07
200.00 849.83 0.36 330.00 737.26 0.33 470.00 594.52 1.41
210.00 841.25 0.30 340.00 728.45 0.38 480.00 580.72 1.52
220.00 832.63 0.25 350.00 719.55 0.43 490.00 566.33 1.56
230.00 823.99 0.21 360.00 710.55 0.49 500.00 551.37 1.53
240.00 815.34 0.18 370.00 701.42 0.54 510.00 535.58 1.46
250.00 806.68 0.16 380.00 692.12 0.60 520.00 518.45 1.41
260.00 798.02 0.16 390.00 682.63 0.65 530.00 499.10 1.37
270.00 789.37 0.16 400.00 672.91 0.71 540.00 476.25 1.37
280.00 780.71 0.17 410.00 662.92 0.76 550.00 447.80 1.41
290.00 772.06 0.19 420.00 652.62 0.82 560.00 409.41 1.56
293.15 769.33 0.20 430.00 641.97 0.88 570.00 340.43 2.22
298.15 765.00 0.21
Cycloheptane [291-64-5] C7H14 MW = 98.19 50
Tc = 604.20 K [96-dau]
c = 278.00 kgm-3 [96-dau]
= 1.0829 (low temperature range), c,w = (3.4892 10-1 combined temperature ranges, weighted),
O

T = 273.15 to 485.00 K T = 485.00 to 604.20 K
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
A 7.98067 102 1.45435
B 1.38830 -4.54351 10-2
C -6.26106 10-3 5.25283 10-4
-6
D 5.70644 10 -1.95959 10-6
cont.
Landolt-Brnstein
New Series IV/8D
Cycloheptane (cont.)
K kg m 3
kg m3 in Fig. 1)
273.15 825.20 2.00 -1.23 02-mar( ) 574.00 491.00 2.00 -2.40 72-you( )
288.15 815.30 2.00 0.53 02-mar1) 580.30 479.00 2.00 2.05 72-you( )
293.15 809.20 2.00 -1.55 02-mar1) 300.45 804.80 0.30 0.04 73-nay/kud()
273.15 825.20 1.00 -1.23 03-mar-1( ) 310.27 796.62 0.30 0.10 73-nay/kud()
293.15 809.20 1.00 -1.55 03-mar-11) 320.89 787.63 0.30 0.22 73-nay/kud()
273.15 827.50 1.50 1.07 08-wil/kam( ) 330.83 779.10 0.30 0.38 73-nay/kud()
273.65 823.90 2.00 -2.16 26-ruz/bru1( ) 340.81 770.41 0.30 0.54 73-nay/kud()
289.25 813.30 0.60 -0.59 38-vog( ) 350.02 762.28 0.30 0.64 73-nay/kud()
293.15 809.80 0.60 -0.95 38-vog1) 359.78 753.54 0.30 0.68 73-nay/kud()
314.15 790.50 0.60 -2.72 38-vog1) 369.70 744.55 0.30 0.63 73-nay/kud()
334.15 773.30 0.60 -2.49 38-vog1) 298.15 806.56 0.30 -0.10 75-ana/gro()
293.15 809.80 0.40 -0.95 52-ano-5( ) 289.23 814.59 0.09 0.68 76-mey/hot( )
293.15 811.00 0.40 0.25 54-ano-8( ) 301.55 804.00 0.09 0.15 76-mey/hot( )
298.15 807.32 0.40 0.66 65-wat/mcl( ) 318.29 789.54 0.10 -0.12 76-mey/hot( )
477.10 639.00 5.00 -15.97 72-you1) 333.52 776.27 0.10 -0.07 76-mey/hot( )
492.20 620.00 5.00 -22.31 72-you1) 349.14 762.52 0.10 0.09 76-mey/hot( )
504.50 606.00 5.00 -15.59 72-you( ) 363.46 749.75 0.10 0.21 76-mey/hot( )
535.90 563.00 2.00 2.83 72-you( ) 376.96 737.52 0.11 0.14 76-mey/hot( )
542.60 547.00 2.00 -1.78 72-you( ) 387.44 727.88 0.13 -0.10 76-mey/hot( )
545.70 544.00 2.00 0.28 72-you( ) 298.15 806.67 0.20 0.01 79-for/dar( ) {
565.00 512.00 2.00 0.10 72-you( ) 298.15 806.75 0.20 0.09 81-mar/sym()
Further references: [16-ros, 26-ruz/bru-1, 29-ros, 30-god/cau, 30-ruz/sto, 46-baz/ste, 47-spi/huf, 52-
kaa/coo, 83-wil/ing].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 828.80 1.83 370.00 743.65 0.30 490.00 645.05 13.33
280.00 821.19 1.08 380.00 734.65 0.17 500.00 629.98 6.96
290.00 813.29 0.57 390.00 725.70 0.14 510.00 610.66 5.29
293.15 810.75 0.45 400.00 716.83 0.24 520.00 590.28 4.64
298.15 806.66 0.30 410.00 708.08 0.39 530.00 570.83 4.33
300.00 805.14 0.25 420.00 699.48 0.60 540.00 553.12 4.18
310.00 796.75 0.11 430.00 691.07 0.86 550.00 536.84 4.11
320.00 788.18 0.08 440.00 682.87 1.19 560.00 520.66 4.09
330.00 779.45 0.12 450.00 674.94 1.60 570.00 502.19 4.12
340.00 770.60 0.19 460.00 667.29 2.08 580.00 477.82 4.25
350.00 761.66 0.28 470.00 659.96 2.64 590.00 441.87 4.61
360.00 752.66 0.33 480.00 652.99 3.30 600.00 379.46 6.32
cont.
Landolt-Brnstein
New Series IV/8D
Cycloheptane (cont.)
2.4 Alkylcycloalkanes, (CnH2n), C8

2.4.1 Cyclopropanes
1-Butyl-2-methylcyclopropane [2511-92-4] C8H16 MW = 112.22 51

T exp 2 est Ref.
K kg m3
293.15 744.5 2.00 63-nef/nov
1-Ethyl-2-propylcyclopropane [500011-08-5] C8H16 MW = 112.22 52

T exp 2 est Ref.
3
K kg m
293.15 735.4 0.80 56-gra/kos
Landolt-Brnstein
New Series IV/8D
1,2-Diethyl-1-methylcyclopropane [98997-51-4] C8H16 MW = 112.22 53

T exp 2 est Ref.
3
K kg m
293.15 738.1 2.00 13-zel/upe
293.15 741.2 0.80 56-gra/kos
293.15 740.8 0.9 Recommended
1,1-Dimethyl-2-propylcyclopropane [41845-48-1] C8H16 MW = 112.22 54

T exp 2 est Ref.
K kg m3
293.15 729.7 0.40 60-kac/tog
(1,2-Dimethylpropyl)cyclopropane [6976-27-8] C8H16 MW = 112.22 55

T exp 2 est Ref.
K kg m3
293.15 750.2 1.00 52-sla-1
(1-Methylbutyl)cyclopropane [5458-16-2] C8H16 MW = 112.22 56

T exp 2 est Ref.
3
K kg m
293.15 742.7 0.20 52-sla/wis-1
1-Methyl-2-(2-methylpropyl)cyclopropane [500030-54-6] C8H16 MW = 112.22 57

T exp 2 est Ref.
K kg m3
293.15 740.3 2.00 13-zel/upe
Pentylcyclopropane [2511-91-3] C8H16 MW = 112.22 58

T exp 2 est Ref.
3
K kg m
293.15 742.7 1.00 63-nef/nov
Landolt-Brnstein
New Series IV/8D
2.4.2 Cyclobutanes
Butylcyclobutane [13152-44-8] C 8H16 MW = 112.22 59

A 995.73
B -0.725

K kg m3
kg m3
293.15 783.2 2.00 0.00 39-pin/ipa

313.15 768.7 2.00 0.00 39-pin/ipa

T exp 2 est
K kg m3
290.00 785.5 2.5
293.15 783.2 2.0
298.15 779.6 2.0
310.00 771.0 2.0
320.00 763.7 2.5
1-(1-Methylethyl)-1-methylcyclobutane [500004-72-8] C8H16 MW = 112.22 60

T exp 2 est Ref.
K kg m3
293.15 722.7 1.00 49-der/gre
trans-1-Methyl-3-propylcyclobutane [500025-80-9] C8H16 MW = 112.22 61

T exp 2 est Ref.
K kg m3
293.15 737.0 0.80 54-kaz/luk
Landolt-Brnstein
New Series IV/8D
2.4.3 Cyclopentanes
1-Ethyl-1-methylcyclopentane [16747-50-5] C8H16 MW = 112.22 62

A 1025.08
B -0.833

K kg m 3
kg m3
293.15 780.6 0.60 -0.28 46-pla/zab

293.15 780.9 0.15 0.03 49-for/ros
298.15 776.7 0.15 -0.04 49-for/ros
303.15 772.6 0.15 0.03 49-for/ros
293.15 782.4 1.00 1.52 57-nov/khr 1)
1)

T exp 2 est
K kg m3
290.00 783.5 0.2
293.15 780.9 0.2
298.15 776.7 0.2
300.00 775.2 0.2
310.00 766.8 0.3

T exp 2 est Ref.
K kg m3
293.15 772.8 4.00 35-nen/van
Landolt-Brnstein
New Series IV/8D
cis-1-Ethyl-2-methylcyclopentane [930-89-2] C8H16 MW = 112.22 64

T = 273.15 to 303.15 K
A 9.54368 102
B -3.48442 10-1
C -7.80948 10-4
K kg m
3
kg m3 in Fig. 1)
273.15 801.10 0.60 0.18 31-chi() 273.15 801.55 0.40 0.63 {

44-chi( )
293.15 784.60 0.60 -0.51 31-chi() 293.15 785.06 0.40 -0.05 {
44-chi( )
273.15 801.10 0.60 0.18 34-chi-1() 293.15 785.20 0.10 0.09
49-for/ros( )
293.15 784.60 0.60 -0.51 34-chi-1() 298.15 781.11 0.10 0.05
49-for/ros( )
293.15 785.06 0.60 -0.05 35-chi() 303.15 776.97 0.10 0.00
49-for/ros( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 803.36 0.60 293.15 785.11 0.20 300.00 779.55 0.12
280.00 795.58 1.00 298.15 781.06 0.11 310.00 771.30 1.16
290.00 787.64 0.40
cont.
Landolt-Brnstein
New Series IV/8D
cis-1-Ethyl-2-methylcyclopentane (cont.)
trans-1-Ethyl-2-methylcyclopentane [930-90-5] C8H16 MW = 112.22 65

T = 273.15 to 298.15 K
A 1.01326 103
B -8.32453 10-1
cont.
Landolt-Brnstein
New Series IV/8D
trans-1-Ethyl-2-methylcyclopentane (cont.)
273.15 786.00 0.60 0.13 31-chi() 273.15 785.48 0.50 -0.39 {

44-chi( )
293.15 769.60 0.60 0.38 31-chi() 293.15 769.10 0.50 -0.12 {
44-chi( )
273.15 786.00 0.60 0.13 34-chi-1() 293.15 769.00 0.40 -0.22
46-for/ros-1( )
293.15 769.60 0.60 0.38 34-chi-1() 298.15 764.90 0.40 -0.16
46-for/ros-1( )
293.15 769.10 0.60 -0.12 35-chi()
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 788.49 0.60 293.15 769.22 0.5 300.00 763.52 0.50
280.00 780.17 0.66 298.15 765.06 0.5 310.00 755.19 0.60
290.00 771.84 0.60
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
289.15 766.9 6.00 02-zel-1
293.15 763.3 4.00 50-boo/gre
293.15 763.1 4.00 56-ano
cis-1-Ethyl-3-methylcyclopentane [2613-66-3] C8H16 MW = 112.22 67

A 1024.51
B -0.860

K kg m 3
kg m3
293.15 772.4 0.40 -0.00 46-for/ros-1

298.15 768.1 0.40 0.00 46-for/ros-1

T exp 2 est
K kg m3
290.00 775.1 0.5
293.15 772.4 0.4
298.15 768.1 0.4
300.00 766.5 0.5
trans-1-Ethyl-3-methylcyclopentane [2613-65-2] C8H16 MW = 112.22 68

A 1008.38
B -0.840
cont.
Landolt-Brnstein
New Series IV/8D
trans-1-Ethyl-3-methylcyclopentane (cont.)

K kg m 3
kg m3
293.15 761.9 0.40 -0.23 46-for/ros-1

298.15 757.7 0.40 -0.23 46-for/ros-1
293.15 762.6 0.40 0.47 54-baz/kop

T exp 2 est
K kg m3
290.00 764.8 0.5
293.15 762.1 0.4
298.15 757.9 0.4
300.00 756.4 0.5
(1-Methylethyl)cyclopentane [3875-51-2] C8H16 MW = 112.22 69

T = 273.15 to 303.15 K
A 9.31678 102
B -2.64716 10-1
C -9.02208 10-4
K 3
kg m3 in Fig. 1)
293.15 776.50 0.40 -0.04 41-ano-1( ) 273.15 792.00 1.50 -0.06 46-gei/can( )
273.15 792.00 0.40 -0.06 44-can() 293.15 776.00 1.50 -0.54 46-gei/can1)
293.15 776.30 0.40 -0.24 44-can1) 313.15 761.00 1.50 0.69 46-gei/can1)
313.15 760.70 0.40 0.39 44-can1) 293.15 776.60 0.40 0.06 49-boo/hen( )
293.15 776.59 0.40 0.05 44-gar() 293.15 776.50 0.40 -0.04 49-foe/fen( )
293.15 776.61 0.40 0.07 44-gar() 293.15 776.51 0.15 -0.03 {
49-for/ros( )
293.15 776.60 0.30 0.06 46-boo/gre() 298.15 772.57 0.15 0.02 {
49-for/ros( )
293.15 776.54 0.05 -0.00
46-for/gla( ) 303.15 768.51 0.15 -0.01 {
49-for/ros( )
298.15 772.55 0.05 -0.00
46-for/gla( )
cont.
Landolt-Brnstein
New Series IV/8D
(1-Methylethyl)cyclopentane (cont.)
Further references: [25-eis/gor, 36-kaz/pla-1, 39-kaz/tat, 39-pin/ipa, 43-ano, 45-cra/boo, 46-baz/ste, 50-
kaz/ter-1].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 794.43 1.05 293.15 776.54 0.22 300.00 771.06 0.12
280.00 786.82 0.72 298.15 772.55 0.17 310.00 762.91 0.25
290.00 779.03 0.42
Landolt-Brnstein
New Series IV/8D
Propylcyclopentane [2040-96-2] C8H16 MW = 112.22 70

T = 273.15 to 313.15 K
A 1.01354 103
B -8.09393 10-1
K kg m
3
kg m3 in Fig. 1)
293.15 775.60 0.60 -0.67 39-pin/ipa1) 293.15 776.35 0.20 0.08 44-gar()
313.15 760.10 0.60 0.02 39-pin/ipa() 299.85 770.98 0.20 0.14 44-gar()
273.15 791.80 0.40 -0.65 44-can() 300.42 770.46 0.20 0.08 44-gar()
293.15 776.00 0.40 -0.27 44-can1) 308.54 763.84 0.20 0.03 44-gar()
313.15 759.70 0.40 -0.38 44-can() 309.15 763.35 0.20 0.03 44-gar()
281.19 786.14 0.20 0.19 44-gar() 293.15 776.23 0.05 -0.04 46-for/gla()
281.53 785.84 0.20 0.17 44-gar() 298.15 772.31 0.05 0.09 46-for/gla()
289.43 779.39 0.20 0.11 44-gar() 293.15 776.31 0.15 0.04 49-for/ros({)
289.88 779.05 0.20 0.14 44-gar() 298.15 772.27 0.15 0.05 49-for/ros({)
293.15 776.35 0.20 0.08 44-gar() 303.15 768.09 0.15 -0.08 49-for/ros({)
Further references: [06-zel, 27-cha/bec, 32-gar/eva, 34-zel/kaz, 35-zel/kaz, 38-eva, 39-tur/pol, 40-ano,
43-ano, 45-boo/gre, 45-cra/boo, 46-baz/ste, 46-boo/gre, 46-gei/can, 49-foe/fen, 51-ano, 54-khr/bal-1].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 795.00 0.41 293.15 776.27 0.14 310.00 762.63 0.33
280.00 786.91 0.29 298.15 772.22 0.13 320.00 754.53 0.84
290.00 778.82 0.16 300.00 770.72 0.14
cont.
Landolt-Brnstein
New Series IV/8D
Propylcyclopentane (cont.)
1,1,2-Trimethylcyclopentane [4259-00-1] C8H16 MW = 112.22 71

T = 277.15 to 303.15 K
A 1.01539 103
B -8.29191 10-1
cont.
Landolt-Brnstein
New Series IV/8D
1,1,2-Trimethylcyclopentane (cont.)
K 3
kg m3 in Fig. 1)
277.15 784.70 2.00 -0.88 06-cro/ren( ) 293.15 772.20 0.40 -0.11 45-ano()
283.15 779.80 2.00 -0.81 06-cro/ren( ) 293.15 772.50 0.15 0.19 49-for/ros( )
288.18 775.50 2.00 -0.94 06-cro/ren1) 298.15 768.15 0.15 -0.02 49-for/ros( )
289.35 774.61 2.00 -0.86 06-cro/ren1) 303.15 763.97 0.15 -0.05 49-for/ros( )
293.15 771.40 2.00 -0.91 06-cro/ren1) 293.15 772.20 0.40 -0.11 51-ano()
298.15 767.10 2.00 -1.07 06-cro/ren1) 293.15 772.20 0.40 -0.11 51-des/fid( ){
289.35 774.60 1.00 -0.87 06-eyk-1( ) 293.15 775.10 0.50 2.79 56-lev/gir-1()
Further references: [01-zel/lep-1, 22-cha].
cont.
Landolt-Brnstein
New Series IV/8D
1,1,2-Trimethylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 791.51 3.00 293.15 772.31 0.41 300.00 766.63 0.11
280.00 783.22 2.11 298.15 768.17 0.09 310.00 758.34 2.57
290.00 774.93 0.90

A 1002.42
B -0.867
K kg m 3
kg m3 K kg m 3
kg m3
293.15 770.3 2.00 22.04 13-zel/usp 1) 293.15 748.3 0.30 0.04 49-boo/gre
293.15 748.2 0.40 -0.06 45-ano-8 293.15 748.23 0.15 -0.03 49-for/ros
293.15 748.3 0.30 0.04 45-boo/gre 298.15 743.90 0.15 -0.02 49-for/ros
293.15 748.1 0.50 -0.16 45-mck/ste 1) 303.15 739.56 0.15 -0.03 49-for/ros
293.15 748.3 0.40 0.04 45-per 293.15 748.2 0.40 -0.03 51-slo
293.15 748.3 0.40 0.04 46-ano-2 293.15 748.2 0.40 -0.06 54-ano-8
298.15 744.2 0.60 0.28 47-gla/wil 1) 293.15 748.4 0.30 0.14 54-baz/kop
293.15 748.4 0.30 0.14 49-boo/gre
1)

T exp 2 est
K kg m3
290.00 751.0 0.2
293.15 748.3 0.2
298.15 743.9 0.2
300.00 742.3 0.2
310.00 733.7 0.3
Landolt-Brnstein
New Series IV/8D

A 1001.83
B -0.830

K kg m3 kg m3
277.15 771.8 5.00 0.01 06-cro/ren

288.15 762.6 5.00 -0.06 06-cro/ren
292.95 758.8 5.00 0.12 06-cro/ren
293.15 758.3 5.00 -0.21 06-cro/ren
298.15 754.5 5.00 0.14 06-cro/ren

T exp 2 est
K kg m3
270.00 777.7 6.0
280.00 769.4 5.0
290.00 761.1 5.0
293.15 758.5 5.0
298.15 754.4 5.0
300.00 752.8 5.0
r-1, c-2, c-3-Trimethylcyclopentane [2613-69-6] C8H16 MW = 112.22 74

A 1019.58
B -0.820

K kg m3
kg m3
293.15 779.2 0.40 0.00 46-for/ros-1

298.15 775.1 0.40 0.00 46-for/ros-1
293.15 776.6 2.00 -2.60 47-kaz/kop 1)
293.15 776.6 2.00 -2.60 48-kop/kaz 1)
1)
cont.
Landolt-Brnstein
New Series IV/8D
r-1, c-2, c-3-Trimethylcyclopentane (cont.)

T exp 2 est
K kg m3
290.00 781.8 0.5
293.15 779.2 0.4
298.15 775.1 0.4
r-1, c-2, t-3-Trimethylcyclopentane [15890-40-1] C8H16 MW = 112.22 75

A 1022.30
B -0.860
Table 2. Experimental values with uncertainties

and deviation from calculated values.
K kg m 3
kg m3
293.15 770.4 0.40 0.21 46-for/ros-1

298.15 766.1 0.40 0.21 46-for/ros-1
293.15 769.5 0.60 -0.69 47-kaz/kop
293.15 769.5 1.00 -0.69 48-kop/kaz

T exp 2 est
K kg m3
290.00 772.9 0.4
293.15 770.2 0.4
298.15 765.9 0.4
300.00 764.3 0.4
r-1, t-2, c-3-Trimethylcyclopentane [19374-46-0] C8H16 MW = 112.22 76

A 1005.76
B -0.860
cont.
Landolt-Brnstein
New Series IV/8D
r-1, t-2, c-3-Trimethylcyclopentane (cont.)

K kg m3 kg m3
293.15 753.5 0.40 -0.15 46-ano

298.15 749.2 0.40 -0.15 46-ano
293.15 754.0 0.60 0.35 47-kaz/kop
293.15 754.0 1.00 0.35 48-kop/kaz
293.15 753.7 0.30 0.05 61-ano-9

T exp 2 est
K kg m3
290.00 756.4 0.5
293.15 753.7 0.5
298.15 749.4 0.5
300.00 747.8 0.5
r-1, c-2, c-4-Trimethylcyclopentane [2613-72-1] C8H16 MW = 112.22 77

T exp 2 est Ref.
3
K kg m
293.15 776.6 1.00 48-kop/kaz
293.15 762.0 1.50 63-ano-3
r-1, c-2, t-4-Trimethylcyclopentane [4850-28-6] C8H16 MW = 112.22 78

A 1009.96
B -0.841
293.15 763.6 0.40 0.18 43-ano 293.15 763.6 0.50 0.18 51-ano
293.15 763.43 0.15 0.01 49-for/ros 293.15 763.4 0.60 -0.02 51-bir/joh1)
298.15 759.18 0.15 -0.03 49-for/ros 293.15 763.5 0.40 0.08 51-slo
303.15 755.02 0.15 0.01 49-for/ros 293.15 763.2 0.30 -0.22 54-baz/kop
293.15 763.5 0.50 0.08 50-boo/gre
1)
cont.
Landolt-Brnstein
New Series IV/8D
r-1, c-2, t-4-Trimethylcyclopentane (cont.)

T exp 2 est
K kg m3
290.00 766.1 0.2
293.15 763.4 0.2
298.15 759.2 0.2
310.00 749.2 0.3
r-1, t-2, t-4-Trimethylcyclopentane [16883-48-0] C8H16 MW = 112.22 79

A 997.58
B -0.854
K kg m 3
kg m3 K kg m 3
kg m3
293.15 747.5 0.40 0.27 43-ano 303.15 738.71 0.10 0.02 49-for/ros
293.15 747.2 0.30 -0.03 49-boo/gre 293.15 747.1 0.60 -0.13 51-bir/joh
293.15 747.25 0.10 0.02 49-for/ros 293.15 747.5 0.40 0.27 51-slo
298.15 743.00 0.10 0.04 49-for/ros 293.15 746.3 0.30 -0.93 54-baz/kop

T exp 2 est
K kg m3
290.00 749.9 0.2
293.15 747.2 0.2
298.15 743.0 0.2
310.00 732.8 0.3
Landolt-Brnstein
New Series IV/8D
2.4.4 Cyclohexanes
Ethylcyclohexane [1678-91-7] C8H16 MW = 112.22 80

T = 273.15 to 313.15 K
A 1.02440 103
B -8.06381 10-1
288.15 791.40 0.40 -0.65 32-gar/eva( ) 291.54 789.62 0.20 0.31 44-gar()
293.15 787.50 0.40 -0.51 32-gar/eva1) 292.19 788.97 0.20 0.18 44-gar()
288.15 791.40 0.40 -0.65 38-eva( ) 293.15 788.21 0.30 0.20 44-gar()
293.15 787.50 0.40 -0.51 38-eva1) 293.15 788.20 0.30 0.19 44-gar()
273.15 803.90 0.50 -0.24 42-gei( ) 302.48 780.74 0.20 0.25 44-gar()
293.15 788.10 0.50 0.09 42-gei1) 302.98 780.31 0.20 0.22 44-gar()
313.15 772.30 0.50 0.41 42-gei( ) 311.00 773.83 0.20 0.21 44-gar()
273.15 803.90 0.30 -0.24 44-can() 293.15 787.90 0.05 -0.11
46-for/gla( )
293.15 788.10 0.30 0.09 44-can() 298.15 783.88 0.05 -0.10
46-for/gla( )
313.15 772.30 0.30 0.41 44-can() 303.15 779.40 0.50 -0.55 64-pra/van( )
273.78 803.80 0.20 0.17 44-gar() 298.15 783.59 0.30 -0.39 90-fer/lap()
283.07 796.33 0.20 0.19 44-gar() 298.15 783.82 0.20 -0.16 {
94-del/fer( )
283.86 795.76 0.20 0.26 44-gar()
Further references: [1899-kur-1, 01-sab/sen, 01-sab/sen-1, 11-leb/ska, 14-vav, 25-eis/gor, 28-ada/mar,

29-str-1, 33-sig/cra, 34-lev/tzu, 35-ros/whi, 37-loz/dya, 39-ano, 40-ano, 46-baz/ste, 46-gei/can, 51-des/fid,
54-chi/maq, 55-bal/tur, 60-qoz/van, 60-yak/vol, 61-pau/yuz, 61-tar/tul, 63-ano-3, 63-pra/van].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 806.68 0.39 293.15 788.01 0.15 310.00 774.43 0.27
280.00 798.62 0.29 298.15 783.98 0.13 320.00 766.36 0.45
290.00 790.55 0.20 300.00 782.49 0.13
cont.
Landolt-Brnstein
New Series IV/8D
Ethylcyclohexane (cont.)
1,1-Dimethylcyclohexane [590-66-9] C8H16 MW = 112.22 81

T = 273.15 to 303.15 K
A 1.01699 103
B -8.05772 10-1
cont.
Landolt-Brnstein
New Series IV/8D
1,1-Dimethylcyclohexane (cont.)
K 3
kg m3 in Fig. 1)
277.15 794.70 1.00 1.03 05-cro/ren( ) 293.15 780.99 0.40 0.21 46-lib/kaz( )
288.15 785.69 1.00 0.88 05-cro/ren1) 293.15 780.60 0.30 -0.18 49-eva()
293.15 781.88 1.00 1.10 05-cro/ren1) 293.15 780.92 0.10 0.14 49-for/ros( )
298.15 777.50 1.00 0.75 05-cro/ren1) 298.15 776.75 0.10 0.00 49-for/ros( )
290.35 782.24 0.50 -0.79 19-eyk( ) 303.15 772.74 0.10 0.02 49-for/ros( )
288.15 784.00 0.60 -0.81 31-cha/mil( ) 293.15 780.75 0.50 -0.03 50-chi/fie1)
273.15 797.07 0.30 0.18 35-mam( ) { 303.15 772.55 0.50 -0.17 50-chi/fie( )
293.15 780.73 0.30 -0.05 35-mam( ) { 293.15 781.00 0.40 0.22 51-ano( )
273.15 797.07 0.60 0.18 35-mil( ) 293.15 780.90 0.40 0.12 56-ano( )
293.15 780.71 0.40 -0.07 35-mil( ) 293.15 780.90 0.40 0.12 56-ano-6()
293.15 780.60 0.30 -0.18 45-boo/gre()
Further references: [13-von/eis, 13-zel/lep, 15-von/lan, 23-zel, 23-zel-2, 35-zel/pac, 36-hib/lin, 48-
sho/cra, 49-baz/ukh, 50-zel/ela, 55-bal/tur, 56-goe/mcc, 66-khr/koc, 68-puz/eid].
cont.
Landolt-Brnstein
New Series IV/8D
1,1-Dimethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 799.43 0.69 293.15 780.78 0.20 300.00 775.26 0.15
280.00 791.37 0.55 298.15 776.75 0.15 310.00 767.20 0.25
290.00 783.32 0.35

3 3
K kg m K kg m
273.15 800.8 4.00 01-sab/sen 293.15 781.4 4,00 37-loz/dya
273.15 800.3 4.00 05-sab/mai-1 288.15 791.2 4.00 38-eva
287.45 788.0 6.00 11-eyk 293.15 787.4 4.00 38-eva
286.15 798.0 6.00 19-cha/sim-1 293.15 783.0 4.00 66-mek/mag
291.00 780.9 4.00 20-von-2 293.15 772.6 4.00 67-mek/mag
566.30 779.0 6.00 20-von-2 298.15 786.1 4.00 90-che/pet
293.15 789.3 4.00 24-zel-2 298.15 786.1 4.00 95-pet/gas
286.65 792.0 5.00 30-god/cau
cis-1,2-Dimethylcyclohexane [2207-01-4] C8H16 MW = 112.22 83

T = 273.15 to 313.15 K
A 1.03175 103
B -8.02866 10-1
cont.
Landolt-Brnstein
New Series IV/8D
cis-1,2-Dimethylcyclohexane (cont.)
273.15 811.23 0.25 -1.22 32-mil() 290.54 798.73 0.20 0.24 44-gar( ){
293.15 796.18 0.25 -0.21 32-mil() 291.19 798.21 0.20 0.25 44-gar( ){
273.15 813.09 0.25 0.64 35-mil() 293.15 796.56 0.20 0.17 44-gar( ){
293.15 796.23 0.25 -0.16 35-mil() 301.43 789.95 0.20 0.21 44-gar( ){
273.15 812.10 0.50 -0.35 42-gei( ) 301.93 789.94 0.20 0.60 44-gar( ){
293.15 795.70 0.50 -0.69 42-gei1) 310.24 782.73 0.20 0.06 44-gar( ){
313.15 780.10 0.50 -0.23 42-gei( ) 310.89 782.20 0.20 0.05 44-gar( ){
273.15 812.10 0.50 -0.35 44-can( ) 293.15 796.25 0.05 -0.14 46-for/gla( )
293.15 795.70 0.50 -0.69 44-can1) 298.15 792.20 0.05 -0.18 46-for/gla( )
313.15 780.10 0.50 -0.23 44-can( ) 298.15 792.86 0.30 0.48 90-che/pet()
282.09 805.64 0.20 0.37 44-gar( ){
Further references: [22-cha/bec, 22-cha/van, 22-ski/sch, 32-gar/eva, 32-zel/mar, 33-mil/pia, 33-sig/cra,
35-mam, 41-ano-1, 45-gre-1, 46-ano, 46-boo/gre, 46-gei/can, 49-baz/ukh, 49-boo/hen, 54-cla/cor, 68-
man/mue, 68-wip/cle, 74-anf/bal, 75-pav/kla, 95-pet/gas].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 814.98 0.40 293.15 796.39 0.18 310.00 782.86 0.32
280.00 806.95 0.31 298.15 792.38 0.16 320.00 774.83 0.75
290.00 798.92 0.20 300.00 790.89 0.17
trans-1,2-Dimethylcyclohexane [6876-23-9] C8H16 MW = 112.22 84

T = 273.15 to 313.15 K
A 9.91644 102
B -6.76113 10-1
C -2.03176 10-4
K kg m 3
kg m3 in Fig. 1)
273.15 791.83 0.25 0.02 32-mil() 283.12 784.05 0.20 0.11 {

44-gar( )
293.15 775.99 0.25 0.01 32-mil() 290.88 777.85 0.20 0.06 {
44-gar( )
293.15 775.84 0.30 -0.14 33-mil/pia( ) 293.15 776.03 0.20 0.05 {
44-gar( )
273.15 791.86 0.20 0.05 35-mil() 301.49 769.43 0.20 0.09 {
44-gar( )
293.15 775.99 0.20 0.01 35-mil() 302.21 768.85 0.20 0.09 {
44-gar( )
298.15 792.02 0.20 20.02 35-mil1) 310.31 762.34 0.20 0.06 {
44-gar( )
293.15 775.65 0.30 -0.33 41-ano-1( ) 293.15 776.04 0.20 0.06 46-ano()
273.15 791.00 0.40 -0.81 44-can1) 293.15 776.04 0.30 0.06 46-boo/gre( )
293.15 775.50 0.40 -0.48 44-can1) 293.15 775.99 0.05 0.01 46-for/gla( )
313.15 759.90 0.40 -0.10 44-can( ) 298.15 772.02 0.05 0.02 46-for/gla( )
282.66 784.42 0.20 0.12 44-gar( ){ 293.15 775.65 0.30 -0.33 49-boo/hen( )
Further references: [21-ski, 22-ski/sch, 25-eis/gor, 29-str-1, 32-zel/mar, 36-mar-1, 46-baz/ste, 46-
gei/can, 49-baz/ukh, 54-cla/cor].
cont.
Landolt-Brnstein
New Series IV/8D
trans-1,2-Dimethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 794.28 0.30 293.15 775.98 0.15 310.00 762.52 0.28
280.00 786.40 0.25 298.15 772.00 0.13 320.00 754.48 0.65
290.00 778.48 0.19 300.00 770.52 0.15
Landolt-Brnstein
New Series IV/8D

3 3
K kg m K kg m
273.15 777.0 4.00 1877-wre 293.15 782.2 4.00 08-ski
293.15 766.0 4.00 1877-wre 294.95 770.1 4.00 10-lei
292.45 766.5 3.00 1884-los/zan 286.15 775.0 4.00 19-cha/sim-1
292.15 764.0 4.00 1884-ren 288.15 775.0 6.00 19-cha/sim-2
290.15 757.3 4.00 1891-asc 293.15 777.0 4.00 26-wei/hen
295.15 764.0 4.00 1892-wal-1 286.65 777.2 5.00 30-god/cau
292.15 768.8 5.00 1895-zel 293.15 770.1 4.00 32-zel/mar
295.15 795.7 4.00 1895-zel/rud 293.15 769.3 4.00 32-zel/mar
291.15 773.6 4.00 1897-kno-1 293.15 772.0 4.00 33-sig/cra
293.15 768.7 4.00 1897-zel 293.15 767.7 4.00 37-loz/dya
273.15 787.4 4.00 01-sab/sen 288.15 776.1 4.00 38-eva
273.15 787.4 4.00 01-sab/sen-1 293.15 772.3 4.00 38-eva
299.15 766.1 4.00 02-zel-1 293.15 770.7 4.00 49-vve/tak
288.15 774.1 6.00 04-bal/ang 293.15 767.6 4.00 66-mek/mag
273.15 786.9 4.00 05-sab/mai-1

T = 273.15 to 313.15 K
A 1.03766 103
B -1.04011
C 3.87507 10-4
K 3
kg m3 in Fig. 1)
273.15 782.49 0.60 0.03 35-mil( ) 293.15 766.01 0.05 -0.04 46-for/gla( )
293.15 766.26 0.40 0.21 35-mil( ) 298.15 761.94 0.05 -0.05 46-for/gla( )
273.15 781.90 0.50 -0.56 42-gei( ) 298.15 762.00 0.30 0.01 47-osb/gin()
293.15 765.90 0.50 -0.15 42-gei( ) 293.15 766.28 0.30 0.23 60-nat()
313.15 749.80 0.50 -0.15 42-gei( ) 293.15 766.00 0.20 -0.05 63-gon/sha( ) {
293.15 766.70 0.30 0.65 43-ano( ) 303.15 757.90 0.20 -0.06 63-gon/sha( ) {
273.15 781.90 0.30 -0.56 44-can() 293.15 766.30 0.50 0.25 68-man/mue( )
293.15 765.90 0.30 -0.15 44-can() 293.15 766.60 0.50 0.55 75-pav/kla( )
313.15 749.80 0.30 -0.15 44-can()
cont.
Landolt-Brnstein
New Series IV/8D
Further references: [15-von/hin, 19-cha/sim-1, 21-ski, 22-cha/bec, 22-cha/van, 22-ski/sch, 25-eis/gor,

26-wei/hen, 32-gar/eva, 32-zel/mar, 35-mam, 36-mar-1, 38-mou/gra, 38-mou/gra-1, 39-mou/pau, 41-ano-
1, 46-ano-4, 46-baz/ste, 46-gei/can, 49-baz/ukh, 51-des/fid, 53-noy/nag].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 785.08 0.34 293.15 766.05 0.34 310.00 752.46 0.29
280.00 776.81 0.60 298.15 761.99 0.22 320.00 744.50 1.06
290.00 768.61 0.42 300.00 760.50 0.19
Landolt-Brnstein
New Series IV/8D
(1R-trans)-1,3-Dimethyl-cyclohexane [69685-68-3] C8H16 MW = 112.22 87

T exp 2 est Ref.
3
K kg m
783.48 0.30 35-mil
1)
293.15
298.15 777.00 0.70 38-mou/gra
298.15 777.00 2.00 38-mou/gra-1
298.15 777.00 0.70 46-mou
293.15 784.90 0.70 68-man/mue
293.15 784.80 0.70 75-pav/kla
1)
This point included in the fit of trans-1,3-Dimethylhexane.

T = 273.15 to 313.15 K
A 1.11135 103
B -1.40304
C 9.84496 10-4
K kg m 3
kg m3 in Fig. 1)
293.15 783.48 0.30 -1.18 35-mil() 313.15 768.70 0.40 0.17 44-can()
298.15 779.28 0.50 -1.27 35-mil1) 293.15 784.70 0.05 0.04 46-for/gla( )
293.15 784.00 0.50 -0.66 41-ano-1( ) 298.15 780.53 0.05 -0.02 46-for/gla( )
273.15 801.60 0.50 0.03 42-gei( ) 298.15 780.60 0.30 0.05 47-osb/gin()
293.15 785.30 0.50 0.64 42-gei( ) 293.15 784.50 0.50 -0.16 49-baz/ukh( )
313.15 768.70 0.50 0.17 42-gei( ) 293.15 784.80 0.20 0.14 63-gon/sha( ) {
273.15 801.60 0.40 0.03 44-can() 303.15 776.60 0.20 0.10 63-gon/sha( ) {
293.15 785.30 0.40 0.64 44-can()
Further references: [21-ski, 32-gar/eva, 32-zel/mar, 35-mam, 36-mar-1, 38-mou/gra, 38-mou/gra-1, 39-
mou/pau, 46-gei/can, 46-mou, 68-man/mue, 75-pav/kla].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 804.30 0.70 293.15 784.66 0.20 310.00 771.02 0.31
280.00 795.69 0.60 298.15 780.55 0.18 320.00 763.19 1.21
290.00 787.27 0.35 300.00 779.05 0.20
*
Data sets 87 and 88 are combined for recommended values.
Landolt-Brnstein
New Series IV/8D

3 3
K kg m K kg m
293.15 769.0 4.00 1898-zel/nou 286.65 775.6 5.00 30-god/cau
293.15 768.8 4.00 1898-zel/nou 293.15 775.0 4.00 33-sig/cra
273.15 786.6 4.00 01-sab/sen 293.15 782.7 4.00 35-mil
293.15 762.6 4.00 01-sub 293.15 766.9 4.00 37-loz/dya
273.15 786.1 4.00 05-sab/mai-1 288.15 776.7 4.00 38-eva
295.35 762.0 4.00 11-eyk 293.15 772.7 4.00 38-eva
286.15 783.0 4.00 19-cha/sim-1 293.15 770.5 4.00 55-bal/tur
288.85 772.2 4.00 20-von-2 293.15 766.6 4.00 66-mek/mag
293.15 769.0 4.00 20-von-2

T = 273.15 to 313.15 K
A 1.02460 103
B -8.24605 10-1
273.15 799.25 0.30 -0.11 35-mil( ) 289.75 785.84 0.20 0.17 {

44-gar( )
293.15 782.71 0.30 -0.16 35-mil( ) 293.15 782.97 0.15 0.10 {
44-gar( )
273.15 799.00 0.50 -0.36 42-gei( ) 300.16 777.22 0.20 0.13 {
44-gar( )
293.15 782.60 0.50 -0.27 42-gei1) 300.39 777.02 0.20 0.12 {
44-gar( )
313.15 766.00 0.50 -0.38 42-gei( ) 308.18 770.54 0.20 0.06 {
44-gar( )
293.15 782.80 0.20 -0.07 43-for-1() 293.15 782.97 0.20 0.10 46-ano()
298.15 778.61 0.20 -0.14 43-for-1() 293.15 782.97 0.30 0.10 46-boo/gre( )
273.15 799.00 0.30 -0.36 44-can( ) 293.15 782.83 0.05 -0.04 46-for/gla( )
293.15 782.60 0.30 -0.27 44-can( ) 298.15 778.68 0.05 -0.07 46-for/gla( )
313.15 766.00 0.30 -0.38 44-can( ) 293.15 782.71 0.30 -0.16 60-nat( )
281.94 792.41 0.20 0.30 {
44-gar( ) 293.15 783.70 0.30 0.83 81-sid/koh()
281.29 792.92 0.20 0.28 {
44-gar( ) 313.15 766.98 0.30 0.60 81-sid/koh()
Further references: [22-ski/sch, 32-zel/mar, 36-mar-1, 41-ano-1, 46-gei/can, 49-boo/hen, 54-baz/kop,

64-doe/hau, 65-zhi/ste, 68-akh/yas, 68-man/mue, 68-wip/cle, 75-pav/kla].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 801.96 0.38 293.15 782.87 0.17 310.00 768.98 0.30
280.00 793.71 0.32 298.15 778.75 0.15 320.00 760.73 0.61
290.00 785.47 0.20 300.00 777.22 0.15
Landolt-Brnstein
New Series IV/8D

T = 273.15 to 313.15 K
A 1.06462 103
B -1.22900
C 6.78048 10-4
273.15 779.11 0.30 -0.39 35-mil() 293.15 762.55 0.15 -0.05 {

44-gar( )
293.15 762.62 0.30 0.02 35-mil1) 293.28 763.39 0.20 0.89 {
44-gar( )
298.15 758.50 0.30 0.04 35-mil1) 293.84 762.98 0.20 0.95 {
44-gar( )
273.15 778.50 0.50 -1.00 42-gei( ) 298.65 758.77 0.20 0.72 {
44-gar( )
293.15 762.30 0.50 -0.30 42-gei1) 298.93 758.99 0.20 1.17 44-gar1)
313.15 746.00 0.50 -0.25 42-gei( ) 302.27 755.08 0.20 0.00 {
44-gar( )
293.15 762.49 0.20 -0.11 43-for-1() 302.68 754.72 0.20 -0.02 {
44-gar( )
298.15 758.28 0.20 -0.18 43-for-1() 310.36 748.34 0.20 -0.16 {
44-gar( )
283.71 770.45 0.20 -0.06 44-gar( ){ 293.15 762.52 0.05 -0.08 46-for/gla( )
284.47 769.86 0.20 -0.01 44-gar( ){ 298.15 758.33 0.05 -0.13 46-for/gla( )
291.94 763.59 0.20 -0.02 44-gar( ){ 293.15 762.87 0.30 0.27 81-sid/koh1)
292.25 763.32 0.20 -0.03 44-gar( ){ 313.15 746.21 0.30 -0.04 81-sid/koh()
Further references: [13-gad/sso, 22-ski/sch, 25-eis/gor, 32-zel/mar, 36-mar-1, 41-ano-1, 46-baz/ste, 46-
boo/gre, 46-gei/can, 49-boo/hen, 54-cla/cor, 60-nat, 68-akh/yas, 68-man/mue, 68-wip/cle, 75-pav/kla].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 782.22 0.51 293.15 762.60 0.16 310.00 748.79 0.31
280.00 773.66 0.28 298.15 758.46 0.17 320.00 740.77 0.56
290.00 765.23 0.17 300.00 756.94 0.18
cont.
Landolt-Brnstein
New Series IV/8D
2.4.5 Cycloheptanes and Cyclooctane
Methylcycloheptane [4126-78-7] C8H16 MW = 112.22 92

A 1052.29
B -0.850
K kg m
3
kg m3 K kg m 3
kg m3
293.15 798.1 2.00 -5.01 05-zel 293.15 805.2 1.00 2.09 36-ruz/sei
286.65 808.7 0.80 0.07 30-god/cau 293.15 800.1 2.00 -3.01 46-baz/ste
286.65 808.2 1.50 -0.43 34-god
cont.
Landolt-Brnstein
New Series IV/8D
Methylcycloheptane (cont.)

T exp 2 est
K kg m3
280.00 814.3 3.0
290.00 805.8 2.5
293.15 803.1 2.5
298.15 798.9 3.0
Cyclooctane [292-64-8] C8H16 MW = 112.22 93

Tc = 647.20 K [96-dau]
c = 274.00 kgm-3 [96-dau]
O

T = 288.15 to 520.00 K T = 520.00 to 647.20 K
[c + A(Tc -T ) + B(Tc - T )2 + C(Tc - T )3
+ D(Tc - T )4]
A 9.98119 102 1.44739
B -1.48110 10-5 -3.59047 10-2
C -3.36957 10-3 3.35402 10-4
-6
D 6.56657 10 -1.04712 10-6
-9
E -5.13236 10
293.15 836.20 0.20 0.13 52-kaa/coo() 638.30 422.00 2.00 15.62 72-you( )
293.15 836.10 0.20 0.03 53-ano-1( ){ 288.15 840.05 0.20 -0.01 73-lev( )
293.10 836.70 0.34 0.59 55-kus1) 298.15 832.01 0.20 -0.05 73-lev( )
298.10 832.60 0.35 0.50 55-kus1) 318.15 815.63 0.20 -0.30 73-lev1)
303.10 828.40 0.36 0.31 55-kus1) 302.24 828.95 0.09 0.17 76-mey/hot( )
313.10 820.20 0.38 0.18 55-kus( ) 318.92 815.33 0.10 0.03 76-mey/hot( )
323.10 812.00 0.40 0.09 55-kus( ) 337.71 799.95 0.10 -0.03 76-mey/hot( )
333.10 804.00 0.42 0.25 55-kus1) 349.62 790.20 0.10 0.02 76-mey/hot( )
343.10 795.60 0.44 0.05 55-kus( ) 363.74 778.49 0.10 0.02 76-mey/hot( )
353.10 787.20 0.46 -0.10 55-kus( ) 383.49 761.94 0.12 0.03 76-mey/hot( )
288.15 840.05 0.20 -0.01 70-ewi/lev( ) 401.89 746.23 0.14 -0.00 76-mey/hot( )
298.15 832.01 0.20 -0.05 70-ewi/lev( ) 298.15 832.10 0.20 0.04 79-for/dar()
308.15 823.80 0.20 -0.22 70-ewi/lev( ) 298.15 831.99 0.20 -0.07 81-mar/sym()
568.60 573.00 2.00 7.52 72-you( ) 293.15 836.07 0.20 0.00 84-tan/tak( )
580.10 553.00 2.00 2.86 72-you( ) 298.15 831.98 0.20 -0.08 84-tan/tak( )
601.40 515.00 2.00 -4.91 72-you( ) 303.15 827.90 0.20 -0.15 84-tan/tak( )
613.30 488.00 2.00 -9.19 72-you( )
1) Not included in Fig. 1. cont.
Landolt-Brnstein
New Series IV/8D
Cyclooctane (cont.)
Further references: [07-wil/bru, 07-wil/ver, 10-wil/was, 11-wil/was, 30-god/cau, 30-ruz/sto, 30-zel/fre,
31-ruz/boe, 33-ruz/boe, 47-spi/huf, 50-zie/wil, 65-tre/mit, 65-wat/mcl, 74-jai/nor, 75-ana/gro, 79-wil/far,
81-kiy/ben, 82-gri/phi, 83-wil/ing].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 846.54 0.21 390.00 756.39 0.17 520.00 635.03 6.40
290.00 838.59 0.19 400.00 747.85 0.16 530.00 622.53 6.90
293.15 836.07 0.20 410.00 739.23 0.22 540.00 607.77 7.20
298.15 832.06 0.21 420.00 730.52 0.37 550.00 592.44 7.30
300.00 830.58 0.21 430.00 721.70 0.60 560.00 577.57 7.40
310.00 822.53 0.23 440.00 712.77 0.90 570.00 563.57 7.50
320.00 814.43 0.25 450.00 703.69 1.29 580.00 550.27 7.60
330.00 806.29 0.26 460.00 694.48 1.78 590.00 536.90 7.70
340.00 798.10 0.26 470.00 685.09 2.38 600.00 522.18 7.78
350.00 789.87 0.25 480.00 675.53 3.11 610.00 504.23 7.86
360.00 781.58 0.24 490.00 665.76 3.97 620.00 480.48 7.90
370.00 773.25 0.22 500.00 655.77 5.00 630.00 447.06 8.10
380.00 764.85 0.20 510.00 645.53 5.80 640.00 395.47 8.60
Landolt-Brnstein
New Series IV/8D

2.5.1 Cyclopropanes - Cyclobutanes
1-Butyl-1-ethylcyclopropane [66688-70-8] C9H18 MW = 126.24 94

T exp 2 est Ref.
3
K kg m
293.15 755.9 0.60 48-sho/cra
1,2-Diethyl-1,2-dimethylcyclopropane [500011-35-8] C9H18 MW = 126.24 95

T exp 2 est Ref.
3
K kg m
293.15 759.5 0.70 52-lev/gla
1,1-Dimethyl-2-(2-methylpropyl) [500030-55-7] C9H18 MW = 126.24 96

cyclopropane

A 954.59
B -0.805

K kg m3 kg m3
293.15 718.6 1.50 0.00 13-kis-5

273.15 734.7 1.50 0.00 13-kis-5

T exp 2 est
K kg m3
270.00 737.2 3.0
280.00 729.2 2.0
290.00 721.1 2.0
293.15 718.6 2.0
298.15 714.6 3.0
Landolt-Brnstein
New Series IV/8D
Hexamethylcyclopropane [2570-81-2] C9H18 MW = 126.24 97

T exp 2 est Ref.
3
K kg m
293.15 768.3 0.40 55-kel/gre
(1-Methylpentyl)cyclopropane [6976-28-9] C9H18 MW = 126.24 98

T exp 2 est Ref.
3
K kg m
293.15 754.2 0.20 52-sla/wis-1
(1-Ethylpropyl)cyclobutane [500025-81-0] C9H18 MW = 126.24 99

T exp 2 est Ref.
K kg m3
292.15 794.5 6.00 05-kis/amo
293.15 781.5 0.80 57-kaz/luk
2.5.2 Cyclopentanes
Butylcyclopentane [2040-95-1] C 9H18 MW = 126.24 100

T = 288.10 to 313.15 K
A 1.01768 103
B -7.95859 10-1
cont.
Landolt-Brnstein
New Series IV/8D
Butylcyclopentane (cont.)
K kg m 3
kg m3 in Fig. 1)
288.15 788.70 0.60 0.34 27-cha( ) 293.15 783.20 0.70 -1.18 39-gro/wac( )
293.35 784.80 0.60 0.58 27-cha( ) 293.15 783.20 0.60 -1.18 39-pin/ipa( )
288.10 788.70 0.60 0.30 27-cha/bec( ) 313.15 768.70 0.60 0.24 39-pin/ipa( )
293.35 784.80 0.60 0.58 27-cha/bec( ) 293.15 784.00 0.50 -0.38 45-cra/boo()
288.15 788.60 0.50 0.24 32-gar/eva( ) 293.15 784.60 0.30 0.22 47-boo/gre( )
293.15 784.70 0.50 0.32 32-gar/eva( ) 293.15 784.60 0.30 0.22 47-boo/gre( )
289.15 786.20 1.00 -1.36 36-kaz/pla( ) 293.15 784.60 0.40 0.22 49-boo/hen( ) {
288.15 788.60 0.40 0.24 38-eva() 293.15 784.40 0.50 0.02 49-foe/fen()
293.15 784.70 0.40 0.32 38-eva() 293.15 784.60 0.50 0.22 50-chi/fie-1( )
Further references: [27-bau, 39-tur/kos, 46-baz/ste, 57-pla/sta, 57-shu/che].
cont.
Landolt-Brnstein
New Series IV/8D
Butylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 794.84 1.00 298.15 780.40 0.44 310.00 770.97 0.44
290.00 786.88 1.07 300.00 778.93 0.44 320.00 763.01 4.20
293.15 784.38 0.51
1,1-Diethylcyclopentane [2721-38-2] C9H18 MW = 126.24 101

T exp 2 est Ref.
K kg m3
293.15 802.7 0.60 11-kis
cis-1,2-Diethylcyclopentane [932-39-8] C9H18 MW = 126.24 102

A 1030.24
B -0.800

K kg m3
kg m3
293.15 795.1 1.00 -0.62 11-kis

293.15 796.0 1.00 0.25 33-chi
273.15 811.6 1.00 -0.07 33-chi
293.15 796.0 0.60 0.25 44-chi
273.15 811.6 0.60 -0.09 44-chi

T exp 2 est
K kg m3
270.00 814.2 0.7
280.00 806.2 0.5
290.00 798.2 0.5
293.15 795.7 0.5
298.15 791.7 0.7
Landolt-Brnstein
New Series IV/8D
trans-1,2-Diethylcyclopentane [932-40-1] C9H18 MW = 126.24 103

A 1011.41
B -0.780

K kg m3 kg m3
293.15 783.2 1.00 0.41 33-chi

273.15 798.6 1.00 0.21 33-chi
293.15 783.1 1.00 0.39 35-chi
293.15 781.7 1.00 -1.05 44-boo/per
293.15 783.2 0.60 0.41 44-chi
273.15 798.6 0.60 0.21 44-chi
293.15 781.7 0.80 -1.05 44-gre/per

T exp 2 est
K kg m3
270.00 800.8 0.8
280.00 793.0 0.9
290.00 785.2 0.6
293.15 782.8 0.6
298.15 778.9 0.8
1,3-Diethylcyclopentane [19398-75-5] C9H18 MW = 126.24 104

T exp 2 est Ref.
K kg m3
293.15 785.0 6.00 05-kis-1
(1,1-Dimethylethyl)cyclopentane [3875-52-3] C9H18 MW = 126.24 105

A 1022.41
B -0.790
cont.
Landolt-Brnstein
New Series IV/8D
(1,1-Dimethylethyl)cyclopentane (cont.)
K kg m3
kg m3 K kg m 3
kg m3
293.15 791.1 0.60 0.28 39-gro/wac 293.15 790.9 0.30 0.08 44-boo/per
293.15 791.1 0.60 0.28 39-pin/ipa 293.15 789.4 0.50 -1.42 45-cra/boo
313.15 775.3 0.60 0.28 39-pin/ipa 293.15 790.9 0.40 0.08 45-per
293.15 791.1 0.50 0.28 39-pin/ipa-1 293.15 790.8 0.30 -0.02 46-boo/gre
313.15 775.3 0.50 0.28 39-pin/ipa-1 293.15 790.8 0.40 -0.02 47-ano-4

T exp 2 est
K kg m3
290.00 793.3 0.5
293.15 790.8 0.4
298.15 786.9 0.4
300.00 785.4 0.5
310.00 777.5 0.6
320.00 769.6 1.0
r-1-Ethyl-c-2, t-4-dimethylcyclopentane [2532-62-9] C9H18 MW = 126.24 106

T exp 2 est Ref.
3
K kg m
293.15 779.5 0.60 54-baz/kop
r-1-Ethyl-t-2, c-4-dimethylcyclopentane [2532-61-8] C9H18 MW = 126.24 107

T exp 2 est Ref.
3
K kg m
293.15 763.7 0.30 54-baz/kop
r-1-Ethyl-t-2, t-3-dimethylcyclopentane [18469-76-6] C9H18 MW = 126.24 108

T exp 2 est Ref.
K kg m3
293.15 763.7 1.00 54-baz/kop
Landolt-Brnstein
New Series IV/8D
1-Methyl-2-(1-methylethyl)cyclopentane [89223-57-4] C9H18 MW = 126.24 109

A 1019.48
B -0.820

K kg m3 kg m3
293.15 779.1 4.00 0.00 12-kis-1

288.15 783.2 4.00 0.00 12-kis-1

T exp 2 est
K kg m3
280.00 789.9 5.0
290.00 781.7 4.0
293.15 779.1 4.0
298.15 775.0 5.0
300.00 773.5 5.0
1-Methyl-3-(1-methylethyl)cyclopentane [53771-88-3] C9H18 MW = 126.24 110

A 1009.31
B -0.800

K kg m3 kg m3
288.35 779.9 5.00 1.27 11-eyk-1

293.15 779.2 6.00 4.41 12-kis-1
295.15 773.0 5.00 -0.19 12-wal/mey
292.15 773.0 5.00 -2.59 13-god/tab-1
291.65 775.0 4.00 -0.99 29-kaz
cont.
Landolt-Brnstein
New Series IV/8D
1-Methyl-3-(1-methylethyl)cyclopentane (cont.)

T exp 2 est
K kg m3
280.00 785.3 6.0
290.00 777.3 5.0
293.15 774.8 4.0
298.15 770.8 5.0
300.00 769.3 5.0
(1-Methylpropyl)cyclopentane [4850-32-2] C9H18 MW = 126.24 111

T = 273.15 to 313.15 K
A 1.02780 103
B -7.95659 10-1
K 3
kg m3 in Fig. 1)
273.15 810.00 2.00 -0.47 13-wil/hei( ) 293.15 794.10 0.60 -0.46 39-pin/ipa()
273.15 810.00 1.00 -0.47 13-wil/kin( ) 313.15 778.70 0.60 0.06 39-pin/ipa()
291.15 797.10 1.00 0.95 36-kaz( ) 293.15 793.40 0.50 -1.16 {
45-cra/boo( )
291.15 797.10 1.00 0.95 36-kaz/pla( ) 293.15 794.70 0.40 0.14
48-ano-6( )
291.15 797.10 0.70 0.95 36-kaz/pla-1( ) 293.15 794.50 0.50 -0.06 49-foe/fen()
293.15 794.10 0.60 -0.46 39-gro/wac()
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit
K kg m3 K kg m3
270.00 812.98 0.65 293.15 794.56 0.52 310.00 781.15 0.80
280.00 805.02 2.30 298.15 790.58 0.50 320.00 773.19 3.50
290.00 797.06 1.12 300.00 789.11 0.60
cont.
Landolt-Brnstein
New Series IV/8D
(1-Methylpropyl)cyclopentane (cont.)
(2-Methylpropyl)cyclopentane [3788-32-7] C9H18 MW = 126.24 112

T exp 2 est Ref.
K kg m3
293.15 779.5 1.00 25-eis-1
293.15 779.5 2.00 25-eis/gor
293.15 780.6 0.60 39-gro/wac
293.15 780.9 0.20 44-boo/per
293.15 780.9 0.40 44-gre
293.15 780.7 0.50 45-cra/boo
293.15 780.8 0.30 Recommended
Landolt-Brnstein
New Series IV/8D
1-Methyl-1-propylcyclopentane [16631-63-3] C9H18 MW = 126.24 113

T exp 2 est Ref.
3
K kg m
293.15 785.1 4.00 57-nov/khr
cis-1-Methyl-2-propylcyclopentane [932-43-4] C9H18 MW = 126.24 114

A 1023.64
B -0.790

K kg m3 kg m3
293.15 792.1 2.00 0.04 34-chi

273.15 807.8 2.00 -0.05 34-chi
293.15 792.1 0.50 0.04 44-chi
273.15 807.8 0.50 -0.05 44-chi

T exp 2 est
K kg m3
270.00 810.3 0.5
280.00 802.4 0.6
290.00 794.5 0.5
293.15 792.1 0.5
298.15 788.1 0.6
trans-1-Methyl-2-propylcyclopentane [932-44-5] C9H18 MW = 126.24 115

A 1009.04
B -0.790
cont.
Landolt-Brnstein
New Series IV/8D
trans-1-Methyl-2-propylcyclopentane (cont.)

K kg m 3
kg m3
293.15 777.4 1.00 -0.05 26-cha-3

293.15 777.4 2.00 -0.04 34-chi
273.15 793.3 2.00 0.01 34-chi
293.15 777.4 2.00 -0.05 35-chi
293.15 777.5 0.60 0.01 44-chi
273.15 793.3 0.60 0.01 44-chi

T exp 2 est
K kg m3
270.00 795.7 0.6
280.00 787.8 0.7
290.00 779.9 0.6
293.15 777.4 0.6
298.15 773.5 0.7
cis-1-Methyl-3-propylcyclopentane [2443-04-1] C9H18 MW = 126.24 116

T exp 2 est Ref.
3
K kg m
293.15 771.7 2.00 33-lov/cam
293.15 771.5 2.00 49-baz/ukh
293.15 771.5 1.00 50-kaz/kop
293.15 771.5 1.00 Recommended
1,1,2,3-Tetramethylcyclopentane [102653-33-8] C9H18 MW = 126.24 117

T exp 2 est Ref.
K kg m3
287.25 782.0 5.00 06-eyk-1
Landolt-Brnstein
New Series IV/8D
cis-1,1,2,3-Tetramethylcyclopentane [62016-69-7] C9H18 MW = 126.24 118

A 999.92
B -0.800

K kg m3 kg m3
287.25 782.0 2.00 11.88 06-eyk-1

273.15 779.5 0.80 -1.90 19-eyk

T exp 2 est
K kg m3
270.00 783.9 1.0
280.00 775.9 3.0
290.00 767.9 6.0
293.15 765.4 8.0

T exp 2 est Ref.
3
K kg m
293.15 764.8 3.00 63-lev/sha

T exp 2 est Ref.
K kg m3
293.15 764.6 0.80 56-ano
trans-1,1,2,4-Tetramethylcyclopentane [62016-72-2] C9H18 MW = 126.24 121

T exp 2 est Ref.
3
K kg m
293.15 764.8 0.80 51-ano-3
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 750.9 0.40 48-ano-3
293.15 750.9 0.40 49-ano-1
293.15 750.9 0.40 51-slo
293.15 750.9 0.40 Recommended

T exp 2 est Ref.
K kg m3
293.15 767.0 0.40 51-ano-3
trans-1,1,3,4-Tetramethylcyclopentane [20309-77-7] C9H18 MW = 126.24 124

T exp 2 est Ref.
K kg m3
293.15 748.9 0.40 51-ano-3
r-1, c-2, c-3, c-4- [2532-65-2] C9H18 MW = 126.24 125

Tetramethylcyclopentane

T exp 2 est Ref.
3
K kg m
293.15 792.4 0.30 61-mil/gre
293.15 792.4 0.30 63-ano-3
r-1, c-2, c-3, t-4- [2532-69-6] C9H18 MW = 126.24 126


T exp 2 est Ref.
K kg m3
293.15 776.3 0.40 61-mil/gre
293.15 776.3 0.40 63-ano-3
Landolt-Brnstein
New Series IV/8D
r-1, c-2, t-3, c-4- [2532-68-5] C9H18 MW = 126.24 127


T exp 2 est Ref.
3
K kg m
293.15 766.9 0.30 61-mil/gre
293.15 766.9 0.30 63-ano-3
r-1, t-2, t-3, c-4- [19907-40-5] C9H18 MW = 126.24 128


T exp 2 est Ref.
3
K kg m
293.15 756.2 0.30 61-mil/gre
293.15 756.2 0.30 63-ano-3
2.5.3 Cyclohexanes
1-Ethyl-1-methylcyclohexane [4926-90-3] C9H18 MW = 126.24 129

T exp 2 est Ref.
3
K kg m
293.15 806.2 0.20 53-ano-1
293.15 806.2 0.20 55-ano-8
293.15 806.5 0.40 55-pin/mar
293.15 806.1 1.00 55-pin/mar
293.15 805.3 1.00 66-khr/koc
298.15 805.0 2.00 70-goo-31)
293.15 806.2 0.20 Recommended
1)

T exp 2 est Ref.
3
K kg m
293.15 803.6 4.00 33-sig/cra
Landolt-Brnstein
New Series IV/8D
cis-1-Ethyl-2-methylcyclohexane [4923-77-7] C9H18 MW = 126.24 131

A 1044.16
B -0.800

K kg m3 kg m3
293.15 809.4 0.40 -0.24 54-bir/dea-1

298.15 805.6 0.40 -0.04 54-bir/dea-1
293.15 809.7 0.20 0.06 58-ano-6
293.15 809.7 0.40 0.06 63-ano-3
298.15 809.0 2.00 3.36 70-goo-31)
1)

T exp 2 est
K kg m3
290.00 812.2 0.5
293.15 809.6 0.4
298.15 805.6 0.5
300.00 804.2 0.6
trans-1-Ethyl-2-methylcyclohexane [4923-78-8] C9H18 MW = 126.24 132

A 1033.03
B -0.800

K kg m 3
kg m3
293.15 797.2 1.00 -1.31 54-bir/dea-1

298.15 793.4 1.00 -1.11 54-bir/dea-1
293.15 798.9 0.40 0.39 58-ano-6
298.15 796.0 2.00 1.49 70-goo-31)
1)
cont.
Landolt-Brnstein
New Series IV/8D
trans-1-Ethyl-2-methylcyclohexane (cont.)

T exp 2 est
K kg m3
290.00 801.0 1.0
293.15 798.5 0.7
298.15 794.5 0.7
300.00 793.0 0.8

T exp 2 est Ref.
K kg m3
290.15 789.6 4.00 02-zel-1

accepted points. Deviation = 0.387.
A 1051.49
B -0.900

K kg m3
kg m3
293.15 788.7 2.00 1.04 33-sig/cra

298.15 783.0 1.00 -0.16 38-mou/gra-1
298.15 783.0 1.00 -0.16 39-mou/pau
298.15 783.0 1.00 -0.16 46-mou
293.15 783.7 3.00 -3.96 63-ano-31)
298.15 784.0 2.00 0.84 70-goo-3
1)

T exp 2 est
K kg m3
290.00 790.5 1.5
293.15 787.7 1.0
298.15 783.2 1.5
300.00 781.5 2.0
Landolt-Brnstein
New Series IV/8D

accepted points. Deviation = 4.831.
A 1047.48
B -0.850

K kg m3 kg m3
298.15 786.0 2.00 -8.05 38-mou/gra-1

298.15 786.0 1.00 -8.05 39-mou/pau
298.15 786.0 1.00 -8.05 46-mou
293.15 801.2 0.40 2.90 63-ano-3

T exp 2 est
K kg m3
290.00 801.0 4.8
293.15 798.3 4.8
298.15 794.1 4.8
300.00 792.5 5.0

accepted point. Deviation = 0.000.
A 1047.73
B -0.900

K kg m 3
kg m3
273.15 804.1 2.00 2.20 01-sab/sen1)

288.15 788.4 1.00 0.00 06-sab/mai
293.15 789.7 2.00 5.80 33-sig/cra1)
1)
cont.
Landolt-Brnstein
New Series IV/8D
1-Ethyl-4-methylcyclohexane (cont.)

T exp 2 est
K kg m3
280.00 795.7 4.0
290.00 786.7 4.0
293.15 783.9 5.0

T exp 2 est Ref.
K kg m3
293.15 789.7 2.00 33-sig/cra1)
293.15 796.9 0.80 55-kaz/lib
293.15 795.6 0.40 63-ano-3
298.15 795.0 2.00 70-goo-31)
293.15 795.9 0.40 Recommended
1)

T exp 2 est Ref.
3
K kg m
293.15 779.4 0.40 63-ano-3
298.15 778.0 2.00 70-goo-3
(1-Methylethyl)cyclohexane [696-29-7] C9H18 MW = 126.24 139

T = 273.15 to 323.15 K
A 1.02537 103
B -7.61832 10-1
cont.
Landolt-Brnstein
New Series IV/8D
(1-Methylethyl)cyclohexane (cont.)
284.15 809.00 1.00 0.10 29-str-1( ) 293.15 802.06 0.20 0.02 44-gar( ){
293.15 802.30 0.30 0.26 39-wib/hoo() 293.15 802.06 0.20 0.02 46-ano()
298.15 798.38 0.30 0.15 39-wib/hoo() 273.15 817.00 1.50 -0.28 46-gei/can( )
293.15 801.60 0.30 -0.44 41-ano-1() 293.15 803.00 1.50 0.96 46-gei/can1)
273.15 816.60 0.40 -0.68 44-can( ) 313.15 786.00 1.50 -0.81 46-gei/can1)
293.15 802.60 0.40 0.56 44-can( ) 293.15 802.19 0.10 0.15 49-for/ros( )
313.15 786.20 0.40 -0.61 44-can( ) 298.15 798.31 0.10 0.08 49-for/ros( )
303.15 794.76 0.40 0.33 44-gar/( )2) 303.15 794.42 0.10 -0.01 49-for/ros( )
313.15 786.88 0.40 0.07 44-gar/( )2) 293.15 801.80 0.50 -0.24 50-chi/fie-1( )
323.15 779.07 0.40 -0.12 44-gar/( )2) 293.15 802.70 0.50 0.66 54-khr/nov( )
2)
Calculated from equation given by author
Further references: [25-eis/gor, 33-sig/cra, 45-gre/vog, 47-nam/vol, 49-vve/tak, 54-chi/maq, 54-eve/bor,

55-bal/tur, 56-tur/kra].
cont.
Landolt-Brnstein
New Series IV/8D
(1-Methylethyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 819.68 1.18 293.15 802.04 0.35 310.00 789.21 0.28
280.00 812.06 0.73 298.15 798.23 0.28 320.00 781.59 0.44
290.00 804.44 0.42 300.00 796.82 0.26 330.00 773.97 0.74
Propylcyclohexane [1678-92-8] C9H18 MW = 126.24 140

T = 273.15 to 313.15 K
A 1.07063 103
B -1.10742
C 5.52915 10-4
K kg m
3
kg m3 in Fig. 1)
273.15 809.10 1.00 -0.29 01-sab/sen( ) 300.82 787.68 0.20 0.15 44-gar()
293.15 793.48 0.20 -0.03 43-for-1() 301.19 787.38 0.20 0.14 44-gar()
298.15 789.56 0.20 -0.04 43-for-1() 309.65 780.76 0.20 0.03 44-gar()
273.15 808.50 0.30 -0.89 44-can1) 310.35 780.21 0.20 0.01 44-gar()
293.15 793.00 0.30 -0.51 44-can1) 293.15 793.47 0.05 -0.04
46-for/gla( )
313.15 777.70 0.30 -0.36 44-can( ) 298.15 789.58 0.05 -0.02
46-for/gla( )
280.88 803.23 0.20 0.03 44-gar() 293.15 793.58 0.15 0.07 {
49-for/ros( )
281.32 802.88 0.20 0.03 44-gar() 298.15 789.75 0.15 0.15 {
49-for/ros( )
289.61 796.37 0.20 0.08 44-gar() 303.15 785.79 0.15 0.06 {
49-for/ros( )
289.97 796.10 0.20 0.10 44-gar() 293.15 793.27 0.20 -0.24 50-chi/fie-1( )
293.15 793.54 0.20 0.03 44-gar() 298.15 789.74 0.20 0.14 94-del/fer()
Further references: [1899-kur, 01-kur-2, 01-sab/sen-1, 25-eis/gor, 27-bou, 29-str-1, 32-gar/eva, 33-
sig/cra, 34-lev/tzu, 37-loz/dya, 38-eva, 41-ano-1, 46-ano, 46-boo/gre, 46-gei/can, 46-gre-1, 48-fie/ber-2,
54-chi/maq, 54-khr/nov, 56-tur/kra, 60-ale/ste, 91-ric/lau].
cont.
Landolt-Brnstein
New Series IV/8D
Propylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 811.93 1.32 293.15 793.51 0.13 310.00 780.47 0.26
280.00 803.90 0.39 298.15 789.60 0.17 320.00 772.87 0.20
290.00 795.98 0.13 300.00 788.17 0.19
Landolt-Brnstein
New Series IV/8D
1,1,2-Trimethylcyclohexane [7094-26-0] C9H18 MW = 126.24 141

T exp 2 est Ref.
3
K kg m
293.15 798.7 0.50 47-ano-2
293.15 798.6 0.80 48-sho/cra
293.15 798.7 0.50 49-eva
293.15 798.6 0.20 56-ano
293.15 798.6 0.20 Recommended

T = 273.15 to 313.15 K
A 9.04924 102
B -9.18282 10-2
C -1.15476 10-3
K 3
kg m3 in Fig. 1)
293.15 779.20 0.30 0.43 41-ano-1() 293.15 778.00 1.50 -0.77 46-gei/can1)
273.15 793.90 0.60 0.22 44-can( ) 313.15 763.00 1.50 0.07 46-gei/can( )
293.15 778.30 0.60 -0.47 44-can( ) 293.15 778.30 0.60 -0.47 46-ipa/pin( )
313.15 762.90 0.60 -0.03 44-can( ) 293.15 778.81 0.15 0.04
49-for/ros( )
293.15 778.67 0.20 -0.10 {
44-gar( ) 298.15 774.95 0.15 0.06
49-for/ros( )
293.15 778.67 0.20 -0.10 46-ano() 303.15 770.98 0.15 0.02
49-for/ros( )
273.15 794.00 1.50 0.32 46-gei/can( ) 293.15 778.78 0.40 0.01 50-chi/fie-1()
Further references: [1897-kno/fis, 20-von-2, 54-lev/shu].
cont.
Landolt-Brnstein
New Series IV/8D
1,1,3-Trimethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 795.95 0.96 293.15 778.77 0.26 310.00 765.48 0.64
280.00 788.68 1.04 298.15 774.89 0.15 320.00 757.29 2.74
290.00 781.18 0.40 300.00 773.45 0.15
Landolt-Brnstein
New Series IV/8D

A 991.56
B -0.750

K kg m3 kg m3
293.15 772.2 1.00 0.50 51-chi/maq

273.15 786.2 1.00 -0.50 51-chi/maq

T exp 2 est
K kg m3
270.00 789.1 1.2
280.00 781.6 1.2
290.00 774.1 0.8
293.15 771.7 0.7
298.15 768.0 0.9

T exp 2 est Ref.
3
K kg m
293.15 793.0 8.00 25-eis/gor
293.15 792.0 6.00 50-chi/fie-1
r-1, c-2, c-3-Trimethylcyclohexane [1839-88-9] C9H18 MW = 126.24 145

T exp 2 est Ref.
K kg m3
293.15 802.1 0.50 56-bus/gre
293.15 802.7 0.40 61-ano-9
293.15 802.7 0.60 62-mah/gre
Landolt-Brnstein
New Series IV/8D
r-1, c-2, t-3-Trimethylcyclohexane [7667-55-2] C9H18 MW = 126.24 146

3 3
K kg m K kg m
293.15 802.9 0.40 56-ano 293.15 803.0 0.25 62-ano-3
293.15 802.9 0.40 56-bus/gre 293.15 803.1 0.60 62-mah/gre
293.15 803.1 0.40 61-ano-9 293.15 803.0 0.30 Recommended
293.15 803.1 0.50 61-ano-9
r-1, t-2, c-3-Trimethylcyclohexane [1678-81-5] C9H18 MW = 126.24 147

T exp 2 est Ref.
K kg m3
293.15 787.0 0.40 56-bus/gre
293.15 787.0 0.60 62-mah/gre

weighted), c,uw = 1.6500 (combined temperature
ranges, unweighted).
T = 273.15 to 298.15 K
A 1.04297 103
B -8.95135 10-1
K 3
kg m3 in Fig. 1)
293.15 780.80 6.00 0.23 1883-mar/ogl( ) 293.15 778.00 4.00 -2.57 20-von-2( )
273.15 783.30 6.00 -15.17 1894-gue( ) 293.15 781.30 4.00 0.73 25-eis-1( )
291.15 780.70 6.00 -1.66 1896-zel/ref( ) 293.15 785.00 5.00 4.43 25-eis/gor( )
273.15 805.20 4.00 6.73 01-sab/sen( ) 286.65 798.10 4.00 11.72 30-god/cau()
289.75 785.00 5.00 1.39 11-eyk-1( ) 293.15 772.00 3.00 -8.57 39-whi/gla()
289.85 784.80 5.00 1.28 11-eyk-1( ) 293.15 782.50 3.00 1.93 50-chi/fie-1( )
293.15 778.00 4.00 -2.57 13-gad/sso() 298.15 781.60 3.00 5.51 95-pet/gas( ) {
290.05 779.90 4.00 -3.44 20-von-2( )
cont.
Landolt-Brnstein
New Series IV/8D
1,2,4-Trimethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 801.29 7.10 293.15 780.57 4.58 300.00 774.43 4.00
280.00 792.34 5.58 298.15 776.09 4.00 310.00 765.48 5.56
290.00 783.39 4.88
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
K kg m3
293.15 790.0 2.00 22-ski/sch
293.15 785.0 2.00 25-eis-1
293.15 791.4 0.50 56-ano-19
293.15 791.0 0.60 Recommended

T exp 2 est Ref.
3
K kg m
293.15 786.0 2.00 22-ski/sch
293.15 782.8 0.50 56-ano-19
293.15 790.8 0.40 61-ano-9
293.15 787.6 2.50 Recommended
r-1, t-2, c-4-Trimethylcyclohexane [7667-59-6] C9H18 MW = 126.24 151

T exp 2 est Ref.
K kg m3
293.15 773.8 0.60 54-ano-13
293.15 774.5 0.50 56-ano-19
293.15 774.2 0.50 Recommended
r-1, t-2, t-4-Trimethylcyclohexane [7667-60-9] C9H18 MW = 126.24 152

T exp 2 est Ref.
3
K kg m
293.15 774.0 2.00 22-ski/sch1)
293.15 772.0 2.00 39-whi/gla1)
283.15 788.4 0.50 56-ano-19
293.15 790.8 0.40 61-ano-9
293.15 790.6 0.40 62-ano-3
293.15 790.1 1.00 Recommended
1)
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
K kg m3
291.15 780.7 2.00 1896-zel/ref
290.05 779.9 3.00 20-von-2

K kg m3 K kg m3
273.15 788.4 4.00 01-sab/sen 293.15 775.7 6.00 33-sig/cra
288.85 774.4 6.00 11-eyk 293.15 771.1 4.00 37-loz/dya
293.15 759.0 4.00 15-pic/bou 293.15 773.8 4.00 55-bal/tur
293.15 772.0 5.00 20-von-2 293.15 772.2 4.00 56-tur/kra
286.25 777.7 4.00 20-von-2

T = 273.15 to 303.15 K
A 9.94516 102
B -7.31800 10-1
K 3
kg m3 in Fig. 1)
293.15 781.70 0.60 1.71 49-ano-2() 293.15 778.85 0.70 -1.14 51-chi()
293.15 778.85 1.00 -1.14 50-chi/fie-1() 303.15 771.08 0.70 -1.59 51-chi()
273.15 794.38 0.70 -0.25 51-chi() 293.15 781.60 0.60 1.61 {
54-ano-5( )
288.15 782.73 0.70 -0.92 51-chi() 293.15 781.70 0.50 1.71 56-ano( )
Further references: [25-eis/gor, 49-ano-2].
cont.
Landolt-Brnstein
New Series IV/8D
r-1, c-3, t-5-Trimethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 796.93 0.96 293.15 779.99 0.69 300.00 774.98 0.74
280.00 789.61 0.78 298.15 776.33 0.72 310.00 767.66 0.90
290.00 782.29 0.69
Landolt-Brnstein
New Series IV/8D

T = 273.15 to 303.15 K
A 1.00232 103
B -7.92266 10-1
K kg m
3
kg m3 in Fig. 1)
293.15 770.00 0.60 -0.06 46-baz/ste() 293.15 770.48 0.70 0.42 51-chi( )
293.15 769.70 0.40 -0.36 49-ano-2( ) 303.15 762.73 0.70 0.59 51-chi( )
293.15 770.48 0.80 0.42 50-chi/fie-1( ) 293.15 769.90 0.50 -0.16 56-ano()
273.15 785.98 0.70 0.07 51-chi( ) 293.15 769.50 0.60 -0.56 56-ano-6()
288.15 774.36 0.70 0.33 51-chi( ) 293.15 769.40 0.50 -0.66 56-lib/pry-2( ){
Further references: [25-eis-1, 25-eis/gor].
cont.
Landolt-Brnstein
New Series IV/8D
r-1, c-3, c-5-Trimethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 788.41 0.83 293.15 770.06 0.59 300.00 764.64 0.64
280.00 780.48 0.92 298.15 766.10 0.59 310.00 756.71 1.45
290.00 772.56 0.66
2.5.4 Cycloheptanes - Cyclononane
Ethylcycloheptane [13151-55-8] C 9H18 MW = 126.24 157

A 1035.14
B -0.750

K kg m3 kg m3
273.15 829.8 1.00 -0.48 02-mar/jak

293.15 815.1 1.00 -0.18 02-mar/jak
273.15 829.8 1.00 -0.48 03-mar-1
293.15 815.2 1.00 -0.08 03-mar-1
293.15 814.8 1.00 -0.48 46-baz/ste
293.15 815.7 0.50 0.42 56-ano

T exp 2 est
K kg m3
270.00 832.6 1.0
280.00 825.1 0.6
290.00 817.6 0.4
293.15 815.3 0.5
298.15 811.5 0.6
Landolt-Brnstein
New Series IV/8D
Methylcyclooctane [1502-38-1] C9H18 MW = 126.24 158

A 1053.21
B -0.750

K kg m3 kg m3
286.65 840.5 0.80 2.28 30-god/cau

293.15 834.9 1.00 1.55 34-god
286.65 839.9 1.00 1.68 34-god
298.15 822.8 1.00 -6.80 52-cop/cam

T exp 2 est
K kg m3
280.00 843.2 3.7
290.00 835.7 3.6
293.15 833.3 3.6
298.15 829.6 3.6
Cyclononane [293-55-0] C9H18 MW = 126.24 159

T exp 2 est Ref.
K kg m3
289.15 773.3 30.00 07-zel

273.15 785.0 30.00 07-zel
293.15 850.2 0.20 52-kaa/coo

1,1-Dimethyl-2-(1,1-dimethylpropyl) [500028-22-8] C10H20 MW = 140.27 160

cyclopropane

T exp 2 est Ref.
K kg m3
293.15 761.9 2.00 65-lev/kos
Landolt-Brnstein
New Series IV/8D
1,1-Dimethyl-2-(1,1,2-trimethylpropyl) [500023-51-8] C10H20 MW = 40.27 161

cyclopropane

T exp 2 est Ref.
3
K kg m
293.15 784.7 1.00 65-lev/kos
1-Methyl-1,2-dipropylcyclopropane [99976-16-6] C10H20 MW = 140.27 162

T exp 2 est Ref.
3
K kg m
293.15 762.1 1.00 56-gra/kos
1-(1-Methylethyl)-2-(2-methylpropyl) [99976-15-5] C10H20 MW = 140.27 163

cyclopropane

T exp 2 est Ref.
K kg m3
293.15 750.8 2.00 56-gra/kos
1-Methyl-1-(4-methylpentyl) [500025-70-7] C10H20 MW = 140.27 164

cyclopropane

T exp 2 est Ref.
K kg m3
293.15 754.4 0.80 57-kaz/luk-1
1,2-bis(1-Methylethyl)cyclobutane [3642-15-7] C10H20 MW = 140.27 165

A 995.16
B -0.750

K kg m 3
kg m3
293.15 775.5 4.00 0.20 11-leb

273.15 790.1 4.00 -0.20 11-leb
cont.
Landolt-Brnstein
New Series IV/8D
1,2-bis(1-Methylethyl)cyclobutane (cont.)

T exp 2 est
K kg m3
270.00 792.7 4.0
280.00 785.2 4.0
290.00 777.7 4.0
293.15 775.3 4.0
298.15 771.6 5.0
1,1,2-Trimethyl-3-(1-methylethyl) [500030-18-2] C10H20 MW = 140.27 166

cyclobutane

A 973.80
B -0.730

K kg m3
kg m3
293.15 759.8 4.00 0.00 11-leb

273.15 774.4 4.00 0.00 11-leb

T exp 2 est
K kg m3
270.00 776.7 4.0
280.00 769.4 4.0
290.00 762.1 4.0
293.15 759.8 4.0
298.15 756.1 5.0
2.6.2 Cyclopentanes
cis-1-Butyl-2-methylcyclopentane [20556-39-2] C10H20 MW = 140.27 167

T exp 2 est Ref.
K kg m3
293.15 798.0 0.80 56-baz/sok
Landolt-Brnstein
New Series IV/8D
trans-1-Butyl-2-methylcyclopentane [53366-35-1] C10H20 MW = 140.27 168

T exp 2 est Ref.
3
K kg m
293.15 784.7 0.80 56-baz/sok
(1-Ethylpropyl)cyclopentane [700001-38-3] C10H20 MW = 140.27 169

A 1043.13
B -0.800

K kg m 3
kg m3
292.15 811.6 1.00 2.19 36-kaz/pla-1

293.15 809.9 0.80 1.29 39-gro/wac
293.15 807.1 0.60 -1.51 39-pin/ipa

T exp 2 est
K kg m3
290.00 811.1 2.5
293.15 808.6 2.0
298.15 804.6 3.0
4-Ethyl-1,1,2-trimethylcyclopentane [91351-91-6] C10H20 MW = 140.27 170

T exp 2 est Ref.
K kg m3
293.15 778.2 2.00 63-lev/sha
1-Butyl-3-methylcyclopentane [500030-24-0] C10H20 MW = 140.27 171

T exp 2 est Ref.
K kg m3
288.15 784.0 4.00 30-cha/mil
Landolt-Brnstein
New Series IV/8D
1,1-Dimethyl-2-(1-methylethyl) [500025-87-6] C10H20 MW = 140.27 172

cyclopentane

T exp 2 est Ref.
3
K kg m
298.15 795.9 0.80 49-ste/spa

cyclopentane

A 1022.63
B -0.800

K 3
kg m kg m3
289.15 786.0 3.00 -5.31 13-god/tab-1

288.15 793.0 2.00 0.89 21-god
294.15 788.0 2.00 0.69 29-kaz
288.15 792.9 2.00 0.79 31-ric/wol

T exp 2 est
K kg m3
280.00 798.6 2.5
290.00 790.6 2.5
293.15 788.1 2.5
298.15 784.1 3.0
r-1, t-2-Dimethyl-c-3-(1-methylethyl) [36208-14-7] C10H20 MW = 140.27 174

cyclopentane

A 1022.69
B -0.800
cont.
Landolt-Brnstein
New Series IV/8D
r-1, t-2-Dimethyl-c-3-(1-methylethyl)cyclopentane (cont.)

K kg m 3
kg m3
294.15 787.7 1.00 0.33 29-kaz

294.15 788.3 1.00 0.93 29-kaz
288.15 792.9 1.00 0.73 31-ric/wol
293.15 788.2 0.60 0.03 53-ipa/hun
293.15 787.2 0.60 -0.97 54-pin/hof
293.15 788.8 1.00 0.63 57-ish/kog

T exp 2 est
K kg m3
280.00 798.7 1.0
290.00 790.7 1.0
293.15 788.2 1.0
298.15 784.2 1.5
r-1, c-2-Dimethyl, c-3-(1-methylethyl) [36208-17-0] C10H20 MW = 140.27 175

cyclopentane

T exp 2 est Ref.
3
K kg m
293.15 804.0 0.60 54-pin/hof
(1,1-Dimethylpropyl)cyclopentane [66291-56-3] C10H20 MW = 140.27 176

A 1024.03
B -0.740

K kg m3 kg m3
293.15 807.1 0.80 0.00 39-gro/wac

293.15 807.1 1.00 0.00 39-pin/ipa-1
313.15 792.3 1.00 0.00 39-pin/ipa-1
cont.
Landolt-Brnstein
New Series IV/8D
(1,1-Dimethylpropyl)cyclopentane (cont.)

T exp 2 est
K kg m3
290.00 809.4 1.0
293.15 807.1 1.0
298.15 803.4 1.0
310.00 794.6 1.0
320.00 787.2 1.5
(1-Methylbutyl)cyclopentane [4737-43-3] C10H20 MW = 140.27 177

T exp 2 est Ref.
K kg m3
293.15 809.9 2.00 00-pin/ipa
313.15 795.5 2.00 00-pin/ipa
293.15 798.7 0.40 49-foe/fen
(3-Methylbutyl)cyclopentane [1005-68-1] C10H20 MW = 140.27 178

A 1022.10
B -0.800

K kg m3
kg m3
298.15 783.7 0.60 0.12 29-har

293.65 786.8 0.60 -0.38 36-kaz/pla
293.15 787.5 0.80 -0.08 57-shu/che
293.15 788.4 1.00 0.82 57-shu/che

T exp 2 est
K kg m3
290.00 790.1 1.0
293.15 787.6 0.7
298.15 783.6 0.6
300.00 782.1 1.0
Landolt-Brnstein
New Series IV/8D
1,1,3,3,4-Pentamethylcyclopentane [500031-17-4] C10H20 MW = 140.27 179

T exp 2 est Ref.
K kg m3
293.15 767.4 1.00 62-lev/sha-1
Pentylcyclopentane [3741-00-2] C10H20 MW = 140.27 180

A 1025.33
B -0.800

K kg m3
kg m3
293.15 802.0 2.00 11.19 27-bau

284.15 816.0 4.00 17.99 29-str-1
293.15 789.8 1.00 -1.01 39-pla
293.15 789.3 1.00 -1.51 39-pla
293.15 785.2 2.00 -5.61 46-baz/ste

T exp 2 est
K kg m3
280.00 801.3 5.0
290.00 793.3 4.9
293.15 790.8 4.9
298.15 786.8 5.0
2.6.3 Cyclohexanes
Butylcyclohexane [1678-93-9] C 10H20 MW = 140.27 181

T = 288.15 to 333.15 K
A 1.12702 103
B -1.46341
C 1.17912 10-3
cont.
Landolt-Brnstein
New Series IV/8D
Butylcyclohexane (cont.)
K 3
kg m3 in Fig. 1)
288.15 803.70 1.00 0.46 32-gar/eva( ) 298.15 795.49 0.15 -0.03 49-for/ros( )
293.15 800.50 1.00 1.15 32-gar/eva1) 303.15 791.74 0.15 -0.01 49-for/ros( )
288.15 803.70 1.00 0.46 38-eva( ) 293.15 799.20 0.60 -0.15 59-dix-1( )
293.15 800.50 1.00 1.15 38-eva1) 313.15 784.50 0.60 0.12 59-dix-1( )
293.15 799.30 0.50 -0.05 43-ano-3( ) 333.15 769.80 0.60 -0.55 59-dix-1( )
293.15 799.40 0.30 0.05 45-boo/gre() 293.15 799.25 0.20 -0.10 87-hol/goe( ) {
293.15 799.40 0.50 0.05 46-boo/gre() 298.15 795.46 0.20 -0.06 94-del/fer()
293.15 799.16 0.15 -0.19 49-for/ros( )
Further references: [27-bou, 29-str-1, 33-sig/cra, 37-lev/pot, 39-loz/dya, 40-sch/gro, 42-sch, 49-boo/hen,
49-lut, 51-sch, 54-naz/kak-1].
cont.
Landolt-Brnstein
New Series IV/8D
Butylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 809.71 2.98 298.15 795.52 0.16 320.00 779.47 0.96
290.00 801.79 0.73 300.00 794.12 0.15 330.00 772.50 0.94
293.15 799.35 0.39 310.00 786.68 0.47 340.00 765.77 0.64
(R)-(+)-(1-Methylpropyl)cyclohexane [29916-19-6] C10H20 MW = 140.27 182

A 1076.20
B -0.900

K kg m 3
kg m3
300.15 805.0 3.00 -1.07 32-lev/mar-1

295.15 810.0 3.00 -0.57 32-lev/mar-1
293.15 814.0 3.00 1.63 35-lev/har

T exp 2 est
K kg m3
290.00 815.2 3.5
293.15 812.4 3.0
298.15 807.9 3.0
310.00 797.2 4.0
1,1-Diethylcyclohexane [78-01-3] C10H20 MW = 140.27 183

T exp 2 est Ref.
K kg m3
293.15 824.9 1.00 57-khr/bal
Landolt-Brnstein
New Series IV/8D

A 1063.57
B -0.900

K kg m3 kg m3
295.15 795.7 2.00 -2.23 1895-zel/rud

284.15 811.8 2.00 3.97 29-str-1
293.15 798.0 2.00 -1.73 33-sig/cra

T exp 2 est
K kg m3
280.00 811.6 3.0
290.00 802.6 2.8
293.15 799.7 2.8
298.15 795.2 2.9

T exp 2 est Ref.
3
K kg m
293.15 800.0 2.00 33-sig/cra
cis-1,4-Diethylcyclohexane [13990-92-6] C10H20 MW = 140.27 186

T exp 2 est Ref.
K kg m3
310.93 794.9 1.20 63-gud/cam
Landolt-Brnstein
New Series IV/8D
(1,1-Dimethylethyl)cyclohexane [3178-22-1] C10H20 MW = 140.27 187

T = 284.15 to 303.15 K
A 1.04183 103
B -7.80906 10-1
284.15 820.50 2.00 0.57 29-str-1() 298.15 808.88 0.15 -0.12 49-for/ros( )
293.15 812.70 0.30 -0.21 {
44-boo/per( ) 303.15 805.11 0.15 0.01 49-for/ros( )
293.15 812.65 0.15 -0.26
49-for/ros( )
Further references: [63-gud/cam].
cont.
Landolt-Brnstein
New Series IV/8D
(1,1-Dimethylethyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 823.17 4.14 293.15 812.91 0.23 300.00 807.56 0.19
290.00 815.36 0.52 298.15 809.00 0.16 310.00 799.75 0.25
1-Ethyl-1,3-dimethylcyclohexane [500032-69-9] C10H20 MW = 140.27 188

T exp 2 est Ref.
K kg m
3
293.15 800.5 1.00 54-lev/shu
1-Ethyl-3,5-dimethylcyclohexane [7045-68-3] C10H20 MW = 140.27 189

A 1012.12
B -0.750

K 3
kg m kg m3
293.15 792.8 2.00 0.54 1893-sub

273.15 807.2 2.00 -0.06 1893-sub
288.15 795.3 2.00 -0.71 1898-rud
273.15 807.5 2.00 0.24 1898-rud

T exp 2 est
K kg m3
270.00 809.6 2.0
280.00 802.1 2.0
290.00 794.6 2.0
293.15 792.3 2.0
298.15 788.5 2.5
Landolt-Brnstein
New Series IV/8D
1-Methyl-1-(1-methylethyl)cyclohexane [16580-26-0] C10H20 MW = 140.27 190

T exp 2 est Ref.
3
K kg m
293.15 826.1 0.80 55-pin/mar
d-1-Methyl-2-(1-methylethyl) [500030-52-4] C10H20 MW = 140.27 191

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 829.7 1.00 24-wei/sch

A 1062.28
B -0.850

K kg m3 kg m3
273.15 832.5 1.50 2.37 13-sab/mur-1

294.15 813.4 1.50 1.12 13-sab/mur-1
293.15 806.9 2.00 -6.20 66-sad/akh

T exp 2 est
K kg m3
270.00 832.8 3.4
280.00 824.3 3.3
290.00 815.8 3.3
293.15 813.1 3.4
298.15 808.9 3.4
Landolt-Brnstein
New Series IV/8D
d-1-Methyl-3-(1-methylethyl) [500030-75-1] C10H20 MW = 140.27 193

cyclohexane

T exp 2 est Ref.
K kg m3
794.7 3.00 11-kis
1)
293.15
823.4 3.00 13-sab/mur
1)
273.15
1)
Not included in fit of 1-methyl-3-(1-methylethyl)cyclohexane.
l-1-Methyl-3-(1-methylethyl) [500030-76-2] C10H20 MW = 140.27 194

cyclohexane

T exp 2 est Ref.
K kg m3
793.7 2.00 11-kis/sav
1)
293.15
807.7 2.00 11-kis/sav
1)
273.15
1)
Included in fit of 1-methyl-3-(1-methylethyl)cyclohexane.

A 1062.51
B -0.900
K kg m3
kg m3
287.15 803.3 2.00 -0.77 01-sab/sen-1

297.15 796.4 3.00 1.30 13-sab/mur-11)
273.15 823.3 2.00 6.60 13-sab/mur-1
296.15 811.5 5.00 15.50 13-sab/mur-11)
293.15 806.8 2.00 8.13 66-sad/akh
1)

T exp 2 est
K kg m3
270.00 819.5 6.7
280.00 810.5 6.6
290.00 801.5 6.6
293.15 798.7 6.6
298.15 794.2 6.7
Landolt-Brnstein
New Series IV/8D

T = 273.15 to 352.35 K
A 1.00813 103
B -7.09194 10-1
K kg m 3
kg m3 in Fig. 1)
273.15 805.60 4.00 -8.82 1887-kon( ) 298.15 806.10 2.50 9.41 28-ada/mar( ) {
293.15 793.00 4.00 -7.23 1887-kon1) 293.15 796.00 3.00 -4.23 37-dya/loz1)
273.15 806.60 6.00 -7.82 1894-wag( ) 293.15 796.00 2.50 -4.23 37-loz/dya()
273.15 813.20 3.00 -1.22 01-sab/sen() 293.15 799.30 2.50 -0.93 47-boo/gre( )
293.05 790.40 4.00 -9.90 06-eyk-11) 293.15 798.70 2.50 -1.53 47-boo/gre( )
293.25 790.40 4.00 -9.76 06-eyk-11) 301.15 808.30 3.00 13.74 47-son/bhu( )
352.35 744.80 4.00 -13.45 06-eyk-1( ) 298.15 808.30 3.00 11.61 47-son/bhu-1( )
288.15 802.23 3.00 -1.55 09-vav( ) 293.15 800.20 2.50 -0.03 49-boo/gre()
273.15 813.27 3.50 -1.15 13-sab/mur-1( ) 293.15 800.20 2.60 -0.03 49-boo/gre()
298.15 802.67 3.50 5.98 13-sab/mur-1( )
Further references: [09-smi, 12-kis-3, 31-ric/wol, 36-bro/dur, 41-ano-1, 46-ano-2, 49-ano-1, 50-her/ruz,
66-sad/akh].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 816.65 5.20 298.15 796.69 3.10 330.00 774.10 6.30
280.00 809.56 3.30 300.00 795.37 3.50 340.00 767.01 7.30
290.00 802.47 2.61 310.00 788.28 4.60 350.00 759.91 8.30
293.15 800.23 3.00 320.00 781.19 5.80 360.00 752.82 10.0
cont.
Landolt-Brnstein
New Series IV/8D
1-Methyl-4-(1-methylethyl)cyclohexane (cont.)
cis-1-Methyl-4-(1-methylethyl) [6069-98-3] C10H20 MW = 140.27 197

cyclohexane

T exp 2 est Ref.
K kg m3
293.15 816.0 2.00 22-ski/sch
293.15 807.6 0.80 53-ano-1
293.15 808.6 0.70 54-oco/gol
293.15 808.7 0.7 Recommended
Landolt-Brnstein
New Series IV/8D
trans-1-Methyl-4-(1-methylethyl) [1678-82-6] C10H20 MW = 140.27 198

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 792.0 2.00 22-ski/sch
293.15 795.0 1.00 34-war/ful
293.15 792.4 0.70 53-ano-1
293.15 793.2 0.70 54-oco/gol
293.15 793.2 0.7 Recommended
(1-Methylpropyl)cyclohexane [7058-01-7] C10H20 MW = 140.27 199

T = 293.15 to 303.15 K
A 1.03394 103
B -7.53139 10-1
K kg m 3
kg m3 in Fig. 1)
293.15 813.10 0.60 -0.06 45-gre-2() 298.15 809.33 0.15 -0.06 49-for/ros( )
293.15 813.30 0.50 0.14 46-ano( ){ 303.15 805.63 0.15 0.01 49-for/ros( )
293.15 813.12 0.15 -0.04 49-for/ros( )
Further references: [29-str-1, 32-lev/mar-1, 33-sig/cra].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 815.53 0.73 298.15 809.39 0.15 310.00 800.47 0.64
293.15 813.16 0.42 300.00 808.00 0.14
cont.
Landolt-Brnstein
New Series IV/8D
(1-Methylpropyl)cyclohexane (cont.)
(2-Methylpropyl)cyclohexane [1678-98-4] C10H20 MW = 140.27 200

A 1020.94
B -0.770
293.15 795.0 2.00 -0.22 25-eis/gor 293.15 795.3 0.40 0.08 49-boo/hen
293.15 785.3 5.00 -9.92 33-sig/cra 1) 293.15 795.19 0.15 -0.03 49-for/ros
293.15 795.3 0.30 0.08 45-boo/gre 298.15 791.39 0.15 0.02 49-for/ros
293.15 795.3 0.50 0.08 46-boo/gre 303.15 787.48 0.15 -0.04 49-for/ros
1)
cont.
Landolt-Brnstein
New Series IV/8D
(2-Methylpropyl)cyclohexane (cont.)

T exp 2 est
K kg m3
290.00 797.6 0.2
293.15 795.2 0.1
298.15 791.4 0.1
310.00 782.2 0.3
1-Methyl-1-propylcyclohexane [4258-93-9] C10H20 MW = 140.27 201

T exp 2 est Ref.
3
K kg m
293.15 807.7 1.00 54-khr/bal-3
293.15 810.1 0.80 55-pin/mar
824.3 5.00 57-khr/bal
1)
293.15
293.15 810.1 1.00 66-khr/koc
293.15 809.4 0.9 Recommended
1)

A 1058.58
B -0.850

K kg m 3
kg m3
292.15 813.0 2.00 2.74 32-kuh/deu

293.15 808.0 2.00 -1.41 33-sig/cra
293.15 806.4 3.00 -3.01 39-loz/dya

T exp 2 est
K kg m3
290.00 812.1 2.4
293.15 809.4 2.4
298.15 805.2 2.4
Landolt-Brnstein
New Series IV/8D
cis-1-Methyl-2-propylcyclohexane [4926-71-0] C10H20 MW = 140.27 203

T exp 2 est Ref.
3
K kg m
293.15 812.6 0.40 56-ano
trans-1-Methyl-2-propylcyclohexane [42806-77-9] C10H20 MW = 140.27 204

T exp 2 est Ref.
3
K kg m
293.15 799.9 0.40 56-ano

T exp 2 est Ref.
K kg m3
293.15 794.0 2.00 33-sig/cra
298.15 781.0 3.00 38-mou/gra
cis-1-Methyl-3-propylcyclohexane [42806-75-7] C10H20 MW = 140.27 206

T exp 2 est Ref.
K kg m3
298.15 791.0 3.00 38-mou/gra
298.15 791.0 3.00 39-mou/pau
trans-1-Methyl-3-propylcyclohexane [34522-19-5] C10H20 MW = 140.27 207

T exp 2 est Ref.
K kg m3
298.15 792.0 2.00 38-mou/gra

T exp 2 est Ref.
3
K kg m
293.15 796.0 2.00 33-sig/cra
Landolt-Brnstein
New Series IV/8D
1,1,3,4-Tetramethylcyclohexane [500032-70-2] C10H20 MW = 140.27 209

T exp 2 est Ref.
3
K kg m
293.15 797.6 1.00 54-chi/maq
cis-1,1,3,5-Tetramethylcyclohexane [50876-32-9] C10H20 MW = 140.27 210

T exp 2 est Ref.
K kg m3
293.15 781.3 1.00 54-chi/maq
trans-1,1,3,5-Tetramethylcyclohexane [50876-31-8] C10H20 MW = 140.27 211

T exp 2 est Ref.
K kg m3
293.15 792.9 1.00 54-chi/maq

T exp 2 est Ref.
K kg m3
293.15 821.9 2.00 33-mit/mar

T exp 2 est Ref.
3
K kg m
293.15 816.6 2.00 25-eis/gor
293.15 814.0 2.00 25-eis/gor
293.15 815.3 2.2 Recommended
Landolt-Brnstein
New Series IV/8D

c,w = 1.1019 101 (combined temperature ranges,
T = 273.15 to 343.15 K
A 1.05204 103
B -8.50015 10-1
273.15 825.00 4.00 5.14 12-wil/hat() 293.15 810.00 7.00 7.14 25-eis/gor()
293.15 811.00 4.00 8.14 12-wil/hat() 293.15 793.40 3.00 -9.46 37-loz/dya( ) {
286.25 791.00 3.00 -17.73 20-von-2( ) 343.15 757.80 3.00 -2.56 37-loz/dya( ) {
293.15 812.20 7.00 9.34 25-eis/gor()
cont.
Landolt-Brnstein
New Series IV/8D
1,2,4,5-Tetramethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 822.54 5.93 298.15 798.61 7.51 330.00 771.54 14.95
280.00 814.04 2.59 300.00 797.04 8.42 340.00 763.04 7.57
290.00 805.54 4.08 310.00 788.54 13.21 350.00 754.54 3.14
293.15 802.86 5.25 320.00 780.04 16.14
2.6.4 Cycloheptanes - Cyclodecane
Propylcycloheptane [13705-36-7] C 10H20 MW = 140.27 215

T exp 2 est Ref.
3
K kg m
291.15 817.5 2.00 06-zel
1,1,2-Trimethylcycloheptane [35099-89-9] C10H20 MW = 140.27 216

T exp 2 est Ref.
K kg m3
293.15 824.3 2.00 36-ruz/sei
1,1,4-Trimethylcycloheptane [2158-55-6] C10H20 MW = 140.27 217

T exp 2 est Ref.
K kg m 3
293.15 801.1 1.00 36-ruz/sei
Ethylcyclooctane [13152-02-8] C10H20 MW = 140.27 218

T exp 2 est Ref.
3
K kg m
298.15 832.8 1.00 51-cra/lar
293.15 837.6 1.00 52-hag
Landolt-Brnstein
New Series IV/8D
Cyclodecane [293-96-9] C10H20 MW = 140.27 219

T = 293.15 to 439.40 K
A 1.29173 103
B -2.61827
C 5.41046 10-3
D -5.19182 10-6
293.15 857.70 0.40 -0.65 44-pla/hul() 319.10 838.22 0.40 -0.24 85-mcl/bar()
293.15 857.50 0.40 -0.85 44-pla/hul() 327.23 832.14 0.60 -0.24 85-mcl/bar()
293.15 857.50 0.40 -0.85 52-blo/bur() 335.73 825.80 0.60 -0.27 85-mcl/bar()
294.82 857.23 0.10 0.19 76-mey/hot( ) 344.39 819.35 0.80 -0.31 85-mcl/bar()
307.72 847.33 0.10 0.25 76-mey/hot( ) 353.37 812.66 0.80 -0.37 85-mcl/bar()
322.28 836.27 0.10 0.19 76-mey/hot( ) 362.39 806.00 1.00 -0.35 85-mcl/bar()
339.39 823.42 0.10 0.06 76-mey/hot( ) 372.18 798.71 1.00 -0.34 85-mcl/bar()
352.56 813.63 0.10 0.00 76-mey/hot( ) 381.95 791.43 1.50 -0.27 85-mcl/bar()
366.88 802.99 0.11 -0.02 76-mey/hot( ) 393.21 782.92 1.50 -0.17 85-mcl/bar()
385.16 789.38 0.13 0.12 76-mey/hot( ) 404.15 774.70 1.50 0.14 85-mcl/bar()
404.42 774.92 0.15 0.57 76-mey/hot( ) 415.44 766.13 2.00 0.60 85-mcl/bar()
298.15 854.69 0.20 0.24 81-mar/sym( ){ 427.12 757.15 2.00 1.24 85-mcl/bar()
298.84 853.62 0.40 -0.29 85-mcl/bar() 439.40 747.60 2.00 2.18 85-mcl/bar()
302.84 850.49 0.40 -0.33 85-mcl/bar() 464.95 727.16 2.00 5.01 85-mcl/bar1)
311.25 844.14 0.40 -0.25 85-mcl/bar()
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 860.83 0.36 340.00 822.91 0.43 400.00 777.82 1.20
293.15 858.35 0.34 350.00 815.52 0.51 410.00 769.91 1.40
298.15 854.45 0.33 360.00 808.12 0.60 420.00 761.81 1.63
300.00 853.01 0.32 370.00 800.68 0.72 430.00 753.48 1.88
310.00 845.34 0.32 380.00 793.17 0.86 440.00 744.90 2.16
320.00 837.79 0.33 390.00 785.56 1.02 450.00 736.02 2.48
330.00 830.32 0.37
cont.
Landolt-Brnstein
New Series IV/8D
146 2.6 Alkylcycloalkanes (CnH2n), C10 - 2.7 Alkylcycloalkanes (CnH2n), C11
Cyclodecane (cont.)
Further references: [33-huc/ger].

1,1-Dimethyl-2-(1,1-dimethylbutyl) [500023-52-6] C10H20 MW = 140.27 220

cyclopropane

T exp 2 est Ref.
3
K kg m
293.15 777.6 1.00 65-lev/kos
Landolt-Brnstein
New Series IV/8D
1,1-Dimethyl-2-hexylcyclopropane [41845-49-2] C11H22 MW = 154.30 221

T exp 2 est Ref.
3
K kg m
293.15 761.2 0.70 60-kac/tog
2.7.2 Cyclopentanes
Hexylcyclopentane [4457-00-5] C 11H22 MW = 154.30 222

T exp 2 est Ref.
K kg m3
293.15 790.3 2.00 33-zel/mic
293.15 795.7 0.70 39-pla
293.15 795.6 0.70 39-pla
293.15 795.7 0.7 Recommended
4-(1-Methylethyl)-1,1,2- [91242-58-9] C11H22 MW = 154.30 223

trimethylcyclopentane

T exp 2 est Ref.
3
K kg m
293.15 786.3 2.00 63-lev/sha
l-(1-Methylbutyl)cyclopentane [500030-78-4] C11H22 MW = 154.30 224

T exp 2 est Ref.
3
K kg m
298.15 823.0 3.00 32-lev/mar-1
300.15 814.0 3.00 32-lev/mar-1
4-(1-Methylethyl)-1,2,3-trimethyl- [500030-25-1] C11H22 MW = 154.30 225

cyclopentane

T exp 2 est Ref.
3
K kg m
286.15 783.3 2.00 21-god
Landolt-Brnstein
New Series IV/8D
4-Propyl-1,1,2-trimethylcyclopentane [91242-59-0] C11H22 MW = 154.30 226

T exp 2 est Ref.
3
K kg m
293.15 788.6 2.00 63-lev/sha
2.7.3 Cyclohexanes
1-Butyl-1-methylcyclohexane [5009-92-7] C11H22 MW = 154.30 227

T exp 2 est Ref.
3
K kg m
293.15 813.3 1.00 54-khr/bal

T exp 2 est Ref.
3
K kg m
293.15 811.0 2.00 33-sig/cra

T exp 2 est Ref.
K kg m3
293.15 799.0 2.00 33-sig/cra

T exp 2 est Ref.
K kg m3
293.15 805.0 2.00 33-sig/cra
1-(1,1-Dimethylethyl)- [61828-22-6] C11H22 MW = 154.30 231

2-methylcyclohexane

T exp 2 est Ref.
K kg m3
293.15 831.5 3.0 49-ser/wis
[73908-41-5] C11H22 MW = 154.30 232

Landolt-Brnstein
New Series IV/8D
1-(1,1-Dimethylethyl)-
3-methylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 817.6 3.00 49-ser/wis
293 15 808.3 3.00 49-ser/wis
293.15 813.0 6.00 Recommended
1-(1,1-Dimethylethyl)- 75736-66-2 C11H22 MW = 154.30 233

4-methylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 817.2 3.0 49-ser/wis
cis-1-(1,1-Dimethylethyl)- [3325-80-2] C11H22 MW = 154.30 234

4-methylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 817.3 1.00 64-lib/ler
trans-1-(1,1-Dimethylethyl)- [4001-94-9] C11H22 MW = 154.30 235

4-methylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 801.6 1.00 64-lib/ler

cyclohexane

T exp 2 est Ref.
3
K kg m
290.15 820.0 2.00 54-cle
Landolt-Brnstein
New Series IV/8D

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 807.8 3.0 66-sad/akh

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 816.3 3.0 66-sad/akh
(1,1-Dimethylpropyl)cyclohexane [31797-64-5] C11H22 MW = 154.30 239

A 1076.90
B -0.850

K kg m3 kg m3
289.15 822.6 1.00 -8.52 15-hal

293.15 819.6 2.00 -8.12 33-sig/cra1)
293.15 828.5 0.70 0.78 50-ano-1
293.15 828.4 0.70 0.68 52-ano-14
293.15 828.7 0.80 0.98 52-ina/gre
293.15 828.8 0.80 1.08 52-ina/gre
293.15 828.3 0.50 0.58 50-boo/gre
1)

T exp 2 est
K kg m3
280.00 838.9 5.0
290.00 830.4 2.6
293.15 827.7 2.6
298.15 823.5 4.0
Landolt-Brnstein
New Series IV/8D
(2,2-Dimethylpropyl)cyclohexane [25446-34-8] C11H22 MW = 154.30 240

A 1024.65
B -0.770

K kg m3 kg m3
293.15 798.9 1.00 0.00 00-pin/ipa

313.15 783.5 1.00 -0.00 00-pin/ipa

T exp 2 est
K kg m3
290.00 801.4 1.5
293.15 798.9 1.0
298.15 795.1 1.0
310.00 786.0 1.0
320.00 778.3 2.0
1,3-Dimethyl-1-propylcyclohexane [500027-65-6] C11H22 MW = 154.30 241

T exp 2 est Ref.
K kg m3
293.15 806.5 1.00 54-lev/shu
1-Ethyl-2-(1-methylethyl)cyclohexane [16580-30-6] C11H22 MW = 154.30 242

T exp 2 est Ref.
K kg m3
293.15 825.1 3.0 66-sad/akh
1-Ethyl-2-propylcyclohexane [62238-33-9] C11H22 MW = 154.30 243

T exp 2 est Ref.
K kg m3
293.15 818.1 3.0 57-els/str-2
Landolt-Brnstein
New Series IV/8D
1-Ethyl-1,3,5-trimethylcyclohexane [500027-66-7] C11H22 MW = 154.30 244

T exp 2 est Ref.
3
K kg m
293.15 803.5 3.0 56-lev/gir
(1-Methylbutyl)cyclohexane [61208-94-4] C11H22 MW = 154.30 245

T exp 2 est Ref.
3
K kg m
300.15 814.0 2.00 32-lev/mar-1
(3-Methylbutyl)cyclohexane [54105-76-9] C11H22 MW = 154.30 246

T exp 2 est Ref.
3
K kg m
813.6 4.00 29-str-1
1)
284.15
293.15 798.0 2.00 33-sig/cra
823.5 4.00 36-nen/cio-1
1)
293.15
293.15 802.3 2.00 39-loz/dya
293.15 792.2 1.00 42-lev
293.15 794.9 2.4 Recommended
1)
1,1,3,3,5-Pentamethylcyclohexane [70810-19-4] C11H22 MW = 154.30 247

T exp 2 est Ref.
K kg m3
293.15 793.2 1.00 54-chi/maq
1,2,3,4,5-Pentamethylcyclohexane [1839-64-1] C11H22 MW = 154.30 248

T exp 2 est Ref.
3
K kg m
295.15 783.8 6.00 13-pic/bou
284.15 808.1 2.00 29-str-1
293.15 820.0 0.50 37-loz/dya
Landolt-Brnstein
New Series IV/8D
Pentylcyclohexane [4292-92-6] C11H22 MW = 154.30 249

A 1052.00
B -0.850

K kg m3 kg m3
293.15 802.0 2.00 -0.83 27-bou

284.15 816.0 4.00 5.52 29-str-1
293.15 802.6 2.00 -0.23 33-sig/cra
293.15 801.8 2.00 -1.03 39-lev/gol
293.15 804.4 3.00 1.57 39-loz/dya

T exp 2 est
K kg m3
280.00 814.0 5.0
290.00 805.5 2.0
293.15 802.8 2.0
298.15 798.6 3.0
2.7.4 Cycloheptanes - Cycloundecane
Butylcycloheptane [13152-41-5] C 11H22 MW = 154.30 250

T exp 2 est Ref.
K kg m3
293.15 819.5 0.80 54-khr/bal-2
Propylcyclooctane [500028-16-0] C11H22 MW = 154.30 251

T exp 2 est Ref.
K kg m3
298.15 887.0 2.00 52-cop/cam
Landolt-Brnstein
New Series IV/8D
Cycloundecane [294-41-7] C11H22 MW = 154.30 252
Table 1. Experimental values with uncertainties

T exp 2 est Ref.
3
K kg m
287.15 800.2 10.00 1883-mar/ogl-2
273.15 811.9 10.00 1883-mar/ogl-2
293.15 812.8 5.00 30-kom

2.8.1 Cyclopropanes - Cyclopentanes
Heptylcyclopentane [5617-42-5] C 12H24 MW = 168.32 253

A 1021.19
B -0.750

K kg m3
kg m3
293.15 800.2 0.70 -1.13 39-pla

293.15 801.3 0.60 -0.01 61-jes/sta
298.15 797.8 0.60 0.20 61-jes/sta
293.15 801.3 0.30 -0.03 63-mea/sta
298.15 797.8 0.30 0.18 63-mea/sta

T exp 2 est
K kg m3
290.00 803.7 0.4
293.15 801.3 0.3
298.15 797.6 0.3
1-Methyl-2,3-bis(1-methylethyl) [500030-26-2] C12H24 MW = 168.32 254

cyclopentane

T exp 2 est Ref.
3
K kg m
290.15 781.0 2.00 13-god/tab-1
Landolt-Brnstein
New Series IV/8D
(1-Methylhexyl)cyclopentane [89216-54-6] C12H24 MW = 168.32 255

T exp 2 est Ref.
3
K kg m
293.15 535.7 0.60 49-foe/fen
(1-Propylbutyl)cyclopentane [5617-43-6] C12H24 MW = 168.32 256

T exp 2 est Ref.
3
K kg m
293.15 812.4 1.00 49-kaz/gak
2.8.2 Cyclohexanes
1,4-Diethyl-2,3-dimethylcyclohexane [91695-26-0] C12H24 MW = 168.32 257

T exp 2 est Ref.
K kg m3
293.15 853.6 2.00 33-mit/mar
(1,1-Dimethylbutyl)cyclohexane [500030-80-0] C12H24 MW = 168.32 258

T exp 2 est Ref.
3
K kg m
289.15 837.2 2.00 15-hal
(1,2-Dimethylbutyl)cyclohexane [61142-37-8] C12H24 MW = 168.32 259

T exp 2 est Ref.
K kg m3
289.15 837.2 2.00 15-hal
cis-1-(1,1-Dimethylethyl)- [1129-24-4] C12H24 MW = 168.32 260

4-ethylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 820.3 1.00 64-lib/ler
293.15 825.3 2.00 65-lib/ler
293.15 821.3 2.0 Recommended
Landolt-Brnstein
New Series IV/8D
trans-1-(1,1-Dimethylethyl)- [1129-23-3] C12H24 MW = 168.32 261

4-ethylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 814.2 1.00 64-lib/ler
293.15 812.8 2.00 65-lib/ler
293.15 813.9 2.0 Recommended
1,3-Dimethyl-5-(2-methylpropyl) [500030-82-2] C12H24 MW = 168.32 262

cyclohexane

T exp 2 est Ref.
3
K kg m
273.15 822.7 2.00 06-sab/sen
1,2-Dipropylcyclohexane [105946-02-9] C12H24 MW = 168.32 263

T exp 2 est Ref.
3
K kg m
293.15 818.8 4.00 57-els/str-2
(1-Ethylbutyl)cyclohexane [4456-99-9] C12H24 MW = 168.32 264

T exp 2 est Ref.
3
K kg m
296.15 823.0 2.00 32-lev/mar-1
292.15 838.0 2.00 45-pet/kru
293.15 823.3 0.30 53-lam/wis
(2-Ethylbutyl)cyclohexane [61828-23-7] C12H24 MW = 168.32 265

T exp 2 est Ref.
K kg m3
293.15 817.3 0.30 53-lam/wis
Landolt-Brnstein
New Series IV/8D
(1-Ethyl-1-methylpropyl)cyclohexane [500027-67-8] C12H24 MW = 168.32 266

T exp 2 est Ref.
3
K kg m
289.15 831.0 1.00 15-hal
1-Ethyl-2-(1-methylethyl)- [500030-83-1] C12H24 MW = 168.32 267

5-methylcyclohexane

A 1034.06
B -0.750

K kg m3 kg m3
293.15 815.9 4.00 1.70 01-kur

273.15 827.5 4.00 -1.70 01-kur

T exp 2 est
K kg m3
270.00 831.6 5.0
280.00 824.1 4.0
290.00 816.6 4.0
293.15 814.2 4.0
298.15 810.5 5.0
Hexamethylcyclohexane [51345-51-8] C12H24 MW = 168.32 268

T exp 2 est Ref.
3
K kg m
293.15 819.4 4.0 54-chi/maq
1,2,3,4,5,6-Hexamethylcyclohexane [1795-13-7] C12H24 MW = 168.32 269

T exp 2 est Ref.
K kg m3
293.15 840.5 5.0 37-dya/loz
293.15 840.5 3.0 37-loz/dya
Landolt-Brnstein
New Series IV/8D
Hexylcyclohexane [4292-75-5] C12H24 MW = 168.32 270

A 1042.85
B -0.800

K kg m3 kg m3
293.15 806.0 2.00 -2.33 27-bou1)

293.15 806.0 2.00 -2.33 51-sch1)
293.15 808.2 0.60 -0.16 61-jes/sta
298.15 804.5 0.60 0.19 61-jes/sta
293.15 808.1 0.30 -0.18 63-mea/sta
298.15 804.5 0.30 0.17 63-mea/sta
1)

T exp 2 est
K kg m3
290.00 810.8 1.0
293.15 808.3 0.8
298.15 804.3 0.4
1,4-bis(1-Methylethyl)cyclohexane [22907-72-8] C12H24 MW = 168.32 271

T exp 2 est Ref.
K kg m 3
293.15 814.5 3.00 52-mek/kam

293.15 823.6 2.00 56-lib/lap
293.15 814.3 2.00 56-lib/lap
293.15 818.1 3.2 Recommended

trimethylcyclohexane

T exp 2 est Ref.
K kg m 3
293.15 837.5 5.00 38-far/pit

293.15 789.2 30.0 56-ano
Landolt-Brnstein
New Series IV/8D
1-Methyl-2-(3-methylbutyl)cyclohexane [500030-81-1] C12H24 MW = 168.32 273

T exp 2 est Ref.
3
K kg m
273.15 825.0 6.00 09-mur
290.15 825.0 6.00 09-mur
(1-Methylpentyl)cyclohexane [66553-51-3] C12H24 MW = 168.32 274

T exp 2 est Ref.
K kg m3
298.15 823.0 2.00 32-lev/mar-1
(3-Methylpentyl)cyclohexane [61142-38-9] C12H24 MW = 168.32 275

T exp 2 est Ref.
K kg m3
300.15 806.0 3.00 35-lev/mar-2
1-Methyl-2-pentylcyclohexane [54411-01-7] C12H24 MW = 168.32 276

T exp 2 est Ref.
K kg m3
293.15 814.0 4.00 33-sig/cra
293.15 814.4 3.00 52-col/ber
293.15 814.3 3.0 Recommended
1,3,5-Trimethyl-1-propylcyclohexane [500027-68-9] C12H24 MW = 168.32 277

T exp 2 est Ref.
3
K kg m
293.15 808.7 4.00 56-lev/gir
r-1, c-3, c-5-Triethylcyclohexane [500032-66-6] C12H24 MW = 168.32 278

T exp 2 est Ref.
3
K kg m
293.15 806.9 0.70 51-chi
Landolt-Brnstein
New Series IV/8D
r-1, t-3, c-5-Triethylcyclohexane [500032-67-7] C12H24 MW = 168.32 279

T exp 2 est Ref.
3
K kg m
293.15 808.1 0.60 51-chi
2.8.3 Cycloheptanes - Cycloundodecane
Butylcyclooctane [16538-93-5] C12H24 MW = 168.32 280

T exp 2 est Ref.
3
K kg m
298.15 826.1 1.00 52-cop/van
Cyclododecane [294-62-2] C12H24 MW = 168.32 281

T = 339.30 to 406.50 K
A 1.05315 103
B -6.58616 10-1
K 3
kg m3 in Fig. 1)
339.30 829.40 0.17 -0.29 76-mey/hot( ) 375.81 805.80 0.17 0.16 76-mey/hot( )
346.52 824.60 0.17 -0.33 76-mey/hot( ) 385.64 800.00 0.17 0.83 76-mey/hot( )
356.81 818.50 0.17 0.35 76-mey/hot( ) 396.81 791.50 0.17 -0.31 76-mey/hot( )
366.02 812.30 0.17 0.21 76-mey/hot( ) 406.50 784.80 0.20 -0.63 76-mey/hot( )
Further references: [30-ruz/sto].
cont.
Landolt-Brnstein
New Series IV/8D
Cyclododecane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
330.00 835.81 0.19 370.00 809.47 0.17 400.00 789.71 0.20
340.00 829.22 0.19 380.00 802.88 0.17 410.00 783.12 0.23
350.00 822.64 0.18 390.00 796.29 0.18 420.00 776.54 0.28
360.00 816.05 0.17
Landolt-Brnstein
New Series IV/8D

2.9.1 Cyclopropanes - Cyclopentanes
Decylcyclopropane [5794-39-8] C 13H26 MW = 182.35 282

A 1002.46
B -0.750

K kg m3 kg m3
293.15 782.6 0.50 0.00 69-rie/hoy

313.15 767.6 0.50 0.00 69-rie/hoy
333.15 752.6 0.50 0.00 69-rie/hoy
353.15 737.6 0.50 0.00 69-rie/hoy

3 3
290.00 785.0 0.5 310.00 770.0 0.5 340.00 747.5 0.5
293.15 782.6 0.5 320.00 762.5 0.5 350.00 740.0 0.5
298.15 778.9 0.5 330.00 755.0 0.5 360.00 732.5 0.6
1-(Methylheptyl)cyclopentane [500025-88-7] C13H26 MW = 182.35 283

T exp 2 est Ref.
3
K kg m
293.15 811.8 1.00 56-tar/tai
Octylcyclopentane [1795-20-6] C13H26 MW = 182.35 284

A 1046.54
B -0.800
cont.
Landolt-Brnstein
New Series IV/8D
Octylcyclopentane (cont.)

K kg m3
kg m3
291.15 815.6 4.00 1.98 33-zel/mic

293.15 812.0 2.00 -0.02 40-sch/gem
293.15 812.0 0.50 -0.02 42-sch
293.15 812.0 0.46 -0.00 49-lut

T exp 2 est
K kg m3
290.00 814.5 1.0
293.15 812.0 0.5
298.15 808.0 1.0
2.9.2 Cyclohexanes
1-Butyl-2,2,6-trimethylcyclohexane [500030-85-3] C 13H26 MW = 182.35 285

T exp 2 est Ref.
3
K kg m
292.15 829.2 2.00 36-ruz/sei
2-Butyl-1,1,3-trimethylcyclohexane [54676-39-0] C13H26 MW = 182.35 286

T exp 2 est Ref.
3
K kg m
292.15 829.2 2.00 36-ruz/sei
(1,1-Diethylpropyl)cyclohexane [500027-76-9] C13H26 MW = 182.35 287

T exp 2 est Ref.
K kg m3
289.15 838.8 1.00 15-hal
1,1-Diethyl-2-propylcyclohexane [500027-77-0] C13H26 MW = 182.35 288

T exp 2 est Ref.
K kg m3
293.15 818.1 1.00 57-els/str-1
Landolt-Brnstein
New Series IV/8D
2,4-Dimethyl-1-(1-ethylpropyl) [500005-03-8] C13H26 MW = 182.35 289

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 828.3 3.00 53-lam/wis
cis-1-Ethyl-4-(1,1-dimethylpropyl) [1130-56-9] C13H26 MW = 182.35 290

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 838.0 1.00 65-lib/ler
trans-1-Ethyl-4-(1,1-dimethylpropyl) [1130-57-0] C13H26 MW = 182.35 291

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 828.2 1.00 65-lib/ler
(1-Ethyl-1-methylbutyl)cyclohexane [500030-84-4] C13H26 MW = 182.35 292

T exp 2 est Ref.
3
K kg m
289.15 840.6 2.00 15-hal
(1-Ethylpentyl)cyclohexane [500027-74-7] C13H26 MW = 182.35 293

T exp 2 est Ref.
3
K kg m
298.15 819.0 2.00 32-lev/mar-1
Landolt-Brnstein
New Series IV/8D
Heptylcyclohexane [5617-41-4] C13H26 MW = 182.35 294

T exp 2 est Ref.
3
K kg m
293.15 812.4 1.00 40-sch/gro
293.15 812.4 0.50 42-sch
293.15 812.4 6.60 49-lut
293.15 810.0 2.00 51-sch
293.15 812.3 1.0 Recommended
(1,1,3-Trimethylbutyl)cyclohexane [500027-75-8] C13H26 MW = 182.35 295

T exp 2 est Ref.
K kg m3
289.15 830.4 2.00 15-hal
2.9.3 Cycloheptanes - Cyclotridecane
Hexylcycloheptane [18208-62-3] C 13H26 MW = 182.35 296

A 1036.47
B -0.720

K kg m3
kg m3
293.15 825.4 0.50 0.00 69-rie/hoy

313.15 811.0 0.50 0.00 69-rie/hoy
333.15 796.6 0.50 0.00 69-rie/hoy
353.15 782.2 0.50 0.00 69-rie/hoy

3 3
290.00 827.7 0.5 310.00 813.3 0.5 340.00 791.7 0.5
293.15 825.4 0.5 320.00 806.1 0.5 350.00 784.5 0.5
298.15 821.8 0.5 330.00 798.9 0.5 360.00 777.3 0.6
Landolt-Brnstein
New Series IV/8D
Cyclotridecane [295-02-3] C13H26 MW = 182.35 297

A 1080.80
B -0.750

K kg m3 kg m3
306.65 851.3 1.00 0.48 30-ruz/sto

289.15 863.6 1.00 -0.34 30-ruz/sto
293.15 860.8 1.00 -0.14 30-ruz/sto

T exp 2 est
K kg m3
280.00 870.8 1.5
290.00 863.3 1.0
293.15 860.9 1.0
298.15 857.2 1.5
310.00 848.3 2.0

2.10.1 Cyclobutanes
1,1,2,2-Tetramethyl-3,4-bis [500030-56-8] C14H28 MW = 196.38 298

(1-methylethyl)cyclobutane

A 1050.20
B -0.850

K kg m3 kg m3
273.15 818.1 3.00 0.08 13-mer-5

290.15 803.5 3.00 -0.07 13-mer-5
cont.
Landolt-Brnstein
New Series IV/8D
1,1,2,2-Tetramethyl-3,4-bis(1-methylethyl)cyclobutane (cont.)

T exp 2 est
K kg m3
270.00 820.7 3.5
280.00 812.2 3.5
290.00 803.7 3.0
293.15 801.0 3.0
298.15 796.8 4.0
2.10.2 Cyclohexanes
1,3-bis(1,1-Dimethylethyl)- [107918-24-1] C14H28 MW = 196.38 299

butylcyclohexane

A 1065.77
B -0.800

K kg m 3
kg m3
293.15 831.2 3.00 -0.05 49-pin/cza

298.15 827.3 3.00 0.05 49-pin/cza

T exp 2 est
K kg m3
290.00 833.8 3.0
293.15 831.2 3.0
298.15 827.2 3.0
1,4-bis(1,1-Dimethylethyl)cyclohexane [34386-82-8] C14H28 MW = 196.38 300

T exp 2 est Ref.
K kg m3
293.15 830.9 3.00 52-mek/kam
Landolt-Brnstein
New Series IV/8D
1,4-bis(1-Methylpropyl)cyclohexane [500027-81-6 ] C14H28 MW = 196.38 301

T exp 2 est Ref.
3
K kg m
293.15 830.5 3.00 52-mek/kam
293.15 831.3 3.00 52-mek/kam
293.15 830.9 3.0 Recommended
1,2-Dibutylcyclohexane [107918-23-0] C14H28 MW = 196.38 302

T exp 2 est Ref.
K kg m3
293.15 824.4 3.00 57-els/str-2
(1,1-Diethylbutyl)cyclohexane [500030-87-7] C14H28 MW = 196.38 303

T exp 2 est Ref.
K kg m3
292.15 854.7 2.00 15-hal
(1-Methylheptyl)cyclohexane [2883-05-8] C14H28 MW = 196.38 304

T = 273.15 to 372.05 K
A 1.02429 103
B -6.75413 10-1
C -3.33100 10-5
K 3
kg m3 in Fig. 1)
273.15 837.30 0.50 -0.02

68-ano-1( ) 333.15 795.60 0.50 0.02 68-ano-1( )
293.15 823.50 0.50 0.07
68-ano-1( ) 372.05 768.40 0.50 0.00 68-ano-1( )
310.95 811.00 0.50 -0.05
68-ano-1( )
Further references: [52-ano]. cont.
Landolt-Brnstein
New Series IV/8D
(1-Methylheptyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 839.50 0.66 300.00 818.67 0.57 350.00 783.82 0.58
280.00 832.57 0.59 310.00 811.72 0.58 360.00 776.83 0.59
290.00 825.62 0.57 320.00 804.75 0.58 370.00 769.83 0.63
293.15 823.43 0.56 330.00 797.78 0.59 380.00 762.83 0.71
298.15 819.96 0.57 340.00 790.80 0.58
(1-Methyl-1-propylbutyl)cyclohexane [500030-86-4] C14H28 MW = 196.38 305

T exp 2 est Ref.
K kg m3
292.15 848.3 2.00 15-hal
Landolt-Brnstein
New Series IV/8D
1,1,2,2,4,4,5,5-Octamethylcyclohexane [500027-83-8] C14H28 MW = 196.38 306

T exp 2 est Ref.
3
K kg m
293.15 790.2 1.00 55-pet
Octylcyclohexane [1795-15-9] C 14H28 MW = 196.38 307

T = 273.15 to 372.05 K
A 1.01827 103
B -6.95723 10-1
K kg m 3
kg m3 in Fig. 1)
293.15 816.50 2.00 2.19 39-wat/lee1) 313.15 792.80 0.50 -7.60 59-dix-11)
343.45 782.20 2.00 2.88 39-wat/lee() 333.15 786.40 0.50 -0.09 59-dix-1( {)
273.15 828.20 1.00 -0.03 47-sch() 273.15 828.20 0.50 -0.03 68-ano-1( )
293.15 813.90 1.00 -0.41 47-sch() 293.15 813.90 0.50 -0.41 68-ano-1( )
310.93 801.70 1.00 -0.24 47-sch() 310.95 801.70 0.50 -0.23 68-ano-1( )
333.15 786.40 1.00 -0.09 47-sch() 333.15 786.40 0.50 -0.09 68-ano-1( )
372.04 759.00 1.00 -0.43 47-sch() 372.05 759.00 0.50 -0.42 68-ano-1( )
293.15 813.90 0.50 -0.41 {
59-dix-1( )
Further references: [39-loz/dya, 51-sch].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 830.42 0.73 300.00 809.55 0.77 350.00 774.76 0.91
280.00 823.46 0.74 310.00 802.59 0.79 360.00 767.81 0.95
290.00 816.51 0.75 320.00 795.63 0.81 370.00 760.85 0.99
293.15 814.31 0.76 330.00 788.68 0.84 380.00 753.89 1.03
298.15 810.84 0.76 340.00 781.72 0.87
cont.
Landolt-Brnstein
New Series IV/8D
Octylcyclohexane (cont.)
(1-Propylpentyl)cyclohexane [500027-79-2] C14H28 MW = 196.38 308

T exp 2 est Ref.
K kg m3
300.15 823.0 1.00 32-lev/mar-1
(1,1,3,3-Tetramethylbutyl)cyclohexane [500027-80-5] C14H28 MW = 196.38 309

T exp 2 est Ref.
3
K kg m
293.15 842.1 1.00 53-dre/har
293.15 842.1 1.00 53-pin/mye
Landolt-Brnstein
New Series IV/8D
(1,1,4-Trimethylpentyl)cyclohexane [500030-88-6] C14H28 MW = 196.38 310

T exp 2 est Ref.
3
K kg m
292.15 851.2 2.00 15-hal
2.10.3 Cycloheptanes - Cyclotetradecane
Heptylcycloheptane [18373-89-2] C14H28 MW = 196.38 311

A 1035.18
B -0.711

K kg m3 kg m3
293.15 826.8 0.50 0.05 69-rie/hoy

313.15 812.5 0.50 -0.03 69-rie/hoy
333.15 798.3 0.50 -0.01 69-rie/hoy
353.15 784.1 0.50 0.01 69-rie/hoy

3 3
290.00 829.0 0.5 310.00 814.8 0.5 340.00 793.4 0.5
293.15 826.8 0.5 320.00 807.7 0.5 350.00 786.3 0.5
298.15 823.2 0.5 330.00 800.6 0.5 360.00 779.2 0.5
Cyclotetradecane [295-17-0] C14H28 MW = 196.38 312

accepted points. Deviation w = 0.250
A 1089.76
B -0.750
cont.
Landolt-Brnstein
New Series IV/8D
Cyclotetradecane (cont.)

K 3
kg m kg m3
352.15 825.9 1.00 0.25 30-ruz/sto

348.15 828.4 1.00 -0.25 30-ruz/sto

T exp 2 est
K kg m3
340.00 834.8 2.0
350.00 827.3 1.0
360.00 819.8 2.0

Dodecylcyclopropane [500032-52-0] C15H30 MW = 210.40 313

accepted points. Deviation w = 0.045
A 1005.22
B -0.729

K kg m 3
kg m3
293.15 791.4 0.50 -0.03 69-rie/hoy

313.15 776.9 0.50 0.06 69-rie/hoy
333.15 762.2 0.50 -0.06 69-rie/hoy
353.15 747.7 0.50 0.03 69-rie/hoy

3 3
290.00 793.7 0.6 310.00 779.1 0.6 340.00 757.3 0.6
293.15 791.4 0.6 320.00 771.8 0.6 350.00 750.0 0.6
298.15 787.8 0.6 330.00 764.6 0.6 360.00 742.7 0.6
Landolt-Brnstein
New Series IV/8D
Decylcyclopentane [1795-21-7] C15H30 MW = 210.40 314

T = 273.15 to 372.05 K
A 1.04276 103
B -8.71253 10-1
C 2.74545 10-4
K kg m3
kg m3 in Fig. 1)
293.15 811.20 0.40 0.25 49-boo/gre() 273.15 824.60 0.50 -0.67 68-ano-1()
293.15 811.00 0.30 0.05 50-boo/gre( ) { 293.15 810.90 0.50 -0.05 68-ano-1()
293.15 811.10 0.30 0.15 51-ano-3() 310.95 798.60 0.50 0.21 68-ano-1()
293.15 810.97 0.06 0.02 54-cam/for( ) 333.15 783.40 0.50 0.42 68-ano-1()
298.15 807.39 0.06 -0.02 54-cam/for( ) 372.05 756.30 0.50 -0.32 68-ano-1()
303.15 803.83 0.06 -0.05 54-cam/for( )
Further references: [40-sch/gem, 42-sch, 49-lut].
cont.
Landolt-Brnstein
New Series IV/8D
Decylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 827.54 0.65 300.00 806.10 0.26 350.00 771.46 0.65
280.00 820.34 0.41 310.00 799.06 0.31 360.00 764.69 0.65
290.00 813.19 0.28 320.00 792.08 0.41 370.00 757.99 0.58
293.15 810.95 0.27 330.00 785.15 0.51 380.00 751.33 0.43
298.15 807.41 0.26 340.00 778.28 0.60
1-Butyl-2-pentylcyclohexane [101452-35-1] C15H30 MW = 210.40 315

T exp 2 est Ref.
K kg m3
293.15 825.1 4.00 57-els/str
293.15 825.1 3.00 57-els/str-2
1-(1,5-Dimethylhexyl)- [29799-19-7] C15H30 MW = 210.40 316

4-methylcyclohexane

T exp 2 est Ref.
K kg m3
293.15 826.4 3.00 13-sem/bec
293.15 824.4 4.00 13-sem/ros
293.15 829.0 4.00 29-ruz/van
288.15 828.0 5.00 29-ruz/van
293.15 826.8 4.0 Recommended
(1-Ethyl-1,3-dimethylpentyl)cyclohexane [500027-86-1] C15H30 MW = 210.40 317

T exp 2 est Ref.
3
K kg m
293.15 851.5 1.00 52-lev/shu-2

T exp 2 est Ref.
K kg m3
292.15 871.7 3.00 15-hal
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
K kg m3
293.15 851.5 1.00 52-lev/shu-2
(1,1-Diethyl-3-methylbutyl)cyclohexane [500032-71-3] C15H30 MW = 210.40 320

T exp 2 est Ref.
3
K kg m
293.15 835.9 0.50 60-sok/she
1-Ethyl-2,4-bis(1-methylethyl)- [500027-89-4] C15H30 MW = 210.40 321

1-methylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 848.0 2.00 54-syk/cer
1-(3-Methylbutyl)-3-(1-methylethyl)- [500027-88-3] C15H30 MW = 210.40 322

6-methylcyclohexane

T exp 2 est Ref.
3
K kg m
295.15 825.0 3.00 17-sem/jon
1-(1-Methylpropyl)-3-(1-methylethyl)- [500027-90-7] C15H30 MW = 210.40 323

6,6-dimethylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 841.2 3.00 53-syk/her
Nonylcyclohexane [2883-02-5] C15H30 MW = 210.40 324

T exp 2 est Ref.
3
K kg m
293.15 817.0 2.00 51-sch
Landolt-Brnstein
New Series IV/8D
Octylcycloheptane [18208-63-4] C15H30 MW = 210.40 325

A 1034.36
B -0.702

K kg m3 kg m3
293.15 828.6 0.50 -0.03 69-rie/hoy

313.15 814.6 0.50 0.01 69-rie/hoy
333.15 800.6 0.50 0.04 69-rie/hoy
353.15 786.5 0.50 -0.02 69-rie/hoy

3 3
290.00 830.8 0.5 310.00 816.8 0.5 340.00 795.7 0.5
293.15 828.6 0.5 320.00 809.8 0.5 350.00 788.7 0.5
298.15 825.1 0.5 330.00 802.8 0.5 360.00 781.7 0.6
Cyclopentadecane [295-48-7] C15H30 MW = 210.40 326

T = 334.65 to 382.15 K
A 1.06236 103
B -6.77165 10-1
K kg m
3
kg m3 in Fig. 1)
334.65 836.40 1.00 0.66

26-ruz/bru-1( ) 351.15 824.00 1.00 -0.57
30-ruz/sto( )
344.15 828.00 1.00 -1.31 30-ruz/sto( ) 382.15 804.80 1.00 1.22
30-ruz/sto( )
cont.
Landolt-Brnstein
New Series IV/8D
Cyclopentadecane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
330.00 838.89 1.39 360.00 818.58 1.04 380.00 805.03 1.51
340.00 832.12 1.14 370.00 811.81 1.23 390.00 798.26 1.84
350.00 825.35 1.01
Landolt-Brnstein
New Series IV/8D

1-Butyl-2-hexylcyclohexane [500027-94-1] C16H32 MW = 224.43 327

T exp 2 est Ref.
K kg m3
293.15 826.4 4.00 57-els/str-1
293.15 826.4 4.00 57-els/str-2
Decylcyclohexane [1795-16-0] C16H32 MW = 224.43 328

T = 273.15 to 372.05 K
A 1.01417 103
B -6.67245 10-1
K 3
kg m3 in Fig. 1)
293.15 819.10 0.60 0.53 49-ano-1() 273.15 831.90 0.50 -0.01 68-ano-1()
293.15 819.10 0.50 0.53 49-boo/gre( ) { 293.15 818.60 0.50 0.03 68-ano-1()
293.15 818.58 0.06 0.01 54-cam/for( ) 310.95 806.70 0.50 0.01 68-ano-1()
298.15 815.17 0.06 -0.06 54-cam/for( ) 333.15 791.80 0.50 -0.08 68-ano-1()
303.15 811.83 0.06 -0.06 54-cam/for( ) 372.05 765.50 0.50 -0.42 68-ano-1()
Further references: [47-tuo/guy, 51-sch, 52-ano].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 834.01 0.63 300.00 814.00 0.10 350.00 780.63 0.65
280.00 827.34 0.47 310.00 807.32 0.15 360.00 773.96 0.67
290.00 820.67 0.26 320.00 800.65 0.40 370.00 767.29 0.69
293.15 818.57 0.15 330.00 793.98 0.54 380.00 760.62 0.71
298.15 815.23 0.10 340.00 787.31 0.61
cont.
Landolt-Brnstein
New Series IV/8D
Decylcyclohexane (cont.)
1,4-Dipentylcyclohexane [65162-15-4] C16H32 MW = 224.43 329

T exp 2 est Ref.
K kg m3
298.15 818.0 6.00 54-cra/dae
(1,1-Dipropylbutyl)cyclohexane [500027-92-9] C 16H32 MW = 224.43 330

T exp 2 est Ref.
K kg m3
292.15 838.2 2.00 15-hal
Landolt-Brnstein
New Series IV/8D
[1-(1-Methylethyl)heptyl]cyclohexane [500027-91-8] C16H32 MW = 224.43 331

T exp 2 est Ref.
3
K kg m
290.15 856.0 1.00 45-pet/kru
[1-(2-Methylpropyl)- [500027-93-0] C16H32 MW = 224.43 332

1,3-dimethylbutyl]cyclohexane

T exp 2 est Ref.
3
K kg m
292.15 839.6 2.00 15-hal
Nonylcycloheptane [18208-64-5] C16H32 MW = 224.43 333

A 1033.23
B -0.692

K kg m3 kg m3
293.15 830.4 0.50 -0.03 69-rie/hoy

313.15 816.6 0.50 0.01 69-rie/hoy
333.15 802.8 0.50 0.04 69-rie/hoy
353.15 788.9 0.50 -0.02 69-rie/hoy

3 3
290.00 832.6 0.6 310.00 818.8 0.5 340.00 798.0 0.6
293.15 830.4 0.5 320.00 811.9 0.6 350.00 791.1 0.5
298.15 827.0 0.5 330.00 804.9 0.5 360.00 784.2 0.7
Methylcyclopentadecane [58259-50-0] C16H32 MW = 224.43 334
Landolt-Brnstein
New Series IV/8D

T = 291.15 to 382.15 K
A 1.03251 103
B -5.95332 10-1
K kg m3
kg m3 in Fig. 1)
291.15 859.40 1.00 0.22 30-ruz/sto( ) 307.65 847.50 1.00 -1.85 33-ruz/boe( ) {
293.15 858.00 1.00 0.01 30-ruz/sto( ) 334.05 833.70 1.00 0.06 33-ruz/boe( ) {
382.15 805.10 1.00 0.10 30-ruz/sto( ) 352.35 822.70 1.00 -0.04 33-ruz/boe( ) {
293.45 859.30 1.00 1.49 33-ruz/boe( {)
cont.
Landolt-Brnstein
New Series IV/8D
2.12 Alkylcycloalkanes (CnH2n), C16 - 2.13 Alkylcycloalkanes (CnH2n), C17 to C18 183
Methylcyclopentadecane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 859.86 1.15 320.00 842.00 1.30 360.00 818.19 1.15
293.15 857.99 1.10 330.00 836.05 1.11 370.00 812.23 1.23
298.15 855.01 1.06 340.00 830.09 1.15 380.00 806.28 1.32
300.00 853.91 1.05 350.00 824.14 1.08 390.00 800.33 1.50
310.00 847.95 1.12
Cyclohexadecane [295-65-8] C16H32 MW = 224.43 335

T exp 2 est Ref.
K kg m3
352.15 819.0 3.00 30-ruz/sto
345.15 824.0 3.00 30-ruz/sto

Tetradecylcyclopropane [500032-53-1] C17H34 MW = 238.46 336

A 1006.04
B -0.710

K kg m3 kg m3
293.15 797.9 0.50 0.00 69-rie/hoy

313.15 783.7 0.50 0.00 69-rie/hoy
333.15 769.5 0.50 0.00 69-rie/hoy
353.15 755.3 0.50 0.00 69-rie/hoy

3 3
290.00 800.1 0.6 310.00 785.9 0.5 340.00 764.6 0.6
293.15 797.9 0.5 320.00 778.8 0.6 350.00 757.5 0.5
298.15 794.3 0.5 330.00 771.7 0.5 360.00 750.4 0.7
Landolt-Brnstein
New Series IV/8D
Dodecylcyclopentane [5634-30-0] C17H34 MW = 238.46 337

T exp 2 est Ref.
3
K kg m
291.15 828.0 5.00 37-von/kam 1)
293.15 818.0 2.00 40-sch/gem
293.15 818.0 0.50 42-sch
293.15 818.1 0.67 49-lut
293.15 818.0 0.6 Recommended
1)
Not included in calculation of linear coefficients
(3-Butylheptyl)cyclohexane [500028-18-2] C17H34 MW = 238.46 338

T exp 2 est Ref.
3
K kg m
293.15 835.1 0.80 37-nes/mar
[1-(3-Methylbutyl)-1,3,3-trimethylbutyl] [500032-73-5] C17H34 MW = 238.46 339

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 839.2 0.50 60-sok/she
(3-Methyl-1,1-dipropylbutyl) [500028-19-3] C17H34 MW = 238.46 340

cyclohexane

T exp 2 est Ref.
3
K kg m
292.15 844.1 1.00 15-hal
Undecylcyclohexane [54105-66-7] C17H34 MW = 238.46 341

T exp 2 est Ref.
3
K kg m
293.15 823.0 2.00 51-sch
Landolt-Brnstein
New Series IV/8D
Decylcycloheptane [18208-65-6] C17H34 MW = 238.46 342

A 1032.15
B -0.683

K kg m3 kg m3
293.15 832.0 0.50 0.02 69-rie/hoy

313.15 818.3 0.50 -0.03 69-rie/hoy
333.15 804.7 0.50 0.03 69-rie/hoy
353.15 791.0 0.50 -0.02 69-rie/hoy

3 3
290.00 834.1 0.6 310.00 820.5 0.5 340.00 800.0 0.6
293.15 832.0 0.5 320.00 813.7 0.6 350.00 793.2 0.5
298.15 828.6 0.5 330.00 806.8 0.5 360.00 786.3 0.6
Nonylcyclooctane [500032-59-7] C17H34 MW = 238.46 343

A 1040.53
B -0.674

K kg m3 kg m3
293.15 842.9 0.50 -0.05 69-rie/hoy

313.15 829.5 0.50 0.03 69-rie/hoy
333.15 816.0 0.50 0.02 69-rie/hoy
353.15 802.5 0.50 -0.00 69-rie/hoy

K kg m 3
K kg m 3
K kg m3
290.00 845.1 0.6 310.00 831.6 0.5 340.00 811.4 0.6
293.15 842.9 0.5 320.00 824.8 0.6 350.00 804.6 0.5
298.15 839.6 0.5 330.00 818.1 0.5 360.00 797.9 0.6
Landolt-Brnstein
New Series IV/8D
Cycloheptadecane [295-97-6] C17H34 MW = 238.46 344

A 1104.22
B -0.800

K kg m 3
kg m3
381.15 802.1 3.00 2.80 30-ruz/sto

374.15 806.2 3.00 1.30 30-ruz/sto
350.15 820.0 3.00 -4.10 30-ruz/sto

T exp 2 est
K kg m3
350.00 824.2 3.0
360.00 816.2 3.5
370.00 808.2 3.0
380.00 800.2 3.0
390.00 792.2 3.6
1,3-Dimethyl-2-(3,7-dimethyloctyl) [500028-20-6] C18H36 MW = 252.48 345

cyclohexane

T exp 2 est Ref.
K kg m3
293.15 826.0 5.00 61-ano-9
293.15 822.00 4.00 63-ano-3
Dodecylcyclohexane [795-17-1] C18H36 MW = 252.48 346

T exp 2 est Ref.
K kg m3
293.15 825.0 1.00 40-sch/gro
293.15 825.0 1.00 42-sch
293.15 825.6 1.50 49-lut
293.15 825.0 2.00 51-sch
293.15 824.0 0.80 66-sha/bek
293.15 824.7 0.9 Recommended
Landolt-Brnstein
New Series IV/8D
Hexaethylcyclohexane [98803-61-3] C18H36 MW = 252.48 347

T exp 2 est Ref.
3
K kg m
310.93 862.7 4.00 63-gud/cam
[1-(3-Methylbutyl)-1,4- [500030-90-0] C18H36 MW = 252.48 348

dimethylpentyl]cyclohexane

T exp 2 est Ref.
3
K kg m
293.65 844.0 2.00 15-hal
(4-Methyl-1,1-dipropylpentyl) [500032-74-6] C18H36 MW = 252.48 349

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 848.9 0.50 60-sok/she
Decylcyclooctane [500032-60-0] C18H36 MW = 252.48 350

A 1040.66
B -0.669

K 3
kg m kg m3
293.15 844.5 0.50 -0.05 69-rie/hoy

313.15 831.2 0.50 0.03 69-rie/hoy
333.15 817.8 0.50 0.01 69-rie/hoy
353.15 804.4 0.50 -0.01 69-rie/hoy

3 3
290.00 846.7 0.6 310.00 833.3 0.5 340.00 813.2 0.6
293.15 844.5 0.5 320.00 826.6 0.6 350.00 806.5 0.5
298.15 841.2 0.5 330.00 819.9 0.5 360.00 799.8 0.6
Landolt-Brnstein
New Series IV/8D
188 2.13 Alkylcycloalkanes (CnH2n), C17 to C18 - 2.14 Alkylcycloalkanes (CnH2n), C19 to C20
Cyclooctadecane [296-18-4] C18H36 MW = 252.48 351

A 1084.94
B -0.750

K kg m3 kg m3
349.15 820.1 2.00 -2.98 30-ruz/sto

384.15 799.8 2.00 2.97 30-ruz/sto

K kg m 3
K kg m 3
K kg m3
340.00 829.9 3.5 360.00 814.9 3.5 380.00 799.9 3.0
350.00 822.4 2.5 370.00 807.4 3.5 390.00 792.4 3.6

Hexadecylcyclopropane [18208-79-2] C19H38 MW = 266.51 352

A 1006.84
B -0.695

K kg m3 kg m3
293.15 803.1 0.50 0.00 69-rie/hoy

313.15 789.2 0.50 0.00 69-rie/hoy
333.15 775.3 0.50 -0.00 69-rie/hoy
353.15 761.4 0.50 -0.00 69-rie/hoy

K kg m 3
K kg m 3
K kg m3
290.00 805.3 0.6 310.00 791.4 0.5 340.00 770.5 0.6
293.15 803.1 0.5 320.00 784.4 0.6 350.00 763.6 0.5
298.15 799.6 0.5 330.00 777.5 0.5 360.00 756.6 0.6
Landolt-Brnstein
New Series IV/8D
1,2-Diheptylcyclopentane [500023-46-1] C19H38 MW = 266.51 353

T exp 2 est Ref.
3
K kg m
293.15 831.0 4.00 55-del/rud
(2-Hexyloctyl)cyclopentane [55044-77-4] C19H38 MW = 266.51 354

T = 273.15 to 372.04 K
A 1.01315 103
B -6.27672 10-1
C -7.46736 10-5
K 3
kg m3 in Fig. 1)
273.15 836.10 1.00 -0.03

52-ano( ) 333.15 795.80 1.00 0.04
52-ano( )
293.15 822.80 1.00 0.06
52-ano( ) 372.04 769.30 1.00 0.00
52-ano( )
310.93 810.70 1.00 -0.07
52-ano( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 838.24 1.22 300.00 818.13 1.02 350.00 784.32 1.30
280.00 831.55 1.15 310.00 811.40 1.05 360.00 777.51 1.30
290.00 824.85 1.05 320.00 804.65 1.10 370.00 770.69 1.10
293.15 822.74 1.02 330.00 797.89 1.10 380.00 763.86 1.30
298.15 819.38 1.01 340.00 791.11 1.20
cont.
Landolt-Brnstein
New Series IV/8D
(2-Hexyloctyl)cyclopentane (cont.)
Tetradecylcyclopentane [1795-22-8] C19H38 MW = 266.51 355

T exp 2 est Ref.
3
K kg m
293.15 822.0 2.00 40-sch/gem
293.15 822.0 0.70 42-sch
293.15 822.0 0.68 49-lut
293.15 822.0 0.7 Recommended
(1,1-Dibutylpentyl)cyclohexane [00028-21-7] C19H38 MW = 266.51 356

T exp 2 est Ref.
3
K kg m
293.15 829.5 0.50 60-sok/she
Landolt-Brnstein
New Series IV/8D
1-Dodecyl-2-methylcyclohexane [39762-41-9] C19H38 MW = 266.51 357

T exp 2 est Ref.
3
K kg m
293.15 823.6 4.00 42-pet/che
1-Dodecyl-3-methylcyclohexane [5452-29-9] C19H38 MW = 266.51 358

T exp 2 est Ref.
3
K kg m
293.15 824.7 4.00 42-pet/che
[1-Ethyl-4-methyl-1- [500028-23-9] C19H38 MW = 266.51 359

(3-methylbutyl)pentyl]cyclohexane

T exp 2 est Ref.
3
K kg m
293.65 868.1 1.00 15-hal
(1-Hexylheptyl)cyclohexane [13151-92-3] C19H38 MW = 266.51 360

T = 273.15 to 372.05 K
A 1.02356 103
B -6.40176 10-1
C -4.91724 10-5
K 3
kg m3 in Fig. 1)
293.15 831.70 0.50 0.03 {)

59-dix-1( 293.15 831.70 0.50 0.03 68-ano-1( )
313.15 818.30 0.50 0.03 {)
59-dix-1( 310.95 819.60 0.50 -0.15 68-ano-1( )
333.15 804.80 0.50 -0.03 {)
59-dix-1( 333.15 804.80 0.50 -0.03 68-ano-1( )
273.15 845.00 0.50 -0.03 )
68-ano-1( 372.05 778.60 0.50 0.02 68-ano-1( )
Further references: [48-ano].
cont.
Landolt-Brnstein
New Series IV/8D
(1-Hexylheptyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 847.13 1.50 300.00 827.09 0.48 350.00 793.48 0.90
280.00 840.46 0.90 310.00 820.38 0.45 360.00 786.73 0.85
290.00 833.78 0.60 320.00 813.67 0.45 370.00 779.97 0.60
293.15 831.67 0.50 330.00 806.95 0.55 380.00 773.20 0.70
298.15 828.32 0.48 340.00 800.22 0.70
Tridecylcyclohexane [6006-33-3] C19H38 MW = 266.51 361

T exp 2 est Ref.
3
K kg m
293.15 830.0 2.00 51-sch
Landolt-Brnstein
New Series IV/8D
[1,1,1-tris(2-Methylpropyl) methyl] [500032-76-8] C19H34 MW = 262.48 362

cyclohexane

T exp 2 est Ref.
K kg m3
293.15 847.3 0.50 60-sok/she
Dodecylcycloheptane [500032-57-5] C19H38 MW = 266.51 363

A 1031.52
B -0.673

K kg m3
kg m3
293.15 834.2 0.50 0.03 69-rie/hoy

313.15 820.7 0.50 -0.01 69-rie/hoy
333.15 807.2 0.50 -0.04 69-rie/hoy
353.15 793.8 0.50 0.02 69-rie/hoy

3 3
290.00 836.3 0.6 310.00 822.8 0.5 340.00 802.6 0.6
293.15 834.2 0.5 320.00 816.1 0.6 350.00 795.9 0.5
298.15 830.8 0.5 330.00 809.4 0.5 360.00 789.2 0.6
Undecylcyclooctane [500032-61-1] C19H38 MW = 266.51 364

A 1040.14
B -0.662
cont.
Landolt-Brnstein
New Series IV/8D
Undecylcyclooctane (cont.)
K kg m 3
kg m3 K kg m 3
kg m3
293.15 846.0 0.50 -0.02 69-rie/hoy 333.15 819.5 0.50 -0.03 69-rie/hoy
313.15 832.8 0.50 0.03 69-rie/hoy 353.15 806.3 0.50 0.02 69-rie/hoy

3 3
290.00 848.1 0.6 310.00 834.9 0.5 340.00 815.0 0.6
293.15 846.0 0.5 320.00 828.2 0.6 350.00 808.4 0.5
298.15 842.7 0.5 330.00 821.6 0.5 360.00 801.7 0.6
1-(1,5-Dimethylhexyl)-4- [56009-20-2] C20H40 MW = 280.54 365

(4-methylpentyl)cyclohexane

T exp 2 est Ref.
K kg m3
293.15 833.1 6.00 14-sem/jon
[4-Methyl-1-(3-methylbutyl)-1- [500028-25-1] C20H40 MW = 280.54 366

propylpentyl]cyclohexane

T exp 2 est Ref.
3
K kg m
293.65 842.1 1.00 15-hal
(1-Methyltridecyl)cyclohexane [500028-24-0] C20H40 MW = 280.54 367

T exp 2 est Ref.
K kg m3
293.15 849.2 1.00 42-pet/che
Tetradecylcyclohexane [1795-18-2] C20H40 MW = 280.54 368

T exp 2 est Ref.
3
K kg m
293.15 825.8 1.00 42-sch
293.15 833.0 2.00 51-sch
293.15 827.2 2.8 Recommended
Landolt-Brnstein
New Series IV/8D

1-Butyl-2-dodecylcyclopentane [500023-47-2] C21H42 MW = 294.56 369

T exp 2 est Ref.
K kg m3
293.15 823.8 4.00 55-del/rud
1-Decyl-2-hexylcyclopentane [500023-48-3] C21H42 MW = 294.56 370

T exp 2 est Ref.
K kg m3
293.15 827.5 4.00 55-del/rud
1,2-Dioctylcyclopentane [500034-49-1] C21H42 MW = 294.56 371

T exp 2 est Ref.
K kg m3
293.15 829.5 4.00 55-del/rud
Hexadecylcyclopentane [6812-39-1] C21H42 MW = 294.56 372

T exp 2 est Ref.
K kg m3
293.15 823.2 2.00 40-sch/gem
293.15 823.2 0.70 42-sch
293.15 823.0 2.50 49-lut
293.15 822.9 1.00 55-del/rud
293.15 823.1 0.9 Recommended
1-Heptyl-2-nonylcyclopentane [500023-49-4] C21H42 MW = 294.56 373

T exp 2 est Ref.
3
K kg m
293.15 826.50 4.00 55-del/rud
Landolt-Brnstein
New Series IV/8D
4-Methyl-1-(2-methylpropyl)-1- [500028-26-2] C21H42 MW = 294.56 374

(3-methylbutyl) pentyl]cyclohexane

T exp 2 est Ref.
3
K kg m
293.65 779.7 4.00 15-hal
Pentadecylcyclohexane [6006-95-7] C21H42 MW = 294.56 375

T exp 2 est Ref.
3
K kg m
293.15 832.3 2.00 31-haa
293.15 833.0 0.80 49-lut
293.15 832.9 0.9 Recommended
(1,1-Dimethyltetradecyl)cyclohexane [500028-28-4] C22H44 MW = 308.59 376

T exp 2 est Ref.
K kg m3
293.15 841.3 1.00 42-pet/che
1-Dodecyl-3-(1-methylethyl)- [500028-29-5] C22H44 MW = 308.59 377

6-methylcyclohexane

A 1028.69
B -0.670

K kg m 3
kg m3
293.15 831.8 4.00 -0.48 40 -tur

293.15 831.8 3.00 -0.48 41 -ney/pil
313.15 819.0 3.00 0.12 41 -ney/pil
333.15 806.1 3.00 0.62 41 -ney/pil
cont.
Landolt-Brnstein
New Series IV/8D
1-Dodecyl-3-(1-methylethyl)-6-methylcyclohexane (cont.)

T exp 2 est
K kg m3
290.00 834.4 3.5
293.15 832.3 3.5
298.15 828.9 4.0
310.00 821.0 3.5
320.00 814.3 4.0
330.00 807.6 3.5
340.00 800.9 4.0
Hexadecylcyclohexane [6812-38-0] C22H44 MW = 308.59 378

T = 293.15 to 323.15 K
A 1.03445 103
B -7.06590 10-1
293.15 828.70 0.50 1.39 {

41-ney/pil( ) 293.15 826.00 2.00 -1.31 42-pet/che()
318.15 812.20 0.50 2.55
42-lar/tho( ) 293.15 826.00 1.00 -1.31 42-sch()
323.15 804.80 0.50 -1.31
42-lar/tho( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 829.54 1.80 300.00 822.47 1.70 320.00 808.34 2.00
293.15 827.31 1.50 310.00 815.41 1.80 330.00 801.27 2.40
298.15 823.78 1.60
cont.
Landolt-Brnstein
New Series IV/8D
Hexadecylcyclohexane (cont.)
(4-Hexyldecyl)cyclohexane [500028-27-3] C22H44 MW = 308.59 379

T exp 2 est Ref.
K kg m3
293.15 853.2 1.00 49-pet/kap
Landolt-Brnstein
New Series IV/8D
1-(1-methylethyl)-3-[5-methyl-2- [500028-30-8] C22H44 MW = 308.59 380

(3-methylbutyl)hexyl]-
4-methylcyclohexane

A 1031.19
B -0.680

K kg m3 kg m3
293.15 831.6 4.00 -0.25 40-tur

293.15 831.6 3.00 -0.25 41-ney/pil
313.15 818.4 3.00 0.15 41-ney/pil
333.15 804.9 3.00 0.25 41-ney/pil

T exp 2 est
K kg m3
290.00 834.0 4.0
293.15 831.9 3.5
298.15 828.5 4.0
310.00 820.4 3.5
320.00 813.6 4.0
330.00 806.8 3.5
340.00 800.0 4.0
Cyclodocosane [296-86-6] C22H44 MW = 308.59 381

T exp 2 est Ref.
K kg m3
348.15 817.40 1.00 30-ruz/sto
Octadecylcyclopentane [62016-53-9] C23H46 MW = 322.62 382

T exp 2 est Ref.
K kg m3
293.15 824.0 2.00 40-sch/gem
293.15 824.0 0.80 42-sch
293.15 824.0 1.30 49-lut
293.15 824.0 0.9 Recommended
Landolt-Brnstein
New Series IV/8D
(1-Octylnonyl)cyclohexane [55124-77-1] C23H46 MW = 322.62 383

T = 273.15 to 372.04 K
A 1.04165 103
B -7.60253 10-1
C 1.73341 10-4
293.15 833.70 0.60 0.02 49-foe/fen( ) 310.93 822.00 0.50 -0.02 52-ano( )
273.15 846.90 0.50 -0.02 52-ano( ) 333.15 807.60 0.50 -0.01 52-ano( )
293.15 833.70 0.50 0.02 52-ano( ) 372.04 782.80 0.50 0.00 52-ano( )
cont.
Landolt-Brnstein
New Series IV/8D
(1-Octylnonyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 849.02 0.70 300.00 829.17 0.54 350.00 796.79 0.57
280.00 842.37 0.59 310.00 822.63 0.56 360.00 790.42 0.59
290.00 835.75 0.54 320.00 816.12 0.57 370.00 784.09 0.65
293.15 833.68 0.54 330.00 809.64 0.58 380.00 777.78 0.78
298.15 830.39 0.54 340.00 803.20 0.57
Cyclotricosane [296-96-8] C23H46 MW = 322.62 384

T = 328.15 to 384.15 K
A 1.02936 103
B -6.03926 10-1

T exp 2 est exp calc Ref. (Symbol
K kg m
3
kg m3 in Fig. 1)
342.15 823.30 1.00 0.58 30-ruz/sto( )

384.15 797.30 1.00 -0.06 30-ruz/sto( )
337.15 825.90 1.00 0.16 33-ruz/sto( )
328.15 830.50 1.00 -0.68 33-ruz/sto( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
320.00 836.10 1.50 350.00 817.98 1.00 380.00 799.86 1.30
330.00 830.06 1.20 360.00 811.94 1.10 390.00 793.82 1.50
340.00 824.02 1.10 370.00 805.90 1.20
cont.
Landolt-Brnstein
New Series IV/8D
Cyclotricosane (cont.)

Octadecylcyclohexane [4445-06-1] C24H48 MW = 336.65 385

T = 293.15 to 363.15 K
A 1.02663 103
B -6.61754 10-1
cont.
Landolt-Brnstein
New Series IV/8D
Octadecylcyclohexane (cont.)
K 3
kg m3 in Fig. 1)
298.15 834.00 2.00 4.67 36-mik( ) 328.15 808.40 1.00 -1.08 42-lar/tho()
293.15 833.50 1.00 0.86 39-sui/gem( ) 314.15 817.80 1.00 -0.94 43-het/shc()
321.15 812.40 2.00 -1.71 39-wat/lee-1() 343.15 799.70 1.00 0.15 48-maz( ) {
343.15 798.30 2.00 -1.25 39-wat/lee-1() 363.15 787.40 1.00 1.09 48-maz( ) {
318.15 814.30 1.00 -1.79 42-lar/tho()
cont.
Landolt-Brnstein
New Series IV/8D
Octadecylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 834.72 1.56 310.00 821.49 1.40 350.00 795.02 1.34
293.15 832.64 1.53 320.00 814.87 1.35 360.00 788.40 1.38
298.15 829.33 1.49 330.00 808.25 1.32 370.00 781.78 1.44
300.00 828.10 1.47 340.00 801.63 1.32
1-Methyl-3-octadecylcyclopentane [500023-50-7] C24H48 MW = 336.65 386

T exp 2 est Ref.
K kg m3
293.15 833.8 1.00 39-sui/gem
(4-Octyldodecyl)cyclopentane [5638-09-5] C25H50 MW = 350.67 387

T = 273.15 to 408.15 K
A 1.02118 103
B -6.54834 10-1
K 3
kg m3 in Fig. 1)
310.95 817.80 1.75 0.24 58-cut/mcm( {) 293.15 829.20 0.50 -0.01 68-ano-1( )
333.15 802.89 1.72 -0.13 58-cut/mcm( {) 310.95 817.80 0.50 0.24 68-ano-1( )
352.55 790.20 1.69 -0.12 58-cut/mcm( {) 333.15 802.90 0.50 -0.12 68-ano-1( )
372.05 777.48 1.66 -0.07 58-cut/mcm( {) 352.59 790.20 0.50 -0.09 68-ano-1( )
388.15 767.22 1.64 0.22 58-cut/mcm( {) 372.05 777.50 0.50 -0.05 68-ano-1( )
408.15 753.92 1.60 0.01 58-cut/mcm( {) 388.15 767.00 0.50 -0.00 68-ano-1( )
273.15 842.20 0.50 -0.11 68-ano-1( ) 408.15 753.90 0.50 -0.01 68-ano-1( )
Further references: [47-sch, 52-ano, 53-ano-7].
cont.
Landolt-Brnstein
New Series IV/8D
(4-Octyldodecyl)cyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 844.37 0.55 310.00 818.18 0.70 370.00 778.89 0.86
280.00 837.83 0.65 320.00 811.63 0.80 380.00 772.34 0.84
290.00 831.28 0.76 330.00 805.08 0.85 390.00 765.79 0.82
293.15 829.21 0.70 340.00 798.54 0.85 400.00 759.24 0.84
298.15 825.94 0.73 350.00 791.99 0.80 410.00 752.70 0.84
300.00 824.73 0.73 360.00 785.44 0.84 420.00 746.15 0.93
Landolt-Brnstein
New Series IV/8D
1-Hexadecyl-2,4,5-trimethylcyclohexane [500028-32-0] C25H50 MW = 350.67 388

T exp 2 est Ref.
3
K kg m
293.15 839.5 4.00 42-pet/che
(3-Octylundecyl)cyclohexane [25446-35-9] C25H50 MW = 350.67 389

T = 273.15 to 408.15 K
A 1.02365 103
B -6.50763 10-1
K 3
kg m3 in Fig. 1)
293.15 832.50 0.30 -0.38

49-foe/fen( ) 293.15 832.70 0.50 -0.18 68-ano-1( {)
310.95 821.63 1.76 0.33 58-cut/mcm() 310.95 821.60 0.50 0.30 68-ano-1( {)
333.15 806.78 1.73 -0.07 58-cut/mcm() 333.15 806.80 0.50 -0.05 68-ano-1( {)
352.55 794.60 1.70 0.37 58-cut/mcm() 352.59 794.60 0.50 0.40 68-ano-1( {)
372.05 781.98 1.67 0.44 58-cut/mcm() 372.05 782.00 0.50 0.46 68-ano-1( {)
388.15 770.77 1.65 -0.29 58-cut/mcm() 388.15 770.80 0.50 -0.26 68-ano-1( {)
408.15 757.40 1.61 -0.64 58-cut/mcm() 408.15 757.40 0.50 -0.64 68-ano-1( {)
273.15 846.10 0.50 0.20 {
68-ano-1( )
Further references: [47-sch, 52-ano, 55-cut].
cont.
Landolt-Brnstein
New Series IV/8D
(3-Octylundecyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 847.95 0.50 310.00 821.92 0.55 370.00 782.87 0.65
280.00 841.44 0.53 320.00 815.41 0.58 380.00 776.36 0.70
290.00 834.93 0.55 330.00 808.90 0.55 390.00 769.85 0.70
293.15 832.88 0.50 340.00 802.39 0.60 400.00 763.35 0.75
298.15 829.63 0.65 350.00 795.89 0.70 410.00 756.84 0.75
300.00 828.42 0.68 360.00 789.38 0.75 420.00 750.33 0.85
Landolt-Brnstein
New Series IV/8D

(1-Decylundecyl)cyclopentane [6703-81-7] C26H52 MW = 364.70 390

T = 273.15 to 372.05 K
A 1.04810 103
B -8.04299 10-1
C 2.43365 10-4
K kg m3
kg m3 in Fig. 1)
293.15 832.90 0.80 -0.34 49-foe/fen( ){ 310.95 821.50 0.50 -0.04 68-ano-1( )
273.15 846.80 0.50 0.23 68-ano-1( ) 333.15 807.50 0.50 0.34 68-ano-1( )
293.15 833.10 0.50 -0.14 68-ano-1( ) 372.05 782.50 0.50 -0.05 68-ano-1( )
Further references: [47-sch].
cont.
Landolt-Brnstein
New Series IV/8D
(1-Decylundecyl)cyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 848.69 0.75 300.00 828.72 0.58 350.00 796.41 0.58
280.00 841.98 0.64 310.00 822.16 0.59 360.00 790.10 0.59
290.00 835.33 0.59 320.00 815.65 0.60 370.00 783.83 0.65
293.15 833.24 0.58 330.00 809.19 0.60 380.00 777.61 0.78
298.15 829.94 0.58 340.00 802.78 0.59
Heneicosylcyclopentane [6703-82-8] C26H52 MW = 364.70 391

T = 273.15 to 372.05 K
A 1.01798 103
B -6.43850 10-1
K kg m
3
kg m3 in Fig. 1)
293.15 829.00 1.50 -0.24 {

45-whi/her( ) 310.95 817.80 0.50 0.02
68-ano-1( )
273.15 842.20 0.50 0.08 68-ano-1( ) 333.15 803.70 0.50 0.21
68-ano-1( )
293.15 829.20 0.50 -0.04 68-ano-1( ) 372.05 778.40 0.50 -0.04
68-ano-1( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 844.14 0.85 300.00 824.83 0.71 350.00 792.64 0.60
280.00 837.71 0.80 310.00 818.39 0.67 360.00 786.20 0.60
290.00 831.27 0.75 320.00 811.95 0.65 370.00 779.76 0.61
293.15 829.24 0.74 330.00 805.51 0.62 380.00 773.32 0.63
298.15 826.02 0.72 340.00 799.08 0.61
cont.
Landolt-Brnstein
New Series IV/8D
Heneicosylcyclopentane (cont.)
(1-Butylhexadecyl)cyclohexane [4443-59-8] C26H52 MW = 364.70 392

T = 273.15 to 372.05 K
A 1.02687 103
B -6.45230 10-1
cont.
Landolt-Brnstein
New Series IV/8D
(1-Butylhexadecyl)cyclohexane (cont.)
293.15 836.40 1.00 -1.32 {

42-pet/che( ) 310.95 826.80 0.50 0.57
68-ano-1( )
273.15 851.50 0.50 0.88 68-ano-1( ) 333.15 811.80 0.50 -0.11
68-ano-1( )
293.15 837.30 0.50 -0.42 68-ano-1( ) 372.05 787.20 0.50 0.39 68-ano-1( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 852.65 0.71 300.00 833.30 0.61 350.00 801.04 0.58
280.00 846.20 0.67 310.00 826.84 0.59 360.00 794.58 0.59
290.00 839.75 0.64 320.00 820.39 0.57 370.00 788.13 0.62
293.15 837.72 0.63 330.00 813.94 0.57 380.00 781.68 0.65
298.15 834.49 0.61 340.00 807.49 0.57
Landolt-Brnstein
New Series IV/8D
1,3-Didecylcyclohexane [55334-19-5] C26H52 MW = 364.70 393

T = 293.15 to 372.05 K
A 1.03311 103
B -7.28326 10-1
C 1.40664 10-4
372.05 781.60 1.00 -0.00 58-cla/dix( ) 333.15 806.10 1.00 0.02 68-ano-1( )
293.15 831.70 1.00 0.01 68-ano-1( ) 372.05 781.60 1.00 -0.00 68-ano-1( )
310.95 820.20 1.00 -0.03 68-ano-1( )
cont.
Landolt-Brnstein
New Series IV/8D
1,3-Didecylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 833.72 1.20 310.00 820.84 1.03 350.00 795.42 1.16
293.15 831.69 1.10 320.00 814.45 1.05 360.00 789.14 1.14
298.15 828.46 1.05 330.00 808.08 1.06 370.00 782.88 1.04
300.00 827.27 1.04 340.00 801.74 1.12 380.00 776.65 1.18
1,4-Didecylcyclohexane [55334-20-8] C26H52 MW = 364.70 394

T = 273.15 to 372.05 K
A 1.02007 103
B -6.38915 10-1
K 3
kg m3 in Fig. 1)
310.95 821.70 0.50 0.30 {

59-dix/cla( ) 310.95 821.70 0.50 0.30
68-ano-1( )
323.15 811.70 1.00 -1.90 66-stu() 333.15 807.60 0.50 0.38
68-ano-1( )
273.15 845.80 0.50 0.25 68-ano-1( ) 372.05 782.70 0.50 0.34
68-ano-1( )
293.15 833.10 0.50 0.33 68-ano-1( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 847.56 0.59 300.00 828.40 0.54 350.00 796.45 0.73
280.00 841.17 0.53 310.00 822.01 0.58 360.00 790.06 0.70
290.00 834.78 0.52 320.00 815.62 0.64 370.00 783.67 0.63
293.15 832.77 0.52 330.00 809.23 0.69 380.00 777.28 0.53
298.15 829.58 0.53 340.00 802.84 0.73
cont.
Landolt-Brnstein
New Series IV/8D
1,4-Didecylcyclohexane (cont.)
1,4-Dimethyl-2-octadecylcyclohexane [55282-02-5] C26H52 MW = 364.70 395

T = 293.15 to 372.05 K
A 1.01544 103
B -6.25066 10-1
cont.
Landolt-Brnstein
New Series IV/8D
1,4-Dimethyl-2-octadecylcyclohexane (cont.)
372.05 782.90 4.00 0.02 58-cla/dix() 310.95 821.00 4.00 -0.07

68-ano-1( )
310.95 821.20 4.00 0.13 {
59-dix/cla( ) 333.15 807.20 4.00 0.00
68-ano-1( )
293.15 832.30 4.00 0.10 68-ano-1( ) 372.05 782.70 4.00 -0.18
68-ano-1( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 834.17 4.40 310.00 821.67 4.12 350.00 796.66 4.08
293.15 832.20 4.35 320.00 815.42 4.04 360.00 790.41 4.19
298.15 829.07 4.27 330.00 809.16 4.00 370.00 784.16 4.33
300.00 827.92 4.25 340.00 802.91 4.02 380.00 777.91 4.50
Landolt-Brnstein
New Series IV/8D
1-Dodecyl-4-octylcyclohexane [500033-05-6] C26H52 MW = 350.67 396

T exp 2 est Ref.
3
K kg m
323.15 811.9 4.00 66-stu
Eicosylcyclohexane [4443-55-4] C26H52 MW = 364.70 397

T = 273.15 to 372.05 K
A 1.01345 103
B -6.04594 10-1
C -4.79159 10-5
K 3
kg m3 in Fig. 1)
293.15 832.00 1.50 -0.09 45-whi/her() 293.15 832.20 0.50 0.11 68-ano-1( )
333.15 806.70 1.00 -0.01 47-sch( ) { 310.95 820.80 0.50 -0.02 68-ano-1( )
372.04 781.90 1.00 0.02 47-sch( ) { 333.15 806.70 0.50 -0.01 68-ano-1( )
273.15 844.70 0.50 -0.03 68-ano-1( ) 372.05 781.90 0.50 0.02 68-ano-1( )
Further references: [57-ano-1, 59-dix/cla].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 846.71 0.89 300.00 827.76 0.77 350.00 795.97 0.78
280.00 840.40 0.81 310.00 821.42 0.78 360.00 789.58 0.79
290.00 834.08 0.77 320.00 815.07 0.79 370.00 783.19 0.83
293.15 832.09 0.77 330.00 808.71 0.79 380.00 776.78 0.92
298.15 828.93 0.77 340.00 802.35 0.78
cont.
Landolt-Brnstein
New Series IV/8D
Eicosylcyclohexane (cont.)
(1-Ethyloctadecyl)cyclohexane [4443-57-6] C26H52 MW = 364.70 398

T = 273.15 to 372.05 K
A 1.02448 103
B -6.34512 10-1
273.15 851.20 0.50 0.04 68-ano-1( ) 333.15 813.20 0.50 0.11 68-ano-1( )
293.15 838.50 0.50 0.03 68-ano-1( ) 372.05 788.40 0.50 -0.01 68-ano-1( )
310.95 827.00 0.50 -0.18 68-ano-1( )
cont.
Landolt-Brnstein
New Series IV/8D
(1-Ethyloctadecyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 853.16 0.59 300.00 834.12 0.51 350.00 802.40 0.55
280.00 846.81 0.55 310.00 827.78 0.50 360.00 796.05 0.58
290.00 840.47 0.53 320.00 821.43 0.50 370.00 789.71 0.61
293.15 838.47 0.52 330.00 815.09 0.51 380.00 783.36 0.65
298.15 835.30 0.51 340.00 808.74 0.52
Landolt-Brnstein
New Series IV/8D
(1-Hexyltetradecyl)cyclohexane [4443-60-1] C26H52 MW = 364.70 399

T = 273.15 to 372.05 K
A 1.03804 103
B -7.23702 10-1
C 1.29455 10-4
K 3
kg m3 in Fig. 1)
293.15 836.70 0.50 -0.32

49-foe/fen( ) 310.95 825.60 0.50 0.07 68-ano-1( )
273.15 850.20 0.50 0.18 68-ano-1( ) 333.15 811.50 0.50 0.19 68-ano-1( )
293.15 836.90 0.50 -0.12 68-ano-1( ) 372.05 786.70 0.50 -0.01 68-ano-1( )
cont.
Landolt-Brnstein
New Series IV/8D
(1-Hexyltetradecyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 852.08 0.60 300.00 832.58 0.55 350.00 800.61 0.60
280.00 845.56 0.53 310.00 826.14 0.52 360.00 794.29 0.58
290.00 839.06 0.52 320.00 819.72 0.56 370.00 788.00 0.55
293.15 837.02 0.51 330.00 813.32 0.53 380.00 781.73 0.65
298.15 833.78 0.55 340.00 806.95 0.56
1-Hexyl-4-tetradecylcyclohexane [500028-12-6] C26H52 MW = 364.70 400

T exp 2 est Ref.
K kg m3
323.15 811.8 4.00 16 -tu -0
8-(4-Methylcyclohexyl)nonadecane [103048-68-6] C26H52 MW = 364.70 401

T = 273.15 to 372.05 K
A 1.02133 103
B -6.28034 10-1
C -2.00171 10-5
K kg m
3
kg m3 in Fig. 1)
273.15 848.30 0.50 0.01

68-ano-1( ) 333.15 809.90 0.50 0.02 68-ano-1( )
293.15 835.50 0.50 -0.01
68-ano-1( ) 372.05 784.90 0.50 -0.00 68-ano-1( )
310.95 824.10 0.50 -0.01
68-ano-1( )
Further references: [59-dix/cla].
cont.
Landolt-Brnstein
New Series IV/8D
8-(4-Methylcyclohexyl)nonadecane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 850.31 0.68 300.00 831.12 0.53 350.00 799.07 0.56
280.00 843.92 0.57 310.00 824.72 0.55 360.00 792.65 0.58
290.00 837.52 0.53 320.00 818.31 0.56 370.00 786.22 0.64
293.15 835.51 0.53 330.00 811.90 0.57 380.00 779.79 0.77
298.15 832.31 0.53 340.00 805.49 0.56
Landolt-Brnstein
New Series IV/8D
(1-Methylnonadecyl)cyclohexane [4443-56-5] C26H52 MW = 364.70 402

T = 273.15 to 372.05 K
A 1.02441 103
B -6.38656 10-1
K kg m3
kg m3 in Fig. 1)
273.15 850.10 0.50 0.14 68-ano-1( ) 333.15 811.80 0.50 0.16 68-ano-1( )
293.15 837.10 0.50 -0.09 68-ano-1( ) 372.05 786.80 0.50 0.00 68-ano-1( )
310.95 825.60 0.50 -0.22 68-ano-1( )
cont.
Landolt-Brnstein
New Series IV/8D
(1-Methylnonadecyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 851.97 0.59 300.00 832.81 0.51 350.00 800.88 0.55
280.00 845.58 0.55 310.00 826.42 0.50 360.00 794.49 0.58
290.00 839.20 0.53 320.00 820.04 0.50 370.00 788.11 0.61
293.15 837.19 0.52 330.00 813.65 0.51 380.00 781.72 0.65
298.15 833.99 0.51 340.00 807.27 0.52
(1-Propylheptadecyl)cyclohexane [4443-58-7] C26H52 MW = 364.70 403

T = 273.15 to 372.05 K
A 1.02692 103
B -6.43821 10-1
273.15 851.00 0.50 -0.06 68-ano-1( ) 333.15 812.40 0.50 -0.03

68-ano-1( )
293.15 838.20 0.50 0.01 68-ano-1( ) 372.05 787.40 0.50 0.01
68-ano-1( )
310.95 826.80 0.50 0.07 68-ano-1( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 853.09 0.56 300.00 833.78 0.53 350.00 801.59 0.53
280.00 846.65 0.54 310.00 827.34 0.52 360.00 795.15 0.55
290.00 840.21 0.53 320.00 820.90 0.52 370.00 788.71 0.58
293.15 838.19 0.53 330.00 814.46 0.51 380.00 782.27 0.65
298.15 834.97 0.53 340.00 808.02 0.52
cont.
Landolt-Brnstein
New Series IV/8D
(1-Propylheptadecyl)cyclohexane (cont.)
(1-Octyldodecyl)cyclohexane [4443-61-2] C26H52 MW = 364.70 404

T = 273.15 to 372.05 K
A 1.03510 103
B -7.02815 10-1
C 9.31364 10-5
cont.
Landolt-Brnstein
New Series IV/8D
(1-Octyldodecyl)cyclohexane (cont.)
273.15 850.10 0.50 0.03 68-ano-1( ) 333.15 811.30 0.50 0.01

68-ano-1( )
293.15 837.00 0.50 -0.07 68-ano-1( ) 372.05 786.50 0.50 -0.01
68-ano-1( )
310.95 825.60 0.50 0.04 68-ano-1( )
Further references: [59-dix/cla].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 852.13 0.68 300.00 832.63 0.53 350.00 800.52 0.57
280.00 845.61 0.57 310.00 826.17 0.55 360.00 794.15 0.58
290.00 839.11 0.53 320.00 819.73 0.56 370.00 787.81 0.64
293.15 837.07 0.53 330.00 813.31 0.57 380.00 781.48 0.77
298.15 833.83 0.53 340.00 806.91 0.57
Landolt-Brnstein
New Series IV/8D
226 2.17 Alkylcycloalkanes (CnH2n), C26 - 2.18 Alkylcycloalkanes (CnH2n), C27 to C28
Cyclohexacosane [297-16-5] C26H52 MW = 364.70 405

A 1041.48
B -0.650

K kg m3 kg m3
351.15 812.0 0.60 -1.24 30-ruz/sto

385.15 792.4 0.60 1.26 30-ruz/sto
331.15 825.5 3.00 -0.74 34-ruz/hur

3 3
330.00 827.0 3.0 360.00 807.5 2.5 380.00 794.5 2.0
340.00 820.5 3.0 370.00 801.0 3.0 390.00 788.0 3.0
350.00 814.0 2.0

(2-Decyldodecyl)cyclopentane [6703-79-3] C27H54 MW = 378.73 406

T = 273.15 to 372.05 K
A 1.04299 103
B -7.82119 10-1
C 2.04732 10-4
K 3
kg m3 in Fig. 1)
273.15 844.80 1.00 0.18 47-sch( {) 273.15 844.60 0.50 -0.02 68-ano-1( )
293.15 831.30 1.00 -0.00 47-sch( {) 293.15 831.10 0.50 -0.20 68-ano-1( )
310.93 819.60 1.00 0.01 47-sch( {) 310.95 819.40 0.50 -0.18 68-ano-1( )
333.15 805.40 1.00 0.25 47-sch( {) 333.15 805.20 0.50 0.05 68-ano-1( )
372.04 780.40 1.00 0.06 47-sch( {) 372.05 780.20 0.50 -0.14 68-ano-1( )
cont.
Landolt-Brnstein
New Series IV/8D
(2-Decyldodecyl)cyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 846.74 0.86 300.00 826.78 0.77 350.00 794.32 0.78
280.00 840.04 0.79 310.00 820.20 0.78 360.00 787.96 0.79
290.00 833.39 0.77 320.00 813.67 0.78 370.00 781.63 0.83
293.15 831.30 0.76 330.00 807.18 0.79 380.00 775.34 0.92
298.15 828.00 0.77 340.00 800.73 0.78
Landolt-Brnstein
New Series IV/8D
(1-Decylundecyl)cyclohexane [6703-99-7] C27H54 MW = 378.73 407

T = 273.15 to 372.05 K
A 1.02149 103
B -6.28259 10-1
K kg m3
kg m3 in Fig. 1)
293.15 837.30 0.40 -0.02 46-par/wes( ){ 310.95 826.10 0.50 -0.03 68-ano-1()
293.15 837.30 0.05 -0.02 49-foe/fen( ) 333.15 812.10 0.50 -0.09 68-ano-1()
273.15 850.10 0.50 0.22 68-ano-1() 372.05 787.50 0.50 -0.25 68-ano-1()
293.15 837.50 0.50 0.18 68-ano-1()
cont.
Landolt-Brnstein
New Series IV/8D
(1-Decylundecyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 851.86 0.42 300.00 833.01 0.44 350.00 801.60 0.51
280.00 845.58 0.39 310.00 826.73 0.45 360.00 795.32 0.53
290.00 839.30 0.30 320.00 820.45 0.46 370.00 789.04 0.55
293.15 837.32 0.20 330.00 814.17 0.48 380.00 782.75 0.58
298.15 834.18 0.35 340.00 807.88 0.50
1,3,5-Trimethyl-2-octadecylcyclohexane [55282-34-3] C27H54 MW = 378.73 408

T = 293.15 to 372.05 K
A 1.03412 103
B -7.30802 10-1
C 1.68875 10-4

K kg m3 kg m3 in Fig. 1)
293.15 834.40 4.00 0.00 68-ano-1( )

310.95 823.20 4.00 -0.01 68-ano-1( )
333.15 809.40 4.00 0.00 68-ano-1( )
372.05 785.60 4.00 -0.00 68-ano-1( )
Further references: [58-cla/dix, 59-dix/cla].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 836.39 4.70 310.00 823.80 4.54 350.00 799.03 4.59
293.15 834.40 4.64 320.00 817.56 4.57 360.00 792.92 4.58
298.15 831.24 4.57 330.00 811.35 4.60 370.00 786.84 4.63
300.00 830.08 4.56 340.00 805.17 4.60 380.00 780.80 4.81
cont.
Landolt-Brnstein
New Series IV/8D
1,3,5-Trimethyl-2-octadecylcyclohexane (cont.)
(1-Butyloctadecyl)cyclohexane [500028-14-8] C28H56 MW = 392.75 409

T exp 2 est Ref.
K kg m3
298.15 839.5 0.50 36-mik
Landolt-Brnstein
New Series IV/8D
(2-Decyldodecyl)cyclohexane [6704-00-3] C28H56 MW = 392.75 410

T = 273.15 to 372.05 K
A 1.01860 103
B -6.27710 10-1

K kg m
3
kg m3 in Fig. 1)
273.15 847.20 0.50 0.06 68-ano-1( )

293.15 834.50 0.50 -0.09 68-ano-1( )
310.95 823.40 0.50 -0.02 68-ano-1( )
333.15 809.60 0.50 0.12 68-ano-1( )
372.05 785.00 0.50 -0.06 68-ano-1( )
cont.
Landolt-Brnstein
New Series IV/8D
(2-Decyldodecyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 849.12 0.57 300.00 830.29 0.53 350.00 798.91 0.58
280.00 842.85 0.55 310.00 824.01 0.51 360.00 792.63 0.60
290.00 836.57 0.53 320.00 817.74 0.55 370.00 786.35 0.58
293.15 834.59 0.51 330.00 811.46 0.52 380.00 780.07 0.65
298.15 831.45 0.52 340.00 805.18 0.55
Docosylcyclohexane [61828-07-7] C28H56 MW = 392.75 411

T exp 2 est Ref.
K kg m3
298.15 832.7 2.00 36-mik
Cyclooctacosane [297-24-5] C28H56 MW = 392.75 412

A 1043.27
B -0.660

K kg m 3
kg m3
353.15 810.3 2.00 0.11 30-ruz/sto

349.15 813.0 3.00 0.17 30-ruz/sto
331.15 824.3 3.00 -0.41 34-ruz/hur

T exp 2 est
K kg m3
330.00 825.5 3.0
340.00 818.9 3.0
350.00 812.3 3.0
360.00 805.7 3.5
Landolt-Brnstein
New Series IV/8D

1-(2-Decyldodecyl)- [55429-26-0] C29H58 MW = 406.78 413
2,4-dimethylcyclopentane

T = 273.15 to 372.05 K
A 1.01213 103
B -6.34881 10-1

K 3
kg m kg m3 in Fig. 1)
273.15 838.80 4.00 0.08 68-ano-1( )

293.15 826.00 4.00 -0.02 68-ano-1( )
310.95 814.60 4.00 -0.12 68-ano-1( )
333.15 800.70 4.00 0.08 68-ano-1( )
372.05 775.90 4.00 -0.03 68-ano-1( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 840.72 4.10 300.00 821.67 4.06 350.00 789.93 4.15
280.00 834.37 4.10 310.00 815.32 4.02 360.00 783.58 4.15
290.00 828.02 4.06 320.00 808.97 4.06 370.00 777.23 4.08
293.15 826.02 4.02 330.00 802.62 4.02 380.00 770.88 4.21
298.15 822.84 4.05 340.00 796.27 4.10
cont.
Landolt-Brnstein
New Series IV/8D
1-(2-Decyldodecyl)-2,4-dimethylcyclopentane (cont.)
(2-Decyldodecyl)-2,4-dimethyl [500023-53-0] C29H58 MW = 406.78 414

cyclopentane

T = 273.15 to 372.04 K
A 1.01220 103
B -6.35102 10-1
cont.
Landolt-Brnstein
New Series IV/8D
(2-Decyldodecyl)-2,4-dimethylcyclopentane (cont.)

K 3
273.15 838.80 4.00 0.08 52-ano( )

293.15 826.00 4.00 -0.02 52-ano( )
310.93 814.60 4.00 -0.13 52-ano( )
333.15 800.70 4.00 0.08 52-ano( )
372.04 775.90 4.00 -0.02 52-ano( )
cont.
Landolt-Brnstein
New Series IV/8D
(2-Decyldodecyl)-2,4-dimethylcyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 840.72 4.10 300.00 821.67 4.06 350.00 789.91 4.16
280.00 834.37 4.10 310.00 815.32 4.03 360.00 783.56 4.19
290.00 828.02 4.05 320.00 808.97 4.10 370.00 777.21 4.14
293.15 826.02 4.03 330.00 802.62 4.05 380.00 770.86 4.21
298.15 822.84 4.05 340.00 796.26 4.10
2-(1-Decylundecyl)- [55429-27-1] C29H58 MW = 406.78 415

1,4-dimethylcyclohexane

T = 273.15 to 372.04 K
A 1.02436 103
B -6.31938 10-1

K 3
273.15 851.80 4.00 0.06 48-ano( )

293.15 839.00 4.00 -0.11 48-ano( )
310.93 827.90 4.00 0.03 48-ano( )
333.15 813.90 4.00 0.07 48-ano( )
372.04 789.20 4.00 -0.05 48-ano( )
cont.
Landolt-Brnstein
New Series IV/8D
2-(1-Decylundecyl)-1,4-dimethylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 853.73 4.10 300.00 834.78 4.06 350.00 803.18 4.16
280.00 847.42 4.10 310.00 828.46 4.02 360.00 796.86 4.15
290.00 841.10 4.06 320.00 822.14 4.10 370.00 790.54 4.08
293.15 839.11 4.02 330.00 815.82 4.04 380.00 784.22 4.21
298.15 835.95 4.05 340.00 809.50 4.12
Landolt-Brnstein
New Series IV/8D
238 2.19 Alkylcycloalkanes (CnH2n), C29 - 2.20 Alkylcycloalkanes (CnH2n), C30 to C32
Cyclononacosane [500028-10-4] C29H58 MW = 406.78 416

A 1045.34
B -0.660
K kg m3 kg m3
337.15 823.2 3.00 0.38 30-ruz/sto

306.15 842.9 3.00 -0.38 30-ruz/sto

T exp 2 est
K kg m3
298.15 848.6 3.5
310.00 840.7 3.0
320.00 834.1 3.5
330.00 827.5 3.5
340.00 820.9 3.5

Cyclotriacontane [297-35-8] C30H60 MW = 420.81 417
T = 331.15 to 384.15 K
A 1.04482 103
B -6.45931 10-1
K kg m
3
kg m3 in Fig. 1)
331.15 830.80 1.00 -0.12 30-ruz/sto( )

342.15 823.30 1.00 -0.52 30-ruz/sto( )
350.15 818.00 1.00 -0.65 30-ruz/sto( )
384.15 797.30 1.00 0.61 30-ruz/sto( )
346.15 821.90 1.00 0.67 34-ruz/hur( )
cont.
Landolt-Brnstein
New Series IV/8D
Cyclotriacontane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
330.00 831.66 1.80 360.00 812.29 1.20 380.00 799.37 2.30
340.00 825.20 1.30 370.00 805.83 1.70 390.00 792.91 3.00
350.00 818.74 1.00
Landolt-Brnstein
New Series IV/8D
(1-Dodecyltridecyl)cyclohexane [6697-15-0] C31H62 MW = 434.83 418

T = 273.15 to 372.05 K
A 1.02465 103
B -6.33029 10-1
K kg m3
kg m3 in Fig. 1)
293.15 839.48 0.50 0.40 46-par/wes() 310.95 827.80 0.50 -0.01 68-ano-1( ) {
293.15 839.00 0.30 -0.08 49-foe/fen( ) 333.15 813.70 0.50 -0.06 68-ano-1( ) {
273.15 851.60 0.50 -0.14 68-ano-1( ) { 372.05 789.10 0.50 -0.03 68-ano-1( ) {
293.15 839.00 0.50 -0.08 68-ano-1( ) {
cont.
Landolt-Brnstein
New Series IV/8D
(1-Dodecyltridecyl)cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 853.73 0.55 300.00 834.74 0.54 350.00 803.09 0.55
280.00 847.40 0.53 310.00 828.41 0.50 360.00 796.76 0.58
290.00 841.07 0.51 320.00 822.08 0.53 370.00 790.43 0.55
293.15 839.08 0.50 330.00 815.75 0.50 380.00 784.10 0.66
298.15 835.91 0.53 340.00 809.42 0.53
(1-Butyldocosyl)cyclohexane [500028-15-9] C32H64 MW = 448.86 419

T exp 2 est Ref.
K kg m3
298.15 837.2 0.50 36-mik
Cyclodotriacontane [297-39-2] C32H64 MW = 448.86 420

T exp 2 est Ref.
K kg m3
343.15 826.1 3.00 34-ruz/hur
1,16-Dimethylcyclotriacontane [500032-27-9] C32H64 MW = 448.86 421

A 1060.96
B -0.700

K kg m3
kg m3
362.45 808.0 3.00 0.76 31-ruz/boe

353.15 813.0 3.00 -0.75 31-ruz/boe
cont.
Landolt-Brnstein
New Series IV/8D
1,16-Dimethylcyclotriacontane (cont.)

T exp 2 est
K kg m3
350.00 816.0 3.5
360.00 809.0 3.0
370.00 802.0 4.0

Cyclotetratriacontane [297-47-2] C34H68 MW = 476.91 422

T exp 2 est Ref.
K kg m3
349.15 822.9 3.00 34-ruz/hur
(1-Tetradecylpentadecyl) cyclohexane [55521-27-2] C35H70 MW = 490.94 423

T = 273.15 to 372.05 K
A 1.02165 103
B -6.18392 10-1

K kg m3 kg m3 in Fig. 1)
273.15 852.70 0.50 -0.04 )

68-ano-1(
293.15 840.40 0.50 0.03 )
68-ano-1(
310.95 829.40 0.50 0.03 )
68-ano-1(
333.15 815.60 0.50 -0.04 )
68-ano-1(
372.05 791.60 0.50 0.02 )
68-ano-1(
cont.
Landolt-Brnstein
New Series IV/8D
(1-Tetradecylpentadecyl) cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 854.69 0.56 300.00 836.14 0.54 350.00 805.22 0.57
280.00 848.51 0.54 310.00 829.95 0.52 360.00 799.03 0.58
290.00 842.32 0.52 320.00 823.77 0.55 370.00 792.85 0.56
293.15 840.37 0.52 330.00 817.59 0.52 380.00 786.67 0.65
298.15 837.28 0.53 340.00 811.40 0.55
Landolt-Brnstein
New Series IV/8D
(1-Hexadecylheptadecyl) cyclohexane [55517-75-4] C39H78 MW = 547.05 424

T = 273.15 to 372.05 K
A 1.02020 103
B -6.08493 10-1

K kg m3
kg m3 in Fig. 1)
273.15 854.00 0.50 0.01 68-ano-1( )

293.15 841.80 0.50 -0.02 68-ano-1( )
310.95 831.00 0.50 0.01 68-ano-1( )
333.15 817.50 0.50 0.02 68-ano-1( )
372.05 793.80 0.50 -0.01 68-ano-1( )
cont.
Landolt-Brnstein
New Series IV/8D
(1-Hexadecylheptadecyl) cyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 855.91 0.56 300.00 837.65 0.55 350.00 807.23 0.57
280.00 849.82 0.56 310.00 831.57 0.51 360.00 801.14 0.58
290.00 843.74 0.54 320.00 825.48 0.53 370.00 795.06 0.56
293.15 841.82 0.52 330.00 819.40 0.51 380.00 788.97 0.61
298.15 838.78 0.54 340.00 813.31 0.55
Landolt-Brnstein
New Series IV/8D
3. Tabulated Data on Density -
Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2)
3.1 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C4 to C5 249
3.1 Alkylcycloalkanes and Alkenylcycloalkanes (CnH2n-2), C4 to C5

Methylenecyclopropane [6142-73-0] C4H6 MW = 54.09 425

T exp 2 est Ref.
K kg m3
273.15 718.0 2.00 53-gra/gre
Cyclobutene [822-35-5] C4H6 MW = 54.09 426

T exp 2 est Ref.
K kg m3
273.15 733.0 3.00 07-wil/bru
Ethenylclopropane [693-86-7] C5H8 MW = 68.12 427

A 1011.16
B -1.000
K 3
kg m kg m3 K kg m 3
kg m3
291.15 723.0 2.00 2.99 22-dem/doj 273.15 741.5 2.00 3.49 22-dem/doj
288.15 726.0 2.00 2.99 22-dem/doj 293.15 716.0 0.80 -2.01 49-van/gre-1
283.15 731.1 2.00 3.09 22-dem/doj

T exp 2 est
K kg m3
270.00 741.2 2.6
280.00 731.2 2.5
290.00 721.2 2.5
293.15 718.0 2.5
298.15 713.0 2.5
Ethylidenecyclopropane [18631-83-9] C5H8 MW = 68.12 428

T exp 2 est Ref.
3
K kg m
291.15 705.2 2.00 1896-gus
273.15 723.5 2.00 1896-gus
Landolt-Brnstein
New Series IV/8D
250 3.1 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C4 to C5
1-Methylcyclobutene [1489-60-7] C5H8 MW = 68.12 429

T exp 2 est Ref.
3
K kg m
296.15 707.5 2.00 13-phi-1
Methylenecyclobutane [1120-56-5] C5H8 MW = 68.12 430

T = 273.15 to 296.15 K
A 1.02166 103
B -9.65797 10-1
K 3
kg m3 in Fig. 1)
296.15 736.00 1.50 0.36 14-phi-2() 273.15 758.30 1.50 0.44 22-dem/doj1-( ) {
273.15 758.50 2.00 0.64 17-dem/doj() 293.15 735.70 1.50 -2.84 51-slo/sho()
283.15 748.70 2.00 0.50 17-dem/doj() 293.15 740.30 1.00 1.76 66-dya/luk( )
288.15 742.50 2.00 -0.87 17-dem/doj()
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 760.90 2.10 290.00 741.58 1.80 298.15 733.71 1.70
280.00 751.24 2.10 293.15 738.54 1.70 300.00 731.92 2.00
cont.
Landolt-Brnstein
New Series IV/8D
Methylenecyclobutane (cont.)
Cyclopentene [142-29-0] C5H8 MW = 68.12 431

T = 259.35 to 308.15 K
A 9.02675 102
B 1.68263 10-1
C -2.09440 10-3
cont.
Landolt-Brnstein
New Series IV/8D
Cyclopentene (cont.)
K kg m 3
kg m3 in Fig. 1)
279.90 786.40 0.60 0.71 18-von-2( ) 308.15 756.00 0.50 0.35 47-huc/har( )
280.25 786.10 0.60 0.76 18-von-2( ) 293.15 771.80 0.40 -0.21 49-foe/fen()
293.15 776.00 2.00 3.99 18-von-21) 303.15 760.60 0.50 -0.61 49-wei( )
290.35 775.60 0.50 0.64 38-vog( ) 293.15 771.97 0.15 -0.04 50-for/cam( )
291.05 775.30 0.50 1.07 38-vog( ) 298.15 766.51 0.15 -0.15 50-for/cam( )
293.15 773.60 0.50 1.59 38-vog1) 303.15 761.22 0.15 0.01 50-for/cam( )
293.15 771.80 0.30 -0.21 43-ano() 273.15 792.27 0.20 -0.10 55-tim/hen( ) {
293.15 772.40 0.40 0.39 46-ger/van() 288.15 776.71 0.20 -0.55 55-tim/hen( ) {
259.35 804.80 0.50 -0.64 47-huc/har( ) 303.15 761.01 0.20 -0.20 55-tim/hen( ) {
289.35 774.80 0.50 -1.21 47-huc/har( )
1)
Not included in Fig. 1.
Further references: [08-har/tan, 14-phi-1, 18-von-1, 26-doj-1, 27-doj, 30-god/cau, 33-hof/lan, 34-god,
38-car/stu, 42-ano-2, 46-mou, 50-kaz/ter, 56-pla/sta, 60-shu/nar, 65-sam/ogl, 72-sid/mir].
cont.
Landolt-Brnstein
New Series IV/8D
3.1 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C4 to C5 - 253
3.2 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C6
Cyclopentene (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
250.00 813.84 0.82 290.00 775.33 0.38 300.00 764.66 0.34
260.00 804.84 0.59 293.15 772.01 0.37 310.00 753.56 0.37
270.00 795.42 0.47 298.15 766.66 0.35 320.00 742.05 0.54
280.00 785.59 0.42

(1-Methylethenyl)cyclopropane [4663-22-3] C6H10 MW = 82.15 432

T exp 2 est Ref.
K kg m3
293.15 751.0 1.00 11-kis/kla
293.15 745.0 1.00 29-van
293.15 751.5 0.50 49-sla/wis
293.15 751.4 0.50 49-van/gre
293.15 751.3 1.00 61-luk/zot
293.15 751.3 0.50 Recommended
(1-Methylethylidene)cyclopropane [4741-86-0] C6H10 MW = 82.15 433

T exp 2 est Ref.
3
K kg m
293.15 753.1 1.50 05-ale
Ethylidenecyclobutane [1528-21-8] C6H10 MW = 82.15 434

T exp 2 est Ref.
3
K kg m
293.15 767.8 0.50 49-der/gre
Landolt-Brnstein
New Series IV/8D
254 3.2 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C6
1-Methylcyclopentene [693-89-0] C6H10 MW = 82.15 435

T = 273.15 to 303.15 K
A 1.05567 103
B -9.40052 10-1
K kg m 3
kg m3 in Fig. 1)
273.15 797.90 0.70 -1.00 28-cha/dev( ) 293.15 780.20 0.50 0.10 43-ano-3( )
286.65 791.20 0.70 4.99 30-god/cau( ) 293.15 780.20 0.60 0.10 46-boo/gre( )
286.65 791.20 0.70 4.99 34-god( ) 293.15 780.20 0.40 0.10 49-boo/hen()
294.15 747.40 0.70 -31.76 34-god1) 293.15 775.80 0.60 -4.30 49-spe( )
293.15 779.00 0.60 -1.10 34-zel/tar( ) 293.15 779.90 0.40 -0.20 51-ano( ){
273.15 798.61 0.15 -0.29 37-tim/hen( ) 293.15 779.50 0.40 -0.60 61-ano-9()
288.15 784.50 0.15 -0.30 37-tim/hen( ) 293.15 780.00 0.60 -0.10 64-shu/kho( )
303.15 770.46 0.15 -0.24 37-tim/hen( ) 293.15 779.50 0.60 -0.60 65-ogl/pot( )
293.15 779.10 0.50 -1.00 39-gro/wac() 293.15 779.50 0.60 -0.60 65-sam/ogl( )
Further references: [1899-mar-1, 02-zel, 12-mey-1, 33-hof/lan, 44-tat/mel, 44-tat/ter, 46-mou, 47-
tat/mel, 48-adk/roe, 49-coo, 51-pet/jur, 51-shu/min, 51-zel, 53-lev/mez, 53-pla/lib, 60-shu/nar, 64-
mar/vel, 72-sad/ali].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 801.86 0.75 293.15 780.10 0.51 300.00 773.66 0.62
280.00 792.46 0.70 298.15 775.40 0.48 310.00 764.26 1.14
290.00 783.06 0.56
cont.
Landolt-Brnstein
New Series IV/8D
3.2 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C6 255
1-Methylcyclopentene (cont.)

A 1057.83
B -1.000
cont.
Landolt-Brnstein
New Series IV/8D
3-Methylcyclopentene (cont.)
293.15 785.1 5.00 20.42 1893-sem1) 293.15 768.2 0.70 3.52 49-coo
291.15 766.3 1.00 -0.38 02-zel 293.15 765.4 1.00 0.72 53-pla/lib
293.15 787.4 5.00 22.72 37-von/kam1) 293.15 763.8 1.00 -0.91 60-cam
293.15 770.5 2.00 5.82 38-vog 298.15 758.6 1.00 -1.10 60-cam
292.05 771.5 2.00 5.72 38-vog 293.15 770.9 1.00 6.22 60-nar/shu
293.15 762.2 1.00 -2.48 41-cra 293.15 764.7 2.00 0.02 60-pla/sta
293.15 762.2 0.50 -2.48 45-cra/boo 293.15 760.0 2.00 -4.68 64-bro/ayy
298.15 769.0 2.00 9.32 46-mou 293.15 764.4 1.00 -0.28 64-mar/vel
293.15 761.6 1.00 -3.08 48-lut/bea-1
1)
Not included in calculation of linear coefficinets.

T exp 2 est
K kg m3
290.00 767.8 3.1
293.15 764.7 3.1
298.15 759.7 3.1

A 1062.22
B -1.000
K kg m 3
kg m3 K kg m 3
kg m3
292.15 772.6 1.00 2.53 02-zel 293.15 764.0 0.70 -5.07 49-coo
289.15 781.0 2.00 7.93 35-god/mou 293.15 781.0 3.00 11.93 51-ano1)
289.15 784.0 2.00 10.93 35-god/mou 293.15 768.4 2.00 -0.71 60-cam
298.15 778.0 2.00 13.93 46-mou 298.15 763.3 2.00 -0.79 60-cam
1)

T exp 2 est
K kg m3
280.00 782.2 6.0
290.00 772.2 6.0
293.15 769.1 6.0
298.15 764.1 6.0
Landolt-Brnstein
New Series IV/8D
Methylenecyclopentane [1528-30-9] C6H10 MW = 82.15 438

T = 293.15 to 317.95 K
A 1.12043 103
B -1.16019
K kg m
3
kg m3 in Fig. 1)
293.15 778.00 1.50 -2.32 12-von/ell( ) 317.95 751.80 1.00 0.26 38-vog( ) {
293.15 778.70 1.00 -1.62 33-vog( ) 293.15 780.60 1.00 0.28 52-van/koo()
293.95 777.80 1.00 -1.59 38-vog( ){ 293.15 780.30 1.00 -0.02 53-lev/mez()
315.85 754.10 1.00 0.12 38-vog( ){ 293.15 785.20 1.00 4.88 53-sor/ber()
cont.
Landolt-Brnstein
New Series IV/8D
Methylenecyclopentane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
290.00 783.97 1.14 298.15 774.52 1.07 310.00 760.77 1.09
293.15 780.32 1.10 300.00 772.37 1.06 320.00 749.17 1.23
Cyclohexene [110-83-8] C6H10 MW = 82.15 439
T = 254.15 to 353.15 K
A 3.30584 103
B -2.33992 101
C 7.53148 10-2
D -8.36824 10-5
K kg m 3
kg m3 in Fig. 1)
323.15 782.30 0.70 -3.04 38-eva( ) 350.75 756.40 0.60 3.16 47-huc/har( )
293.15 808.80 0.80 -1.74 38-vog1) 293.15 810.94 0.15 0.40 50-for/cam( )
295.85 806.40 0.80 -1.95 38-vog1) 298.15 806.07 0.15 -0.42 50-for/cam( )
314.35 789.60 0.80 -3.61 38-vog1) 303.15 801.39 0.15 -1.07 50-for/cam( )
315.05 789.00 0.80 -3.61 38-vog1) 273.15 828.93 0.20 0.71 55-tim/hen( )
332.95 773.10 0.80 -2.40 38-vog( ) 288.15 815.04 0.20 0.37 55-tim/hen( )
334.25 772.00 0.80 -2.09 38-vog( ) 303.15 801.34 0.20 -1.12 55-tim/hen( )
334.95 771.30 0.80 -2.01 38-vog( ) 298.15 810.40 0.50 3.91 60-wri1) 2)
293.15 810.75 0.20 0.21 41-ano-1() 313.15 790.90 0.70 -3.33 60-wri1) 2)
273.15 831.00 0.70 2.78 44-can( ) 333.15 771.40 0.70 -3.88 60-wri( )2)
293.15 812.90 0.70 2.36 44-can1) 353.15 751.90 0.80 2.22 60-wri( )2)
313.15 793.90 0.70 -0.33 44-can1) 273.15 829.90 0.40 1.68 60-wri( )2)
291.85 810.50 0.50 -1.10 44-fri/har1) 273.15 829.90 0.50 1.68 61-wri( )2)
314.75 789.20 0.50 -3.67 44-fri/har( ) 298.15 805.66 0.20 -0.83 70-har/dun()
323.15 781.90 0.50 -3.44 44-fri/har( ) 299.29 814.50 0.30 8.93 74-let/mar1)
333.35 771.60 0.50 -3.47 44-fri/har( ) 307.25 806.70 0.30 7.56 74-let/mar( )
342.90 762.10 0.50 -1.78 44-fri/har( ) 315.28 799.30 0.30 6.89 74-let/mar( )
352.75 752.50 0.50 2.22 44-fri/har( ) 323.61 790.70 0.30 5.79 74-let/mar( )
254.15 848.10 0.60 -1.85 47-huc/har( ) 298.15 806.00 0.20 -0.49 75-let()
287.85 815.80 0.60 0.87 47-huc/har1) 298.15 805.88 0.20 -0.61 86-tar/dia( ){
319.15 785.50 0.60 -3.51 47-huc/har( )
1) 2)
Not included in Fig. 1. Calculated from equation given by author. cont.
Landolt-Brnstein
New Series IV/8D
Cyclohexene (cont.)
Further references: [1894-bru-1, 1898-for, 1898-mar, 1898-mar-1, 01-zel/zel-1, 07-eyk, 09-eyk, 10-ipa,
11-ski/rit, 15-rot/von, 15-von/hin, 21-far/gar, 24-nam, 24-zel, 26-mat, 26-wei/hen, 28-tre/sch, 29-bod, 30-
god/cau, 34-god, 35-mam, 37-car/stu, 38-car/stu, 39-gro/wac, 42-gei, 46-gei/can, 48-adk/roe, 49-foe/fen,
49-wei, 51-ano, 60-jef, 69-rod/hsu, 82-gro/ing, 86-cod/mon, 87-let/bax, 89-bec/ric, 89-mat/gon, 93-
jan/xie].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
250.00 855.69 1.60 293.15 810.54 0.44 330.00 778.61 1.75
260.00 842.54 0.85 298.15 806.49 0.46 340.00 767.47 2.60
270.00 831.40 0.58 300.00 805.00 0.47 350.00 754.32 3.30
280.00 821.76 0.46 310.00 796.87 0.67 360.00 738.66 3.60
290.00 813.13 0.43 320.00 788.24 1.10
Landolt-Brnstein
New Series IV/8D

(1-Ethyl-1-propenyl)cyclopropane [500030-92-2] C7H12 MW = 96.17 440

T exp 2 est Ref.
K kg m3
293.15 764.4 3.00 09-bru
293.15 791.5 3.00 29-van
(1-Methyl-1-propenyl)cyclopropane [500030-91-1] C7H12 MW = 96.17 441

T exp 2 est Ref.
K kg m3
293.15 780.4 1.50 29-van
(1-Propylethenyl)cyclopropane [5809-54-1] C7H12 MW = 96.17 442

T exp 2 est Ref.
K kg m3
293.15 777.2 1.50 29-van
(1-Methylethylidene)cyclobutane [1528-22-9] C7H12 MW = 96.17 443

T exp 2 est Ref.
3
K kg m
293.15 782.3 0.50 49-der/gre
293.15 784.2 1.00 55-kaz/luk
293.15 782.7 0.8 Recommended
1,2-Dimethylcyclopentene [765-47-9] C7H12 MW = 96.17 444

T = 273.15 to 303.15 K
A 1.05315 103
B -8.81671 10-1
cont.
Landolt-Brnstein
New Series IV/8D
1,2-Dimethylcyclopentene (cont.)
K 3
kg m3 in Fig. 1)
293.15 792.20 1.00 -2.49 08-kis( ) 288.15 799.50 0.60 0.40 {

38-chi-1( )
286.65 799.10 3.00 -1.32 08-kis-3( ) 293.15 795.00 0.60 0.31 {
38-chi-1( )
293.15 792.20 3.00 -2.49 08-kis-31) 303.15 786.10 0.60 0.23 {
38-chi-1( )
293.15 792.00 2.00 -2.69 12-von/moo-1( ) 293.15 793.00 2.00 -1.69 41-tur/vse( )
293.15 795.30 0.70 0.61 28-cha/dev() 293.15 797.60 0.50 2.91 45-ano( )
288.15 799.80 1.00 0.70 30-cha() 293.15 795.40 1.00 0.71 50-kaz/kop( )
293.15 794.70 0.70 0.01 30-cha() 293.15 796.10 1.00 1.41 52-pla/sav()
273.15 812.80 0.60 0.48 {
38-chi-1( ) 293.15 795.10 2.00 0.41 64-mir/kos-1( )
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 815.10 0.57 293.15 794.69 1.11 300.00 788.65 0.65
280.00 806.28 1.86 298.15 790.28 0.71 310.00 779.83 1.81
290.00 797.47 1.44

T exp 2 est Ref.
3
K kg m
293.15 771.5 4.00 50-kaz/kop
293.15 771.4 4.00 50-kop/noz
293.15 774.8 4.00 52-naz/kot
293.15 772.6 4.2 Recommended

T = 273.15 to 303.15 K
A 1.04621 103
B -9.07246 10-1
K 3
kg m3 in Fig. 1)
293.15 783.10 3.00 2.85 30-cha() 303.15 771.60 0.60 0.43 38-chi-1( )
273.15 798.50 0.60 0.11
38-chi-1( ) 298.15 771.00 2.00 -4.71 48-adk/roe()
288.15 785.10 0.60 0.32
38-chi-1( ) 293.15 780.90 1.00 0.65 64-mir/kos-1( ) {
293.15 780.60 0.60 0.35
38-chi-1( )
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 801.25 2.67 293.15 780.25 1.58 300.00 774.03 1.65
280.00 792.18 0.32 298.15 775.71 1.89 310.00 764.96 0.50
290.00 783.10 0.96

T exp 2 est Ref.
3
K kg m
293.15 757.9 1.00 08-kis
293.15 758.0 2.00 12-von/moo
293.15 757.9 1.0 Recommended
Landolt-Brnstein
New Series IV/8D

A 1037.60
B -0.800
K kg m 3
kg m3 K kg m 3
kg m3
291.15 800.5 4.00 -4.18 1897-kno 291.55 807.4 4.00 3.04 10-von/pet-2
293.75 806.5 4.00 3.90 10-von/pet-2 294.25 797.0 4.00 -5.20 15-von/hin
292.55 806.2 4.00 2.64 10-von/pet-2 288.75 800.9 4.00 -5.70 15-von/hin
291.25 810.1 4.00 5.50 10-von/pet-2 293.15 759.0 20.00 -44.08 51-lev/skv-21)
1)

T exp 2 est
K kg m3
280.00 813.6 4.5
290.00 805.6 4.5
293.15 803.1 4.5
298.15 799.1 4.5
Ethenylcyclopentane [3742-34-5] C7H12 MW = 96.17 449

T exp 2 est Ref.
K kg m 3
293.15 779.6 1.00 50-pla/sha

293.15 783.5 1.00 52-van/koo
293.15 783.4 1.00 53-lev/mez
293.15 782.2 1.2 Recommended
1-Ethylcyclopentene [2146-38-5] C7H12 MW = 96.17 450

A 1032.07
B -0.800
cont.
Landolt-Brnstein
New Series IV/8D
1-Ethylcyclopentene (cont.)
K kg m3
kg m3 K kg m 3
kg m3
293.15 797.5 0.70 -0.05 09-wal/mar 293.15 796.8 1.00 -0.75 51-shu/min
293.15 796.0 2.00 -1.55 12-von/moo1) 293.15 796.8 1.00 -0.75 51-zel
288.15 804.1 1.00 2.55 27-cha/bec 293.15 796.3 0.70 -1.25 52-van/koo
293.15 800.0 1.00 2.45 27-cha/bec 293.15 801.5 2.00 3.95 53-lev/mez1)
293.15 792.0 2.00 -5.55 35-huc/kum1) 293.15 797.9 0.40 0.35 59-pla/mel
293.15 805.3 2.00 7.75 39-gro/wac1) 293.15 797.6 0.60 0.05 60-nar/shu
293.15 797.0 0.30 -0.55 43-ano-3 293.15 796.4 1.50 -1.15 65-ogl/pot
293.15 798.2 0.40 0.65 46-ano 293.15 796.4 1.50 -1.15 65-sam/ogl
1)

T exp 2 est
K kg m3
280.00 808.1 1.1
290.00 800.1 0.9
293.15 797.6 0.8
298.15 793.6 0.9
3-Ethylcyclopentene [694-35-9] C7H12 MW = 96.17 451

K kg m3 K kg m3
293.15 787.4 2.00 37-von/kam1) 293.15 782.7 0.40 53-ano-1
293.15 783.0 0.50 45-cra/boo 293.15 783.5 1.00 53-lev/mez
298.15 784.0 4.00 48-adk/roe1) 293.15 792.8 4.00 53-lev/tan-11)
293.15 783.0 0.40 53-ano-1 293.15 782.9 0.4 Recommended
1)
Ethylidenecyclopentane [2146-37-4] C7H12 MW = 96.17 452

T exp 2 est Ref.
3
K kg m
293.15 802.0 2.00 09-wal/mar
293.15 803.0 1.00 52-van/koo
293.15 802.8 1.0 Recommended
Landolt-Brnstein
New Series IV/8D
1-Methyl-3-methylenecyclopentane [53366-56-6] C7H12 MW = 96.17 453

T exp 2 est Ref.
3
K kg m
292.15 773.4 1.00 01-zel-2
289.15 775.0 1.00 02-spe
Methylenecyclohexane [1192-37-6] C7H12 MW = 96.17 454

T = 273.15 to 334.15 K
A 1.03175 103
B -7.78988 10-1
K kg m 3
kg m3 in Fig. 1)
273.15 818.40 6.00 -0.57 07-fav/bor( ) 314.05 787.20 1.50 0.09 38-vog( )
288.75 805.50 1.00 -1.31 15-von/hin() 314.65 786.70 1.50 0.06 38-vog( )
290.75 803.60 1.00 -1.66 15-von/hin() 334.15 770.40 1.50 -1.05 38-vog( )
290.95 803.40 1.00 -1.70 15-von/hin() 293.15 801.60 1.00 -1.79 52-van/koo()
293.15 803.40 1.50 0.01 33-ale-1( ) 293.15 805.50 1.00 2.11 53-lev/mez( ) {
293.15 801.80 2.00 -1.59 33-vog1) 293.15 804.30 1.00 0.91 53-sor/ber( )
290.75 809.70 1.50 4.44 38-vog( ) 298.15 798.00 1.00 -1.49 55-bai/hew()
293.15 807.40 1.50 4.01 38-vog( ) 293.15 801.30 0.50 -2.09 62-ano-3( )
Further references: [08-wal-1, 12-von/ell].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 821.42 7.65 298.15 799.49 0.87 320.00 782.47 1.85
280.00 813.63 3.28 300.00 798.05 0.89 330.00 774.68 1.68
290.00 805.84 1.58 310.00 790.26 1.35 340.00 766.89 2.00
293.15 803.39 1.02
cont.
Landolt-Brnstein
New Series IV/8D
Methylenecyclohexane (cont.)
1-Methylcyclohexene [591-49-1] C7H12 MW = 96.17 455

T = 273.15 to 315.25 K
A 7.24928 101
B 5.83494
C -1.13084 10-2
cont.
Landolt-Brnstein
New Series IV/8D
1-Methylcyclohexene (cont.)
K kg m 3
kg m3 in Fig. 1)
273.15 817.10 3.00 -5.48 04-mar-2( ) 293.15 812.70 1.50 1.50 38-vog1)
293.15 799.80 3.00 -11.40 04-mar-21) 315.25 791.20 1.50 3.10 38-vog( )
293.15 802.90 3.00 -8.30 04-mar-21) 335.25 773.40 1.50 15.72 38-vog1)
273.15 821.00 2.00 -1.58 05-sab/mai( ) 293.15 810.10 0.50 -1.10 43-ano-3()
287.15 812.30 1.00 -3.26 07-eyk( ) 293.15 810.10 0.40 -1.10 49-boo/hen( ) {
273.15 823.00 2.50 0.42 07-sab/mai-4( ) 293.15 811.46 0.05 0.26 60-cam/ros( )
287.95 814.50 0.80 -0.53 12-von/ell() 298.15 806.58 0.05 -0.36 60-cam/ros( )
291.65 811.50 0.80 -0.86 12-von/ell() 303.15 802.28 0.05 0.16 60-cam/ros( )
293.15 810.30 0.80 -0.90 12-von/ell1) 293.15 810.30 0.80 -0.90 61-ano-91)
286.65 825.70 0.80 9.81 30-god/cau( ) 293.15 811.70 0.60 0.50 66-khr/koc()
Further references: [02-wal-1, 06-zel/gut, 12-ipa-1, 12-von/moo, 23-nam/bru, 24-zel, 26-gou/hun, 33-
sig/cra, 34-god, 35-huc/kum, 38-kaz/glu, 39-cow/jef, 48-adk/roe, 50-til, 53-lev/mez, 53-pla/lib, 61-shu/tul,
65-sam/ogl].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 823.55 2.78 293.15 811.20 0.39 310.00 794.59 0.60
280.00 819.70 1.75 298.15 806.94 0.12 320.00 781.70 2.79
290.00 813.59 0.66 300.00 805.22 0.08 330.00 766.54 7.24
(+)-(R)-3-Methylcyclohexene [500032-90-6] C7H12 MW = 96.17 456

T exp 2 est Ref.
K kg m3
803.0 2.00 38-mou/gra-1
1)
287.15
803.0 2.00 46-mou/ric
1)
287.15
1)
Values included in the fit of 3-methylcyclohexene.

T = 287.15 to 299.15 K
A 9.45780 102
B -4.91219 10-1
K kg m
3
kg m3 in Fig. 1)
293.45 804.80 2.00 3.17 1897-kno( ) 292.65 803.00 1.50 0.97 39-gui()
293.15 800.00 2.00 -1.78 00-kon/sch( ) 299.15 799.00 2.00 0.17 41-ber( )
292.15 803.20 1.00 0.93 01-zel/zel-1() 287.15 803.00 2.00 -1.73 42-ber( )
293.15 801.90 1.00 0.12 01-zel/zel-1() 298.15 799.00 2.00 -0.32 42-ber( )
293.15 805.00 2.00 3.22 12-von/moo( ) 293.15 810.10 0.60 8.32 {
46-boo/gre( )
293.15 800.90 0.80 -0.88 24-zel() 298.15 796.00 2.00 -3.32 48-adk/roe( )
299.15 795.00 2.00 -3.83 26-gou/hun( ) 293.15 800.20 0.20 -1.58
62-ano-3( )
287.15 803.00 2.00 -1.73 34-god/mou( )
Further references: [1895-wal-2].
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 808.24 5.00 293.15 801.78 1.25 300.00 798.41 2.00
290.00 803.33 1.60 298.15 799.32 2.13 310.00 793.50 2.16
(+)-(R)-4-Methylcyclohexene [500032-89-3] C7H12 MW = 96.17 458

T exp 2 est Ref.
K kg m 3
287.15 805.0 2.00 38-mou/gra-1

287.15 805.0 2.00 46-mou/ric
Landolt-Brnstein
New Series IV/8D

T = 273.15 to 293.15 K
A 3.62077 102
B 4.23781
C -9.36895 10-3
273.15 820.60 1.00 -0.01 03-mar( ) 290.75 802.30 0.70 0.09 07-eyk( )
288.15 803.40 1.00 -1.89 03-mar( ) 293.15 800.10 0.60 0.85 23-nam/bru()
293.15 798.50 1.00 -0.75 03-mar1) 286.65 808.60 0.80 1.58 30-god/cau( )
273.15 820.70 1.00 0.09 04-mar-2( ) 286.65 808.60 1.00 1.58 34-god( )
288.15 804.70 1.00 -0.59 04-mar-2( ) 293.15 800.10 0.50 0.85 49-foe/fen()
293.15 798.60 1.00 -0.65 04-mar-21) 293.15 799.20 0.60 -0.05 50-ano-1()
273.15 820.60 1.00 -0.01 04-mar-3( ) 293.15 798.90 0.40 -0.35 {
50-boo/gre( )
293.15 798.50 1.00 -0.75 04-mar-31) 293.15 799.00 0.60 -0.25 {
50-boo/gre( )
293.15 798.90 1.00 -0.35 04-mar-31) 293.15 798.30 0.60 -0.95 61-hue/mau( )
288.25 804.20 0.70 -0.98 07-eyk( ) 293.15 799.30 0.20 0.05
62-ano-3( )
Further references: [04-zel, 29-mid/hen, 34-god/mou, 36-dup-2, 61-shu/tul, 65-mus/bar, 66-gan/kha, 74-
aga/aly, 77-fer/lys].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 823.29 1.19 290.00 803.11 0.77 298.15 792.74 0.66
280.00 814.14 1.15 293.15 799.25 0.52 300.00 790.21 0.93
cont.
Landolt-Brnstein
New Series IV/8D
Cycloheptene [628-92-2] C7H12 MW = 96.17 460

T = 273.15 to 335.25 K
A 1.09030 103
B -9.03934 10-1
cont.
Landolt-Brnstein
New Series IV/8D
Cycloheptene (cont.)
K 3
kg m3 in Fig. 1)
273.15 840.60 2.00 -2.79 1894-mar-1( ) 293.15 825.40 0.60 0.09

36-ruz/sei( )
293.15 823.10 2.00 -2.21 1894-mar-1( ) 291.05 827.20 1.00 -0.01 38-vog()
293.15 823.00 2.00 -2.31 08-har/tan( ) 293.15 825.50 1.00 0.19 38-vog()
293.15 822.80 2.00 -2.51 16-ros( ) 314.55 805.90 1.00 -0.06 38-vog()
293.15 823.90 1.50 -1.41 29-ros-1() 315.25 805.20 1.00 -0.13 38-vog()
286.65 835.90 0.80 4.72 30-god/cau( ){ 335.15 788.50 1.00 1.16 38-vog()
286.65 835.30 2.00 4.12 34-god() 335.25 788.40 1.00 1.15 38-vog()
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 846.23 2.10 298.15 820.79 1.29 330.00 792.00 1.10
280.00 837.19 1.75 300.00 819.12 1.26 340.00 782.96 1.20
290.00 828.16 1.47 310.00 810.08 1.12 350.00 773.92 1.36
293.15 825.31 1.40 320.00 801.04 1.07
Landolt-Brnstein
New Series IV/8D

3.4.1 3 and 4 Member Rings
[1-(1-Methylethyl)ethenyl]cyclopropane [5405-78-7] C 8H14 MW = 110.20 461

T exp 2 est Ref.
3
K kg m
293.15 773.9 1.00 52-sla-1
3.4.2 5-Member Rings
Ethenylidenecyclohexane [5664-20-0] C8H12 MW = 108.18 462

A 1105.74
B -0.870

K kg m3 kg m3
293.15 850.7 2.00 0.00 11-jeg-1

273.15 868.1 2.00 0.00 11-jeg-1

T exp 2 est
K kg m3
270.00 870.8 2.5
280.00 862.1 2.5
290.00 853.4 2.0
293.15 850.7 2.0
298.15 846.3 2.5
1-Ethylidene-2-methylcyclopentane [98428-04-7] C8H14 MW = 110.20 463

T exp 2 est Ref.
3
K kg m
293.15 799.5 1.50 35-nen/van
Landolt-Brnstein
New Series IV/8D
1-Ethyl-2-methylcyclopentene [19780-56-4] C8H14 MW = 110.20 464

A 1051.18
B -0.850

K kg m3 kg m3
293.15 802.0 2.00 -0.00 31-chi

273.15 819.0 2.00 -0.00 31-chi

T exp 2 est
K kg m3
270.00 821.7 2.5
280.00 813.2 2.0
290.00 804.7 2.0
293.15 802.0 2.0
298.15 797.8 2.5
1-(1-Methylethyl)cyclopentene [1462-07-3] C8H14 MW = 110.20 465

T exp 2 est Ref.
K kg m3
293.15 814.1 4.00 14-mee

293.15 818.3 4.00 51-nam/vol
293.15 816.2 4.3 Recommended
3-(1-Methylethyl)cyclopentene [4276-45-3] C8H14 MW = 110.20 466

T exp 2 est Ref.
K kg m3
293.15 794.1 1.00 45-cra/boo
293.15 794.1 0.40 49-boo/hen
Landolt-Brnstein
New Series IV/8D
(1-Methylethylidene)cyclopentane [765-83-3] C8H14 MW = 110.20 467

T exp 2 est Ref.
3
K kg m
293.15 817.0 2.00 07-wal/fle
2-Propenylcyclopentane [3524-75-2] C8H14 MW = 110.20 468

T exp 2 est Ref.
3
K kg m
296.15 793.0 2.00 35-pia/bou 1)
293.15 794.0 0.60 45-whi/her
293.15 791.2 1.00 53-lev/mez
293.15 793.3 1.2 Recommended
1)
1-Propylcyclopentene [3074-61-1] C8H14 MW = 110.20 469

T exp 2 est Ref.
K kg m3
293.15 806.2 3.00 25-eis-2
288.15 805.6 4.00 27-cha/bec 1)
293.15 801.5 1.00 27-cha/bec
293.15 806.2 1.50 39-gro/wac
293.15 795.9 3.00 53-lev/mez
293.15 802.5 1.00 60-nar/shu
293.15 802.7 1.0 Recommended
1)
3-Propylcyclopentene [34067-75-9] C8H14 MW = 110.20 470

T exp 2 est Ref.
K kg m3
293.15 791.0 0.60 46-boo/gre
293.15 791.0 0.60 49-boo/hen
293.15 791.8 1.00 53-lev/tan-1
293.15 791.1 0.7 Recommended
Landolt-Brnstein
New Series IV/8D
1,2,3-Trimethylcyclopentene [473-91-6] C8H14 MW = 110.20 471

equation (based on data sets 471 and 472). Standard
deviations (see introduction):c,w = 1.0785 (combined
temperature ranges, weighted), c,uw = 3.2835 10-1
(combined temperature ranges, unweighted).
T = 277.15 to 298.15 K
A -2.12414 102
B 7.94356
C -1.53551 10-2

K kg m
3
kg m3 in Fig. 1)
293.15 795.00 3.00 -1.67 {
01-zel/lep-1( )
288.15 803.50 3.00 1.92 10-noy/kyr()
292.55 796.20 4.00 -1.10 19-eyk( )
Data sets 471 and 472 were combined for the graph of 1,2,3-trimethylcyclopentene.
cont.
Landolt-Brnstein
New Series IV/8D
1,2,3-Trimethylcyclopentene (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 812.96 7.53 290.00 799.86 3.40 298.15 790.99 3.84
280.00 807.94 3.56 293.15 796.67 3.30 300.00 788.70 4.49
(R)-1,2,3-Trimethylcyclopentene [74190-02-6] C8H14 MW = 110.20 472

K kg m 3
kg m3 in Fig. 1)
290.65 800.80 4.00 1.58 00-tie( ) 293.15 796.10 3.00 -0.57 06-cro/ren()
291.65 798.80 3.00 0.57 {
01-zel/lep-1( ) 298.15 791.60 3.00 0.61 06-cro/ren()
277.15 809.70 3.00 0.01 06-cro/ren() 288.15 803.00 4.00 1.42 09-noy/der( )
283.15 804.60 3.00 -1.13 06-cro/ren() 293.15 797.70 4.00 1.03 10-noy/der()
288.15 800.30 3.00 -1.28 06-cro/ren() 293.15 796.00 2.50 -0.67 37-von/kam( )
292.65 796.50 3.00 -0.70 06-cro/ren()

T exp 2 est Ref.
K kg m3
293.15 787.6 2.00 51-slo
cis-1,3,5-Trimethylcyclopentene [500031-65-2] C8H16 MW = 112.22 474

T exp 2 est Ref.
K kg m3
293.15 775.0 2.00 51-slo
trans-1,3,5-Trimethylcyclopentene [500031-66-3] C8H16 MW = 112.22 475

T exp 2 est Ref.
K kg m 3
293.15 774.5 2.00 51-slo
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 768.7 1.00 45-ano-8
293.15 768.7 1.00 51-bir/joh
293.15 767.7 1.00 51-slo
293.15 764.8 2.00 54-aut
293.15 768.1 1.4 Recommended

T = 277.15 to 298.15 K
A 1.03164 103
B -8.51814 10-1
K 3
kg m3 in Fig. 1)
293.15 783.00 2.00 1.07 1895-beh( ) 293.15 781.70 2.00 -0.23 06-cro/ren()
293.15 781.20 2.00 -0.73 01-zel/lep-1() 298.15 777.20 2.00 -0.47 06-cro/ren()
277.15 795.30 2.00 -0.26 06-cro/ren() 288.15 786.70 1.00 0.51 10-kis-3()
283.15 790.50 2.00 0.05 06-cro/ren() 293.15 782.30 1.00 0.37 10-kis-3()
288.15 786.00 2.00 -0.19 06-cro/ren() 293.15 782.00 1.00 0.07 {
18-von-2( )
289.25 785.10 2.00 -0.15 06-cro/ren() 293.15 781.90 0.60 -0.03
45-ano( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 801.65 1.82 293.15 781.93 1.48 300.00 776.10 2.60
280.00 793.13 2.31 298.15 777.67 2.10 310.00 767.58 9.17
290.00 784.61 1.53
cont.
Landolt-Brnstein
New Series IV/8D
2,3,3-Trimethylcyclopentene (cont.)

T exp 2 est Ref.
K kg m3
293.15 750.6 0.40 51-bir/joh
293.15 750.3 0.60 51-slo
293.15 750.5 0.4 Recommended
Landolt-Brnstein
New Series IV/8D
1,2-Dimethylcyclohexene [1674-10-8] C8H14 MW = 110.20 479

T = 273.15 to 303.15 K
A 1.06372 103
B -8.16712 10-1
273.15 841.10 1.00 0.46 05-sab/mai1() 293.15 823.00 2.00 -1.30 18-mee/fle( )
288.15 826.90 1.00 -1.48 08-zel/gor() 293.15 824.00 2.00 -0.30 33-sig/cra( )
293.15 822.60 1.00 -1.70 08-zel/gor() 288.15 827.30 0.80 -1.08 38-chi()
293.15 824.00 2.00 -0.30 13-wal( ) 293.15 823.20 0.80 -1.10 38-chi()
293.15 824.00 2.00 -0.30 14-mee( ) 303.15 815.00 0.80 -1.13 38-chi()
286.65 831.70 1.50 2.09 15-von/hin( ) 293.15 826.20 0.50 1.90 {
53-ano-1( )
286.85 831.50 1.50 2.05 15-von/hin( ) 293.15 826.50 0.50 2.20
56-ano( )
Further references: [56-goe/mcc].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 843.21 1.30 293.15 824.30 1.25 300.00 818.71 1.24
280.00 835.04 1.29 298.15 820.22 1.18 310.00 810.54 1.50
290.00 826.87 1.32
cont.
Landolt-Brnstein
New Series IV/8D
1,2-Dimethylcyclohexene (cont.)

T = 273.15 to 303.15 K
A 1.04523 103
B -8.19450 10-1
cont.
Landolt-Brnstein
New Series IV/8D
K 3
kg m3 in Fig. 1)
273.15 821.00 2.00 -0.40 05-sab/mai() 303.15 794.50 1.00 -2.32 38-chi()
273.15 821.00 1.00 -0.40 {
05-sab/mai1( ) 298.15 807.00 2.00 6.08 39-mou/pau( )
293.15 800.60 3.00 -4.41 31-ruz/koo( ) 298.15 807.00 2.00 6.08 46-mou()
288.15 806.80 1.00 -2.31 38-chi() 293.15 805.10 1.00 0.09
50-nic/hei( )
293.15 802.60 1.00 -2.41 38-chi()
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 823.98 1.69 293.15 805.01 1.60 300.00 799.40 1.80
280.00 815.79 1.65 298.15 800.92 1.90 310.00 791.20 1.98
290.00 807.59 1.60
Landolt-Brnstein
New Series IV/8D

T = 273.15 to 303.15 K
A 1.07934 103
B -9.46497 10-1
273.15 820.70 2.00 -0.10 05-sab/mai( ) 295.55 798.50 1.50 -1.10 15-von/hin( )
273.15 820.80 1.00 -0.00 05-sab/mai1() 293.15 802.40 1.00 0.53 24-nam/bry( ) {
273.15 820.70 2.00 -0.10 06-sab/mai( ) 293.15 800.50 1.00 -1.37 24-zel/pav( )
287.15 811.10 2.00 3.55 06-sab/mai( ) 288.15 804.70 1.00 -1.91 38-chi()
293.15 800.50 2.00 -1.37 08-zel/gor( ) 293.15 800.60 1.00 -1.27 38-chi()
293.15 800.50 2.00 -1.37 08-zel/gor1( ) 303.15 792.40 1.00 -0.01 38-chi()
292.65 802.00 1.00 -0.35 13-wal() 293.15 803.00 1.00 1.13 38-kaz/glu( )
295.15 798.90 1.50 -1.08 15-von/hin( ) 298.15 802.00 2.00 4.86 47-mou/win( )
Further references: [30-god/cau, 34-god, 46-mou].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 823.79 1.86 293.15 801.87 1.80 300.00 795.39 2.00
280.00 814.32 1.92 298.15 797.14 1.80 310.00 785.93 2.50
290.00 804.86 2.00
cont.
Landolt-Brnstein
New Series IV/8D

T = 273.15 to 298.15 K
A 1.04388 103
B -8.18614 10-1
cont.
Landolt-Brnstein
New Series IV/8D
K kg m 3
kg m3 in Fig. 1)
291.15 800.50 3.00 -5.04 1897-kno( ) 295.75 799.80 1.50 -1.98 15-von/hin()
273.15 820.90 3.00 0.62 07-sab/mai-4( ) 293.15 803.00 2.00 -0.90 33-sig/cra()
285.15 812.20 3.00 1.75 07-sab/mai-4( ) 293.15 805.60 1.00 1.70 38-kaz/glu( )
294.15 802.50 1.00 -0.59 13-wal( ){ 298.15 803.00 2.50 3.19 38-mou/gra( )
295.55 800.00 1.50 -1.94 15-von/hin() 298.15 803.00 2.00 3.19 39-mou/pau()
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 822.85 4.11 293.15 803.90 1.97 300.00 798.30 1.94
280.00 814.67 3.04 298.15 799.81 1.86 310.00 790.11 2.80
290.00 806.48 2.16
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
K kg m3
288.15 765.00 20.00 31-cha/mil
294.15 797.00 1.00 35-zel/pac
3,4-Dimethyl-1-cyclohexene [2808-72-2] C8H14 MW = 110.20 484

A 1055.54
B -0.850

K kg m3
kg m3
292.35 807.5 2.00 0.46 20-von-2

293.15 805.9 2.00 -0.46 20-von-2

T exp 2 est
K kg m3
290.00 809.0 2.5
293.15 806.4 2.0
298.15 802.1 2.5

A 1048.98
B -0.850
cont.
Landolt-Brnstein
New Series IV/8D

K kg m 3
kg m3
293.75 805.5 3.00 6.21 10-von/pet-2

292.55 806.2 3.00 5.89 10-von/pet-2
291.55 807.4 3.00 6.24 10-von/pet-2
294.25 797.0 2.00 -1.87 15-von/hin
288.75 800.9 2.00 -2.64 15-von/hin
288.75 800.9 2.00 -2.64 15-von/hin
291.15 800.5 2.00 -1.00 31-kom/kaw

T exp 2 est
K kg m3
280.00 811.0 3.6
290.00 802.5 3.6
293.15 799.8 3.6
298.15 795.6 3.6

T = 277.15 to 298.15 K
A 1.07995 103
B -9.51614 10-1
K 3
kg m3 in Fig. 1)
277.15 812.90 1.00 -3.31 05-cro/ren( ) 293.15 803.00 2.00 2.02 15-von/lan( )
288.15 803.28 1.00 -2.46 05-cro/ren( ) 294.15 797.00 1.00 -3.03 35-zel/pac()
298.15 794.65 1.00 -1.58 05-cro/ren( ) 289.75 809.20 0.80 4.98 36-hib/lin()
286.65 808.90 1.00 1.73 15-von/lan( ) 293.15 799.90 0.60 -1.08 47-ano-2()
289.35 805.60 1.00 1.00 15-von/lan( ) 293.15 799.90 0.60 -1.08 49-eva( ){
293.15 804.00 2.00 3.02 15-von/lan( ) 293.15 800.80 0.50 -0.18 56-ano( )
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 823.01 1.60 290.00 803.98 1.10 298.15 796.23 1.30
280.00 813.50 1.40 293.15 800.98 1.10 300.00 794.47 1.51
Landolt-Brnstein
New Series IV/8D
Ethenylcyclohexane [695-12-5] C8H14 MW = 110.20 487

A 1052.93
B -0.850

K kg m3 kg m3
292.15 816.6 1.50 12.00 36-lev/zur

293.15 813.4 1.50 9.65 37-lev/pot
293.15 801.2 1.00 -2.55 52-van/koo
293.15 809.1 1.00 5.35 53-lev/mez
293.15 801.8 0.40 -1.99 62-sla/mag

T exp 2 est
K kg m3
290.00 806.4 5.6
293.15 803.7 5.0
1-Ethylcyclohexene [1453-24-3] C8H14 MW = 110.20 488

T = 288.40 to 303.15 K
A 1.97564 103
B -6.89646
C 1.01037 10-2
cont.
Landolt-Brnstein
New Series IV/8D
1-Ethylcyclohexene (cont.)
K 3
kg m3 in Fig. 1)
293.15 826.00 1.00 3.78 08-wal/eva1) 293.15 821.50 0.50 -0.72 53-ano-1()
293.15 823.50 1.00 1.28 08-wal/eva( ) 293.15 821.50 0.50 -0.72 54-ano-1()
292.25 823.80 1.00 0.70 12-von/ell( ) 293.15 821.20 0.50 -1.02 56-ano( ){
293.15 823.10 1.00 0.88 12-von/ell( ) 293.15 822.12 0.06 -0.10 60-cam/ros( )
288.40 827.00 1.00 -0.07 15-rot/von( ) 298.15 817.65 0.06 0.04 60-cam/ros( )
288.65 826.80 1.00 -0.00 15-rot/von( ) 303.15 813.48 0.06 -0.02 60-cam/ros( )
293.15 821.70 1.00 -0.52 35-eis( ) 293.15 822.50 0.60 0.28 66-khr/koc()
Further references: [33-sig/cra, 38-kaz/glu, 53-lev/mez, 56-ohl/far].
cont.
Landolt-Brnstein
New Series IV/8D
1-Ethylcyclohexene (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 836.76 1.73 293.15 822.22 0.26 300.00 816.03 0.18
290.00 825.38 0.50 298.15 817.61 0.18 310.00 808.70 0.51
3-Ethylcyclohexene [2808-71-1] C8H14 MW = 110.20 489

T exp 2 est Ref.
K kg m 3
299.15 810.0 2.00 41-ber

299.15 810.0 2.00 42-ber
293.15 810.4 1.00 53-lev/mez
Ethylidenecyclohexane [1003-64-1] C8H14 MW = 110.20 490

A 1071.20
B -0.850

K kg m 3
kg m3
293.15 823.0 2.00 0.97 08-wal-1

291.15 823.0 2.00 -0.73 08-wal/eva
293.15 822.5 2.00 0.47 08-wal/eva
293.15 822.0 2.00 -0.03 08-wal/eva
290.45 823.9 1.50 -0.42 15-von/hin
290.75 823.7 1.50 -0.37 15-von/hin
293.15 822.5 1.00 0.47 28-god/cau-1
292.15 823.5 1.00 0.62 28-god/cau-1
293.15 821.1 1.00 -0.93 52-van/koo

T exp 2 est
K kg m3
290.00 824.7 2.5
293.15 822.0 2.0
Landolt-Brnstein
New Series IV/8D
1-Methylene-2-methylcyclohexane [500030-97-7] C8H14 MW = 110.20 491

T exp 2 est Ref.
3
K kg m
295.15 808.0 2.00 06-wal/bes

T = 289.45 to 335.05 K
A 1.04429 103
B -8.45746 10-1
K 3
kg m3 in Fig. 1)
291.15 797.00 2.00 -1.05 06-wal() 293.15 797.00 1.50 0.64 38-vog( )
293.15 794.00 2.00 -2.36 06-wal() 315.25 777.80 1.50 0.13 38-vog( )
293.15 798.00 2.00 1.64 {
08-wal-1( ) 334.65 761.40 1.50 0.14 38-vog( )
289.45 800.30 1.50 0.81 38-vog( ) 335.05 761.00 1.50 0.07 38-vog( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 807.48 2.52 298.15 792.13 1.76 320.00 773.65 1.64
290.00 799.03 2.06 300.00 790.57 1.74 330.00 765.20 1.68
293.15 796.36 1.86 310.00 782.11 1.66 340.00 756.74 1.77
cont.
Landolt-Brnstein
New Series IV/8D
1-Methylene-3-methylcyclohexane (cont.)

T = 289.05 to 360.45 K
A 1.03424 103
B -8.16240 10-1
cont.
Landolt-Brnstein
New Series IV/8D
K 3
kg m3 in Fig. 1)
295.15 792.50 2.00 -0.83 06-wal( ){ 289.05 803.30 1.50 4.99 38-vog( )
293.15 792.50 2.00 -2.46 08-wal-1() 293.15 799.60 1.50 4.64 38-vog( )
293.15 790.70 3.00 -4.26 08-wal-5() 334.05 763.40 1.50 1.82 38-vog( )
292.15 791.00 3.00 -4.78 11-per/pop( ) 359.85 741.20 1.50 0.68 38-vog( )
293.15 794.50 2.00 -0.46 33-ale-1() 360.45 740.70 1.50 0.67 38-vog( )
cont.
Landolt-Brnstein
New Series IV/8D
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 805.70 3.22 300.00 789.37 2.16 340.00 756.72 1.80
290.00 797.53 2.89 310.00 781.21 2.30 350.00 748.56 1.75
293.15 794.96 2.45 320.00 773.05 2.40 360.00 740.40 1.70
298.15 790.88 2.18 330.00 764.88 1.90 370.00 732.23 2.30
Methylenecycloheptane [2505-03-5] C8H14 MW = 110.20 494

T exp 2 est Ref.
K kg m3
293.15 824.0 2.00 06-wal-4
293.15 825.7 1.00 53-sor/ber
293.15 825.4 1.0 Recommended
1-Methylcycloheptene [1453-25-4] C8H14 MW = 110.20 495

A 1076.48
B -0.850
K kg m 3
kg m3 K kg m 3
kg m3
292.65 824.0 2.00 -3.73 06-wal-4 286.65 835.6 0.80 2.77 30-god/cau
288.15 829.4 1.00 -2.16 27-god/bed 286.65 834.4 2.00 1.57 34-god
293.15 826.0 1.00 -1.31 27-god/bed 295.15 824.3 2.00 -1.31 36-ruz/sei

T exp 2 est
K kg m3
280.00 838.5 2.8
290.00 830.0 2.3
293.15 827.3 2.3
298.15 823.1 2.5
Landolt-Brnstein
New Series IV/8D
Cyclooctene [931-88-4] C8H14 MW = 110.20 496

T = 273.15 to 293.15 K
A 1.09025 103
B -8.24730 10-1
K kg m
3
kg m3 in Fig. 1)
273.15 871.00 4.00 6.03 10-wil/was( ) 286.65 849.70 2.00 -4.14 30-god/cau()
293.15 855.00 4.00 6.52 10-wil/was( ) 292.15 848.60 2.00 -0.70 31-ruz/boe()
290.15 848.70 2.00 -2.25 27-god/cau( ){ 293.15 850.00 1.00 1.52 48-rep/sch1( )
293.15 841.50 3.00 -6.98 29-ros-1()
cont.
Landolt-Brnstein
New Series IV/8D
Cyclooctene (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 867.57 5.00 290.00 851.08 2.00 298.15 844.35 5.50
280.00 859.32 4.50 293.15 848.48 2.71
(Z)-Cyclooctene [931-87-3] C8H14 MW = 110.20 497

T exp 2 est Ref.
3
K kg m
293.15 847.2 2.00 50-zie/eim
293.15 850.1 1.00 65-tre/mit
293.15 849.5 1.5 Recommended
(E)-Cyclooctene [931-89-5] C8H14 MW = 110.20 498

A 1089.38
B -0.820

K kg m 3
kg m3
293.15 848.3 2.00 -0.70 50-zie/eim

298.15 845.6 2.00 0.70 53-cop/pik

T exp 2 est
K kg m3
290.00 851.6 2.5
293.15 849.0 2.0
298.15 844.9 2.0
Landolt-Brnstein
New Series IV/8D

1,1-Dimethyl-2-(2-methyl-1-propenyl) [33422-32-1] C9H16 MW = 124.23 499

cyclopropane

T exp 2 est Ref.
3
K kg m
293.15 767.7 1.50 13-kis-5
(1-Ethylpropylidene)cyclobutane [500030-93-3] C9H16 MW = 124.23 500

T exp 2 est Ref.
3
K kg m
293.15 809.1 1.50 05-kis/amo
(2-Butenyl)cyclopentane [5860-29-7] C 9H16 MW = 124.23 501

T exp 2 est Ref.
3
K kg m
297.65 806.0 2.00 35-gre-1
1-Butylcyclopentene [2423-01-0] C9H16 MW = 124.23 502

A 1029.33
B -0.750

K kg m 3
kg m3
288.15 810.1 1.00 -3.11 27-cha/bec

290.95 812.3 1.00 1.19 27-cha/bec
293.15 813.8 1.50 4.34 39-gro/wac
cont.
Landolt-Brnstein
New Series IV/8D
1-Butylcyclopentene (cont.)

T exp 2 est
K kg m3
280.00 819.3 2.9
290.00 811.8 2.8
293.15 809.5 2.8
298.15 805.7 2.8
3-Butylcyclopentene [22531-00-6] C9H16 MW = 124.23 503

T exp 2 est Ref.
K kg m3
293.15 799.0 0.70 45-cra/boo
1,2-Diethylcyclopentene [500019-09-0] C9H16 MW = 124.23 504

A 1059.07
B -0.840

K kg m 3
kg m3
293.15 812.3 3.00 -0.52 11-kis1)

298.15 813.6 2.00 4.98 28-cas/rei
273.15 833.1 2.00 3.48 28-cas/rei
293.15 808.8 2.00 -4.02 33-chi
273.15 825.2 2.00 -4.42 33-chi
1)

T exp 2 est
K kg m3
270.00 832.3 4.3
280.00 823.9 4.3
290.00 815.5 4.3
293.15 812.8 4.3
298.15 808.6 4.3
Landolt-Brnstein
New Series IV/8D
3,3-Diethylcyclopentene [500031-47-0] C9H16 MW = 124.23 505

T exp 2 est Ref.
3
K kg m
293.15 808.3 2.00 11-kis
293.15 808.4 2.00 11-kis
293.15 808.3 2.00 Recommended
1-(1,1-Dimethylethyl)cyclopentene [3419-67-8] C9H16 MW = 124.23 506

T exp 2 est Ref.
3
K kg m
293.15 802.1 1.00 39-gro/wac
3-(1,1-Dimethylethyl)cyclopentene [6189-88-4] C9H16 MW = 124.23 507

T exp 2 est Ref.
3
K kg m
293.15 806.6 0.60 45-cra/boo
2-Ethyl-1,3-dimethylcyclopentene [500031-27-6] C9H16 MW = 124.23 508

T exp 2 est Ref.
K kg m3
293.15 803.0 2.00 18-von-2
1-Methyl-3-(1-methylethyl)cyclopentene [13828-12-1] C9H16 MW = 124.23 509

T exp 2 est Ref.
K kg m3
293.15 801.0 2.00 04-sem
Landolt-Brnstein
New Series IV/8D
3-Methyl-1-(1-methylethyl)cyclopentene [51115-02-7] C9H16 MW = 124.23 510

T exp 2 est Ref.
3
K kg m
295.15 791.0 2.00 03-wal/col
1-Methyl-2-(1-methylethylidene) [500030-94-4] C9H16 MW = 124.23 511

cyclopentane

T exp 2 est Ref.
3
K kg m
293.15 810.3 1.50 12-kis-4
(R)-1-Methyl-4-(1-methylethyl) [2699-04-9] C9H16 MW = 124.23 512

cyclopentene

A 1041.54
B -0.840

K kg m3 kg m3
273.15 812.0 2.00 -0.10 08-bou/lev

294.15 794.5 1.50 0.04 09-wal-6

T exp 2 est
K kg m3
270.00 814.7 2.4
280.00 806.3 2.0
290.00 797.9 1.8
293.15 795.3 1.6
298.15 791.1 2.0
Landolt-Brnstein
New Series IV/8D
1-(1-Methylethenyl)- [98880-18-3] C9H16 MW = 124.23 513

2-methylcyclopentane

T exp 2 est Ref.
3
K kg m
293.15 800.5 1.50 12-kis-4
1-Methyl-1-(2-propenyl)cyclopentane [500023-43-8] C9H16 MW = 124.23 514

T exp 2 est Ref.
3
K kg m
293.15 809.3 0.70 57-nov/khr
1-Methyl-3-propylcyclopentene [500031-16-3] C9H16 MW = 124.23 515

T exp 2 est Ref.
3
K kg m
293.15 792.4 1.00 50-kaz/kop
3-(1-Methylpropyl)cyclopentene [500019-12-5] C9H16 MW = 124.23 516

T exp 2 est Ref.
3
K kg m
293.15 809.2 0.80 45-cra/boo
3-(2-Methylpropyl)cyclopentene [37689-12-6] C9H16 MW = 124.23 517

T exp 2 est Ref.
3
K kg m
293.15 793.6 2.00 41-cra
293.15 793.6 2.00 45-cra/boo
Landolt-Brnstein
New Series IV/8D
1,2,3,3-Tetramethylcyclopentene [65378-75-8] C9H16 MW = 124.23 518

T = 273.15 to 352.05 K
A 1.13685 103
B -1.16276
K kg m3
kg m3 in Fig. 1)
287.65 803.40 2.00 1.02 1893-thi( ) 288.15 803.50 2.00 1.70 07-bla-2()
273.15 813.40 2.00 -5.84 1895-beh( ){ 352.05 723.20 3.00 -4.30 19-eyk()
293.15 803.40 3.00 7.42 1897-tie()
cont.
Landolt-Brnstein
New Series IV/8D
1,2,3,3-Tetramethylcyclopentene (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 822.90 4.01 298.15 790.17 4.10 330.00 753.14 9.05
280.00 811.27 3.40 300.00 788.02 4.73 340.00 741.51 9.47
290.00 799.65 2.80 310.00 776.39 7.58 350.00 729.88 5.00
293.15 795.98 3.60 320.00 764.76 8.58 360.00 718.25 6.00
3,3,5,5-Tetramethylcyclopentene [38667-10-6] C9H16 MW = 124.23 519

T exp 2 est Ref.
K kg m3
293.15 748.4 2.00 51-slo
3,3-Dimethyl-1-methylenecyclohexane [52291-22-2] C9H16 MW = 124.23 520
Table 1. Fit with estimated coefficient for 2

A 1013.95
B -0.750

K kg m3
kg m3
289.65 797.0 1.50 0.29 26-esc-1

283.15 801.3 1.50 -0.29 26-esc-1

T exp 2 est
K kg m3
280.00 803.9 1.8
290.00 796.4 1.6
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
287.25 792.2 4.00 15-von/hin
287.75 791.8 4.00 15-von/hin
287.75 792.0 4.00 Recommended

T exp 2 est Ref.
K kg m3
287.25 792.2 4.00 15-von/hin
1-Ethenyl-3-methylcyclohexane [500029-68-5] C9H16 MW = 124.23 523

T exp 2 est Ref.
K kg m3
293.15 813.0 2.00 08-wal-1
293.15 813.0 2.00 08-wal/eva-1
298.15 793.6 1.00 59-ove/mul
1-Ethenyl-4-methylcyclohexane [500029-69-6] C9H16 MW = 124.23 524

T exp 2 est Ref.
K kg m3
293.15 812.5 2.00 08-wal-1
293.15 811.0 2.00 08-wal/eva-2
292.15 812.5 1.00 08-wal/eva-2
1-Ethylidene-2-methylcyclohexane [500031-01-6] C9H16 MW = 124.23 525

T exp 2 est Ref.
3
K kg m
273.15 823.0 2.00 14-mur/amo
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 813.0 2.00 08-wal/eva-1
292.15 812.2 2.00 11-haw/per

T exp 2 est Ref.
K kg m3
294.15 810.0 2.00 09-wal/ren
292.15 812.0 2.00 09-wal/ren
1-Ethyl-2-methylcyclohexene [19780-54-2] C9H16 MW = 124.23 528

T exp 2 est Ref.
K kg m3
293.15 830.3 2.00 33-sig/cra

A 1033.45
B -0.750
K 3
kg m kg m3 K kg m 3
kg m3
273.15 827.8 1.00 -0.79 06-sab/mai 295.15 814.5 1.50 2.41 13-wal/aug
289.15 816.9 1.00 0.31 06-sab/mai 293.15 813.3 1.00 -0.29 24-nam/bry
293.15 814.0 2.00 0.41 12-von/moo 293.15 812.0 2.00 -1.59 33-sig/cra

T exp 2 est
K kg m3
270.00 831.0 1.8
280.00 823.5 1.5
290.00 816.0 1.2
293.15 813.6 1.2
298.15 809.8 1.8
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 813.0 2.00 33-sig/cra
298.15 812.0 3.00 38-mou/gra

T exp 2 est Ref.
K kg m3
293.15 816.5 2.00 56-pin/esc
(1-Methylethylidene)cyclohexane [5749-72-4] C9H16 MW = 124.23 532

T exp 2 est Ref.
K kg m3
293.15 836.0 2.00 08-wal-1
293.15 836.0 2.00 08-wal/mal
1-(1-Methylethyl)cyclohexene [4292-04-0] C9H16 MW = 124.23 533

A 1076.19
B -0.850
K kg m 3
kg m3 K kg m 3
kg m3
293.15 829.0 2.00 1.98 08-wal/mal 286.05 832.0 2.00 -1.05 12-von/ell
293.15 826.0 2.00 -1.02 12-von/ell 293.15 828.0 2.00 0.98 33-sig/cra
288.35 830.2 2.00 -0.90 12-von/ell 293.15 821.9 3.00 -5.12 47-nam/vol1)
1)
cont.
Landolt-Brnstein
New Series IV/8D
1-(1-Methylethyl)cyclohexene (cont.)

T exp 2 est
K kg m3
280.00 838.2 2.6
290.00 829.7 2.0
293.15 827.0 2.0
298.15 822.8 3.0
(1-Propenyl)cyclohexane [5364-83-0] C9H16 MW = 124.23 534

T exp 2 est Ref.
K kg m3
293.15 821.0 2.00 08-wal-1
292.15 821.0 0.80 08-wal/chu
3-Propylcyclohexene [3983-06-0] C9H16 MW = 124.23 535

T exp 2 est Ref.
3
K kg m
292.15 824.0 2.00 28-fuj
(2-Propenyl)cyclohexane [2114-42-3] C9H16 MW = 124.23 536

T = 273.15 to 314.65 K
A 1.02642 103
B -7.15170 10-1
273.15 831.20 1.50 0.13 {

10-der( ) 301.65 811.70 0.70 1.02
33-hur/bol( )
286.15 819.60 1.50 -2.17 10-der1) 314.65 801.00 0.70 -0.39
33-hur/bol( )
293.15 816.00 0.70 -0.76
33-hur/bol( )
Further references: [27-bou, 36-lev/tra, 53-lev/mez].
cont.
Landolt-Brnstein
New Series IV/8D
2-Propenylcyclohexane (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 833.32 1.97 293.15 816.76 0.70 310.00 804.71 0.85
280.00 826.17 1.14 298.15 813.19 0.69 320.00 797.56 0.97
290.00 819.02 0.75 300.00 811.86 0.71
Landolt-Brnstein
New Series IV/8D
1-Propylcyclohexene [2539-75-5] C9H16 MW = 124.23 537

T exp 2 est Ref.
3
K kg m
292.15 838.0 3.00 08-wal/chu
293.15 824.0 2.00 33-sig/cra
293.15 827.9 1.00 53-lev/mez
293.15 824.0 1.00 66-khr/koc
293.15 825.7 1.50 Recommended
1,3,3-Trimethylcyclohexene [503-47-9] C9H16 MW = 124.23 538

T exp 2 est Ref.
K kg m3
293.15 812.3 2.00 54-lev/shu
298.15 788.5 2.00 56-opp/day

T exp 2 est Ref.
K kg m3
293.15 812.4 2.00 50-nic/hei

A 1045.83
B -0.850
K 3
kg m kg m3 K kg m 3
kg m3
294.15 796.5 1.50 0.69 13-wal/sch 286.25 805.4 1.50 2.88 15-von/hin
297.85 794.1 1.50 1.44 15-von/hin 287.45 802.5 1.50 1.00 15-von/hin
287.45 802.5 1.50 1.00 15-von/hin 286.65 803.1 1.50 0.92 15-von/hin
286.65 803.1 1.50 0.92 15-von/hin 293.15 795.8 0.40 -0.86 49-ano-1
286.95 804.8 1.50 2.87 15-von/hin 293.15 797.0 1.50 0.34 50-nic/hei
cont.
Landolt-Brnstein
New Series IV/8D
1,3,5-Trimethylcyclohexene (cont.)

T exp 2 est
K kg m3
280.00 807.8 1.8
290.00 799.3 1.5
293.15 796.7 1.5
298.15 792.4 1.6

A 1068.11
B -0.900

K kg m 3
kg m3
287.95 809.8 1.00 0.85 15-von/lan

288.25 809.6 1.00 0.92 15-von/lan
291.95 803.2 1.00 -2.15 15-von/lan
293.15 804.0 1.00 -0.27 15-von/lan
296.30 802.1 1.00 0.66 15-von/lan

T exp 2 est
K kg m3
280.00 816.1 1.8
290.00 807.1 1.4
293.15 804.3 1.4
298.15 799.8 1.4

A 1068.41
B -0.900
cont.
Landolt-Brnstein
New Series IV/8D

K kg m3
kg m3
289.30 807.8 1.50 -0.24 20-von-2

293.15 805.0 2.00 0.43 20-von-2

T exp 2 est
K kg m3
280.00 816.4 1.6
290.00 807.4 1.7
293.15 804.6 1.8
298.15 800.1 2.0
cis-1,4,5-Trimethylcyclohexene [30631-18-6] C9H16 MW = 124.23 543

T exp 2 est Ref.
K kg m3
293.15 814.0 2.00 22-ski/sch
trans-1,4,5-Trimethylcyclohexene [87954-39-0] C9H16 MW = 124.23 544

T exp 2 est Ref.
3
K kg m
293.15 805.0 2.00 22-ski/sch

T exp 2 est Ref.
3
K kg m
298.15 828.5 3.00 47-mou/win
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 822.5 0.60 47-ano-2

A 1086.47
B -0.900

K kg m3 kg m3
293.45 821.7 2.00 -0.66 15-von/lan

288.15 827.8 2.00 0.66 15-von/lan

T exp 2 est
K kg m3
280.00 834.5 2.5
290.00 825.5 2.0
293.15 822.6 2.2
298.15 818.1 3.0

A 1051.39
B -0.850
cont.
Landolt-Brnstein
New Series IV/8D

K 3
kg m kg m3
296.15 798.1 3.00 -1.56 1897-kno

294.65 791.1 3.00 -9.83 04-har/wei
288.15 807.8 3.00 1.34 10-cro/gil
290.95 809.4 3.00 5.32 12-von/moo
287.55 811.7 3.00 4.73 12-von/moo

T exp 2 est
K kg m3
280.00 813.4 5.5
290.00 804.9 5.5
293.15 802.2 5.5
298.15 798.0 5.5

T exp 2 est Ref.
3
K kg m
293.15 788.6 0.40 50-boo/gre
293.15 788.7 0.40 51-ano-3
293.15 788.7 0.40 Recommended

T exp 2 est Ref.
3
K kg m
293.15 815.9 0.40 62-ano-3
r-3, t-4, c-5-Trimethylcyclohexene [73156-88-4] C9H16 MW = 124.23 551

T exp 2 est Ref.
3
K kg m
293.15 811.4 0.40 56-bus/gre
293.15 811.4 1.00 62-mah/gre
Landolt-Brnstein
New Series IV/8D
r-3, t-4, t-5-Trimethylcyclohexene [500031-82-3] C9H16 MW = 124.23 552

T exp 2 est Ref.
K kg m3
293.15 812.9 1.00 62-mah/gre

T exp 2 est Ref.
3
K kg m
293.15 797.8 2.00 1893-tie/sem
293.15 793.9 0.50 50-boo/gre
293.15 794.3 2.00 51-ano-3
293.15 794.1 0.50 Recommended
3.5.4 7 to 9 Member Rings
1,2-Dimethylcycloheptene [20053-89-8] C9H16 MW = 124.23 554

T exp 2 est Ref.
3
K kg m
293.15 836.0 1.00 55-cri/ker
Methylenecyclooctane [3618-18-6] C9H16 MW = 124.23 555
Table 1. Experimental value with uncertainty

T exp 2 est Ref.
K kg m3
293.15 848.5 1.00 53-sor/ber
(E)-Cyclononene [3958-38-1] C9H16 MW = 124.23 556

T exp 2 est Ref.
3
K kg m
293.15 861.5 2.00 52-blo/liu
(Z)-Cyclononene [933-21-1] C9H16 MW = 124.23 557

T exp 2 est Ref.
K kg m3
293.15 867.1 2.00 52-blo/liu
Landolt-Brnstein
New Series IV/8D

1,3-Diethyl-2-methylcyclopentene [500031-29-8] C10H18 MW = 138.25 558

T exp 2 est Ref.
3
K kg m
293.15 811.0 2.00 18-von-2
1,1-Dimethyl-2-(1-methylethenyl) [500025-86-5] C10H18 MW = 138.25 559

cyclopentane

T exp 2 est Ref.
3
K kg m
298.15 794.8 0.80 49-ste/spa
1-(1,1-Dimethylpropyl)cyclopentene [500032-63-3] C10H18 MW = 138.25 560

T exp 2 est Ref.
3
K kg m
293.15 825.6 1.00 39-gro/wac
4-(1-Methylethyl)-2,3- [500031-28-7] C10H18 MW = 138.25 561

dimethylcyclopentene

A 1043.89
B -0.800

K kg m3 kg m3
293.15 804.6 4.00 -4.77 04-tsc-11)

291.65 810.0 3.00 -0.57 15-wal-2
294.15 808.4 3.00 -0.17 15-wal-2
295.15 808.5 3.00 0.73 15-wal-2
1)
cont.
Landolt-Brnstein
New Series IV/8D
4-(1-Methylethyl)-2,3-dimethylcyclopentene (cont.)

T exp 2 est
K kg m3
290.00 811.9 4.6
293.15 809.4 4.0
298.15 805.4 4.0
1-Ethylidene-3-(1-methylethyl) [500030-95-5] C10H18 MW = 138.25 562

cyclopentane

T exp 2 est Ref.
3
K kg m
293.15 809.0 2.00 11-wal-4
1-Ethylidene-2,2,3- [500030-96-6] C10H18 MW = 138.25 563

trimethylcyclopentane

T exp 2 est Ref.
3
K kg m
297.15 802.4 1.50 28-von/hey
1-(3-Methylbutyl)cyclopentene [37689-15-9] C10H18 MW = 138.25 564

T exp 2 est Ref.
3
K kg m
298.15 801.0 1.00 29-har
293.15 815.1 1.00 57-shu/che
3-(3-Methylbutyl)cyclopentene [37689-16-0] C10H18 MW = 138.25 565

T exp 2 est Ref.
3
K kg m
295.15 796.9 1.00 37-von/kam
Landolt-Brnstein
New Series IV/8D
1-Pentylcyclopentene [4291-98-9] C10H18 MW = 138.25 566

T exp 2 est Ref.
3
K kg m
293.15 812.8 1.00 39-pla
293.15 805.2 2.00 40-tur/tar
293.15 811.3 3.5 Recommended
(2-Butenyl)cyclohexane [500031-03-8] C 10H18 MW = 138.25 567

A 1062.23
B -0.850

K kg m3 kg m3
294.15 813.0 2.00 0.80 27-bou

286.15 818.0 2.00 -1.00 27-bou
293.15 813.1 1.00 0.05 37-lev/pot

T exp 2 est
K kg m3
280.00 824.2 2.8
290.00 815.7 2.5
293.15 813.0 2.5
298.15 808.8 2.6
1-Butylcyclohexene [3282-53-9] C10H18 MW = 138.25 568

T exp 2 est Ref.
3
K kg m
293.15 826.0 2.00 33-sig/cra
293.15 822.9 1.00 66-khr/koc
293.15 823.5 1.5 Recommended
Landolt-Brnstein
New Series IV/8D
1,2-Diethylcyclohexene [103394-01-0] C10H18 MW = 138.25 569

T exp 2 est Ref.
3
K kg m
298.15 831.0 3.00 49-dic/lov
293.15 845.1 2.00 50-nic/hei

T exp 2 est Ref.
3
K kg m
293.15 805.1 1.00 50-nic/hei-1

T exp 2 est Ref.
3
K kg m
293.15 830.0 1.50 11-hen/boy
1-(1,1-Dimethylethyl)cyclohexene [3419-66-7] C10H18 MW = 138.25 572

T exp 2 est Ref.
3
K kg m
298.15 827.6 1.00 56-goe/ree

T exp 2 est Ref.
3
K kg m
298.15 820.3 2.00 56-goe/ree
Landolt-Brnstein
New Series IV/8D

A 1051.46
B -0.750

K 3
kg m kg m3
293.15 831.5 2.00 -0.10 00-pin/ipa

313.15 817.3 2.00 0.70 00-pin/ipa
293.15 831.5 0.80 -0.10 39-gro/wac

T exp 2 est
K kg m3
290.00 834.0 2.0
293.15 831.6 1.3
298.15 827.8 1.8
310.00 819.0 2.0
320.00 811.5 2.0
2-Ethyl-4,4-dimethylcyclohexene [500031-35-6] C10H18 MW = 138.25 575

T exp 2 est Ref.
3
K kg m
293.15 832.0 2.00 12-von/moo
3-Ethyl-1,3-dimethylcyclohexene [99191-29-4] C10H18 MW = 138.25 576

T exp 2 est Ref.
3
K kg m
293.15 827.8 2.00 54-lev/shu
Landolt-Brnstein
New Series IV/8D
1-Methylene-4-(1-methylethyl) [1124-24-9] C10H18 MW = 138.25 577

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 866.7 2.00 37-isk
1-Methyl-1-(1-methylethenyl) [16580-19-1] C10H18 MW = 138.25 578

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 844.7 0.50 55-pin/mar

cyclohexene

T exp 2 est Ref.
3
K kg m
293.15 834.5 1.00 66-sad/akh

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 834.5 0.80 08-wal/chu-3
d-1-Methyl-3-(1-methylethenyl) [500031-11-8] C10H18 MW = 138.25 581

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 817.7 2.00 11-kis/saw
Landolt-Brnstein
New Series IV/8D
l-1-Methyl-3-(1-methylethenyl) [500031-12-9] C10H18 MW = 138.25 582

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 818.4 2.00 11-kis-1

cyclohexane

T exp 2 est Ref.
K kg m3
293.15 825.0 2.00 08-wal-1
293.15 825.0 1.00 08-wal/chu-2
293.15 825.0 1.00 08-wal/chu-3
293.15 821.4 2.00 11-kis/saw
293.15 824.6 1.4 Recommended

cyclohexane

A 1071.51
B -0.850

K kg m3
kg m3
293.15 831.0 4.00 8.67 08-wal-1

294.15 831.0 4.00 9.52 08-wal/chu-1
293.65 817.5 3.00 -4.41 10-beh
294.15 819.0 3.00 -2.48 10-beh
295.15 817.3 3.00 -3.33 14-sem/fel-1

T exp 2 est
K kg m3
290.00 825.0 5.6
293.15 822.3 5.6
298.15 818.1 5.6
Landolt-Brnstein
New Series IV/8D
1-Methyl-4-(1-methylethyl)cyclohexene [5502-88-5] C10H18 MW = 138.25 585

T exp 2 est Ref.
3
K kg m
294.15 821. 0 2.00 11-wal
(R)-1-Methyl-4-(1-methylethyl) [1195-31-9] C10H18 MW = 138.25 586

cyclohexene

T exp 2 est Ref.
3
K kg m
293.15 829.0 5.00 03-sem
293.15 825.8 5.00 08-bac
291.15 824.6 5.00 11-vav
293.15 810.0 4.00 18-bro/hum
293.15 821.2 5.1 Recommended

cyclohexane

A 1068.92
B -0.850

K kg m 3
kg m3
293.15 810.4 6.00 -9.34 06-sem/rim1)

293.15 814.1 6.00 -5.64 11-kis-71)
294.15 821.7 3.00 2.81 14-sem/fel-1
288.15 809.3 5.00 -14.69 36-lev/tra
293.15 823.4 5.00 3.66 66-sad/akh
1)

T exp 2 est
K kg m3
280.00 830.9 7.6
290.00 822.4 7.5
293.15 819.7 7.5
298.15 815.5 7.6
Landolt-Brnstein
New Series IV/8D
cis-1-Methyl-4-(1-methylethenyl) [1879-07-8] C10H18 MW = 138.25 588

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 816.0 2.00 22-ski/sch
trans-1-Methyl-4-(1-methylethenyl) [1124-25-0] C10H18 MW = 138.25 589

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 792.0 2.00 22-ski/sch

cyclohexane

T exp 2 est Ref.
3
K kg m
294.15 831.0 2.00 06-wal-6

T exp 2 est Ref.
3
K kg m
293.15 828.0 4.00 01-sem-1
293.15 820.8 4.00 20-hen/sme
293.15 824.4 4.00 Recommended

T exp 2 est Ref.
3
K kg m
293.15 824.0 5.00 09-sem-3
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
273.15 827.0 2.00 02-sab/sen-1
273.15 823.0 2.00 07-sab/mai-4
273.15 825.0 2.4 Recommended
1-Methyl-3-(1-propenyl)cyclohexane [500029-71-0] C10H18 MW = 138.25 594

T exp 2 est Ref.
3
K kg m
293.15 814.0 2.00 08-wal-1
292.15 814.00 2.00 08-wal/ren
1-Methyl-4-(1-propenyl)cyclohexane [500029-72-1] C10H18 MW = 138.25 595

T exp 2 est Ref.
K kg m3
293.15 815.0 2.00 08-wal-1
292.15 813.5 1.00 08-wal/ren-1
293.15 815.0 2.50 08-wal/ren-1
1-Methyl-2-propylcyclohexene [93168-17-3] C10H18 MW = 138.25 596

T exp 2 est Ref.
K kg m3
293.15 830.0 2.00 33-sig/cra
1-Methyl-3-propylidenecyclohexane [500031-09-4] C10H18 MW = 138.25 597

T exp 2 est Ref.
K kg m3
292.15 814.0 2.00 08-wal/ren
Landolt-Brnstein
New Series IV/8D
1-Methyl-4-propylidenecyclohexane [500031-13-0] C10H18 MW = 138.25 598

T exp 2 est Ref.
3
K kg m
292.15 813.5 2.00 08-wal/ren
293.15 811.0 2.00 18-wal/aug

T exp 2 est Ref.
3
K kg m
298.15 813.0 3.00 39-mou/pau

A 1041.43
B -0.750

K kg m3 kg m3
273.15 838.7 2.00 2.13 06-sab/mai

289.15 827.0 2.00 2.43 06-sab/mai
293.15 817.0 2.00 -4.57 33-sig/cra

T exp 2 est
K kg m3
270.00 838.9 3.3
280.00 831.4 3.2
290.00 823.9 3.2
293.15 821.6 3.3
298.15 817.8 3.3
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 814.0 2.00 33-sig/cra

T exp 2 est Ref.
3
K kg m
298.15 814.0 3.00 39-mou/pau
1,2,3,3-Tetramethylcyclohexene [500032-79-1] C10H18 MW = 138.25 603

T exp 2 est Ref.
3
K kg m
298.15 835.0 2.00 56-opp/day

A 1034.47
B -0.750
K kg m 3
kg m3 K kg m 3
kg m3
273.15 825.0 2.00 -4.61 12-wil/hat 293.15 817.0 2.00 2.39 20-von-2
293.15 811.0 2.00 -3.61 12-wil/hat 293.15 812.2 2.00 -2.41 25-eis/gor
289.65 819.9 1.00 2.66 20-von-2 293.15 812.2 2.00 -2.41 25-eis/gor

T exp 2 est
K kg m3
270.00 832.0 3.2
280.00 824.5 3.0
290.00 817.0 3.0
293.15 814.6 3.0
298.15 810.9 3.0
Landolt-Brnstein
New Series IV/8D
1,2, cis-4,5-Tetramethylcyclohexene [500031-36-7] C10H18 MW = 138.25 605

T exp 2 est Ref.
3
K kg m
293.15 828.0 2.00 22-ski/sch
1,2, trans-4,5-Tetramethylcyclohexene [500031-37-8] C10H18 MW = 138.25 606

T exp 2 est Ref.
3
K kg m
293.15 817.0 2.00 22-ski/sch

T exp 2 est Ref.
3
K kg m
293.15 799.1 2.00 52-von/sch-1

T exp 2 est Ref.
3
K kg m
293.15 828.0 2.00 01-sem-1
293.15 819.4 3.00 22-maj/kub
293.15 825.4 3.9 Recommended

T exp 2 est Ref.
3
K kg m
293.15 800.5 2.00 54-chi/maq
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 789.0 2.00 54-chi/maq
1,1,2-Trimethyl-3-methylenecyclohexane [500031-14-1] C10H18 MW = 138.25 611

T exp 2 est Ref.
3
K kg m
284.15 832.0 2.00 26-esc-1
1,4,4-Trimethylcycloheptene [4755-36-6] C10H18 MW = 138.25 612

T exp 2 est Ref.
3
K kg m
293.15 818.5 1.00 36-ruz/sei
1-Ethylcyclooctene [49660-70-0] C10H18 MW = 138.25 613

T exp 2 est Ref.
3
K kg m
293.15 846.2 1.00 52-hag
(Z)-Cyclodecene [935-31-9] C10H18 MW = 138.25 614

T exp 2 est Ref.
3
K kg m
293.15 874.3 1.00 52-pre/sch
(E)-Cyclodecene [2198-20-1] C10H18 MW = 138.25 615

T exp 2 est Ref.
3
K kg m
293.15 868.1 1.00 52-pre/sch
Landolt-Brnstein
New Series IV/8D

1-Hexylcyclopentene [4291-99-0] C11H20 MW = 152.28 616

T exp 2 est Ref.
3
K kg m
293.15 807.9 2.00 33-zel/mic
293.15 815.8 2.00 39-pla
293.15 811.8 3.4 Recommended

trimethylcyclopentene

T exp 2 est Ref.
K kg m3
292.15 809.5 3.00 34-von/kur
1-Butyl-2-methylcyclohexene [56608-70-9] C11H20 MW = 152.28 618

T exp 2 est Ref.
K kg m3
293.15 831.0 2.00 33-sig/cra

T exp 2 est Ref.
K kg m3
293.15 816.0 3.00 33-sig/cra

T exp 2 est Ref.
K kg m3
293.15 818.0 2.00 33-sig/cra
4-(1,1-Dimethylpropyl)cyclohexene [500031-72-1] C11H20 MW = 152.28 621
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 841.0 1.00 39-gro/wac
1,3-Dimethyl-3-propylcyclohexene [500031-75-4] C11H20 MW = 152.28 622

T exp 2 est Ref.
K kg m3
293.15 826.0 2.00 54-lev/shu
2-(1-Methylethyl)-1,5- [500031-42-5] C11H20 MW = 152.28 623

dimethylcyclohexene

T exp 2 est Ref.
3
K kg m
298.15 855.0 1.50 29-rea/wat
1-(1-Methylethenyl)-2,3- [16580-20-4] C11H20 MW = 152.28 624

dimethylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 828.4 3.00 66-sad/akh
1-(1-Methylethenyl)-3,5- [16580-21-5] C11H20 MW = 152.28 625

dimethylcyclohexane

T exp 2 est Ref.
3
K kg m
293.15 836.0 3.00 66-sad/akh
4,4-Dimethyl-3-(1-methylethyl)-1- [500025-85-4] C11H20 MW = 152.28 626
Landolt-Brnstein
New Series IV/8D
cyclohexene

T exp 2 est Ref.
3
K kg m
298.15 826.0 1.00 49-ste/spa
1-Ethyl-2,2-dimethyl-6- [500031-99-2] C11H20 MW = 152.28 627

methylenecyclohexane

T exp 2 est Ref.
3
K kg m
283.15 816.0 2.00 26-esc-1
1-Ethyl-2-propylcyclohexene [500031-74-3] C11H20 MW = 152.28 628

T exp 2 est Ref.
3
K kg m
298.15 843.0 2.00 49-dic/lov
1-Ethyl-1-(2-propenyl)cyclohexane [500019-84-1] C11H20 MW = 152.28 629

T exp 2 est Ref.
K kg m3
293.15 837.9 0.80 57-khr/bal
1-(1-Methylbutyl)cyclohexene [169265-89-8] C11H20 MW = 152.28 630

T exp 2 est Ref.
K kg m3
273.15 856.0 2.00 04-sab/mai
1-(3-Methylbutyl)cyclohexene [3983-04-8] C11H20 MW = 152.28 631

T exp 2 est Ref.
3
K kg m
293.15 824.0 2.00 33-sig/cra
(3-Pentenyl)cyclohexane [6881-53-4] C11H20 MW = 152.28 632
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
K kg m3
298.15 832.2 2.00 35-mul/wak
293.11 871.6 3.00 63-gen/pet
1-Methyl-3-methylene-4- [500031-98-1] C11H20 MW = 152.28 633

(1-methylethyl)cyclohexane

T exp 2 est Ref.
K kg m3
289.15 827.3 2.00 22-oga/miz
1-Methyl-3- [500031-97-0] C11H20 MW = 152.28 634

(2-methyl-2-propenyl)cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 812.0 2.00 12-wal/von
1-Pentylcyclohexene [15232-85-6] C11H20 MW = 152.28 635

T exp 2 est Ref.
3
K kg m
293.15 829.0 2.00 33-sig/cra
4-Methyl-2-(2-methylpropyl)cyclohexene [500018-93-9] C11H20 MW = 152.28 636

T exp 2 est Ref.
K kg m3
293.15 810.0 2.00 33-sig/cra
1-(2-Methylpropyl)-5- [500031-73-2] C11H20 MW = 152.28 637

methylcyclohexene
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 810.6 2.00 33-sig/cra
1,3,3,5,5-Pentamethylcyclohexene [500031-81-2] C11H20 MW = 152.28 638

A 1053.40
B -0.850

K kg m3 kg m3
292.15 805.2 1.00 0.12 52-von/sch

293.15 804.1 1.00 -0.13 54-chi/maq

T exp 2 est
K kg m3
290.00 806.9 1.2
293.15 804.2 1.1
298.15 800.0 1.4
(1-Propylethenyl)cyclohexane [500031-15-2] C11H20 MW = 152.28 639

T exp 2 est Ref.
3
K kg m
293.15 822.0 2.00 27-bou
1,1,2,2-Tetramethyl-3- [500032-00-8] C11H20 MW = 152.28 640

methylenecyclohexane

T exp 2 est Ref.
3
K kg m
284.15 824.6 2.00 26-esc-1
1,2,4-Trimethyl-4- [73156-90-8] C11H20 MW = 152.28 641

(1-methylethyl)cyclohexene
Landolt-Brnstein
New Series IV/8D

A 1094.46
B -0.850

K kg m3 kg m3
298.15 842.3 1.50 1.28 11-ric

273.15 860.0 2.00 -2.28 11-ric

T exp 2 est
K kg m3
270.00 865.0 2.1
280.00 856.5 1.8
290.00 848.0 1.7
293.15 845.3 1.7
298.15 841.0 1.8
6,6-Dimethylcyclononene [500031-80-1] C11H20 MW = 152.28 642

T exp 2 est Ref.
K kg m3
298.15 853.1 1.00 55-blo/whe
(E)-Cycloundecene [500033-21-6] C11H20 MW = 152.28 643

T exp 2 est Ref.
K kg m3
293.15 870.6 2.00 54-zie/sau
Landolt-Brnstein
New Series IV/8D
3.8 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C12 to C13

1-Heptylcyclopentene [4292-00-6] C12H22 MW = 166.31 644

T exp 2 est Ref.
3
K kg m
293.15 817.6 2.00 39-pla
293.15 820.6 1.00 56-pet/ser
293.15 820.0 1.5 Recommended
3-Heptylcyclopentene [66553-63-7] C12H22 MW = 166.31 645

T exp 2 est Ref.
K kg m3
294.15 807.2 2.00 41-von/rei
1,1-Dimethyl-3-methylene-2- [500032-02-0] C12H22 MW = 166.31 646

propylcyclohexane

T exp 2 est Ref.
K kg m3
283.15 812.6 2.00 26-esc-1
1,2-Dipropylcyclohexene [100383-97-9] C12H22 MW = 166.31 647

T exp 2 est Ref.
K kg m3
298.15 868.0 3.00 49-dic/lov
2-Ethyl-1-(1-methylethyl)-4- [500031-44-7] C12H22 MW = 166.31 648

methylcyclohexene

T exp 2 est Ref.
K kg m3
298.15 830.2 1.50 29-rea/wat
(+)-1-Ethylidene-2-(1-methylethyl)-5- [500032-01-9] C12H22 MW = 166.31 649

methylcyclohexane

T exp 2 est Ref.
3
K kg m
289.15 830.4 2.00 22-oga/miz
Landolt-Brnstein
New Series IV/8D
1-Hexylcyclohexene [3964-66-7] C12H22 MW = 166.31 650

T exp 2 est Ref.
3
K kg m
293.15 824.4 2.00 56-pet/ser
1-Methyl-2-pentylcyclohexene [93915-87-8] C12H22 MW = 166.31 651

T exp 2 est Ref.
3
K kg m
293.15 832.0 2.00 33-sig/cra
4-Methyl-1-(3-methylbutyl)cyclohexene [500030-58-0] C12H22 MW = 166.31 652

A 1038.16
B -0.750

K kg m 3
kg m3
273.15 833.3 4.00 0.00 06-sab/mai

289.15 821.3 4.00 0.00 06-sab/mai
289.15 821.3 3.00 0.00 07-sab/mai-4
273.15 833.3 3.00 0.00 07-sab/mai-4

T exp 2 est
K kg m3
270.00 835.7 3.5
280.00 828.2 3.0
290.00 820.7 3.0
1,2,4-Triethylcyclohexene [500031-77-6] C12H22 MW = 166.31 653

T exp 2 est Ref.
K kg m3
293.15 837.0 2.00 50-nic/hei
Landolt-Brnstein
New Series IV/8D
1,1,3-Trimethyl-2-propylcyclohexene [500032-81-5] C12H22 MW = 166.31 654

T exp 2 est Ref.
3
K kg m
298.15 839.4 2.00 56-opp/day
Cyclododecene [1501-82-2] C12H22 MW = 166.31 655

T exp 2 est Ref.
K kg m3
293.15 877.6 5.00 67-tep/far
(Z)-Cyclododecene [1129-89-1] C12H22 MW = 166.31 656

T exp 2 est Ref.
K kg m3
293.15 882.3 1.00 65-zak/kor
(E)-Cyclododecene [1486-75-5] C12H22 MW = 166.31 657

T exp 2 est Ref.
K kg m3
293.15 871.7 1.00 65-zak/kor

(2-methylpropyl)cyclohexane

T exp 2 est Ref.
K kg m3
284.15 811.2 2.00 26-esc-1
1-Methyl-4-(1-methylethyl)-3- [500032-04-2] C13H24 MW = 180.33 659

propylidenecyclohexane

T exp 2 est Ref.
K kg m3
289.65 812.9 2.00 22-oga/miz
Landolt-Brnstein
New Series IV/8D
340 3.8 Alkylcycloalkenes and Alkenylcycloalkanes (CnH2n-2), C12 to C13 -
1-Isopropyl-2-propyl-4- [500031-45-8] C13H24 MW = 180.33 660
methylcyclohexene

T exp 2 est Ref.
3
K kg m
298.15 834.8 1.50 29-rea/wat
1-Octylcyclopentene [52315-44-3] C13H24 MW = 180.33 661

T exp 2 est Ref.
3
K kg m
293.15 826.9 1.00 40-sch/gem
293.15 826.9 0.50 42-sch
293.15 826.9 0.68 49-lut
293.15 826.9 0.50 Recommended
(1-Propyl-2-butenyl)cyclohexane [500032-03-1] C13H24 MW = 180.33 662

T exp 2 est Ref.
K kg m3
298.15 835.5 2.00 36-lev/zur

1-Octylcyclohexene [15232-87-8] C14H26 MW = 194.36 663

T exp 2 est Ref.
3
K kg m
293.15 841.6 2.00 42-sch/sch
1,3,3,5,5-Pentamethyl-4- [96850-42-9] C14H26 MW = 194.36 664

(1-methylethyl)cyclohexene

A 1071.90
B -0.700
cont.
Landolt-Brnstein
New Series IV/8D
1,3,3,5,5-Pentamethyl-4-(1-methylethyl)cyclohexene (cont.)

K kg m3
kg m3
290.15 869.6 2.00 0.80 13-mer-1

273.15 879.9 2.00 -0.80 13-mer-1

T exp 2 est
K kg m3
270.00 882.9 2.5
280.00 875.9 2.5
290.00 868.9 2.0
293.15 866.7 2.0
298.15 863.2 2.5
4-(1,1,3,3-Tetramethylbutyl)cyclohexene [500031-46-9] C14H26 MW = 194.36 665

T exp 2 est Ref.
K kg m3
298.15 856.5 1.50 37-nie/smi
1-Decylcyclopentene [62184-75-2] C15H28 MW = 208.39 666

T exp 2 est Ref.
K kg m3
293.15 829.0 1.00 40-sch/gem
293.15 829.0 0.50 42-sch
293.15 829.0 0.69 49-lut
293.15 829.0 0.50 Recommended
Landolt-Brnstein
New Series IV/8D
(1-Ethyl-1,3-dimethyl-1-pentenyl) [500011-27-8] C15H28 MW = 208.39 667

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 866.0 1.00 52-lev/shu-2
Cyclopentadecene [6573-72-4] C15H28 MW = 208.39 668

A 1097.74
B -0.750

K kg m 3
kg m3
341.65 841.6 1.00 0.10 31-ruz/boe

339.65 842.9 1.00 -0.10 31-ruz/boe

T exp 2 est
K kg m3
330.00 850.2 2.5
340.00 842.7 1.0
350.00 835.2 3.0
1-Methylcyclopentadecene [500032-40-6] C16H30 MW = 222.41 669

T exp 2 est Ref.
K kg m3
295.15 869.7 2.00 28-ruz/sch
Landolt-Brnstein
New Series IV/8D
1-Methylene-2,2,6,6- [500032-09-7] C19H36 MW = 264.49 670

tetrapropylcyclohexane

T exp 2 est Ref.
3
K kg m
289.15 861.8 3.00 35-cor/bor
Tetradecylcyclopentene [500031-78-7] C19H36 MW = 264.49 671

T exp 2 est Ref.
3
K kg m
293.15 833.5 0.69 49-lut
1-Methyl-3-octadecylcyclopentene [500032-62-2] C24H46 MW = 334.63 672

T exp 2 est Ref.
3
K kg m
293.15 848.2 1.00 39-gro/wac
1-Octadecylcyclohexene [500031-76-5] C24H46 MW = 334.63 673

T exp 2 est Ref.
K kg m3
293.15 845.8 2.00 39-sui/gem
Landolt-Brnstein
New Series IV/8D
4. Tabulated Data on Density - Monocyclic Hydrocarbons
(CnH2n-4)
4.1 Monocyclic Hydrocarbons (CnH2n-4), C5 - C6 347
4.1 Monocyclic Hydrocarbons (CnH2n-4), C5 - C6

1,3-Cyclopentadiene [542-92-7] C5H6 MW = 66.10 674

A 1037.12
B -0.800
K 3
kg m kg m3 K kg m 3
kg m3
293.15 803.0 3.00 0.40 1891-eta/lam 289.25 807.0 2.00 1.28 10-von/eis-1
291.75 804.7 2.00 1.01 1896-kra/spi 289.25 808.5 2.00 2.78 10-von/eis-1
291.75 814.3 4.00 10.55 1896-kra/spi1) 292.65 798.3 1.00 -4.70 33-zel/lev
287.25 808.3 1.50 0.98 07-eyk 293.15 803.5 0.60 0.90 49-foe/fen
288.85 807.1 1.50 1.06 07-eyk
1)

T exp 2 est
K kg m3
280.00 813.1 2.8
290.00 805.1 2.2
293.15 802.6 2.2
298.15 798.6 2.5
1,2-bis(Methylene)cyclobutane [14296-80-1] C6H8 MW = 80.13 675

T exp 2 est Ref.
K kg m 3
293.15 769.8 2.00 13-leb-2
1-Methyl-1,3-cyclopentadiene [96-39-9] C6H8 MW = 80.13 676

T exp 2 est Ref.
3
K kg m
293.15 770.9 1.00 60-nar/shu
Landolt-Brnstein
New Series IV/8D
348 4.1 Monocyclic Hydrocarbons (CnH2n-4), C5 - C6
2-Methyl-1,3-cyclopentadiene [3727-31-9] C6H8 MW = 80.13 677

T exp 2 est Ref.
3
K kg m
293.15 808.5 1.00 63-mir/sob
1,3-Cyclohexadiene [592-57-4] C6H8 MW = 80.13 678

T = 277.15 to 323.43 K
A 1.07128 103
B -7.97815 10-1
K kg m 3
kg m3 in Fig. 1)
277.15 847.60 3.00 -2.57 04-cro( ) 295.15 834.70 3.00 -1.11 38-kaz/vol( )
288.15 836.90 3.00 -4.49 04-cro( ) 293.15 841.10 1.00 3.70 45-arb/zel()
288.55 836.57 3.00 -4.50 04-cro( ) 286.15 840.00 1.00 -2.99 54-dom/bel()
298.15 827.27 3.00 -6.14 04-cro1) 298.18 837.70 0.50 4.31 74-let/mar( )
283.15 845.40 2.00 0.02 27-sen( ) 306.93 828.50 0.50 2.09 74-let/mar( )
291.65 834.00 3.00 -4.60 27-zel/koz( ) 314.32 820.70 0.50 0.19 74-let/mar( )
289.15 842.10 2.00 1.51 29-far/sco( ) 323.43 810.90 0.50 -2.34 74-let/mar( )
293.15 840.00 2.00 2.60 30-cri() 298.15 841.60 0.60 8.19 86-tar/dia( ){
Further references: [1898-for, 25-hof/dam, 38-car/stu, 87-let/bax].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 855.87 2.35 293.15 837.40 1.82 310.00 823.96 0.43
280.00 847.89 2.68 298.15 833.41 1.34 320.00 815.98 0.46
290.00 839.92 2.11 300.00 831.94 1.16 330.00 808.00 1.59
cont.
Landolt-Brnstein
New Series IV/8D
4.1 Monocyclic Hydrocarbons (CnH2n-4), C5 - C6 349
1,3-Cyclohexadiene (cont.)
1,4-Cyclohexadiene [628-41-1] C6H8 MW = 80.13 679

T = 283.15 to 323.61 K
A 1.14463 103
B -9.88394 10-1
cont.
Landolt-Brnstein
New Series IV/8D
350 4.1 Monocyclic Hydrocarbons (CnH2n-4), C5 - C6
1,4-Cyclohexadiene(cont.)
283.15 860.50 2.00 -4.26 27-sen( ) 315.28 833.80 0.30 0.79 74-let/mar( ) {
293.15 855.40 0.50 0.52 42-ano-2() 323.61 824.80 0.30 0.03 74-let/mar( ) {
293.15 855.70 0.20 0.82 62-ano-3( ) 298.15 851.03 0.40 1.09 86-tar/dia()
299.29 849.70 0.30 0.89 {
74-let/mar( ) 298.15 849.00 1.00 -0.94 91-luk/tim-1()
307.25 842.00 0.30 1.06 74-let/mar( ) {
Further references: [08-zel/gor-2, 35-zel/den, 87-let/bax].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
280.00 867.88 4.00 298.15 849.94 1.00 320.00 828.34 1.00
290.00 857.99 1.40 300.00 848.11 1.10 330.00 818.46 1.60
293.15 854.88 1.00 310.00 838.22 1.20
Landolt-Brnstein
New Series IV/8D
4.2 Monocyclic Hydrocarbons (CnH2n-4), C7 351
4.2 Monocyclic Hydrocarbons (CnH2n-4), C7

1-Ethenylcyclopentene [28638-58-6] C 7H10 MW = 94.16 680

T exp 2 est Ref.
3
K kg m
291.15 824.0 2.00 34-uri
2-Ethyl-1,3-cyclopentadiene [22516-12-7] C7H10 MW = 94.16 681

T exp 2 est Ref.
3
K kg m
293.15 823.1 1.00 60-nar/shu
Ethynylcyclopentane [930-51-8] C7H10 MW = 94.16 682

T exp 2 est Ref.
3
K kg m
295.15 825.0 2.00 34-gre-2
1-Methyl-1,4-cyclohexadiene [4313-57-9] C7H10 MW = 94.16 683

T exp 2 est Ref.
3
K kg m
293.15 845.2 0.30 43-ano-3

T exp 2 est Ref.
3
K kg m
293.15 829.2 2.00 08-zel/gor
Landolt-Brnstein
New Series IV/8D
352 4.2 Monocyclic Hydrocarbons (CnH2n-4), C7

T exp 2 est Ref.
3
K kg m
295.65 825.2 2.00 13-har/sei-1
(R)-5-Methyl-1,3-cyclohexadiene [78939-20-5] C7H10 MW = 94.16 686

T exp 2 est Ref.
K kg m3
293.15 827.4 2.00 08-zel/gor-2
1,2-Cycloheptadiene [6577-10-2] C7H10 MW = 94.16 687

T exp 2 est Ref.
K kg m3
293.15 853.2 2.00 36-fav
1,3-Cycloheptadiene [4054-38-0] C7H10 MW = 94.16 688

A 1114.40
B -0.850

K kg m 3
kg m3
273.15 882.3 2.00 0.08 01-wil

273.15 881.5 2.00 -0.72 01-wil-1
290.75 867.9 2.00 0.64 01-wil-1

T exp 2 est
K kg m3
270.00 884.9 2.7
280.00 876.4 2.6
290.00 867.9 2.8
293.15 865.2 2.9
298.15 861.0 3.5
Landolt-Brnstein
New Series IV/8D

2,4-Dimethyl-3-methylenecyclopentene [500031-05-0] C8H12 MW = 108.18 689

T exp 2 est Ref.
K kg m3
293.15 813.80 1.00 64-mir/kos
1-(1-Propenyl)cyclopentene [36193-53-0] C8H12 MW = 108.18 690

T exp 2 est Ref.
3
K kg m
294.15 835.0 2.00 34-uri
1-Propyl-1,3-cyclopentadiene [62247-85-2] C8H12 MW = 108.18 691

T exp 2 est Ref.
K kg m3
293.15 828.8 1.00 60-nar/shu
(1-Propynyl)cyclopentane [5623-79-0] C8H12 MW = 108.18 692

T exp 2 est Ref.
3
K kg m
295.15 843.0 2.00 34-gre-2
(2-Propynyl)cyclopentane [116279-08-4] C8H12 MW = 108.18 693

T exp 2 est Ref.
3
K kg m
297.15 828.0 2.00 34-gre-1
1,3-Dimethyl-1,3-cyclohexadiene [4573-05-1] C8H12 MW = 108.18 694

A 1082.07
B -0.850
cont.
Landolt-Brnstein
New Series IV/8D
1,3-Dimethyl-1,3-cyclohexadiene (cont.)
K kg m 3
kg m3 K kg m 3
kg m3
290.75 827.0 5.00 -7.93 10-von/eis-21) 293.15 832.4 2.00 -0.49 18-pic/kai
289.75 835.6 2.00 -0.18 10-von/eis-2 293.15 830.8 2.00 -2.09 54-lev/shu
289.35 836.5 2.00 0.38 10-von/eis-2 293.15 833.0 1.00 0.11 63-tho/sto
293.15 837.3 3.00 4.41 13-haw
1)

T exp 2 est
K kg m3
280.00 844.1 2.5
290.00 835.6 2.3
293.15 832.9 2.3
298.15 828.6 2.3

A 1081.56
B -0.850

K kg m 3
kg m3
292.15 830.6 2.00 -2.64 10-von/eis

289.45 835.8 1.00 0.27 14-rot/von
288.65 836.6 1.00 0.39 15-von/hin-1

T exp 2 est
K kg m3
280.00 843.6 1.5
290.00 835.1 1.0
293.15 832.4 1.0
298.15 828.1 1.8
Landolt-Brnstein
New Series IV/8D

A 1068.12
B -0.850

K kg m3 kg m3
291.15 819.2 2.00 -1.44 03-har/ant

292.95 818.9 2.00 -0.21 10-von/pet-2
291.55 820.5 2.00 0.20 10-von/pet-2
291.15 822.1 2.00 1.46 10-von/pet-2

T exp 2 est
K kg m3
290.00 821.6 2.0
293.15 818.9 2.0
298.15 814.7 3.5

T exp 2 est Ref.
K kg m3
293.15 852.1 2.00 13-haw

T exp 2 est Ref.
K kg m3
293.15 822.3 2.00 08-zel/gor
Landolt-Brnstein
New Series IV/8D

A 1071.70
B -0.850

K kg m3 kg m3
293.15 822.5 2.00 -0.02 08-zel/gor

288.15 826.8 2.00 0.03 08-zel/gor

T exp 2 est
K kg m3
280.00 833.7 3.5
290.00 825.2 2.0
293.15 822.5 2.0
298.15 818.3 3.5

T exp 2 est Ref.
K kg m3
291.15 842.1 2.00 03-har/ant

T = 277.15 to 298.15 K
A 1.07458 103
B -9.01931 10-1
cont.
Landolt-Brnstein
New Series IV/8D
5,5-Dimethyl-1,3-cyclohexadiene (cont.)
K 3
kg m3 in Fig. 1)
277.15 824.60 2.00 -0.01 02-cro/les-1() 293.15 810.30 2.00 0.12 02-cro/les-1()
283.15 819.10 2.00 -0.10 02-cro/les-1() 298.15 805.90 2.00 0.23 02-cro/les-1()
287.15 815.71 2.00 0.12 02-cro/les-1() 288.15 814.60 2.00 -0.09 {
03-har/ant( )
288.15 814.60 2.00 -0.09 02-cro/les-1() 293.15 810.00 1.00 -0.18
10-von/eis2( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 831.06 2.92 293.15 810.18 1.87 300.00 804.00 2.08
280.00 822.04 2.20 298.15 805.67 2.00 310.00 794.98 2.74
290.00 813.02 1.86
Landolt-Brnstein
New Series IV/8D

T exp 2 est Ref.
3
K kg m
293.15 837.3 3.00 14-mee
3-Ethenylcyclohexene [766-03-0] C8H12 MW = 80.13 703

equation. References 60-wri and 61-wri for T =
298.15 to 402 K.
T = 277.15 to 298.15 K
A 8.465
B -8.317 10-1
C -4.722 10-4
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
298.15 825.4 2.00 340.00 788.8 2.00 380.00 752.2 2.50
300.00 823.8 2.00 360.00 770.7 2.50 400.00 733.4 2.50
320.00 806.5 2.00
4-Ethenylcyclohexene [100-40-3] C8H12 MW = 108.18 704

T = 273.15 to 343.28 K
A 1.08518 103
B -8.67508 10-1
cont.
Landolt-Brnstein
New Series IV/8D
4-Ethenylcyclohexene (cont.)
K 3
kg m3 in Fig. 1)
273.15 848.40 1.50 0.18 11-leb/ska-1() 311.41 815.00 0.40 -0.03 73-var/bul( )
293.15 832.00 1.50 1.13 11-leb/ska-1() 321.58 806.10 0.50 -0.11 73-var/bul( )
293.15 831.00 1.00 0.13 35-leb/ser( ){ 332.89 796.20 0.50 -0.20 73-var/bul( )
293.07 830.40 0.40 -0.54 73-var/bul( ) 343.28 787.20 0.50 -0.18 73-var/bul( )
298.10 826.20 0.40 -0.38 73-var/bul( )
cont.
Landolt-Brnstein
New Series IV/8D
4-Ethenylcyclohexene (cont.)
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 850.95 1.71 298.15 826.53 0.73 330.00 798.90 0.48
280.00 842.28 1.29 300.00 824.93 0.69 340.00 790.23 0.59
290.00 833.60 0.95 310.00 816.25 0.52 350.00 781.55 0.77
293.15 830.87 0.85 320.00 807.58 0.45
Ethynylcyclohexane [931-48-6] C8H12 MW = 108.18 705

A 1094.91
B -0.870

K kg m 3
kg m3
293.15 842.3 3.00 2.43 11-jeg-1

273.15 860.1 3.00 2.83 11-jeg-1
296.15 832.0 3.00 -5.26 34-gre-2

T exp 2 est
K kg m3
270.00 860.0 3.8
280.00 851.3 3.7
290.00 842.6 3.7
293.15 839.9 3.7
298.15 835.5 3.8
1-Methyl-3-methylenecyclohexene [23611-15-6] C8H12 MW = 108.18 706

T exp 2 est Ref.
K kg m3
291.95 838.9 2.00 11-von/eis-1
293.15 834.7 1.00 63-tho/sto
Landolt-Brnstein
New Series IV/8D
1-Methyl-6-methylenecyclohexene [23611-14-5] C8H12 MW = 108.18 707

T exp 2 est Ref.
3
K kg m
293.15 852.1 2.00 14-haw/fyf
1,3-Cyclooctadiene [1700-10-3] C8H12 MW = 108.18 708

T exp 2 est Ref.
3
K kg m
273.15 884.0 2.00 07-wil/ver
1,5-Cyclooctadiene [111-78-4] C8H12 MW = 108.18 709

T exp 2 est Ref.
3
K kg m
293.85 856.4 6.00 02-doe
298.15 881.8 3.00 48-cop/bai
298.15 876.0 3.00 50-cop/hoc
(Z,Z)-1,5-Cyclooctadiene [1552-12-1] C8H12 MW = 108.18 710

T exp 2 est Ref.
3
K kg m
293.15 882.0 1.00 63-zak/zhi
293.15 881.5 1.00 65-tre/mit
814.3 60.00 90-kar/kar
1)
293.15
809.4 60.00 90-kar/kar
1)
313.15
800.7 60.00 90-kar/kar
1)
333.15
794.1 60.00 90-kar/kar
1)
353.15
293.15 881.8 1.0 Recommended
1)
Landolt-Brnstein
New Series IV/8D

(2-Butynyl)cyclopentane [30628-30-9] C9H14 MW = 122.21 711

T exp 2 est Ref.
3
K kg m
299.15 842.0 2.00 34-gre-1
3-(1-Methylethyl)-1-methyl- [25148-02-1] C9H14 MW = 122.21 712

1,3-cyclopentadiene

T exp 2 est Ref.
3
K kg m
293.15 840.0 2.00 33-tre
1,5-Dimethyl-3-methylenecyclohexene [500031-67-4] C9H14 MW = 122.21 713

T exp 2 est Ref.
3
K kg m
290.25 830.0 2.00 15-von/tre
293.25 828.0 2.00 15-von/tre
1-Ethyl-4-methyl-1,3-cyclohexadiene [62088-32-8] C9H14 MW = 122.21 714

A 1086.87
B -0.850

K kg m 3
kg m3
292.65 837.1 2.00 -1.02 09-von-2

291.95 840.8 2.00 2.08 09-von-2
291.55 839.3 2.00 0.25 09-von-2
288.75 840.8 2.00 -0.63 14-rot/von
288.35 841.1 2.00 -0.67 14-rot/von
cont.
Landolt-Brnstein
New Series IV/8D
1-Ethyl-4-methyl-1,3-cyclohexadiene (cont.)

T exp 2 est
K kg m3
280.00 848.9 2.2
290.00 840.4 2.1
293.15 837.7 2.1
298.15 833.4 2.2

cyclopentene

T exp 2 est Ref.
K kg m3
293.15 851.5 1.00 13-haw
1-(1-Methylethyl)-3-methyl-1,3- [45676-10-6] C9H14 MW = 122.21 716

cyclopentadiene

T exp 2 est Ref.
K kg m3
288.15 825.0 2.00 33-tre-1
5-(1-Methylethyl)-1,3-cyclohexadiene [35776-64-8] C9H14 MW = 122.21 717

T exp 2 est Ref.
3
K kg m
293.15 846.0 2.00 33-tre-1
1-(2-Methyl-1-propenyl)cyclohexene [500031-68-5] C9H14 MW = 122.21 718

T exp 2 est Ref.
3
K kg m
293.15 853.7 1.50 14-haw/fyf
1-(2-Methyl-3-propenyl)cyclohexene [500031-69-6] C9H14 MW = 122.21 719

T exp 2 est Ref.
3
K kg m
293.15 860.7 1.50 14-haw/fyf
Landolt-Brnstein
New Series IV/8D
(1,2-Propadienyl)cyclohexane [5664-17-5] C9H14 MW = 122.21 720

T exp 2 est Ref.
3
K kg m
293.15 823.9 2.00 36-lev/tra
1-(2-Propenyl)cyclohexene [13511-13-2] C9H14 MW = 122.21 721

T exp 2 est Ref.
K kg m3
293.15 842.6 1.00 36-lev/tra
(1-Propynyl)cyclohexane [18736-95-3] C9H14 MW = 122.21 722

T exp 2 est Ref.
K kg m3
295.15 851.0 2.00 34-gre-2
(2-Propynyl)cyclohexane [17715-00-3] C9H14 MW = 122.21 723

A 1091.93
B -0.850

K kg m 3
kg m3
293.15 836.0 4.00 -6.76 23-bou-2

291.15 844.0 2.00 -0.46 25-bou
293.15 844.9 2.00 2.14 36-lev/tra

T exp 2 est
K kg m3
290.00 845.4 3.5
293.15 842.8 2.7
298.15 838.5 3.5
Landolt-Brnstein
New Series IV/8D
4.4 Monocyclic Hydrocarbons (CnH2n-4), C9 - 4.5 Monocyclic Hydrocarbons (CnH2n-4), C10 365
1,3,5-Trimethyl-1,3-cyclohexadiene [1731-26-6] C9H14 MW = 122.21 724

T exp 2 est Ref.
3
K kg m
293.15 846.50 3.00 18-pic/kai

1,2-bis(1-Methylethylidene)cyclobutane [3642-16-8] C10H16 MW = 136.24 725

accepted points. Deviation w= 0.050
A 1062.01
B -0.750

K kg m 3
kg m3
293.15 842.2 3.00 0.05 11-leb

273.15 857.1 3.00 -0.05 11-leb

T exp 2 est
K kg m3
270.00 859.5 0.7
280.00 852.0 0.2
290.00 844.5 0.3
293.15 842.2 0.5
298.15 838.4 0.8
1,2-Diethenyl-3,4-dimethylcyclobutane [32587-61-4] C10H16 MW = 136.24 726

T exp 2 est Ref.
3
K kg m
293.15 811.3 2.00 13-leb/mer-1
Landolt-Brnstein
New Series IV/8D

(1-methylethylidene)cyclobutane

A 1035.60
B -0.810

K kg m3 kg m3
273.15 814.3 2.00 -0.05 11-leb

293.15 798.2 2.00 0.05 11-leb

T exp 2 est
K kg m3
270.00 816.9 0.7
280.00 808.8 0.2
290.00 800.7 0.3
293.15 798.1 0.5
298.15 794.1 0.8
1,1,2,2-Tetramethyl-3,4- [500032-28-0] C10H16 MW = 136.24 728

dimethylenecyclobutane

T exp 2 est Ref.
K kg m 3
293.15 792.7 2.00 13-leb-3
1-(3-Butenyl)cyclohexene [1911-19-9] C 10H16 MW = 136.24 729

T exp 2 est Ref.
K kg m 3
291.15 844.5 1.00 37-lin/wan
Landolt-Brnstein
New Series IV/8D
3-(3-Butenyl)cyclohexene [104286-35-3] C10H16 MW = 136.24 730

T exp 2 est Ref.
3
K kg m
293.15 812.0 1.00 57-pla/sta
(3-Butynyl)cyclohexane [500032-34-8] C10H16 MW = 136.24 731

T exp 2 est Ref.
K kg m3
293.15 846.2 2.00 37-lev/iva
1,5-Diethyl-1,3-cyclohexadiene [500032-21-3] C10H16 MW = 136.24 732

T exp 2 est Ref.
K kg m3
293.15 864.4 2.00 11-hen/boy
3-Ethenyl-1,5-dimethylcyclohexene [62184-85-4] C10H16 MW = 136.24 733

T exp 2 est Ref.
K kg m3
294.45 836.0 2.00 10-von/pet
293.15 833.2 2.00 11-von/eis-1
5-Ethenyl-1,5-dimethylcyclohexene [1611-21-8] C10H16 MW = 136.24 734

A 1052.86
B -0.750

K kg m3
kg m3
293.15 833.0 3.00 0.00 13-leb-1

273.15 848.0 3.00 0.00 13-leb-1
cont.
Landolt-Brnstein
New Series IV/8D
5-Ethenyl-1,5-dimethylcyclohexene (cont.)

T exp 2 est
K kg m3
270.00 850.4 3.7
280.00 842.9 3.2
290.00 835.4 3.3
293.15 833.0 3.5
298.15 829.2 3.8
1-Methylene-4-(1-methylethenyl) [499-97-8] C10H16 MW = 136.24 735

cyclohexane

T exp 2 est Ref.
K kg m3
293.15 872.0 2.00 37-isk
1-Methylene-4-(1-methylethylidene) [6876-10-4] C10H16 MW = 136.24 736

cyclohexane

T exp 2 est Ref.
K kg m3
289.15 850.7 2.00 30-ric/wol

cyclohexane

A 1085.68
B -0.800

K kg m 3
kg m3
283.15 855.8 3.00 -3.36 1886-pes

293.15 852.0 1.50 0.84 11-fra/ser
cont.
Landolt-Brnstein
New Series IV/8D
3-Methylene-6-(1-methylethenyl)cyclohexane (cont.)

T exp 2 est
K kg m3
280.00 861.7 1.9
290.00 853.7 1.7
293.15 851.2 1.7
298.15 847.2 1.8

cyclohexane

T exp 2 est Ref.
K kg m3
295.15 839.0 2.00 08-wal-7

cyclohexene

A 1094.66
B -0.850

K kg m3
kg m3
290.35 848.6 2.00 0.74 10-von/rot

293.15 845.3 1.00 -0.18 28-asc

T exp 2 est
K kg m3
290.00 848.2 0.4
293.15 845.5 0.4
298.15 841.2 0.5
Landolt-Brnstein
New Series IV/8D

cyclohexene
Table 1. Coefficients of the polynomial expansion equation

(based on data sets 740, 741, and 742). Standard deviations
(see introduction):c,w = 2.4024 (combined temperature
ranges, weighted), c,uw = 7.0520 10-1 (combined
T = 273.15 to 449.65 K
A 1.08541 103
B -8.14635 10-1
2293.14 845.00 3.00 -1.61 1888-wal-2 351.45 796.20 3.00 -2.91 07-eyk( )
277.15 862.66 1.00 3.02 06-kay/per() 291.15 846.40 2.00 -1.83 09-von-2
287.55 854.55 1.00 3.39 06-kay/per() 273.15 865.70 1.00 2.80 10-del()
288.15 854.03 1.00 3.35 06-kay/per() 293.15 853.50 1.00 6.90 10-del()
298.15 846.10 1.00 3.57 06-kay/per() 293.15 845.00 3.00 -1.60 28-tre/sch
294.00 840.20 1.50 -5.71 07-bru-1 293.15 845.00 3.00 -1.60 31-kaf/noz-2
289.75 845.00 2.00 -4.37 07-eyk 293.15 844.60 0.60 -2.00 42-ano-2( ) {
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 865.46 2.03 330.00 816.58 1.25 400.00 759.56 4.86
280.00 857.31 1.19 340.00 808.44 1.80 410.00 751.41 4.91
290.00 849.17 0.69 350.00 800.29 2.41 420.00 743.27 4.71
293.15 846.60 0.60 360.00 792.14 3.04 430.00 735.12 4.21
298.15 842.53 0.51 370.00 784.00 3.65 440.00 726.97 3.39
300.00 841.02 0.49 380.00 775.85 4.18 450.00 718.83 2.24
310.00 832.88 0.55 390.00 767.71 4.60 460.00 710.68 3.00
320.00 824.73 0.82
cont.
Landolt-Brnstein
New Series IV/8D
1-Methyl-4-(1-methylethenyl)cyclohexene (cont.)
Data sets 740, 741, and 742 were combined to produce graph of 1-methyl-4-(1-methylethenyl)cyclohexene.
(R)-(+)-1-Methyl-4-(1-methylethenyl) [5989-27-5] C10H16 MW = 136.24 741

cyclohexene
282.95 853.00 2.00 -1.91 1883-sch-3 291.15 846.40 2.00 -1.83 09-von-2
449.65 713.50 2.00 -5.61 1883-sch-3( ) 287.85 846.80 3.00 -4.12 10-von/rot
273.15 858.36 2.00 -4.54 1899-god/ros( ) 292.75 842.50 3.00 -4.43 10-von/rot
293.15 842.65 2.00 -3.95 1899-god/ros 293.15 846.00 2.00 -0.60 11-per
277.15 857.60 3.00 -2.04 02-per 298.15 837.10 2.00 -5.43 23-von/lem
288.75 853.20 3.00 3.01 02-per 293.15 845.60 2.00 -1.00 31-hen/pag
298.15 841.20 3.00 -1.33 02-per 298.15 840.90 2.00 -1.63 35-pad/jat
294.15 840.20 1.50 -5.59 07-bru-1 293.15 841.90 2.00 -4.70 50-her/ruz
303.15 835.60 2.00 -2.86 08-clo 293.15 842.30 2.00 -4.30 50-her/ruz
Landolt-Brnstein
New Series IV/8D
(S)-(-)-1-Methyl-4-(1-methylethenyl) [5989-54-8] C10H16 MW = 136.24 742

cyclohexene
K kg m 3
kg m3 in Fig. 1)
293.15 846.00 2.00 -0.60 1888-wal-3 293.75 841.70 2.00 -4.41 30-ric/wol-1
283.15 854.64 1.00 -0.11 02-per() 293.15 845.20 0.30 -1.40 90-rib/ber( )
288.15 844.34 1.00 -6.34 02-per() 298.15 841.80 0.30 -0.73 90-rib/ber( )
293.15 846.87 1.00 0.27 02-per() 303.15 838.20 0.30 -0.26 90-rib/ber( )
298.15 842.81 1.00 0.28 02-per() 308.15 833.50 0.30 -0.88 90-rib/ber( )
293.65 840.70 1.50 -5.50 07-bru-1 313.15 830.40 0.30 0.09 90-rib/ber( )
293.15 842.20 2.00 -4.40 23-von/lem 318.15 826.90 0.30 0.66 90-rib/ber( )
287.15 847.20 2.00 -4.29 30-ric/wol-1 323.15 822.60 0.30 0.44 90-rib/ber( )

cyclohexene

T exp 2 est Ref.
K kg m 3
293.15 848.1 2.00 08-fis/per

293.15 847.6 1.00 24-asc/kro
293.15 847.7 1.0 Recommended
(R)-1-Methyl-5-(1-methylethenyl) [1461-27-4] C10H16 MW = 136.24 744

cyclohexene

T exp 2 est Ref.
3
K kg m
287.15 865.8 4.00 1884-gla

cyclohexene

T exp 2 est Ref.
K kg m 3
293.15 846.7 3.00 11-per
Landolt-Brnstein
New Series IV/8D
(+)-3-Methyl-1-(1-methylethenyl) [500032-36-0] C10H26 MW = 146.32 746

cyclohexene

T exp 2 est Ref.
3
K kg m
290.15 862.9 2.00 11-haw/per

cyclohexene

A 1108.95
B -0.850

K 3
kg m kg m3
293.15 859.4 2.00 -0.33 10-luf/per

293.15 860.9 2.00 1.17 11-haw/per
295.15 854.9 3.00 -3.17 38-god/cau
290.15 862.9 2.00 0.58 11-haw/per

T exp 2 est
K kg m3
290.00 862.5 1.4
293.15 859.8 1.4
298.15 855.5 1.4

cyclohexene

T exp 2 est Ref.
3
K kg m
290.15 848.0 2.00 11-per
Landolt-Brnstein
New Series IV/8D
(3R-trans)-3-Methyl-6-(1-methylethenyl) [5113-87-1] C10H16 MW = 136.24 749

cyclohexene

T exp 2 est Ref.
3
K kg m
293.65 838.2 2.00 07-tsc/pok
295.65 838.0 2.00 33-doe
(3S-trans)-3-Methyl-6-(1-methylethenyl) [19956-40-2] C10H16 MW = 136.24 750

cyclohexene

T exp 2 est Ref.
3
K kg m
293.15 837.0 2.00 37-pig/kan
292.65 839.0 2.00 37-pig/kan

cyclohexene

A 1065.93
B -0.790

K kg m3 kg m3
283.15 842.2 2.50 -0.00 06-kay/per

288.15 838.2 2.50 -0.05 06-kay/per
293.15 834.3 2.00 0.04 06-kay/per

T exp 2 est
K kg m3
280.00 844.7 0.4
290.00 836.8 0.1
293.15 834.3 0.2
298.15 830.4 0.5
Landolt-Brnstein
New Series IV/8D

cyclohexene

T = 277.15 to 298.15 K
A 9.48544 102
B -3.00450 10-1
277.15 871.20 3.00 5.93 06-kay/per( ) 289.15 864.05 2.00 2.38 {

11-cho/per( )
285.85 864.81 3.00 2.15 06-kay/per( ) 293.15 851.00 3.00 -9.47 33-doe()
288.15 862.62 3.00 0.65 06-kay/per( ) 287.35 858.50 2.00 -3.71
34-gru/rea( )
298.15 854.87 3.00 -4.10 06-kay/per( ) 297.15 867.90 2.00 8.63 37-god/cau()
293.15 858.00 3.00 -2.47 10-per/wal()
Further references: [06-sem/rim].
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 867.42 5.00 293.15 860.47 2.64 300.00 858.41 3.24
280.00 864.42 3.60 298.15 858.97 3.00 310.00 855.40 4.87
290.00 861.41 3.00
cont.
Landolt-Brnstein
New Series IV/8D
(+)-4-Methyl-1-(1-methylethenyl)cyclohexene (cont.)

cyclohexene

T exp 2 est Ref.
K kg m3
293.15 859.4 2.00 10-luf/per
cis-4-Methyl-5-(1-methylethenyl) [500031-87-8] C10H16 MW = 136.24 754

cyclohexene

T exp 2 est Ref.
K kg m3
293.15 849.3 2.00 11-per-1
Landolt-Brnstein
New Series IV/8D
trans-4-Methyl-5-(1-methylethenyl) [500031-88-9] C10H16 MW = 136.24 755

cyclohexene

T exp 2 est Ref.
3
K kg m
293.15 846.3 2.00 11-per-1

cyclohexene

A 1108.53
B -0.850

K kg m3 kg m3
293.15 854.0 3.00 -5.35 09-sem/sch1)

288.15 862.5 1.50 -1.08 31-hen/pag
288.15 862.5 1.50 -1.08 31-hen/pag
293.15 857.0 2.00 -2.35 31-kaf/noz
293.15 858.3 1.00 -1.05 37-cha/day
298.15 857.7 1.00 2.60 60-mat/sai
1)

T exp 2 est
K kg m3
280.00 870.5 1.9
290.00 862.0 1.8
293.15 859.4 1.8
298.15 855.1 1.8
1-Methyl-5-(1-methylethyl)- [16755-34-3] C10H16 MW = 136.24 757

1,3-cyclohexadiene

T exp 2 est Ref.
K kg m3
293.15 850.1 2.00 20-hen/sme
Landolt-Brnstein
New Series IV/8D

1,3-cyclohexadiene

A 1091.72
B -0.850
K kg m 3
kg m3 K kg m 3
kg m3
300.15 841.2 4.00 4.61 03-har1) 292.75 836.1 4.00 -6.78 09-von-21)
291.65 841.1 2.00 -2.72 03-har/ant 289.15 840.8 4.00 -5.14 09-von/von1)
293.15 846.0 3.00 3.46 06-wal-5 292.05 835.3 4.00 -8.18 14-rot/von1)
291.15 845.3 2.00 1.06 08-har/maj 291.65 846.1 3.00 2.28 15-har/mor
289.15 847.0 2.00 1.06 08-pic 296.15 851.2 4.00 11.21 29-els/gib1)
293.15 845.0 3.00 2.46 09-sem-2 292.75 837.5 3.00 -5.38 30-ric/wol
293.35 844.3 2.00 1.93 09-sem-3 291.45 838.2 3.00 -5.79 30-ric/wol
1)

T exp 2 est
K kg m3
280.00 853.7 3.0
290.00 845.2 2.9
293.15 842.5 2.9
298.15 838.3 2.9

1,4-cyclohexadiene

A 1096.94
B -0.850

K kg m 3
kg m3
289.15 850.7 2.00 -0.46 27-ric/wol

293.15 849.0 2.00 1.24 30-ric/wol
288.15 853.0 2.00 0.99 30-ric/wol
293.15 846.0 2.00 -1.76 35-kaf/ike
cont.
Landolt-Brnstein
New Series IV/8D
1-Methyl-4-(1-methylethyl)-1,4-cyclohexadiene (cont.)

T exp 2 est
K kg m3
280.00 858.9 1.4
290.00 850.4 1.2
293.15 847.8 1.2
298.15 843.5 1.3

1,3-cyclohexadiene

T exp 2 est Ref.
K kg m3
295.15 841.0 2.00 08-wal-4
(R)-2-Methyl-5-(1-methylethyl)- [4221-98-1] C10H16 MW = 136.24 761

1,3-cyclohexadiene

A 1092.73
B -0.850

K kg m3
kg m3
295.15 842.6 3.00 0.75 10-von/eis

290.25 849.0 3.00 2.98 10-von/eis
293.15 842.5 2.00 -1.05 23-smi/hur
298.15 838.7 2.00 -0.60 23-smi/hur
Table 3. Recommended values. *

T exp 2 est
K kg m3
290.00 846.2 1.4
293.15 843.6 1.4
298.15 839.3 1.4
*
Data sets 760, 761, and 762 were combined.
Landolt-Brnstein
New Series IV/8D
(S)-2-Methyl-5-(1-methylethyl)- [2243-33-6] C10H16 MW = 136.24 762

1,3-cyclohexadiene

A 1092.73
B -0.850
292.15 844.0 2.00 -0.41 04-wal/bes 290.25 849.0 3.00 2.98 10-von/eis
293.15 844.7 2.00 1.14 05-har/joh 293.15 842.5 2.00 -1.06 23-smi/hur
303.15 832.4 3.00 -2.66 08-clo 298.15 838.7 2.00 -0.61 23-smi/hur
295.15 842.6 3.00 0.74 10-von/eis 293.15 844.0 2.00 0.44 28-tre/sch
Table 3. Recommended values. *

T exp 2 est
K kg m3
290.00 846.2 1.3
293.15 843.6 1.3
298.15 839.3 1.3
310.00 829.2 1.6
*
Data sets 760, 761, and 762 were combined.
(+)-4-Methyl-2-(2-propenyl)cyclohexene [500031-85-6] C10H16 MW = 136.24 763

T exp 2 est Ref.
K kg m 3
293.15 836.1 2.00 15-sai
1-Methyl-4-propyl-1,3-cyclohexadiene [113768-25-5] C10H16 MW = 136.24 764

T exp 2 est Ref.
K kg m 3
293.15 835.3 2.00 14-rot/von
1,2,3,4-Tetramethyl-1,3-cyclohexadiene [500032-22-4] C10H16 MW = 136.24 765

T exp 2 est Ref.
K kg m 3
293.15 849.1 3.00 18-pic/kai
Landolt-Brnstein
New Series IV/8D
1,3,5,5-Tetramethyl-1,3-cyclohexadiene [4724-89-4] C10H16 MW = 136.24 766

T exp 2 est Ref.
3
K kg m
293.15 814.4 1.00 62-lev/sha-1
2,4,4-Trimethyl-3-methylenecyclohexene [500031-89-0] C10H16 MW = 136.24 767

T exp 2 est Ref.
3
K kg m
294.15 843.0 2.00 34-kuh/hof
1,6,7-Trimethyl-1,3-cycloheptadiene [500031-07-2] C10H16 MW = 136.24 768

T exp 2 est Ref.
3
K kg m
293.15 892.4 1.00 67-kut/tis
3,4-Dimethyl-1,5-cyclooctadiene [21284-05-9] C10H16 MW = 136.24 769

T exp 2 est Ref.
3
K kg m
286.15 862.3 2.00 02-doe
Cyclodecyne [500019-39-6] C10H16 MW = 136.24 770

T exp 2 est Ref.
3
K kg m
293.15 897.3 1.00 52-pre/sch
Landolt-Brnstein
New Series IV/8D
382 4.6 Monocyclic Hydrocarbons (CnH2n-4), C11 to C12
4.6 Monocyclic Hydrocarbons (CnH2n-4), C11 to C12

4.6.1 C11H18
1-(3-Butenyl)-2-methylcyclohexene [500031-90-3] C11H18 MW = 150.26 771

T exp 2 est Ref.
K kg m3
288.65 876.9 1.00 36-hib/lin
2,6-Diethyl-5-methyl-1,3-cyclohexadiene [91250-79-2] C11H18 MW = 150.26 772

T exp 2 est Ref.
K kg m3
295.15 833.9 2.00 64-bla/per
3,5-Dimethyl-5-(1-methylethenyl) [500032-07-5] C11H18 MW = 150.26 773

cyclohexene

T exp 2 est Ref.
3
K kg m
298.15 858.5 2.00 29-rea/wat
1,3-Dimethyl-4-(1-methylethyl)- [500032-23-5] C11H18 MW = 150.26 774

1,3-cyclohexadiene

T exp 2 est Ref.
3
K kg m
298.15 858.5 1.00 29-rea/wat
1,3-Dimethyl-5-(1-methylethyl)- [91250-83-8] C11H18 MW = 150.26 775

1,3-cyclohexadiene
T exp 2 est Ref.
3
K kg m
293.15 839.8 1.00 62-lev/sha
(-)-1,3-Dimethyl-4-(1-methylethylidene) [500031-95-8] C11H18 MW = 150.26 776

cyclohexene
T exp 2 est Ref.
K kg m3
293.15 840.2 2.00 08-rup/emm-1
Landolt-Brnstein
New Series IV/8D
4.6 Monocyclic Hydrocarbons (CnH2n-4), C11 to C12 383
1,5-Dimethyl-3-(1-methylethylidene) [500031-96-9] C11H18 MW = 150.26 777

cyclohexene

A 1097.26
B -0.850

K kg m
3
kg m3
292.15 844.8 3.00 -4.14 10-von/pet

294.55 839.5 3.00 -7.40 10-von/pet
295.55 846.5 3.00 0.45 10-von/pet
296.75 856.1 3.00 11.07 10-von/pet

T exp 2 est
K kg m3
290.00 850.8 7.0
293.15 848.1 7.0
298.15 843.8 7.0
2,4-Dimethyl-4-(2-propenyl)cyclohexene [500032-06-4] C11H18 MW = 150.26 778

A 1057.67
B -0.750

K kg m
3
kg m3
289.15 841.5 2.00 0.69 1896-tie/sch

273.15 852.5 2.00 -0.31 01-gri-2
283.05 845.0 2.00 -0.38 01-gri-2

T exp 2 est
K kg m3
270.00 855.2 2.9
280.00 847.7 2.5
290.00 840.2 2.7
Landolt-Brnstein
New Series IV/8D
5-Propyl-1,3-dimethyl- [91250-80-5] C11H18 MW = 150.26 779

1,3-cyclohexadiene

T exp 2 est Ref.
3
K kg m
293.15 842.0 1.00 62-lev/sha
1-Ethyl-4-(1-methylethenyl)cyclohexene [500031-94-7] C11H18 MW = 150.26 780

T exp 2 est Ref.
3
K kg m
291.15 854.5 2.00 07-wal-7
6-Ethyl-1,3,5-trimethyl- [91250-81-6] C11H18 MW = 150.26 781

1,3-cyclohexadiene

T exp 2 est Ref.
3
K kg m
295.15 917.0 2.00 64-bla/per
(+)-3-Methyl-1-(2-methyl-1-propenyl) [500031-91-4] C11H18 MW = 150.26 782

cyclohexene

T exp 2 est Ref.
K kg m3
288.15 853.1 2.00 14-haw/fyf

cyclohexene

T exp 2 est Ref.
K kg m3
288.15 844.5 2.00 14-haw/fyf

cyclohexene

T exp 2 est Ref.
K kg m3
288.15 846.0 2.00 14-haw/fyf
Landolt-Brnstein
New Series IV/8D
1,2-Dimethyl-3,4- [500032-29-1] C12H20 MW = 164.29 785

bis(1-methylethylidene)cyclobutane

T exp 2 est Ref.
3
K kg m
293.15 824.7 2.00 13-leb/mer
4,4-Dimethyl-6-(2-methyl-1-propenyl) [500032-12-2] C12H20 MW = 164.29 786

cyclohexene

T exp 2 est Ref.
3
K kg m
296.15 824.6 3.00 06-kno/sch
4-Ethyl-6-methyl-4-(1-methylethenyl) [500032-13-3] C12H20 MW = 164.29 787

cyclohexene

T exp 2 est Ref.
3
K kg m
298.15 863.1 2.00 29-rea/wat
1-Methyl-3-ethyl-4-(1-methylethyl)- [500032-24-6] C12H20 MW = 164.29 788

1,3-cyclohexadiene

T exp 2 est Ref.
3
K kg m
298.15 863.1 1.00 29-rea/wat
1,2,4-Trimethyl-4-(1-methylethenyl) [16195-58-7] C12H20 MW = 164.29 789

cyclohexene

A 1103.15
B -0.850
cont.
Landolt-Brnstein
New Series IV/8D
1,2,4-Trimethyl-4-(1-methylethenyl)cyclohexene (cont.)

K kg m 3
kg m3
273.15 872.0 3.00 1.02 11-ric

298.15 835.2 2.00 -14.53 11-ric
273.15 874.1 2.00 3.12 13-leb-1
293.15 859.7 2.00 5.72 13-leb-1
289.15 862.6 2.00 5.22 38-far/pit

T exp 2 est
K kg m3
270.00 873.7 8.0
280.00 865.2 8.0
290.00 856.7 8.0
293.15 854.0 8.0
298.15 849.7 8.0
2,3,3-Trimethyl-1-(2-methyl-1-propenyl) [500031-55-0] C12H20 MW = 164.29 790

cyclopentene

A 1061.52
B -0.800

K kg m 3
kg m3
273.15 842.1 2.00 -0.90 04-beh

289.15 831.1 2.00 0.90 04-beh

T exp 2 est
K kg m3
270.00 845.5 2.5
280.00 837.5 2.5
290.00 829.5 2.5
Landolt-Brnstein
New Series IV/8D
4.6 Monocyclic Hydrocarbons (CnH2n-4), C11 to C12 - 387
1,5-Cyclododecadiene [1502-04-1] C 12H20 MW = 164.29 791

T exp 2 est Ref.
3
K kg m
293.15 885.6 1.00 67-tep/far
Cyclododecyne [1129-90-4] C12H20 MW = 164.29 792

T exp 2 est Ref.
3
K kg m
293.15 901.9 2.00 65-zak/kor

1,2-bis(1-Methylethyl)-4-methyl- [500032-25-7] C13H22 MW = 178.32 793
1,3-cyclohexadiene

T exp 2 est Ref.
3
K kg m
298.15 887.2 2.00 29-rea/wat
3-(1-Butenyl)-2,4,4- [500032-16-6] C13H22 MW = 178.32 794

trimethylcyclohexene

T exp 2 est Ref.
3
K kg m
293.15 853.0 3.00 11-kis-5
(+)-1-(1-Methylethenyl)-2- [500032-14-4] C13H22 MW = 178.32 795

(1-methylethyl)-5-methylcyclohexene

T exp 2 est Ref.
3
K kg m
293.15 855.1 3.00 15-sai
Landolt-Brnstein
New Series IV/8D
4-(1-Methylethenyl)-4-(1-methylethyl)- [500032-15-5] C13H22 MW = 178.32 796

6-methylcyclohexene

T exp 2 est Ref.
3
K kg m
298.15 887.2 2.00 29-rea/wat
1,2-bis(1-Ethylpropylidene)cyclobutane [500032-30-4] C14H24 MW = 192.34 797

T exp 2 est Ref.
3
K kg m
289.65 856.9 2.00 13-mer-1
3,4-bis(1-Methylethylidene)-1,1,2,2- [500032-31-5] C14H24 MW = 192.34 798

tetramethylcyclobutane

A 1061.71
B -0.750

K kg m 3
kg m3
288.75 845.7 2.00 0.55 13-mer-1

273.15 856.3 2.00 -0.55 13-mer-1

T exp 2 est
K kg m3
270.00 859.2 2.8
280.00 851.7 2.6
290.00 844.2 2.7
1-(2-Ethyl-1-butenyl)-2,3,3- [500031-56-1] C14H24 MW = 192.34 799

trimethylcyclopoentene

A 1087.09
B -0.750
cont.
Landolt-Brnstein
New Series IV/8D
1-(2-Ethyl-1-butenyl)-2,3,3-trimethylcyclopoentene(cont.)

K 3
kg m kg m3
273.15 881.4 2.00 -0.83 04-beh

292.15 868.8 2.00 0.82 04-beh

T exp 2 est
K kg m3
270.00 884.6 2.5
280.00 877.1 2.5
290.00 869.6 2.0
293.15 867.2 2.0
1,3,3,5,5-Pentamethyl-4- [500032-17-7] C14H24 MW = 192.34 800

(1-methylethenyl)cyclohexene

A 1094.44
B -0.780

K 3
kg m kg m3
273.15 879.9 2.00 -1.48 13-mer-1

290.15 869.6 2.00 1.48 13-mer-1

T exp 2 est
K kg m3
270.00 883.8 2.6
280.00 876.0 2.5
290.00 868.2 2.5
293.15 865.8 2.6
Landolt-Brnstein
New Series IV/8D
3-(1-4-Dimethyl-5-hexenyl)- [500032-18-8] C15H26 MW = 206.37 801

6-methylcyclohexene

T exp 2 est Ref.
3
K kg m
293.15 855.7 2.00 13-sem/bec
293.15 865.0 3.00 29-ruz/van
293.15 858.6 4.1 Recommended
(-)-(3,7-Dimethyl)-1,6-octadienyl) [500032-33-7] C16H28 MW = 220.40 802

cyclohexane

T exp 2 est Ref.
3
K kg m
293.15 846.8 2.00 13-rup
Landolt-Brnstein
New Series IV/8D
(CnH2n-6)

Cycloheptatriene [544-25-2] C7H8 MW = 92.14 803

T exp 2 est Ref.
K kg m3
273.15 912.9 3.00 1883-lad
290.65 892.9 2.00 10-von/eis-2
273.15 908.2 2.00 10-von/eis-2
5-(1-Methylethylidene)- [2175-91-9] C8H10 MW = 106.17 804

1,3-cyclopentadiene

T exp 2 est Ref.
K kg m3
290.15 885.8 2.00 00-thi
293.15 881.0 2.00 13-wil/hei
1,3,5-Cyclooctatriene [1871-52-9] C8H10 MW = 106.17 805

T exp 2 est Ref.
K kg m3
298.15 897.1 1.00 48-cop/bai
298.15 897.0 2.00 50-cop/hoc-1
298.15 901.3 2.00 50-cop/hoc-1
298.15 897.8 1.70 Recommended
1,3,6-Cyclooctatriene [3725-30-2] C8H10 MW = 106.17 806

T exp 2 est Ref.
3
K kg m
298.15 894.0 2.00 50-cop/hoc-1
5-(1-Methylpropylidene)-1,3- [3141-02-4] C9H12 MW = 120.19 807

cyclopentadiene

A 1112.48
B -0.800
cont.
Landolt-Brnstein
New Series IV/8D
5-(1-Methylpropylidene)-1,3-cyclopentadiene (cont.)

K kg m 3
kg m3
294.05 877.2 2.00 -0.04 11-von/eis-1

293.15 878.0 2.00 0.04 13-wil/hei

T exp 2 est
K kg m3
290.00 880.5 2.4
293.15 878.0 2.0
3,3-Dimethyl-6-methylene-1,4- [29304-70-9] C9H12 MW = 120.19 808

cyclohexadiene

T exp 2 est Ref.
K kg m3
288.35 843.0 2.00 11-von/mul
5-(1-Ethylpropylidene)-1,3- [7301-16-8] C10H14 MW = 134.22 809

cyclopentadiene

T exp 2 est Ref.
3
K kg m
289.55 881.2 2.00 11-von/eis-1
1-(1,3-Butadienyl)cyclohexene [500032-93-9] C10H14 MW = 134.22 810

T exp 2 est Ref.
3
K kg m
293.15 885.6 1.00 54-naz/kak-1
Landolt-Brnstein
New Series IV/8D
6,6-Dimethyl-3-ethylidene [500032-39-3] C10H14 MW = 134.22 811

cyclohexadiene

A 1091.30
B -0.800

K kg m3 kg m3
293.15 857.0 2.00 0.22 21-von/zie

288.65 861.4 2.00 1.02 21-von/zie
285.95 861.3 2.00 -1.24 21-von/zie

T exp 2 est
K kg m3
280.00 867.3 2.7
290.00 859.3 2.1
293.15 856.8 2.1
298.15 852.8 2.8
3-Methylene-1,6,6-trimethyl-1,4- [94925-96-9] C10H14 MW = 134.22 812

cyclohexadiene

T exp 2 est Ref.
K kg m3
283.85 873.5 2.00 21-von/zie
2-Methylene-1,5-dimethyl-3,5- [500032-78-0] C10H14 MW = 134.22 813

cycloheptadiene

T exp 2 est Ref.
K kg m3
293.15 908.1 1.00 67-kut/tis
Landolt-Brnstein
New Series IV/8D
3,3-Dimethyl-6-(1-propenyl)-1,4- [500032-46-2] C11H16 MW = 148.25 814

cyclohexadiene

T exp 2 est Ref.
3
K kg m
288.35 861.8 2.00 21-von/zie
3-Ethenyl-2,6,6-trimethyl-1,4- [500032-47-3] C11H16 MW = 148.25 815

cyclohexadiene

T exp 2 est Ref.
3
K kg m
285.85 884.4 2.00 21-von/zie
6-Methylene-1,3,3,4-tetramethyl-1,4- [14069-96-6] C11H16 MW = 148.25 816

cyclohexadiene

T exp 2 est Ref.
3
K kg m
288.35 880.9 2.00 21-von/zie
5-(Methylethenyl)-2,3-dimethyl-1,3- [103986-54-5] C11H16 MW = 148.25 817

cyclohexadiene

A 1108.16
B -0.800

K kg m3 kg m3
294.25 872.4 2.00 -0.36 06-kla

288.15 877.6 2.00 -0.04 07-kla
293.15 874.7 2.00 1.06 08-rup/emm
292.15 873.8 2.00 -0.65 10-von/eis-2
cont.
Landolt-Brnstein
New Series IV/8D
5-(Methylethenyl)-2,3-dimethyl-1,3-cyclohexadiene (cont.)

T exp 2 est
K kg m3
280.00 884.2 2.6
290.00 876.2 2.1
293.15 873.6 2.0
298.15 869.6 3.0
3-Methylene-1,5,6,6-tetramethyl-1,4- [89549-36-0] C11H16 MW = 148.25 818

cyclohexadiene

T exp 2 est Ref.
K kg m3
296.45 876.5 2.00 21-von/zie
2-Methyl-6-methylene-2,7-octadiene [500027-42-9] C11H16 MW = 148.25 819

A 1047.50
B -0.850
K 3
kg m kg m3 K kg m 3
kg m3
294.15 799.0 3.00 1.53 01-sem 288.15 801.3 3.00 -1.27 07-enk
288.15 802.3 2.00 -0.27 01-sem 293.15 793.7 3.00 -4.62 11-sem/may
288.15 804.6 3.00 2.03 03-cha 293.15 798.2 3.00 -0.12 13-leb
288.95 802.8 3.00 0.91 06-eyk-2 288.15 804.7 3.00 2.13 34-arb/abr

T exp 2 est
K kg m3
280.00 809.5 3.0
290.00 801.0 2.6
293.15 798.3 2.5
298.15 794.1 3.0
Landolt-Brnstein
New Series IV/8D

1,5-Dimethyl-3-(2-methylpropen-2-ylidene) [500032-41-7] C12H18 MW = 162.27 820
cyclohexene

T exp 2 est Ref.
3
K kg m
295.35 861.9 2.00 10-von/pet-1
3-Ethenyl-2,5,6,6-tetramethyl-1,4- [500032-49-5] C12H18 MW = 162.27 821

cyclohexadiene

T exp 2 est Ref.
3
K kg m
288.55 883.7 2.00 21-von/zie
(E,E,Z)-1,5,9-Cyclododecatriene [706-31-0] C12H18 MW = 162.27 822

T exp 2 est Ref.
3
K kg m
298.15 889.5 1.00 63-tak/yam
298.15 889.2 0.40 89-lai/rod
298.15 889.2 0.40 Recommended
2-Ethyl-3-methyl-6-(1-methylethenyl)- [500032-48-4] C13H20 MW = 176.30 823

1,3-cyclohexadiene

A 1104.19
B -0.750

K kg m 3
kg m3
291.15 885.9 2.00 0.07 06-kla/som

288.15 888.0 2.00 -0.08 07-kla
cont.
Landolt-Brnstein
New Series IV/8D
2-Ethyl-3-methyl-6-(1-methylethenyl)-1,3-cyclohexadiene (cont.)

T exp 2 est
K kg m3
280.00 894.2 2.8
290.00 886.7 2.2
293.15 884.3 2.5
298.15 880.6 3.5
2-Methyl-5-(1-methyethenyl)-3-propyl- [500032-50-8] C13H20 MW = 176.30 824

1,3-hexadiene

T exp 2 est Ref.
K kg m3
288.15 880.4 2.00 07-kla
4-(1,5-Dimethyl-4-hexenylidene)-1- [495-62-5] C15H24 MW = 204.36 825

methylcyclohexene

A 1090.71
B -0.750

K kg m3
kg m3
288.15 873.0 2.00 -1.60 04-bur/pag

294.15 871.7 2.00 1.60 32-sim-1

T exp 2 est
K kg m3
280.00 880.7 2.8
290.00 873.2 2.2
293.15 870.9 2.0
298.15 867.1 2.8
Landolt-Brnstein
New Series IV/8D
1-Methyl-4-(1,5-dimethyl-2,4- [500032-42-8] C15H24 MW = 204.36 826

hexadieneyl)cyclohexene

A 1119.67
B -0.850

K kg m3 kg m3
293.15 873.1 2.00 2.61 01-sch/kre

293.15 868.4 2.00 -2.09 13-sem/bec
289.15 873.3 1.00 -0.59 22-ruz/mey-1
303.15 860.0 2.00 -1.99 28-mou
290.15 874.0 1.00 0.96 29-ruz/van-2

T exp 2 est
K kg m3
280.00 881.7 2.8
290.00 873.2 2.4
293.15 870.5 2.2
298.15 866.2 2.4
310.00 856.2 3.0
2-(3-Methylbutyl)-3-methyl-6- [500032-51-9] C15H24 MW = 204.36 827

(1-methylethenyl)-1,3-cyclohexadiene

T exp 2 est Ref.
K kg m3
293.15 867.9 2.00 17-sem/jon
293.15 870.3 2.00 17-sem/jon-1
293.15 869.1 2.20 Recommended
4-(1-Methylethenyl)-1- [83212-57-1] C15H24 MW = 204.36 828

(4-methyl-3-pentenyl)cyclohexene

A 1121.80
B -0.800
cont.
Landolt-Brnstein
New Series IV/8D
4-(1-Methylethenyl)-1-(4-methyl-3-pentenyl)cyclohexene (cont.)

K kg m3
kg m3
292.15 881.7 3.00 -6.38 31-ruz/bos

293.15 905.0 5.00 17.72 32-die/kai

T exp 2 est
K kg m3
290.00 889.8 8.6
293.15 887.3 8.6
1-(3-Propyl-3-hexen-1-yne)cyclohexene [500032-43-9] C15H24 MW = 204.36 829

T exp 2 est Ref.
K kg m3
293.15 879.6 2.00 37-nes/mar
Landolt-Brnstein
New Series IV/8D
(CnH2n-8)
6. Monocyclic Hydrocarbons (CnH2n-8), C8 - C17 405
1,3,5,7-Cyclooctatetraene [629-20-9] C8H8 MW = 104.15 830

T = 273.15 to 353.10 K
A 1.24187 103
B -1.25701
C 5.32581 10-4
273.15 938.20 1.00 -0.05 {

48-rep/sch1( ) 323.10 891.20 0.49 -0.12 55-kus( )
293.10 919.20 0.42 0.01 55-kus( ) 333.10 882.20 0.51 -0.05 55-kus( )
298.10 914.50 0.44 0.02 55-kus( ) 343.10 873.40 0.53 0.12 55-kus( )
303.10 909.00 0.45 -0.79 55-kus1) 353.10 864.40 0.56 -0.02 55-kus( )
313.10 900.60 0.47 0.09 55-kus( )
+ B(Tc - T )2 + C(Tc - T )3 + D(Tc - T )4] ).
T fit T fit T fit
270.00 941.30 1.34 298.15 914.43 0.50 330.00 885.05 0.56
280.00 931.66 0.85 300.00 912.70 0.50 340.00 876.05 0.60
290.00 922.12 0.56 310.00 903.37 0.50 350.00 867.15 0.64
293.15 919.14 0.52 320.00 894.16 0.51 360.00 858.37 0.71
cont.
Landolt-Brnstein
New Series IV/8D
406 6. Monocyclic Hydrocarbons (CnH2n-8), C8 - C17
1,3,5,7-Cyclooctatetraene (cont.)
Methyl-1,3,5,7-cyclooctatetraene [500032-99-5] C9H10 MW = 118.18 831

T exp 2 est Ref.
K kg m3
298.15 897.8 1.00 52-cop/cam
1,2-Dimethyl-1,3,5,7-cyclooctatetraene [500033-01-2] C10H12 MW = 132.21 832

T exp 2 est Ref.
K kg m3
298.15 895.0 1.00 52-cop/cam
Landolt-Brnstein
New Series IV/8D
6. Monocyclic Hydrocarbons (CnH2n-8), C8 - C17 407
1-Ethyl-1,3,5,7-cyclooctatetraene [13402-35-2] C10H12 MW = 132.21 833

T exp 2 est Ref.
3
K kg m
298.15 899.6 1.00 52-cop/van
Propyl-1,3,5,7-cyclooctatetraene [500033-00-1] C11H14 MW = 146.23 834
Table 1. Experimental value with uncertaintys.

T exp 2 est Ref.
3
K kg m
298.15 887.0 1.00 52-cop/cam
1-(3-Methylene-4,4-dimethyl-1- [500031-08-3] C14H20 MW = 188.31 835

pentynyl)cyclohexene

T exp 2 est Ref.
3
K kg m
293.15 876.7 2.00 61-gve/pap
1-(3-Butyl-3-hepten-1-yne)cyclohexene [500032-45-1] C17H26 MW = 230.39 836

T exp 2 est Ref.
K kg m3
293.15 872.4 2.00 37-nes/mar
Landolt-Brnstein
New Series IV/8D
References
Reference codes are those used in the TRC SOURCE database.

A reference code consists of the year prior to 1900, or the last
two digits of the year after 1899, the first three letters of the first
author, the first three letters of the second author. An additional
sequence number is used when more than one reference in the
database has an identical code.
References 411
**-pin/ipa Pines, H.; Ipatieff, V. N.; Unpublished data.
1825-far Faraday, M.; Philos. Trans. R. Soc. London 115 (1825) 440.
1877-wre Wreden, F.; Justus Liebigs Ann. Chem. 187 (1877) 153.
1883-lad Ladenburg, A.; Justus Liebigs Ann. Chem. 217 (1883) 74.
1883-mar/ogl Markownikov, W.; Oglobin; Zh. Russ. Fiz.-Khim. O-va. 15 (1883) 331.
1883-mar/ogl-2 Markownikov, W.; Ogloblin; Zh. Russ. Fiz.-Khim. O-va. 15 (1883) 335.
1883-sch-3 Schiff, R.; Justus Liebigs Ann. Chem. 220 (1883) 71.
1884-gla Gladstone, J. H.; J. Chem. Soc., Trans. 45 (1884) 241.

1884-los/zan Lossen, W.; Zander, A.; Justus Liebigs Ann. Chem. 225 (1884) 109.
1884-ren Renard, A.; Ann. Chim. Phys. 1 (1884) 223.
1886-pes Pesci, L.; Gazz. Chim. Ital. 16 (1886) 225.
1887-kon Konovalov, M.; Zh. Russ. Fiz.-Khim. O-va. 19 (1887) 255.
1888-wal-2 Wallach, O.; Justus Liebigs Ann. Chem. 245 (1888) 191.
1889-hof Hofmann, A. W.; Chem. Ber. 22 (1889) 699.
1891-asc Aschan, O.; Ber. Dtsch. Chem. Ges. 24 (1891) 2710.

1891-eta/lam Etard, A.; Lambert, P.; C. R. Hebd. Seances Acad. Sci. 112 (1891) 945.
1892-ber Berkenheim, A.; Ber. Dtsch. Chem. Ges. 25 (1892) 686.

1892-wal-1 Wallach, O.; Ber. Dtsch. Chem. Ges. 25 (1892) 916.
1893-sem Semmler, F. W.; Chem. Ber. 26 (1893) 774.

1893-sub Subkov; Zh. Russ. Fiz.-Khim. O-va. 25 (1893) 383.
1893-thi Thiel, W.; Ber. Dtsch. Chem. Ges. 26 (1893) 922.
1893-tie/sem Tiemann, F.; Semmler, F. W.; Ber. Dtsch. Chem. Ges. 26 (1893) 2708.
1893-wis/hen Wislicenus, J.; Hentschel, W.; Justus Liebigs Ann. Chem. 275 (1893) 322.
1894-bru-1 Bruhl, J. W.; J. Prakt. Chem. 50 (1894) 119.

1894-bru-2 Bruhl, J. W.; Ber. Dtsch. Chem. Ges. 27 (1894) 1065.
1894-gue Guerbet, M.; C. R. Hebd. Seances Acad. Sci. 118 (1894) 286.
1894-mar-1 Markownikov, W.; J. Prakt. Chem. 49 (1894) 409.
1894-wag Wagner, G.; Ber. Dtsch. Chem. Ges. 27 (1894) 1636.
1895-beh Behal, A.; Bull. Soc. Chim. Fr. 13 (1895) 841.

1895-dem Demjanoff, N.; Ber. Dtsch. Chem. Ges. 28 (1895) 21.
1895-zel Zelinskii, N. D.; Ber. Dtsch. Chem. Ges. 28 (1895) 780.
1895-zel/rud Zelinskii, N. D.; Rudewitsch, W.; Ber. Dtsch. Chem. Ges. 28 (1895) 1341.
1896-gus Gustavson, G.; J. Prakt. Chem. 54 (1896) 99.

1896-kra/spi Kraemer, G.; Spilker, A.; Ber. Dtsch. Chem. Ges. 29 (1896) 552.
1896-tie/sch Tiemann, F.; Schmidt, R.; Ber. Dtsch. Chem. Ges. 29 (1896) 694.
1896-zel/ref Zelinskii, N. D.; Reformatskii, S.; Chem. Ber. 29 (1896) 214.
Landolt-Brnstein
New Series IV/8D
412 References
1897-kno Knoevenagel, E.; Justus Liebigs Ann. Chem. 297 (1897) 113.
1897-kno-1 Knoevenagel, E.; Justus Liebigs Ann. Chem. 297 (1897) 159.
1897-kno/fis Knoevenagel, E.; Fischer, C.; Justus Liebigs Ann. Chem. 297 (1897) 185.
1897-mar-2 Markownikov, W.; Chem. Ber. 30 (1897) 1222.
1897-tie Tiemann, F.; Ber. Dtsch. Chem. Ges. 30 (1897) 594.
1897-zel-1 Zelinskii, N. D.; Ber. Dtsch. Chem. Ges. 30 (1897) 387.
1898-for Fortey, E. C.; J. Chem. Soc. 73 (1898) 932.

1898-gus/pop Gustavson, G.; Popper, O.; J. Prakt. Chem. 58 (1898) 458.
1898-mar Markownikov, W.; Justus Liebigs Ann. Chem. 302 (1898) 1.
1898-mar-1 Markownikov, W.; Justus Liebigs Ann. Chem. 302 (1898) 19.
1898-rud Rudewitsch, W.; Zh. Russ. Fiz.-Khim. O-va. 30 (1898) 587.
1898-zel/nou Zelinskii, N. D.; Noumow, S.; Ber. Dtsch. Chem. Ges. 31 (1898) 3206.
1899-god/ros Godlewsky, B.; Roshanoivitsch; Zh. Russ. Fiz.-Khim. O-va. 31 (1899) 201.
1899-kur Kursanov, D.; Zh. Russ. Fiz.-Khim. O-va. 31 (1899) 161.
1899-kur-1 Kurssanow, N.; Ber. Dtsch. Chem. Ges. 32 (1899) 2972.
1899-mar-1 Markownikov, W.; Zh. Russ. Fiz.-Khim. O-va. 31 (1899) 214.
1899-you/for Young, S.; Fortey, E. C.; J. Chem. Soc., Trans. 75 (1899) 873.
00-gus Gustavson, G.; J. Prakt. Chem. 62 (2) (1900) 271.

00-kon/sch Kondakow, I.; Schindelmeiser, J.; J. Prakt. Chem. 61 (1900) 477.
00-thi Thiele, J.; Ber. Dtsch. Chem. Ges. 33 (1900) 666.
00-tie Tiemann, F.; Ber. Dtsch. Chem. Ges. 33 (1900) 2935.
00-you/for-1 Young, S.; J. Chem. Soc. 77 (1900) 372.
01-gri-2 Grignard, V.; Ann. Chim. 24 (1901) 433.

01-kur Kursanov, D.; Zh. Russ. Fiz.-Khim. O-va. 33 (1901) 301.
01-kur-2 Kurssanow, N.; Ber. Dtsch. Chem. Ges. 34 (1901) 2035.
01-sab/sen Sabatier, P.; Senderens, J. B.; C. R. Hebd. Seances Acad. Sci. 132 (1901) 1254.
01-sab/sen-1 Sabatier, P.; Senderens, J. B.; C. R. Hebd. Seances Acad. Sci. 132 (1901) 566.
01-sch/kre Schreiner, O.; Kremers, R. E.; Pharm. Arch. 4 (1901) 141.
01-sem Semmler, F. W.; Chem. Ber. 34 (1901) 3126.
01-sem-1 Semmler, F. W.; Ber. Dtsch. Chem. Ges. 34 (1901) 3122.
01-sub Subkov; Zh. Russ. Fiz.-Khim. O-va. 33 (1901) 711.
01-wil Willstatter, R.; Ber. Dtsch. Chem. Ges. 34 (1901) 129.
01-wil-1 Willstatter, R.; Justus Liebigs Ann. Chem. 317 (1901) 204.
01-zel/lep-1 Zelinskii, N. D.; Lepeschkin, N.; Justus Liebigs Ann. Chem. 319 (1901) 303.
01-zel/zel Zelinskii, N. D.; Zelikov, J.; Ber. Dtsch. Chem. Ges. 34 (1901) 2856.
01-zel/zel-1 Zelinskii, N. D.; Zelikov, J.; Ber. Dtsch. Chem. Ges. 34 (1901) 3249.
02-cro/les-1 Crossley, A. W.; LeSueur, H.; J. Chem. Soc. 81 (1902) 821.

02-doe Doebner, O.; Ber. Dtsch. Chem. Ges. 35 (1902) 2129.
02-mar Markownikov, W.; Zh. Russ. Fiz.-Khim. O-va. 34 (1902) 904.
02-mar/jak Markownikov, W.; Jakub; Zh. Russ. Fiz.-Khim. O-va. 34 (1902) 914.
02-per Perkin, W. H.; J. Chem. Soc. 81 (1902) 292.
02-sab/sen-1 Sabatier, P.; Senderens, J. B.; C. R. Hebd. Seances Acad. Sci. 134 (1902) 1130.
02-spe Speransky, N.; Zh. Russ. Fiz.-Khim. O-va. 34 (1902) 24.
Landolt-Brnstein
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References 413

02-zel/mos Zelinskii, N. D.; Moser, A.; Ber. Dtsch. Chem. Ges. 35 (1902) 2684.
03-cha Chapman, A. C.; J. Chem. Soc. 83 (1903) 506.

03-eyk Eykman, J. F.; Chem. Weekbla. 1 (1903) 7.
03-har Harries, C.; Justus Liebigs Ann. Chem. 328 (1903) 322.
03-har/ant Harries, C.; Antoni, W.; Justus Liebigs Ann. Chem. 328 (1903) 88.
03-mar Markownikov, W.; Zh. Russ. Fiz.-Khim. O-va. 35 (1903) 389.
03-sab/mai Sabatier, P.; Mailhe, A.; C. R. Hebd. Seances Acad. Sci. 137 (1903) 240.
03-sem Semmler, F. W.; Ber. Dtsch. Chem. Ges. 36 (1903) 1033.
03-wal/col Wallach, O.; Collmann, Fr.; Thede, J.; Justus Liebigs Ann. Chem. 327 (1903) 131.
04-bal/ang Balbiano, L.; Angeloni, L.; Atti Accad. Naz. Lincei, Cl. Sci. Fis., Mat. Nat., Rend. 13
(1904) 142.
04-beh Behal, A.; Bull. Soc. Chim. Fr. 31 (1904) 461.
04-bur/pag Burgess, H. E.; Page, T. H.; J. Chem. Soc. 85 (1904) 414.
04-cro Crossley, A. W.; J. Chem. Soc. 85 (1904) 1404.
04-har/wie Harries, C.; Weil, R.; Ber. Dtsch. Chem. Ges. 37 (1904) 845.
04-sem Semmler, F. W.; Ber. Dtsch. Chem. Ges. 37 (1904) 234.
04-tsc-1 Tschugaev, L.; Ber. Dtsch. Chem. Ges. 37 (1904) 1481.
04-wal/bes Wallach, O.; Beschke, E.; Justus Liebigs Ann. Chem. 336 (1904) 9.
04-zel Zelikov, J.; Ber. Dtsch. Chem. Ges. 37 (1904) 1374.
05-ale Alexejewa, D.; Zh. Russ. Fiz.-Khim. O-va. 37 (1905) 419.

05-cro/ren Crossley, A. W.; Renouf, N.; J. Chem. Soc. 87 (1905) 1487.
05-har/joh Harries, C.; Johnson, M.; Ber. Dtsch. Chem. Ges. 38 (1905) 1832.
05-kis-1 Kishner, N.; Zh. Russ. Fiz.-Khim. O-va. 37 (1905) 517.
05-kis-2 Kishner, N.; J. Soc. Chim. St. Petersbourg 37 (1905) 514.
05-kis/amo Kishner, N.; Amosow, P.; Zh. Russ. Fiz.-Khim. O-va. 37 (1905) 518.
05-sab/mai-1 Sabatier, P.; Mailhe, A.; C. R. Hebd. Seances Acad. Sci. 141 (1905) 20.
05-sab/mai-1 Sabatier, P.; Mailhe, A.; C. R. Hebd. Seances Acad. Sci. 141 (1905) 20.
05-sab/sen-1 Sabatier, P.; Senderens, J. B.; Ann. Chim. Phys. 4 (1905) 358.
05-zel Zelinskii, N. D.; Zh. Russ. Fiz.-Khim. O-va. 37 (1905) 962.
05-zel-1 Zelinskii, N. D.; Zh. Russ. Fiz.-Khim. O-va. 38 (1905) 625.
06-cro/ren Crossley, A. W.; Renouf, N.; J. Chem. Soc., Trans. 89 (1906) 26.
06-eyk-1 Eykman, J. F.; Chem. Weekbl. 3 (1906) 685.
06-kay/per Kay, F. W.; Perkin, W. H.; J. Chem. Soc. 89 (1906) 839.
06-kla Klages, A.; Chem. Ber. 39 (1906) 2306.
06-kla/som Klages, A.; Sommer, P.; Ber. Dtsch. Chem. Ges. 39 (1906) 2306.
06-kno/sch Knoevenagel, E.; Schwartz, R.; Ber. Dtsch. Chem. Ges. 39 (1906) 3441.
06-sab/sen Sabatier, P.; Senderens, J. B.; Ann. Chim. 4 (1906) 365.
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414 References
06-sem/rim Semmler, F. W.; Rimpel, C.; Ber. Dtsch. Chem. Ges. 39 (1906) 2582.
06-wal Wallach, O.; Justus Liebigs Ann. Chem. 347 (1906) 316.
06-wal/bes Wallach, O.; Beschke, E.; Justus Liebigs Ann. Chem. 347 (1906) 338.
06-zel Zelinskii, N. D.; Zh. Russ. Fiz.-Khim. O-va. 38 (1906) 473.
06-zel/gut Zelinskii, N. D.; Gutt, J.; Zh. Russ. Fiz.-Khim. O-va. 38 (1906) 476.
07-bla-2 Blanc, G.; C. R. Hebd. Seances Acad. Sci. 145 (1907) 681.
07-bru-1 Bruhl, J. W.; J. Chem. Soc. 91 (1907) 115.
07-enk Enklaar, C. J.; Rec. Trav. Chim. Pays-Bas 26 (1907) 166.
07-eyk Eykman, J. F.; Chem. Weekbl. 4 (1907) 41.
07-fav/bor Favorskii, A. E.; Borgmann, I.; Ber. Dtsch. Chem. Ges. 40 (1907) 4863.
07-kla Klages, A.; Chem. Ber. 40 (1907) 2360.
07-sab/mai-4 Sabatier, P.; Mailhe, A.; Ann. Chim. Phys. 10 (1907) 527.
07-tsc/pok Tschugaev, L.; Pokrowski; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 39 (1907) 1338.
07-wal/fle Wallach, O.; Fleischer, A.; Justus Liebigs Ann. Chem. 353 (1907) 304.
07-will/bru Willstatter, R.; Bruce, J.; Chem. Ber. 40 (1907) 3979.
07-will/ver Willstatter, R.; Veraguth, H.; Ber. Dtsch. Chem. Ges. 40 (1907) 957.
07-zel Zelinskii, N. D.; Chem. Ber. 40 (1907) 3277.
08-bac Bacon, R. F.; Philippine J. Sci. 3 (1908) 49.

08-bou/lev Bouveault, L.; Levallois, F.; C. R. Hebd. Seances Acad. Sci. 146 (1908) 180.
08-clo Clover, A. M.; Am. Chem. J. 39 (1908) 613.
08-fis/per Fisher, K.; Perkin, W. H.; J. Chem. Soc. 93 (1908) 1876.
08-har/maj Harries, C.; Majema, B.; Ber. Dtsch. Chem. Ges. 41 (1908) 2516.
08-har/tan Harries, C.; Tank, L.; Ber. Dtsch. Chem. Ges. 41 (1908) 1701.
08-kis Kishner, N.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 40 (1908) 994.
08-kis-3 Kishner, N.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 40 (1908) 676.
08-pic Pickles, S. S.; J. Chem. Soc. 93 (1908) 862.
08-rup/emm Rupe, H.; Emmerich, F.; Ber. Dtsch. Chem. Ges. 41 (1908) 1393.
08-rup/emm-1 Rupe, H.; Emmerich, F.; Ber. Dtsch. Chem. Ges. 41 (1908) 1750.
08-ski Skita, A.; Chem. Ber. 41 (1908) 2938.
08-wal/chu Wallach, O.; Churchill, J. B.; Rentschler, M.; Justus Liebigs Ann. Chem. 360 (1908) 55.
08-wal/chu-1 Wallach, O.; Churchill, J. B.; Justus Liebigs Ann. Chem. 360 (1908) 70.
08-wal/eva Wallach, O.; Evans, E.; Justus Liebigs Ann. Chem. 360 (1908) 44.
08-wal/eva-1 Wallach, O.; Evans, E.; Justus Liebigs Ann. Chem. 360 (1908) 51.
08-wal/eva-2 Wallach, O.; Evans, E.; Justus Liebigs Ann. Chem. 360 (1908) 52.
08-wal/mal Wallach, O.; Mallison, H.; Justus Liebigs Ann. Chem. 360 (1908) 68.
08-wal/ren Wallach, O.; Rentschler, M.; Justus Liebigs Ann. Chem. 360 (1908) 59.
08-wal/ren-1 Wallach, O.; Rentschler, M.; Justus Liebigs Ann. Chem. 360 (1908) 64.
08-will/kam Willstatter, R.; Kametaka, T.; Chem. Ber. 41 (1908) 1480.
08-zel/gor Zelinskii, N. D.; Gorskii, A.; Chem. Ber. 41 (1908) 2630.
08-zel/gor-1 Zelinskii, N. D.; Gorskii, A.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 40 (1908) 1399.
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References 415
08-zel/gor-2 Zelinskii, N. D.; Gorsky, A.; Ber. Dtsch. Chem. Ges. 41 (1908) 2479.
08-zel/gut Zelinskii, N. D.; Gutt, J.; Chem. Ber. 41 (1908) 2431.
09-bru Bruylants, P.; Recl. Trav. Chim. Pays-Bas Belg. 28 (1909) 188.
09-mur Murat, M.; Ann. Chim. Phys. 16 (1909) 108.
09-noy/der Noyes, W. A.; Derick, C. G.; J. Am. Chem. Soc. 31 (1909) 669.
09-sem/sch Semmler, F. W.; Schossberger, E; Ber. Dtsch. Chem. Ges. 42 (1909) 4644.
09-smi Smirnow, V.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 41 (1909) 1375.
09-vav Vavon, M. G.; C. R. Hebd. Seances Acad. Sci. 149 (1909) 997.
09-von-2 Von Auwers, K.; Ber. Dtsch. Chem. Ges. 42 (1909) 2424.
09-von/von Von Auwers, K.; Von Heyden, F.; Ber. Dtsch. Chem. Ges. 42 (1909) 2404.
09-wal/mar Wallach, O.; Martins, V.; Justus Liebigs Ann. Chem. 365 (1909) 272.
09-wal/ren Wallach, O.; Rentschler, M.; Justus Liebigs Ann. Chem. 365 (1909) 269.
10-beh Behal, A.; C. R. Hebd. Seances Acad. Sci. 150 (1910) 1764.
10-cro/gil Crossley, A. W.; Gilling, C.; J. Chem. Soc. 97 (1910) 2218.
10-del Delepine, M.; Bull. Soc. Chim. Fr. 7 (1910) 468.
10-der De Resseguier, B.; Bull. Soc. Chim. Fr. 7 (1910) 432.
10-eng/hal Engler, C.; Halmai, B.; Chem. Ber. 43 (1910) 397.
10-ipa Ipatieff, W.; Chem. Ber. 43 (1910) 3383.
10-lei Leiser, H.; Abh. Dtsch. Bunsen-Ges. No. 4 (1910) 69.
10-luf/per Luff, B.; Perkin, W. H.; J. Chem. Soc. 97 (1910) 2154.
10-noy/der Noyes, W. A.; Derick, C. G.; J. Am. Chem. Soc. 32 (1910) 1061.
10-noy/kyr Noyes, W. A.; Kyriakides, L. P.; J. Am. Chem. Soc. 32 (1910) 1064.
10-per/wal Perkin, W. H.; Wallach, O.; Justus Liebigs Ann. Chem. 374 (1910) 198.
10-von/eis Von Auwers, K.; Eisenlohr, F.; J. Prakt. Chem. 82 (1910) 65.
10-von/eis-1 Von Auwers, K.; Eisenlohr, F.; Ber. Dtsch. Chem. Ges. 43 (1910) 806.
10-von/eis-2 Von Auwers, K.; Eisenlohr, F.; Ber. Dtsch. Chem. Ges. 43 (1910) 827.
10-von/pet Von Auwers, K.; Peters, G.; Chem. Ber. 43 (1910) 3076.
10-von/pet-1 Von Auwers, K.; Peters, G.; Ber. Dtsch. Chem. Ges. 43 (1910) 3094.
10-von/pet-2 Von Auwers, K.; Peters, G.; Ber. Dtsch. Chem. Ges. 43 (1910) 3111.
10-von/rot Von Auwers, K.; Roth, W.; Eisenlohr, F.; Justus Liebigs Ann. Chem. 373 (1910) 267.
10-will/was Willstatter, R.; Waser, E.; Chem. Ber. 43 (1910) 1176.
10-you-1 Young, S.; Sci. Proc. R. Dublin Soc. 12 (1910) 374.
11-cho/per Chou, T.; Perkin, W. H.; J. Chem. Soc. 99 (1911) 530.

11-dra Drapier, P.; Bull. Cl. Sci., Acad. R. Belg. 1 (1911) 621.
11-fra/ser Francesconi, L.; Sernagiotto, E.; Atti accad. Lincei 20 (1911) 329.
11-haw/per Haworth, W. N.; Perkin, W. H.; Wallach, O.; Justus Liebigs Ann. Chem. 379 (1911) 131.
11-hen/boy Henderson, G. G.; Boyd, R.; J. Chem. Soc. 99 (1911) 2159.
11-jeg-1 Jegorowa, W.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 43 (1911) 1119.
11-kis Kishner, N.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 43 (1911) 1149.
11-kis-4 Kishner, N.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 43 (1911) 582.
Landolt-Brnstein
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416 References
11-kis/kla Kishner, N.; Klawikordow, V.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 43 (1911) 597.
11-kis/sav Kishner, N.; Savadosky, A.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 43 (1911) 1132.
11-kis/saw Kishner, N.; Sawadowski, A.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 43 (1911) 1137.
11-leb Lebedev. S. V.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 43 (1911) 820.
11-leb/ska Lebedev, S.; Skawronskaja, F.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 43 (1911) 1124.
11-leb/ska-1 Lebedev, S.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 43 (1911) 1136.
11-per Perkin, W. H.; J. Chem. Soc. 99 (1911) 727.
11-per-1 Perkin, W. H.; J. Chem. Soc. 99 (1911) 741.
11-per/pop Perkin, W. H.; Pope, W. J.; J. Chem. Soc. 99 (1911) 1514.
11-ric Richard, A. H.; C. R. Hebd. Seances Acad. Sci. 153 (1911) 116.
11-ric Richard, A. H.; C. R. Hebd. Seances Acad. Sci. 153 (1911) 116.
11-sem/may Semmler, F. W.; Mayer, E. W.; Chem. Ber. 44 (1911) 2009.
11-ski/rit Skita, A.; Ritter, H.; Ber. Dtsch. Chem. Ges. 44 (1911) 668.
11-vav Vavon, M. G.; C. R. Hebd. Seances Acad. Sci. 152 (1911) 1675.
11-von/eis-1 Von Auwers, K.; Eisenlohr, F.; J. Prakt. Chem. 84 (1911) 1.
11-von/mul Von Auwers, K.; Muller, K.; Ber. Dtsch. Chem. Ges. 44 (1911) 1595.
11-will/was Willstatter, R.; Waser, E.; Chem. Ber. 44 (1911) 3423.
12-ipa-1 Ipatieff, V. N.; Ber. Dtsch. Chem. Ges. 45 (1912) 3205.

12-kis Kishner, N.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 44 (1912) 165.
12-kis-1 Kishner, N.; Zh. Russ. Fiz. Khim. O-va., Chast Khim. 44 (1912) 849.
12-mey-1 Meyerfeld, J.; Chem.-Ztg. 36 (1912) 549.
12-ost Ostling, G. J.; J. Chem. Soc. 101 (1912) 457.
12-von/ell Von Auwers, K.; Ellinger, P.; Justus Liebigs Ann. Chem. 387 (1912) 200.
12-von/moo Von Auwers, K.; Moosbrugger, W.; Justus Liebigs Ann. Chem. 387 (1912) 167.
12-von/moo-1 Von Auwers, K.; Moosbrugger, W.; Justus Liebigs Ann. Chem. 387 (1912) 191.
12-wal/mey Wallach, O.; Meyer, E.; Justus Liebigs Ann. Chem. 392 (1912) 58.
12-wal/von Wallach, O.; Von Rechenberg, W.; Justus Liebigs Ann. Chem. 394 (1912) 362.
12-will/hat Willstatter, R.; Hatt, D.; Ber. Dtsch. Chem. Ges. 40 (1912) 1471.
12-zel/sch Zelinskii, N. D.; Schtscherbak, B.; J. Russ. Phys. Chem. Soc. 44 (1912) 1880.
13-dem/doj Demjanoff, N.; Dojarenko, M.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913) 176.
13-gad/sso Gadaskin, D.; Ssorkina, S.; Chem.-Ztg. 37 (1913) 724.
13-god/tab-1 Godchot, M.; Taboury, F.; C. R. Hebd. Seances Acad. Sci. 156 (1913) 470.
13-har/sei-1 Harries, C.; Seitz, R.; Justus Liebigs Ann. Chem. 395 (1913) 211.
13-haw Haworth, W. N.; J. Chem. Soc. 103 (1913) 1242.
13-kis Kishner, N.; Chem. Zentralbl. 84, 2 (1913) 2132.
13-kis/amo Kishner, N.; Amosow, P.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913) 957.
13-leb Lebedev, S.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 45 (1913) 1249.
13-leb-1 Lebedev, S.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913) 1296.
Landolt-Brnstein
New Series IV/8D
References 417
13-leb/mer Lebedev, S.; Mereshkowsky, L.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913)
1348.
13-leb/mer-1 Lebedev, S.; Mereshkowsky, B.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913)
1354.
13-mer-1 Merezhkovskii, B. K.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913) 1940.
13-mer-5 Mereshkowsky, L.; J. Russ. Phys. Chem. Soc. 45 (1913) 1925.
13-phi-1 Philipov, O.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913) 1464.
13-pic/bou Pictet, A.; Bouvier, M.; C. R. Hebd. Seances Acad. Sci. 157 (1913) 1438.
13-rup Rupe, H.; Justus Liebigs Ann. Chem. 402 (1913) 176.
13-sab/mur-1 Sabatier, P.; Murat, M.; C. R. Hebd. Seances Acad. Sci. 156 (1913) 184.
13-sem/bec Semmler, F. W.; Becker, A.; Ber. Dtsch. Chem. Ges. 46 (1913) 1814.
13-sem/ros Semmler, F. W.; Rosenberg., I.; Ber. Dtsch. Chem. Ges. 46 (1913) 768.
13-von/eis Von Auwers, K.; Eisenlohr, F.; Z. Phys. Chem. Stoechiom. Verwandtschaftsl. 83 (1913)
429.
13-wal/aug Wallach, O.; Augspurger, L.; Justus Liebigs Ann. Chem. 396 (1913) 281.
13-wal/sch Wallach, O.; Schlubach, H.; Justus Liebigs Ann. Chem. 396 (1913) 283.
13-will/hei Willstatter, R.; Heidelberger, M.; Ber. Dtsch. Chem. Ges. 46 (1913) 517.
13-will/kin Willstatter, R.; King, V. L.; Ber. Dtsch. Chem. Ges. 46 (1913) 527.
13-zel/lep Zelinskii, N. D.; Lepeschin, W. L.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 45 (1913) 613.
13-zel/sch Zelinskii, N. D.; Schtscherbak, B.; Chem. Ber. 46 (1913) 169.
13-zel/upe Zelinskii, N. D.; Upenskii, A. E.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 45 (1913) 831.
13-zel/usp Zelinskii, N. D.; Uspenskii, A.; Chem. Ber. 46 (1913) 1470.
14-haw/fyf Haworth, W. N.; Fyfe, A.; J. Chem. Soc. 105 (1914) 1659.
14-mee Meerwein, H.; Justus Liebigs Ann. Chem. 405 (1914) 125.
14-mur/amo Murat, M.; Amouroux, G.; Bull. Soc. Chim. Fr. 15 (1914) 159.
14-phi-1 Philipov, O.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 46 (1914) 1141.
14-phi-2 Philipov, O.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 46 (1914) 1163.
14-phi-3 Philipov, O.; Zh. Rus. Fiz.-Khim. O-va 46 (1914) 1185.
14-rot/von Roth, W.; Von Auwers, K.; Justus Liebigs Ann. Chem. 407 (1914) 145.
14-sem/fel-1 Semmler, F. W.; Feldstein, J.; Ber. Dtsch. Chem. Ges. 47 (1914) 384.
14-sem/jon Semmler, F. W.; Jonas, K. G.; Ber. Dtsch. Chem. Ges. 47 (1914) 2068.
14-vav Vavon, G.; Ann. Chim. (Paris) 1 (1914) 144.
15-hal Halse, O. M.; J. Prakt. Chem. 92 (1915) 40.

15-har/mor Harries, C.; Morrell, G.; Justus Liebigs Ann. Chem. 410 (1915) 71.
15-pic/bou Pictet, A.; Bouvier, M.; Ber. Dtsch, Chem. Ges. 48 (1915) 926.
15-ros Rosanov, N. A.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 47 (1915) 591.
15-rot/von Roth, W. A.; Von Auwers, K.; Justus Liebigs Ann. Chem. 407 (1915) 145.
15-sai Saijew, M.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 47 (1915) 2128.
15-von/hin Von Auwers, K.; Hinterseber, R.; Treppman, W.; Justus Liebigs Ann. Chem. 410 (1915)
257.
15-von/hin-1 Von Auwers, K.; Hinterseber, R.; Ber. Dtsch. Chem. Ges. 48 (1915) 1357.
15-von/lan Von Auwers, K.; Lange, E.; Justus Liebigs Ann. Chem. 409 (1915) 149.
15-von/tre Von Auwers, K.; Treppman, W.; Ber. Dtsch. Chem. Ges. 48 (1915) 1207.
16-phi Philipov, O.; J. Prakt. Chem. 93 (1916) 162.

16-phi-1 Philipov, O.; J. Prakt. Chem. 2 (1916) 179.
16-ric/shi Richards, T. W.; Shipley J. W.; J. Am. Chem. Soc. 38. (1916) 989.
Landolt-Brnstein
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418 References
16-ros Rosanov, N. A.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 48 (1916) 309.
16-ros-1 Rosanov, N. A.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 48 (1916) 168.
17-dem/doj Demjanow, N. J.; Dojarenko, M.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 49 (1917) 199.
17-jae Jaeger, F. M.; Z. Anorg. Allg. Chem. 101 (1917) 130.
17-sem/jon Semmler, F. W.; Jonas, K. G.; Roenisch, P.; Ber. Dtsch. Chem. Ges. 50 (1917) 1823.
17-sem/jon-1 Semmler, F. W.; Jonas, K. G.; Oelsner, K.; Ber. Dtsch. Chem. Ges. 50 (1917) 1838.
18-bro/hum Brooks, B. T.; Humphrey, I.; J. Am. Chem. Soc. 40 (1918) 822.
18-mee/fle Meerwein, H.; Fleischhauer, Cl.; Justus Liebigs Ann. Chem. 417 (1918) 263.
18-pic/kai Pictet, A.; Kaiser, M.; Ann. Chim. 10 (1918) 299.
18-von-1 Von Auwers, K.; Justus Liebigs Ann. Chem. 415 (1918) 142.
18-wal/aug Wallach, O.; Augspurger, L.; Justus Liebigs Ann. Chem. 414 (1918) 212.
19-cha/sim-1 Chavanne, G.; Simon, L. J.; C. R. Hebd. Seances Acad. Sci. 168 (1919) 1324.
19-cha/sim-2 Chavanne, G.; Simon, L. J.; C. R. Hebd. Seances Acad. Sci. 168 (1919) 1111.
19-eyk Eykman, J. F.; Natuurkd. Verh. Hollandsche Maatschappij Wet. Haarlem 8 (1919) 438.
19-eyk-1 Eykman, J. F.; Natuurkd. Verh. Hollandsche Maatschappij Wet. Haarlem 8 (1919) 505.
19-ric/shi Richards, T. W.; Shipley, J. W.; J. Am. Chem. Soc. 41 (1919) 2002.
20-hen/sme Henderson, G. G.; Smeaton, T. F.; J. Chem. Soc. 117 (1920) 144.
20-mou/bou Moureu, C.; Boutaric, A.; J. Chim. Phys. Phys.-Chim. Biol. 18 (1920) 348.
21-far/gar Faragher, W. F.; Garner, F. H.; J. Am. Chem. Soc. 43 (1921) 1715.
21-god Godchot, M.; C. R. Hebd. Seances Acad. Sci. 172 (1921) 686.
21-ski Skita, A.; Angew. Chem. 34 (1921) 230.
21-von/zie Von Auwers, K.; Ziegler, K.; Justus Liebigs Ann. Chem. 425 (1921) 217.
22-cha Chavanne, G.; Bull. Soc. Chim. Belg. 31 (1922) 331.

22-cha/bec Chavanne, G.; Becker, P.; Bull. Soc. Chim. Belg. 31 (1922) 95.
22-cha/van Chavanne, G.; Van Risseghem, H.; Bull. Soc. Chim. Belg. 31 (1922) 87.
22-dem/doj Demjanow, N. J.; Dojarenko, M.; Ber. Dtsch. Chem. Ges. 55 (1922) 2718.
22-dem/doj-1 Demjanow, N. J.; Dojarenko, M.; Ber. Dtsch. Chem. Ges. 55 (1922) 2727.
22-maj/kub Majima, R.; Kubota, B.; Japan J. Chem. 1 (1922) 19.
22-oga/miz Ogata, A.; Mizashita, C.; J. Pharm. Soc. Jpn. No. 484 (1922) 4.
22-ruz/mey-1 Ruzicka, L.; Meyer, J.; Mingazzini, M.; Helv. Chim. Acta 5 (1922) 345.
22-ski/sch Skita, A.; Schneck, A; Chem. Ber. 55 (1922) 144.
22-tim/van Timmermans, J.; Van der Horst, H; Onnes, H. K.; C. R. Hebd. Seances Acad. Sci. 174
(1922) 365.
22-tra/win-1 Trautz, M.; Winkler, K.; J. Prakt. Chem. 104 (1922) 37.
23-bou-2 Bourguel, M.; C. R. Hebd. Seances Acad. Sci. 177 (1923) 688.
23-nam/bru Nametkin, S. S.; Bruessoff, L.; Chem. Ber. 56 (1923) 1807.
23-smi/hur Smith, H. G.; Hurst, E.; Read, J.; J. Chem. Soc. 123 (1923) 1657.
23-tim/van Timmermans, J.; Van der Horst, H; Onnes, H. K.; Arch. Neerl. Sci. Exactes Nat., Ser. 3A
6 (1923) 180.
23-von/lem Von Braun, J.; Lemke, G.; Ber. Dtsch. Chem. Ges. 56 (1923) 1562.
Landolt-Brnstein
New Series IV/8D
References 419
24-asc/kro Aschan, O.; Krohn, F.; Ber. Dtsch. Chem. Ges. 57 (1924) 1959.
24-nam Nametkin, S. S.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 55-56 (1924) 47.
24-wie/sch Weinhaus, H.; Schumm, P.; Justus Liebigs Ann. Chem. 439 (1924) 20.
24-zel/pav Zelinskii, N. D.; Pavlov, G.; Chem. Ber. 57 (1924) 1066.
25-bou Bourguel, M.; Ann. Chim. (Paris) 3 (1925) 191.

25-eis-1 Eisenlohr, F.; Fortschr. Chem., Phys. Phys. Chem. 18 (1925) 521.
25-eis-2 Eisenlohr, F.; Fortschr. Chem., Phys. Phys. Chem. 18 (1925) 1.
25-eis/gor Eisenlohr, F.; Gorr, G.; Fortschr. Chem., Phys. Phys. Chem. 18 (1925) 10.
25-hof/dam Hofmann, F.; Damm, P.; Kaiser-Wilhelm Soc. 2 (1925) 97.

26-cha-3 Chavanne, G.; Bull. Cl. Sci., Acad. R. Belg. 12 (1926) 105.
26-des Dessart, A.; Bull. Soc. Chim. Belg. 35 (1926) 9.
26-doj-1 Dojarenko, M.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 58 (1926) 27.
26-esc-1 Escourrou, R.; Bull. Soc. Chim. Fr. 39 (1926) 1460.
26-esc-1 Escourrou, R.; Bull. Soc. Chim. Fr. 39 (1926) 1460.
26-gou/hun Gough, G. A. C.; Hunter, H.; Kenyon, J.; J. Chem. Soc. 129 (1926) 2052.
26-mat Mathews, J. H.; J. Am. Chem. Soc. 48 (1926) 562.
26-pav Pavlova, G. S.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 58 (1926) 1302.
26-ruz/bru-1 Ruzicka, L.; Brugger, W.; Pfeiffer; Schinz; Stoll; Helv. Chim. Acta 9 (1926) 499.
26-ruz/bru-1 Ruzicka, L.; Brugger, W.; Pfeiffer; Schinz; Stoll; Helv. Chim. Acta 9 (1926) 499.
26-tim/mar Timmermans, J.; Martin, F.; J. Chim. Phys. Phys.-Chim. Biol. 23 (1926) 733.
26-tim/mar-1 Timmermans, J.; Martin, F.; J. Chim. Phys. Phys.-Chim. Biol. 23 (1926) 747.
26-wie/hen Weissenberger, G.; Henke, R.; Katschinka, H.; Z. Anorg. Allg. Chem. 153 (1926) 33.
27-bau Baurguel, M.; Bull. Soc. Chim. Belg. 41 (1927) 1475.

27-bou Bourguel, M.; Bull. Soc. Chim. Fr. 41 (1927) 1475.
27-bra/hun Brame, J. S. S.; Hunter, T. G.; J. Inst. Pet. Technol. 13 (1927) 794.
27-cha Charonnat, R.; C. R. Hebd. Seances Acad. Sci. 185 (1927) 284.
27-cha/bec Chavanne, G.; Becker, P.; Bull. Soc. Chim. Belg. 36 (1927) 591.
27-doj Dojarenko, M.; Ber. Dtsch. Chem. Ges. 60 (1927) 1543.
27-god/bed Godchot, M.; Bedos, P.; C. R. Hebd. Seances Acad. Sci. 184 (1927) 208.
27-god/cau Godchot, M.; Cauquil, G.; C. R. Hebd. Seances Acad. Sci. 185 (1927) 1202.
27-ric/wol Richter, F.; Wolff, W.; Ber. Dtsch. Chem. Ges. 60 (1927) 477.
27-sen Senderens, J. B.; C. R. Hebd. Seances Acad. Sci. 177 (1927) 1183.
27-zel/kaz Zelinskii, N. D.; Kazanskii, B. A.; Ber. Dtsch. Chem. Ges. 60 (1927) 1101.
27-zel/koz Zelinskii, N. D.; Kozeshkov, K.; Ber. Dtsch. Chem. Ges. 60 (1927) 1102.
28-ada/mar Adams, R.; Marshall, J. R.; J. Am. Chem. Soc. 50 (1928) 1970.
28-asc Aschan, O.; Justus Liebigs Ann. Chem. 461 (1928) 1.
28-cas/rei Case, F. H.; Reid, E. E.; J. Am. Chem. Soc. 50 (1928) 3062.
28-cha/dev Chavanne, G.; Devogel, L.; Bull. Soc. Chim. Belg. 37 (1928) 141.
28-fuj Fujise, S.; Sci. Papers Inst. Phys. Chem. Res. Tokyo 8 (1928) 185.
28-god/cau-1 Godchot, M.; Cauquil, G.; C. R. Hebd. Seances Acad. Sci. 186 (1928) 375.
28-mou Moudgill, K.; J. Indian Chem. Soc. 5 (1928) 251.
28-ruz/sch Ruzicka, L.; Schinz, H.; Pfeiffer, M.; Helv. Chim. Acta 11 (1928) 686.
28-tre/sch Treibs, W.; Schmidt, H.; Chem. Ber. 61B (1928) 459.
28-von/hey Von Braun, J.; Heymons, A.; Ber. Dtsch. Chem. Ges. 61 (1928) 2276.
Landolt-Brnstein
New Series IV/8D
420 References
29-bau-1 Baudreghien, J.; Bull. Soc. Chim. Belg. 38 (1929) 172.

29-bod Bodroux, D.; Ann. Chim. 11 (1929) 511.
29-els/gib Elson, L. A.; Gibson, C. S.; Simonsen, J. L.; J. Chem. Soc. (1929) 2732.
29-far/sco Farmer, E.; Scott, W.; J. Chem. Soc. (1929) 172.
29-har Harris, J. M.; J. Am. Chem. Soc. 51 (1929) 2591.
29-kaz Kazanskii, B. A.; Chem. Ber. 62 (1929) 2205.
29-mid/hen Midgley, T.; Henne, A. L.; J. Am. Chem. Soc. 51 (1929) 1215.
29-rea/wat Read, J.; Watters, A.; J. Chem. Soc. (1929) 2165.
29-ros Rosanov, N. A.; Zh. Russ. Fiz.-Khim. O-va., Chast Fiz. 61 (1929) 2291.
29-ros-1 Rosanov, N. A.; Zh. Russ. Fiz.-Khim. O-va., Chast Khim. 61 (1929) 2313.
29-ruz/van Ruzicka, L.; VanVeen, A. G.; Justus Liebigs Ann. Chem. 468 (1929) 133.
29-ruz/van-2 Ruzicka, L.; VanVeen, A. G.; Justus Liebigs Ann. Chem. 468 (1929) 133.
29-smy/sto Smyth, C. P.; Stoops, W. N.; J. Am. Chem. Soc. 51 (1929) 3312.
29-str-1 Stratford, R.; Ann. Off. Natl. Combust. Liq. (Fr.) 4 (1929) 83.
29-van Van Keersbilck, N.; Bull. Soc. Chim. Belg. 38 (1929) 205.

30-cha/mil Chavanne, G.; Miller, O.; Bull. Soc. Chim. Belg. 39 (1930) 287.
30-cri Criegee, B.; Justus Liebigs Ann. Chem. 481 (1930) 263.
30-kom Komppa, G.; Ann. Acad. Sci. Fenn., Ser. A 30 (16) (1930) 15.
30-les-1 Lespieau, R.; Bull. Soc. Chim. Fr. 47 (1930) 847.
30-ric/wol Richter, F.; Wolff, W.; Chem. Ber. 63 (1930) 1714.
30-ric/wol-1 Richter, F.; Wolff, W.; Chem. Ber. 63 (1930) 1721.
30-ruz/sto Ruzicka, L.; Stoll, M.; Huyser, H.; Boekenoogen, H. A.; Helv. Chim. Acta 13 (1930)
1152.
30-tau/sta Tausz, J.; Staab, A.; Pet. Z. 26 (1930) 1129.
30-zel/fre Zelinskii, N. D.; Freimann, M. G.; Chem. Ber. 63 (1930) 1485.
31-bru/hic-1 Bruun, J. H.; Hicks-Brunn, M. M.; J. Res. Natl. Bur. Stand. (U. S.) 7 (1931) 607.
31-cha/mil Chavanne, G.; Miller, O.; Cornet; Bull. Soc. Chim. Belg. 40 (1931) 673.
31-chi Chiurdoglu, G.; Bull. Cl. Sci., Acad. R. Belg. 17 (1931) 1404.
31-haa Haagen-Smit, A. J.; Proc. K. Ned. Akad. Wet. 34 (1931) 165.
31-hen/pag Henry, T.; Paget, H.; J. Chem. Soc. (1931) 25.
31-hic Hicks-Brunn, M. M.; J. Res. Natl. Bur. Stand. (U. S.) 7 (1931) 799.
31-kaf/noz Kafuku, K.; Nozoe, T.; Bull. Chem. Soc. Jpn. 6 (1931) 111.
31-kaf/noz-2 Kafuku, K.; Nozoe, T.; Hata, C.; Bull. Chem. Soc. Jpn. 6 (1931) 40.
31-kag Kagehira, I.; Bull. Chem. Soc. Jpn. 6 (1931) 241.
31-kom/kaw Komatsu, S.; Kawamoto, T.; Nippon Kagaku Kaishi 52 (1931) 685.
31-ric/wol Richter, F.; Wolff, W.; Presting, W.; Ber. Dtsch. Chem. Ges. 64 (1931) 871.
31-ruz/boe Ruzicka, L.; Boekenoogen, H. A.; Helv. Chim. Acta 14 (1931) 1319.
31-ruz/bos Ruzicka, L.; Bosch, W.; Helv. Chim. Acta 14 (1931) 1336.
31-ruz/koo Ruzicka, L.; Koolhaas; Wind; Helv. Chim. Acta 14 (1931) 1151.
32-die/kai Dieterle, H.; Kaiser, P. H.; Arch. Pharm. Ber. Dtsch. Pharm. 270 (1932) 413.
32-gar/eva Garner, F. H.; Evans, E. B.; J. Inst. Pet. Technol. 18 (1932) 751.
32-hic/bru Hicks-Brunn, M. M.; Bruun, J. H.; J. Res. Natl. Bur. Stand. (U. S.) 8 (1932) 525.
32-kuh/deu Kuhn, R.; Deutsch, A.; Chem. Ber. 65 (1932) 43.
32-les/wak Lespieau, R.; Wakeman, R. L.; Bull. Soc. Chim. Fr. 51 (1932) 384
32-lev/mar-1 Levene, P. A.; Marker, R. E.; J. Biol. Chem. 97 (1932) 563.
32-mil Miller, O.; Bull. Soc. Chim. Belg. 41 (1932) 217.
32-sim-1 Simonsen, J. L.; The Terpenes Vol. 2, University Press: Cambridge, p 493, (1932).
Landolt-Brnstein
New Series IV/8D
References 421
32-ton/fen Tongberg, C. O.; Fenske, M. R.; Ind. Eng. Chem. 24 (1932) 814.
32-vor/fis Vorlander, D.; Fischer, J.; Chem. Ber. 65 (1932) 1756.
32-zel/mar Zelinskii, N. D.; Margolis, E. I.; Ber. Dtsch. Chem. Ges. A 65 (1932) 1613.
32-zel/tur-1 Zelinskii, N. D.; Turova-Pollak, M. B.; J. Gen. Chem. (U.S.S.R.) 2 (1932) 666.
33-ale-1 Alexandrovitch, N.; Zh. Obshch. Khim. 3 (1933) 48.

33-azi/bha Azim, M. A.; Bhatnagar, S. S.; Mathur, R. N.; Philos. Mag. 16 (1933) 580.
33-bro/qui Bromiley, E. C.; Quiggle, D.; Ind. Eng. Chem. 25 (1933) 1136.
33-bru/hic Bruun, J. H.; Hicks-Brunn, M. M.; J. Res. Natl. Bur. Stand. (U. S.) 10 (1933) 465.
33-chi Chiurdoglu, G.; Bull. Soc. Chim. Belg. 42 (1933) 347.
33-doe Doeuvre, J.; Bull. Soc. Chim. Fr. 53 (1933) 170.
33-hof/lan Hofmann, F.; Lang, K. F.; Berlin, K.; Schmidt, A. W.; Brennst.-Chem. 14 (1933) 103.
33-huc/ger Huckel, W.; Gercke, A.; Gross, A.; Chem. Ber. 66b (1933) 563.
33-hur/bol Hurd, C. D.; Bollman, H. T.; J. Am. Chem. Soc. 55 (1933) 699.
33-lov/cam Lovell, W. G.; Campbell, J. M.; Boyd, T. A.; Ind. Eng. Chem. 25 (1933) 1108.
33-mil/pia Miller, O.; Piaux, L.; C. R. Hebd. Seances Acad. Sci. 197 (1933) 412.
33-mit/mar Mitchell, D. T.; Marvel, C. S.; J. Am. Chem. Soc. 55 (1933) 4276.
33-ruz/boe Ruzicka, L.; Boekenoogen, H. A.; Edelman, H. J.; Helv. Chim. Acta 16 (1933) 487.
33-ruz/sto Ruzicka, L.; Stoll, M.; Helv. Chim. Acta 16 (1933) 493.
33-sig/cra Signaigo, F. K.; Cramer, P. L.; J. Am. Chem. Soc. 55 (1933) 3326.
33-tre Treibs, W.; Ber. Dtsch. Chem. Ges. A 66 (1933) 1483.
33-tre-1 Treibs, W.; Ber. Dtsch. Chem. Ges. A 66 (1933) 610.
33-vog Vogel, A. I.; J. Chem. Soc. (1933) 1028.
33-zel/kaz Zelinskii, N. D.; Kazanskii, B. A.; Plate, A. F.; Chem. Ber. 66 (1933) 1415.
33-zel/lev Zelinskii, N. D.; Levina, R. Ya.; Ber. Dtsch. Chem. Ges. A 66 (1933) 477.
33-zel/mic Zelinskii, N. D.; Michlina, S. E.; Eventova, M. S.; Ber. Dtsch. Chem. Ges. B 66 (1933)
1422.
34-arb/abr Arbuzov, B.; Abramov, W. F.; Chem. Ber. 67B (1934) 1942.
34-car/jon Carter, E. G.; Jones, D. C.; Trans. Faraday Soc. 30 (1934) 1027.
34-chi-1 Chiurdoglu, G.; Bull. Sci. Acad. R. Belg. 17 (1934) 1404.
34-god Godchot, M.; Bull. Soc. Chim. Fr. 1 (1934) 1153.
34-god/mou Godchot, M.; Mousseron, M.; Granger; C. R. Hebd. Seances Acad. Sci. 198 (1934) 480.
34-gre-1 Gredy, B.; C. R. Hebd. Seances Acad. Sci. 199 (1934) 1129.
34-gre-2 Gredy, B.; C. R. Hebd. Seances Acad. Sci. 199 (1934) 153.
34-gru/rea Grubb, W.; Read, J.; J. Chem. Soc. (1934) 242.
34-kuh/hof Kuhn, R.; Hoffer, M.; Ber. Dtsch. Chem. Ges. A 67 (1934) 357.
34-lev/tzu Levina, R. Ya.; Tzurikov, F. F.; Zh. Obshch. Khim. 4 (1934) 1250.
34-rot/nag Rotinyantz, L.; Nagornov, N. N.; Z. Phys. Chem., Abt. A 169 (1934) 20.
34-ruz/hur Ruzicka, L.; Hurbin, M.; Furter, M.; Helv. Chim. Acta 17 (1934) 78.
34-uri Urion, E.; Ann. Chim. 1 (1934) 5.
34-von/kur Von Braun, J.; Kurta, P.; Ber. Dtsch. Chem. Ges. A 67 (1934) 225.
34-war/ful Ward, A. L.; Fulweiler, W. H.; Ind. Eng. Chem., Anal. Ed. 6 (1934) 396.
34-was/spe Washburn, E. R.; Spencer, H. C,; J. Am. Chem. Soc. 56 (1934) 361.
34-zel/kaz Zelinskii, N. D.; Kazanskii, B. A.; Dokl. Akad. Nauk SSSR 3 (1934) 168.
34-zel/tar Zelinskii, N. D.; Tarassova, E. M.; Justus Liebergs Ann. Chem 508 (1934) 115.

35-cor/bor Cornubert, R.; Borrel, C.; Demo, M. D.; Garnier, J.; Humeau, R.; LeBihan, H.; Sarkis, G.;
Bull. Soc. Chim. Fr. 2 (1935) 195.
35-ear/gla Earp, D. P.; Glasstone, S.; J. Chem. Soc. (1935) 1709.
Landolt-Brnstein
New Series IV/8D
422 References
35-eis Eisenlohr, F.; Fortschr. Chem. Physik. 18 (9) (1935) 1

35-god/mou Godchot, M.; Mousseron, M.; Richaud, R.; C. R. Hebd. Seances Acad. Sci. 200 (1935)
1599.
35-gre-1 Gredy, B.; Bull. Soc. Chim. Fr. 2 (1935) 1029.
35-huc/kum Huckel, W.; Kumetat, K.; Severin, H.; Justus Liebigs Ann. Chem. 517 (1935) 184.
35-kaf/ike Kafuku, K.; Ikeda, T.; Hata, C.; Nippon Kagaku Kaishi 56 (1935) 1186.
35-leb/ser Lebedev, S.; Sergjenko, S.; Compt. Rend. Acad. Sci. URSS (1935) II 78.
35-lev/har Levene, P. A.; Harris, S. A.; J. Biol. Chem. 112 (1935) 195.
35-lev/mar-2 Levene, P. A.; Marker, R. E.; J. Biol. Chem. 110 (1935) 311.
35-mam Maman, A.; Publ. Sci. Tech. Minist. Air (Fr.) No. 66, 55 pp, (1935).
35-mil Miller, O.; Bull. Soc. Chim. Belg. 44 (1935) 513.
35-mul/wak Mulliken, S. P.; Wakeman, R. L.; Gerry, H. T.; J. Am. Chem. Soc. 57 (1935) 1605.
35-nen/van Nenitzescu, C. D.; Vantu, G. G.; Bull. Soc. Chim. 2 (1935) 2209.
35-pad/jat Padmanabhan, R.; Jatkar, S. K. K.; J. Am. Chem. Soc. 57 (1935) 334.
35-pia/bou Piaux, L.; Bourguel, M.; Ann. Chim. 4 (1935) 147.
35-ros/whi Rose, F. W.; White, J. D.; J. Res. Natl. Bur. Stand. (U. S.) 15 (1935) 151.
35-wel Wellm, J.; Z. Phys. Chem., Abt. B 28 (1935) 119.
35-zel/den Zelinskii, N. D.; Denissenko, J.; Eventova, M.; Dokl. Akad. Nauk SSSR 1 (1935) 313.
35-zel/kaz Zelinskii, N. D.; Kazanskii, B. A.; Plate, A. F.; Chem. Ber. 68 (1935) 1869.
35-zel/pac Zelinskii, N. D.; Packendorff, K.; Ghochllowa, E. G.; Ber. Dtsch. Chem. Ges. 68 (1935)
98.
36-bro/dur Brown, J. H.; Durand, H. W.; Marvel, C. S.; J. Am. Chem. Soc. 58 (1936) 1594.
36-dup-2 DuPont, R.; Bull. Soc. Chim. Belg. 45 (1936) 57.
36-fav Favorskii, A. E.; Zh. Obshch. Khim. 6 (1936) 720.
36-hib/lin Hibbit, D. C.; Linstead, R. P.; J. Chem. Soc. (1936) 470.
36-kaz Kazanskii, B. A.; Ber. Dtsch. Chem. Ges. B 69 (1936) 950.
36-kaz/pla Kazanskii, B. A.; Plate, A. F.; Chem. Ber. 69 (1936) 1862.
36-kaz/pla-1 Kazanskii, B. A.; Plate, A. F.; Gnatenko, K. M.; Chem. Ber. 69 (1936) 954.
36-lev/tra Levina, R. Ya.; Trakhtenberg, D. M.; Zh. Obshch. Khim. 6 (1936) 764.
36-lev/zur Levina, R. Ya.; Zurikow, F. F.; Zh. Obshch. Khim. 6 (1936) 1250.
36-mar-1 Margolis, E. I.; Ber. Dtsch. Chem. Ges. A 69 (1936) 1710.
36-mas Massart, L.; Bull. Soc. Chim. Belg. 45 (1936) 76.
36-mik Mikeska, L. A.; Ind. Eng. Chem. 28 (1936) 970.
36-nen/cio-1 Nenitzescu, C. D.; Cioranescu, E.; Chem. Ber. 69 (1936) 1820.
36-roz Rozental, D.; Bull. Soc. Chim. Belg. 45 (1936) 585.
36-ruz/sei Ruzicka, L.; Seidel, C. F.; Helv. Chim. Acta 19 (1936) 424.
37-boe/tak Boeseken, J.; Takes, H. V.; Recl. Trav. Chim. Pays-Bas 56 (1937) 858.
37-car/stu Carr, E. R.; Stucklen, H.; J. Am. Chem. Soc. 59 (1937) 2138.
37-cha/day Charlton, R.; Day, A.; Ind. Eng. Chem. 29 (1937) 92.
37-dya/loz Dyakova, M. K.; Lozovoi, A. V.; Stepantseva, T. G.; Zh. Obshch. Khim. 7 (1937) 722.
37-gro Grosse, A. V.; J. Am. Chem. Soc. 59 (1937) 2739.
37-gro/ipa Grosse, A. V.; Ipatieff, V. N.; J. Org. Chem. 2 (1937) 447.
37-isk Iskenderov, M. A.; Zh. Obshch. Khim. 7 (1937) 1435.
37-lev/iva Levina, R. Ya.; Ivanov, A.; Zh. Obshch. Khim. 7 (1937) 1866.
37-lev/pot Levina, R. Ya.; Potapova, A. A.; Zh. Obshch. Khim. 7 (1937) 353.
37-lin/wan Linstead, R. P.; Wang, A.; Williams, J.; Errington, K. D.; J. Chem. Soc. (1937) 1136.
37-loz/dya Lozovoi, A. V.; Dyakova, M. K.; Stepantseva, T. G.; Zh. Obshch. Khim. 7 (1937) 1119.
37-nes/mar Nesty, G. A.; Marvel, C. S.; J. Am. Chem. Soc. 59 (1937) 2662.
37-nie/smi Niederl, J. B.; Smith, R. A.; J. Am. Chem. Soc. 59 (1937) 715.
Landolt-Brnstein
New Series IV/8D
References 423
37-pig/kann Pigulevskii, G. V.; Kanetskaya, E. T.; Platonova, M. A.; Zh. Obshch. Khim. 7 (1937)
873.
37-tim/hen Timmermans, J.; Hennaut-Roland, M.; J. Chim. Phys. Phys.-Chim. Biol. 34 (1937) 693.
37-von/kam Von Braun, J.; Kamp, E.; Kopp, J.; Chem. Ber. 70 (1937) 1750.
38-car/stu Carr, E. P.; Stucklen, H.; J. Chem. Phys. 6 (1938) 55.

38-chi-1 Chiurdoglu, G.; Bull. Soc. Chim. Belg. 47 (1938) 363.
38-eva Evans, E. B.; J. Inst. Pet. Technol. 24 (1938) 321.
38-far/pit Farmer, E. H.; Pitkethly, R. C.; J. Chem. Soc. (1938) 11.
38-gro/wak Grosse, A. V.; Wackher, R.; Unpublished Data (1938).
38-ipa/pin-2 Ipatieff, V. N.; Pines, H.; Corson; J. Am. Chem. Soc. 60 (1938) 577.
38-kaz/glu Kazanskii, B. A.; Glushnev; Zh. Obshch. Khim. 8 (1938) 642.
38-kaz/vol Volfson, L.; Zh. Obshch. Khim. 8 (1938) 1685.
38-mou/gra Mousseron, M.; Granger, R.; Bull. Soc. Chim. Belg. 5 (1938) 1618.
38-mou/gra-1 Mousseron, M.; Granger, R.; C. R. Hebd. Seances Acad. Sci. 207 (1938) 366.
38-pau/nik Pauchkov, P. V.; Nikolaeva, A. F.; Zh. Obshch. Khim. 8 (1938) 1153.
38-will/lan Wilbaut, J. P.; Langedijk, S. L.; Smittenberg, J.; Hoog, H.; Chem. Ind. (London) (1938)
753.
39-ano Am. Pet. Inst. Hydrocarbon Res. Proj., First Annu. Rep., Ohio State Univ., Aug. 31,
(1939).
39-cow/jef Cowan, D. M.; Jeffery, G. H.; Vogel, A. I.; J. Chem. Soc. (1939) 1862.
39-gro/lin Grosse, A. V.; Linn, C. B.; J. Am. Chem. Soc. 61 (1939) 751.
39-gro/wac Grosse, A. V.; Wackher, R. C.; Ind. Eng. Chem., Anal. Ed. 11 (1939) 614.
39-gui Guillemonat, A.; Ann. Chim. (Paris) 11 (1939) 143.
39-kaz/tat Kazanskii, B. A.; Tatevosyan, G. T.; Zh. Obshch. Khim. 9 (1939) 2248.
39-lev/gol Levina, R. Ya.; Golub, G. B.; Smirnov, K. M.; Zh. Obshch. Khim. 9 (1939) 825.
39-loz/dya Lozovoi, A. V.; Dyakova, M. K.; Stepantseva, T. G.; Zh. Obshch. Khim. 9 (1939) 540.
39-mou/pau Mousseron, M.; Paulet, M.; Parfum. Mod. 33 (1939) 101.
39-phi-1 Philip, N. M.; Proc. - Indian Acad. Sci., Sect. A 9 (1939) 109.
39-pin/ipa Pines, H.; Ipatieff, V. N.; J. Am. Chem. Soc. 61 (1939) 1076.
39-pin/ipa-1 Pines, H.; Ipatieff, V. N.; J. Am. Chem. Soc. 61 (1939) 2728.
39-pla Plate, A. F.; Dokl. Akad. Nauk SSSR 24 (1939) 257.
39-sui/gem Suida, H.; Gemassmer, A.; Chem. Ber. 72 (1939) 1168.
39-tur/kos Turova-Pollak, M. B.; Koshelev, A. F.; J. Gen. Chem. (U.S.S.R.) 9 (1939) 2179.
39-tur/mak Turova-Pollak, M. B.; Makaeva, Z.; J. Gen. Chem. (U.S.S.R) 9 (1939) 1279.
39-tur/pol Turova-Pollak, M. B.; Polyakova, O. I.; Zh. Obshch. Khim. 9 (1939) 233.
39-wat/lee Waterman, H. I.; Leendertse, J. J.; Van Krevelen, D. W.; Rev. Pet. Technol. (London) 25
(1939) 801.
39-wat/lee-1 Waterman, H. I.; Leendertse, J. J.; Sirks, J. F.; J. Inst. Pet. 25 (1939) 809.
39-wat/lee-2 Waterman, H. I.; Leendertse, J. J.; Rev. Pet. Technol. (London) 25 (1939) 89.
39-whi/gla White, J. D.; Glasgow, A. R.; J. Res. Natl. Bur. Stand. (U. S.) 22 (1939) 137.
39-whi/pop Whitmore, F. C.; Popkin, A. H.; Pfister, J. R.; J. Am. Chem. Soc. 61 (1939) 1616.
39-wib/hoo Wibaut, J. P.; Hoog, H.; Langedijk, S. L.; Overhoff, J.; Smittenberg, J.; Benninga, N.;
Bouman, G. P.; van Dijk, H.; Gaade, W.; Geldof, H.; Hackmann, J. Th.; Jonker, E. W.;
Paap, T.; Zuiderweg, F. J.; Recl. Trav. Chim. Pays-Bas 58 (1939) 329.
40-ano Am. Pet. Inst. Hydrocarbon Res. Proj., Second Annu. Rep., Ohio State Univ., Aug. 31,
(1940).
Landolt-Brnstein
New Series IV/8D
424 References
40-gla Glasgow, A. R.; J. Res. Natl. Bur. Stand. (U. S.) 24 (1940) 509.
40-moo/ren Moore, G. E.; Renquist, M. L.; Parks, G. S.; J. Am. Chem. Soc. 62 (1940) 1505.
40-sch/gem Schmidt, A. W.; Gemassmer, A.; Ber. Dtsch. Chem. Ges. B 73 (1940) 359.
40-sch/gro Schmidt, A. W.; Grosser, A.; Ber. Dtsch. Chem. Ges. A 73 (1940) 930.
40-tur Turkiewicz, N.; Chem. Ber. 73 (1940) 861.
40-tur/tar Turova-Pollak, M. B.; Tarasova, G. A.; J. Gen. Chem. (U.S.S.R.) 10 (1940) 172.
41-ano-1 Am. Pet. Inst. Hydrocarbon Res. Proj., Third Annu. Rep., Ohio State Univ., Aug. 31,
(1941).
41-ben-1 Benson, S. W.; Anal. Chem. 13 (1941) 502.
41-ber Berlande, A.; C. R. Hebd. Seances Acad. Sci. 213 (1941) 437.
41-cra Crane, G.; Ph.D. Thesis, Ohio State Univ., Columbus, OH, (1941).
41-ney/pil Neyman-Pilat, E.; Pilat, S.; Ind. Eng. Chem. 33 (1941) 1382.
41-tur/vse Turova-Pollak, M. B.; Vsevolzhshaya, E. V.; Zh. Obshch. Khim. 11 (1941) 817.
41-von/rei Von Braun, J.; Reitz-Kopp, J.; Chem. Ber. 74 (1941) 1105.
41-whi/car Whitmore, F. C.; Carney, T. P.; J. Am. Chem. Soc. 63 (1941) 2633.
41-whi/pop Whitmore, F. C.; Popkin, A. H.; Bernstein, H. I.; Wilkins, J. P.; J. Am. Chem. Soc. 63
(1941) 124.
42-ano-2 Am. Pet. Inst. Hydrocarbon Res. Proj., Fourth Annu.Rep., Ohio State Univ., Aug. 31,
(1942).
42-ben Benson, S. W.; Ind. Eng. Chem., Anal. Ed. 14 (1942) 189.
42-ber Berlande, A.; Bull. Soc. Chim. Fr. 9 (1942) 642.
42-gei Geist, J. M.; Ph.D. Thesis, Penn. State Univ., Univ. Park, PA, (1942).
42-lar/tho Larsen, R. G.; Thorpe, R. E.; Armfield, F. A.; Ind. Eng. Chem. 34 (1942) 183.
42-lev Levina, R. Ya.; Zh. Obshch. Khim. 12 (1942) 422.
42-pet/che Petrov, A. D.; Chel'tsova, M. A.; J. Gen. Chem. USSR (Engl. Transl.) 12 (1942) 87.
42-sch Schmidt, A. W.; Ber. Dtsch. Chem. Ges. B 75 (1942) 1399.
42-sch Schmidt, A. W.; Ber. Dtsch. Chem. Ges. B 75 (1942) 1399.
42-sch/sch Schmidt, A. W.; Schoeller, V.; Brennst.-Chem. 23 (1942) 235.
42-van/mee Van Arkel, A. E.; Meerburg, P.; v. d. Handel, C. R.; Recl. Trav. Chim. Pays-Bas 61
(1942) 767.
43-ano Sunbury Rep. No. 2176, Anglo-Iranian Oil Co., May (1943).
43-ano-2 Am. Pet. Inst. Res. Proj. 6, Unpublished, (1943).
43-ano-3 Am. Pet. Inst. Hydrocarbon Res. Proj., Fifth Annu. Rep.,Ohio State Univ., Aug. 31,
(1943).
43-for-1 Forziati, A. F.; Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., March (1943).
43-gri/lud Griswold, J.; Ludwig, E. E.; Ind. Eng. Chem. 35 (1943) 117.
43-het/shc Hetling, V. A.; Shchekin, V. V.; Zh. Obshch. Khim. 13 (1943) 717.
43-too Tooke, J. W.; Ind. Eng. Chem. 35 (1943) 992.
44-boo Boord, C. E.; Am. Pet. Inst. Hydrocarbon Res. Proj. No. 123-S, OhioState Univ., May
(1944).
44-boo/per Boord, C. E.; Perilstein, W. L.; Greenlee, K. W.; Am. Pet. Inst. Hydrocarbon Res. Proj.,
Sixth Annu. Ref.,Ohio State Univ., Aug. 31, (1944).
44-can Cannon, M. R.; Am. Pet. Inst. Res. Proj. 42 Penn. State Univ., (1944).
44-fri/har Friend, J. N.; Hargreaves, W. D.; Philos. Mag. 35 (1944) 136.
44-fri/har-1 Friend, J. N.; Hargreaves, W. D.; Philos. Mag. 35 (1944) 57.
44-gar Garrett, A. B.; Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., unpub-lished, (1944).
44-gre Greenlee, K. W.; Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., Nov. (1944).
Landolt-Brnstein
New Series IV/8D
References 425
44-gre-1 Greenlee, K. W.; Am. Pet. Inst. Res. Proj. 45, No. 111-S, Ohio State Univ.June (1944).
44-gre/per Greenlee, K. W.; Perilstein, W. L.; Boord, C. E.; Personal Commun., Am. Pet. Inst. Res.
Proj. 45, March-June (1944).
44-huc Huckel, W.; Suom. Kemistil. B 17 (1944) 7.
44-pla/hul Plattner; Hulstkamp; Helv. Chim. Acta 27 (1944) 220.
44-tat/mel Tatevosyan, G. T.; Melikyan, M. I.; Bull. Armenian Branch Acad. Sci. U.S.S.R. No. 5/6
(1944) 23.
44-tat/ter Tatevosyan, G. T.; Terzyan, A. G.; Bull. Armenian Branch Acad. Sci. U.S.S.R. No. 1/2
(1944) 73.
45-ano Sunbury Rep. No. 2777, Anglo-Iranian Oil Co. Ltd., Nov. (1945).
45-ano-8 Sunbury Summarizing Rept. No. 2731, April (1945).
45-arb/zel Arbuzov, Yu. A.; Zelinskii, N. D.; Shuikin, N. I.; Bull. Acad. Sci. U.R.S.S. Classe Sci.
Chim. (1945) 163.
45-boo/gre Boord, C. E.; Greenlee, K. W.; Perilstein, W. L.; Am. Pet. Inst. Res. Proj. 45, Seventh
Annu. Rep., Ohio State Univ., June 30, (1945).
45-cra/boo Crane, G.; Boord, C. E.; Henne, A. L.; J. Am. Chem. Soc. 67 (1945) 1237.
45-fid Fidler, F. A.; Sunbury Rep. No. 2731, Anglo-Iranian Oil Co., April (1945).
45-gre Greenlee, K. W.; Am. Pet. Inst. Res. Proj. 45 Ohio State Univ., Sept. (1945).
45-gre-1 Greenlee, K. W.; Am. Pet. Inst. Res. Proj. 45 Ohio State Univ., December (1945).
45-gre-2 Greenlee, K. W.; Am. Pet. Inst. Res. Proj. 45 Ohio State Univ., June (1945).
45-gre/vog Greensfelder, B. S.; Voge, H. H.; Ind. Eng. Chem. 37 (1945) 1038.
45-gre/waa Greenlee, K. W.; Waalkes, T. P.; Am. Pet. Inst. Res. Proj. 45 No. 123A, Ohio State
Univ.,May (1945).
45-mck/ste McKinley, J. B.; Stevens, D. R.; Baldwin, W. E.; J. Am. Chem. Soc. 67 (1945) 1455.
45-per Perilstein, W. L.; Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., Dec. (1945).
45-pet/kru Petrov, A. D.; Krutov, K. M.; Khrenov, I. M.; Zh. Obshch. Khim. 15 (1945) 799.
45-whi/her Whitmore, F. C.; Herr, C. H.; Clarke, D. G.; Rowland, C. S.; Schiessler, R. W.; J. Am.
Chem. Soc. 67 (1945) 2059.
45-zel/arb Zelinskii, N. D.; Arbuzov, Yu. A.; Batu'ev, M. I.; Bull. Acad. Sci. U.R.S.S. (1945) Classe
Sci. Chim. 486.
46-ano Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., June (1946).
46-ano-2 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., Dec. (1946).
46-ano-4 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., August (1946).
46-bar/bur Bartleson, R. M.; Burk, F.; Lankelma, M.; J. Am. Chem. Soc. 68 (1946) 2513.
46-baz/ste Bazhulin, P. A.; Sterin, K. E.; Bulanova, T. F.; Solovova, O. P.; Turova-Pollak, M. B.;
Kazanskii, B. A.; Izv. Akad. Nauk SSSR Ser. Khim. (1946) 7.
46-boo/gre Boord, C. E.; Greenlee, K. W.; Perilstein, W. L.; Am. Pet. Inst. Res. Proj. 45, Eighth
Annu. Rep., OhioState Univ., June 30, (1946).
46-for/gla Forziati, A. F.; Glasgow, A. R.; Willingham, C. B.; Rossini, F. D.; J. Res. Natl. Bur.
Stand. (U. S.) 36 (1946) 129.
46-for/ros-1 Forziati, A. F.; Rossini, F. D.; Am. Pet. Inst. Res. Proj. 6, unpublished, Dec. (1946).
46-gei/can Geist, J. M.; Cannon, M. R.; Ind. Eng. Chem., Anal. Ed. 18 (1946) 611.
46-ger/van Gerding, H.; van der Vet, A. P.; Recl. Trav. Chim. Pays-Bas 64 (1946) 257.
46-gre-1 Greenlee, K. W.; Am. Pet. Inst. Res. Proj. 34, Ohio State Univ., Feb. (1946).
46-ipa/pin Ipatieff, V. N.; Pines, H.; Olberg, R. C.; J. Am. Chem. Soc. 68 (1946) 1709.
46-kay-1 Kay, W. B.; The Vapor Pressure and Saturated Liquid and Vapor Densities of Isomeric
Hexanes, Standard Oil Company: Whiting, IN, (1946).
46-lib/kaz Liberman, A. L.; Kazanskii, B. A.; Izv. Akad. Nauk SSSR Ser. Khim. (1946) 77.
46-mou Mousseron, M.; Bull. Soc. Chim. Fr. (1946) 218.
46-mou/ric Mousseron, M.; Richaud, R.; Granger; Bull. Soc. Chim. Fr. (1946) 222.
Landolt-Brnstein
New Series IV/8D
426 References
46-par/wes Parks, G. S.; West, T. J.; Naylor, B. F.; Fujii, P. S.; McClaine, L. A.; J. Am. Chem. Soc.
68 (1946) 2524.
46-pla/zab Plate; Zabezhenskaya; Izv. Akad. Nauk SSSR Ser. Khim. (1946) 651.
46-ser/spu Serijan, K. T.; Spurr, R. A.; Gibbons, L. C.; J. Am. Chem. Soc. 68 (1946) 1763.
47-ano-1 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., April -June (1947).
47-ano-2 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., July -Sept. (1947).
47-ano-4 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 8th Annu.Rep., (1947).
47-boo/gre Boord, C. E.; Greenlee, K. W.; Perilstein, W. L.; Derfer, J. M.; Am. Pet. Inst. Res. Proj.
45, Ninth Annu. Rep., OhioState Univ., June 30, (1947).
47-gla/wil Glasgow, A. R.; Willingham, C. B.; Rossini, F. D.; J. Res. Natl. Bur. Stand. (U. S.) 38
(1947) 621.
47-huc/har Huckel, W.; Harder, H.; Chem. Ber. 80 (1947) 357.
47-kay Kay, W. B.; J. Am. Chem. Soc. 69 (1947) 1273.
47-kaz/kop Kazanskii, B. A.; Koperina, A. V.; Batu'ev, M. I.; Doklady Akad. Nauk S.S.S.R. 56
(1947) 819.
47-mou/win Mousseron, M.; Winternitz; Jacquier; C. R. Hebd. Seances Acad. Sci. 224 (1947) 1062.
47-nam/vol Nametkin, S. S.; Volodina, M. A.; Zh. Obshch. Khim. 17 (1947) 325.
47-osb/gin Osborne, N. S.; Ginnings, D. C.; J. Res. Natl. Bur. Stand. (U. S.) 39 (1947) 453.
47-sch Schiessler, R. W.; Am. Pet. Inst. Res. Proj. 42, twelfth meeting, June (1947).
47-son/bhu Sondhi, H. K.; Bhushan, B.; Gulati, K. C.; Joshi, M. L.; J. Indian Chem. Soc., Ind. &
News Ed. 10 (1947) 17.
47-son/bhu-1 Sondhi, H. K.; Bhushan, B.; Gulati, K. C.; Joshi, M. L.; J. Indian Chem. Soc., Ind. &
News Ed. 10 (1947) 24.
47-spi/huf Spitzer, R.; Huffman, H. M.; J. Am. Chem. Soc. 69 (1947) 211.
47-tat/mel Tatevosyan; Melikyan; Terzyan; Zh. Obshch. Khim. 17 (1947) 981.
47-tuo/guy Tuot, M.; Guyard, M.; Bull. Soc. Chim. Fr. (1947) 1087.
48-adk/roe Adkins, H.; Roebuck, A. K.; J. Am. Chem. Soc. 70 (1948) 4041.
48-ano Patent, Brit. 607,499, Brit. Thomson-Houston Co., Sept. 1, (1948).
48-ano-4 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., June (1948).
48-ano-6 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., May (1948).
45, Tenth Annu. Rep., OhioState Univ., June (1948).
48-cop/bai Cope, A. C.; Bailey, W. J.; J. Am. Chem. Soc. 70 (1948) 2305.
48-fie/ber-2 Fieser, L. F.; Berliner, E.; Bondhus, F. J.; Chang, F. C.; Dauben, W. G.; Ettilnger, M. G.;
Fawaz, G.; Fields, M.; Heidelberger, C.; Heymann, H.; Vaughan, W. R.; Wilson, A. G.;
Wilson, E.; Wu, M.; Leffler, M. T.; Hamlin, K. E.; Matson, E. J.; Moore, E. E.; Moore,
M. B.; Zaugg, H. E.; J. Am. Chem. Soc. 70 (1948) 3181.
48-kop/kaz Koperina, A. V.; Kazanskii, B. A.; Izv. Akad. Nauk S.S.S.R. (1948) Otdel Khim. Nauk
302.
48-lev Levina, R. Ya.; Vestnik Moskov. Univ. 3 (1948) 123.
48-lut/bea-1 Lutz, G. A.; Bearse, A. E.; Leonard, J. E.; Croxton, F. C.; J. Am. Chem. Soc. 70 (1948)
4139.
48-maz Mazee, W. M.; Recl. Trav. Chim. Pays-Bas 67 (1948) 197.
48-rep/sch-1 Reppe, W.; Schlichting, O.; Klager, K.; Toepel, T.; Justus Liebigs Ann. Chem. 560
(1948) 1.
48-sho/cra Shortridge, R. W.; Craig, R. A.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am.
Chem. Soc. 70 (1948) 946.
48-tur/luk Turova-Pollak, M. B.; Lukina, M. Y.; Zh. Obshch. Khim. 18 (1948) 179.
Landolt-Brnstein
New Series IV/8D
References 427
49-ano-1 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., July (1949).
49-ano-4 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., Feb. (1949).
49-baz/ukh Bazhulin, P. A.; Ukholin, S. A.; Bulanova, T. F.; Koperina, A. V.; Plate, A. F.; Kazanskii,
B. A.; Izv. Akad. Nauk SSSR Ser. Khim. (1949) 481.
45, Eleventh Annu. Rep., OhioState Univ., June (1949).
49-boo/hen Boord, C. E.; Henne, A. L.; Greenlee, K. W.; Perilstein, W. L.; Derfer, J. M.; Ind. Eng.
Chem. 41 (1949) 609.
49-coo Cook, N. C.; Penn. State Univ., March 12 (1949).
49-den/fid Denyer, R. L.; Fidler, F. A.; Lowry, R. A.; Ind. Eng. Chem. 41 (1949) 2727.
49-der/gre Derfer, J. M.; Greenlee, K. W.; Boord, C. E.; J. Am. Chem. Soc. 71 (1949) 175.
49-dic/lov Dice, J. R.; Loveless, L. E., Jr.; Cates, H. L., Jr.; J. Am. Chem. Soc. 71 (1949) 3546.
49-eva Evans, G. L.; Ph.D. Thesis, Ohio State Univ., Columbus, OH, (1949).
49-foe/fen Foehr, E. G.; Fenske, M. R.; Ind. Eng. Chem. 41 (1949) 1956.
49-for/ros Forziati, A. F.; Rossini, F. D.; J. Res. Natl. Bur. Stand. (U. S.) 43 (1949) 473.
49-gel/mar Gelus, E.; Marple, S.; Miller, M. E.; Ind. Eng. Chem. 41 (1949) 1757.
49-kaz/gak Kazanskii, B. A.; Gakhanov, F. N.; Dokl. Akad. Nauk SSSR 64 (1949) 521.
49-kaz/luk Kazanskii, B. A.; Lukina, M. Y.; Dokl. Akad. Nauk SSSR 65 (1949) 693.
49-lev/gla Levina, R. Ya.; Gladshtein, B. M.; Akishin, P. A.; Zh. Obshch. Khim. 19 (1949) 1077.
49-lut Luther, H.; Brennst.-Chem. 30 (1949) 258.
49-pet/kap Petrov, A. D.; Kaplan, E. P.; Izv. Akad. Nauk SSSR Ser. Khim. (1949) 539.
49-pin/cza Pines, H.; Czajkowski, G. J.; Ipatieff, V. N.; J. Am. Chem. Soc. 71 (1949) 3798.
49-ser/wis Serijan, K. T.; Wise, P. H.; Gibbons, L. C.; J. Am. Chem. Soc. 71 (1949) 2265.
49-she/wis Sherijan, K. T.; Wise, P. H.; Gibbons, L. C.; J. Am. Chem. Soc. 71 (1949) 2265.
49-sla/wis Slabey, V. A.; Wise, P. H.; Gibbons, L. C.; J. Am. Chem. Soc. 71 (1949) 1518.
49-spe Sperling, R.; J. Chem. Soc. (1949) 1925.
49-ste/spa Stevens, P. G.; Spalding, S. C.; J. Am. Chem. Soc. 71 (1949) 1687.
49-van/gre Van Volkenburgh, R.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am. Chem. Soc.
71 (1949) 172.
49-van/gre-1 Van Volkenburgh, R.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am. Chem. Soc.
71 (1949) 3595.
49-vve/tak Vvedenskii, A. A.; Takhlareva, N. K.; Zh. Obshch. Khim. 19 (1949) 1083.
49-wie Weissler, A.; J. Am. Chem. Soc. 71 (1949) 419.
50-ano-1 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., Aug. (1950).
50-boo/gre Boord, C. E.; Greenlee, K. W.; Derfer, J. M.; Am. Pet. Inst. Res. Proj. 45, Twelfth Annu.
Rep., OhioState Univ., June (1950).
50-bro/ewa Brown, I.; Ewald, A. H.; Aust. J. Chem. 3 (1950) 306.
50-chi/fie Chiurdoglu, G.; Fierens, P. J. C.; Henkert, C.; Bull. Soc. Chim. Belg. 59 (1950) 140.
50-chi/fie-1 Chiurdoglu, G.; Fierens, P. J. C.; Henkert, C.; Bull. Soc. Chim. Belg. 59 (1950) 156.
50-cop/hoc Cope, A. C.; Stevens, C. L.; Hochstein, F. A.; J. Am. Chem. Soc. 72 (1950) 2510.
50-cop/hoc-1 Cope, A. C.; Hochstein, F. A.; J. Am. Chem. Soc. 72 (1950) 2515.
50-for/cam Forziati, A. F.; Camin, D. L.; Rossini, F. D.; J. Res. Natl. Bur. Stand. (U. S.) 45 (1950)
406.
50-her/ruz Herout, V.; Ruzicuka, V.; Vrany, M.; Sorm, F.; Collect. Czech. Chem. Commun. 15
(1950) 373.
50-kaz/kop Kazanskii, B. A.; Koperina, A. V.; Zemskaya, O. A.; Zh. Obshch. Khim. 20 (1950) 1212.
50-kaz/ter Kazanskii, B. A.; Terenteva, E. M.; Bulanova, T. F.; Akad. Nauk S.S.S.R., Inst. Org.
Khim. Sintegy Org.Sodinenil Sbornik I (1950) 161.
50-kaz/ter-1 Kazanskii, B. A.; Terenteva, E. M.; Akad. Nauk S.S.S.R., Inst. Org. Khim. Sintegy
Org.Sodinenil Sbornik I (1950) 97.
Landolt-Brnstein
New Series IV/8D
428 References
50-kop/noz Koperina, A. V.; Nazarova, L. M.; Kazanskii, B. A.; Zh. Obshch. Khim. 20 (1950) 1498.
50-nic/hei Nickels, J. E.; Heintz, W.; J. Org. Chem. 15 (1950) 1142.
50-nic/hei-1 Nickels, J. E.; Heintzelman; Tech. Report, Koppers Company, Inc., April 3, (1950).
50-pet Petrov, A. D.; Dokl. Akad. Nauk SSSR 73 (1950) 1205.
50-pla/sha Plate, A. F.; Shafran, R. N.; Batuev, M. I.; Zh. Obshch. Khim. 20 (1950) 472.
50-til Tilichenko, M. N.; Zh. Obshch. Khim. 20 (1950) 2152.
50-zel/ela Zelinskii, N. D.; Elagina, N. V.; Dokl. Akad. Nauk SSSR 73 (1950) 705.
50-zie/eim Ziegler, K.; Eimers, E.; Hechelhammer, W.; Wilms, H.; Justus Liebigs Ann. Chem. 567
(1950) 43.
50-zie/will Ziegler, K.; Wilms, H.; Justus Liebigs Ann. Chem. 567 (1950) 1.
51-ano Sunbury Rep. No. 4199, Anglo-Iranian Oil Co. (1951) June (1951).
51-ano-3 Am. Pet. Inst. Res. Proj. 45, Thirteenth Annu. Rep., OhioState Univ., June (1951).
51-ano-5 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., Sept. (1951).
51-bir/joh Birch; Johnson; J. Chem. Soc. (1951) 1493.
51-chi/maq Chiurdoglu, G.; Maquestiau, A.; Bull. Soc. Chim. Belg. 60 (1951) 47.
51-cra/lar Craig, L. E.; Larrab, C. E.; J. Am. Chem. Soc. 73 (1951) 1191.
51-des/fid Desty, D. H.; Fidler, F. A.; Ind. Eng. Chem. 43 (1951) 905.
51-lev/skv-2 Levina, R. Ya.; Skvarchenko, V. R.; Tantsyreva, T. I.; Vestn. Mosk. Univ., Ser. Fiz.-Mat.
Estestv. Nauk. No. 1 (1951) 137.
51-nam/vol Nametkin, S. S.; Volodina; Zh. Obshch. Khim. 21 (1951) 331.
51-pet/jur Petru, F.; Jurecek, M.; Kovar, J.; Chem. Listy 45 (1951) 300.
51-sch Schlenk, W.; Justus Liebigs Ann. Chem. 573 (1951) 142.
51-shu/min Shuikin, N. I.; Minachev, K. M.; Zelinskii, N. D.; Izv. Akad. Nauk SSSR Ser. Khim.
(1951) 554.
51-slo Slomp, G.; Ph.D. Thesis, Ohio State Univ., Columbus, OH, (1951).
51-slo/sho Slobodin, Ya. M.; Shokhor, I. N.; Zhur. Obshchei Khim. 21 (1951) 2005.
51-tur/ada Turova-Pollak, M. B.; Adamova, V. A.; Treshchova, E. G.; Zh. Obshch. Khim. 21 (1951)
250.
51-zel Zelinskii, N. D.; Izv. Akad. Nauk SSSR Ser. Khim. (1951) 554.
52-ano Patent, Brit. 668,609, Brit. Thomson-Houston Co., March19, (1952).

52-ano-4 Am. Pet. Inst. Res. Proj. 6, Carnegie-Mellon Univ., Oct. (1952).
52-ano-5 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., Sept. (1952).
52-ano-14 Am. Pet. Inst. Res. Proj. 45, 13th Annu. Rep., OhioState Univ., July (1952).
52-blo/bur Blomquist, A. T.; Burge, R. E.; Sucsy, A. C.; J. Am. Chem. Soc. 74 (1952) 3636.
52-blo/liu Blomquist, A. T.; Liu, L. H.; Bohrer, J. C.; J. Am. Chem. Soc. 74 (1952) 3643.
52-cla/har Clark, I. T.; Harris, E. E.; J. Am. Chem. Soc. 74 (1952) 1030.
52-col/ber Colonge, J.; Berthoud, J.; Bull. Soc. Chim. Fr. (1952) 211.
52-cop/cam Cope, A. C.; Campbell, H. C.; J. Am. Chem. Soc. 74 (1952) 179.
52-cop/van Cope, A. C.; Van Orden, H. O.; J. Am. Chem. Soc. 74 (1952) 175.
52-hag Hagihara, N.; Nippon Kagaku Zasshi 73 (1952) 373.
52-ina/gre Inatome, M.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am. Chem. Soc. 74 (1952)
292.
52-kaa/coo Kaarsemaker, S.; Coops, J.; Recl. Trav. Chim. Pays-Bas 71 (1952) 261.
52-kaz/luk Kazanskii, B. A.; Lukina, M. Y.; Izv. Akad. Nauk SSSR Ser. Khim. (1952) 314.
52-kel/gre Kelso, R. G.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am. Chem. Soc. 74 (1952)
287.
52-lev/gla Levina, R. Ya.; Gladshtein, B. M.; Zh. Obshch. Khim. 22 (1952) 585.
52-lev/shu-2 Levina, R. Ya.; Shusherina, N. P.; Zh. Obshch. Khim. 22 (1952) 577.
52-mek/kam Mekhtiev; Kambarow; Zeinalova; Dokl. Akad. Nauk SSSR 86 (1952) 547.
Landolt-Brnstein
New Series IV/8D
References 429
52-naz/kot Nazarov, I. N.; Kotlyarevskii, P. A.; Kuznetsov, E. V.; Zh. Obshch. Khim. 22 (1952)
1147.
52-pla/sav Plate; Saveleva; Dokl. Akad. Nauk SSSR 82 (1952) 919.
52-pre/sch Prelog, V.; Schenker, K.; Guenthard, H. H.; Helv. Chim. Acta 35 (1952) 1598.
52-sla-1 Slabey, V. A.; J. Am. Chem. Soc. 74 (1952) 4963.
52-sla/wis-1 Slabey, V. A.; Wise, P. H.; J. Am. Chem. Soc. 74 (1952) 3887.
52-van/koo Van derbij, J. R.; Kooijman, E. C.; Recl. Trav. Chim. Pays-Bas 71 (1952) 837.
52-von/sch Vonderwahl, R.; Schinz, H.; Helv. Chim. Acta 35 (1952) 2368.
52-von/sch-1 Vonderwahl, R.; Schinz, H.; Helv. Chim. Acta 35 (1952) 1997.
53-ano-1 Am. Pet. Inst. Res. Proj. 45, Fifteenth Annu. Rep., Ohio State Univ., June (1953).
53-ano-7 Patent, Brit. 701,097, Wm. Butler & Co., Dec. 16, (1953).
53-ano-11 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., July (1953).
53-bir/dea Birch, S. F.; Dean, R. A.; J. Chem. Soc. (1953) 2477.
53-car/tem Carter, G. F.; Templeton, D. H.; Acta Cryst. 6 (1953) 805.
53-cop/pik Cope, A. C.; Pike, R. A.; Spencer, C. F.; J. Am. Chem. Soc. 75 (1953) 3212.
53-der/har Dreiding, A. S.; Hartman, J. A.; J. Am. Chem. Soc. 75 (1953) 939.
53-gra/gre Gragson, J. T.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am. Chem. Soc. 75
(1953) 3344.
53-ipa/hun Ipatieff, V. N.; Huntsman, W. D.; Pines, H.; J. Am. Chem. Soc. 75 (1953) 6222.
53-lam/wis Lamberti, J. M.; Wise, P. H.; J. Am. Chem. Soc. 75 (1953) 4787.
53-lev/mez Levina, R. Ya.; Mezentsova, N. N.; Akishin, P. A.; Zh. Obshch. Khim. 23 (1953) 562.
53-lev/tan-1 Levina, R. Ya.; Tantsyreva, T. I.; Treshchova, E. G.; Zh. Obshch. Khim. 23 (1953) 729.
53-noy/nag Noyce, D. S.; Nagle, R. J.; J. Am. Chem. Soc. 75 (1953) 127.
53-par/cha Parthasarathy, P. S.; Chari, S. S.; Srinivasan, D.; J. Phys. Radium 14 (1953) 541.
53-pin/mye Pines, H.; Myerholtz, R.; Ipatieff, V. N.; J. Am. Chem. Soc. 75 (1953) 937.
53-pla/lib Plate; Liberman; Momma; Izv. Akad. Nauk SSSR Ser. Khim. (1953) 689.
53-slo/gri Slobodin, Ya. M.; Grigoreva, V. I.; Shmulyakovskii, Ya. E.; Zh. Obshch, Khim. 23
(1953) 1480.
53-slo/gri-1 Slobodin, Ya. M.; Grigoreva, V. I.; Shmulyakovskii, Ya. E.; Zh. Obshch. Khim. 23
(1953) 1665.
53-sor/ber Sorm, F.; Beranek, J.; Chem. Listy 47 (1953) 708.
53-syk/her Sykora, V.; Herout, V.; Pliva, J.; Sorm, F.; Chem. Listy 47 (1953) 889.
54-ano-1 Am. Pet. Inst. Res. Proj. 45, Tech. Rep. 13, Ohio StateUniv., (1954).
54-ano-8 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., March (1954).
54-ano-10 Nat. Advis. Comm. Aeronaut. Lewis Flight Propulsion Lab., Cleveland, OH, April
(1954).
54-aut Auterinen, A.; Suom. Kemistil. B 27 (1954) 29.
54-baz/kop Bazhulin, P. A.; Koperina, A. V.; Liberman, A. L.; Ovodova, V. A.; Kazanskii, B. A.;
Izv. Akad. Nauk SSSR Ser. Khim. (1954) 709.
54-bir/dea Birch, S. F.; Dean, R. A.; Justus Liebigs Ann. Chem. 585 (1954) 234.
54-bir/dea-1 Birch, S. F.; Dean, R. A.; Whitehead, E. V.; J. Org. Chem. 19 (1954) 1449.
54-cam/for Camin, D. L.; Forziati, A. F.; Rossini, F. D.; J. Phys. Chem. 58 (1954) 440.
54-chi/maq Chiurdoglu, G.; Maquestiau, A.; Bull. Soc. Chim. Belg. 63 (1954) 357.
54-cla/cor Claudon, M. M.; Cornubert, R.; Lemoine, G.; Malzieu; C. R. Hebd. Seances Acad. Sci.
238 (1954) 309.
54-cle Clement, G.; Bull. Soc. Chim. Fr. (1954) 228.
54-cra/dae Cram, D. J.; Daeniker, H. U.; J. Am. Chem. Soc. 76 (1954) 2743.
54-dix/sch Dixon, J. A.; Schiessler, R. W.; J. Am. Chem. Soc. 76 (1954) 2197.
Landolt-Brnstein
New Series IV/8D
430 References
54-dom/bel Domnin, N. A.; Beletskaya, A. S.; Zh. Obshch. Khim. 24 (1954) 1636.
54-eve/bor Eventova, M. S.; Borisov, P. P.; Osipova, L. V.; Vestn. Mosk. Univ. 9, No. 6, Ser. Fiz.-
Mat. Estestven. Nauk No. 4 (1954) 91.
54-kaz/luk Kazanskii, B. A.; Lukina, M. Y.; Izv. Akad. Nauk SSSR Ser. Khim. (1954) 173
54-kaz/luk-1 Kazanskii, B. A.; Lukina, M. Y.; Ovodova, V. A.; Izv. Akad. Nauk SSSR Ser. Khim.
(1954) 878.
54-kaz/luk-3 Kazanskii, B. A.; Lukina, M. Y.; Doklady Akad. Nauk. S.S.S.R. 94 (1954) 887.
54-khr/bal Khromov, S. I.; Balenkova, E. S.; Akishin, P. A.; Kazanskii, B. A.; Dokl. Akad. Nauk
SSSR 97 (1954) 103.
54-khr/bal-1 Khromov, S. I.; Balenkova, E. S.; Akishin, P. A.; Kazanskii, B. A.; Zh. Obshch. Khim. 24
(1954) 1360.
54-khr/bal-2 Khromov, S. I.; Balenkova, E. S.; Kazanskii, B. A.; Zh. Obshch. Khim. 24 (1954) 1562.
54-khr/bal-3 Khromov, S. I.; Balenkova, E. S.; Kazanskii, B. A.; Doklady Akad. Nauk S.S.S.R. 96
(1954) 295.
54-khr/nov Khromov, S. I.; Novikov, S. S.; Petrova, G. B.; Zelinskii, N. D.; Dokl. Akad. Nauk SSSR
96 (1954) 1175.
54-lev/shu Levina, R. Ya.; Shusherina, N. P.; Gir, K. D.; Treshchova, E. G.; Zh. Obshch. Khim. 24
(1954) 1551.
54-luk/ovo Lukina, M. Y.; Ovodova, V. A.; Kazanskii, B. A.; Doklady Akad Nauk 97 (1954) 683.
54-naz/kak-1 Nazarov, I. N.; Kakhniashvili, A. I.; Sb. Statei Obshch. Khim. 2 (1954) 896.
54-oco/gol OConnor, R. T.; Goldblatt, L. A.; Anal. Chem. 26 (1954) 1726.
54-pin/hof Pines, H.; Hoffman, N. E.; Ipatieff, V. N.; J. Am. Chem. Soc. 76 (1954) 4412.
54-pin/hof-1 Pines, H.; Hoffman, N. E.; J. Am. Chem. Soc. 76 (1954) 4417.
54-pom/foo-1 Pomerantz, P.; Fookson, A.; Mears, T. W.; Rothberg, S.; Howard, F. L.; J. Res. Natl. Bur.
Stand. (U. S.) 52 (1954) 59.
54-seu Seubold, F. H.; J. Am. Chem. Soc. 76 (1954) 3732.
54-smi/otv Smith, V. N.; Otvos, J. W.; Anal. Chem. 26 (1954) 359.
54-syk/cer Sykora, V.; Cerny, C.; Herout, V.; Sorm, F.; Chem. Listy 48 (1954) 76.
54-wec/hun Weck, H. I.; Hunt, H.; Ind. Eng. Chem. 46 (1954) 2521.
55-ano-8 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., April (1955).
55-bai/hew Bailey, W. J.; Hewitt, J. J.; King, C.; J. Am. Chem. Soc. 77 (1955) 357.
55-bal/tur Balandin, A. A.; Turova-Pollak, M. B.; Kann, S.; Dokl. Akad. Nauk SSSR 105 (1955)
716.
55-blo/whe Blomquist, A. T.; Wheeler, E. S.; Chu, Y.; J. Am. Chem. Soc. 77 (1955) 6307.
55-cri/ker Criegee, R.; Kerckow, A.; Zinke, H.; Chem. Ber. 88 (1955) 1878.
55-cut Cutler, W.; Ph.D. Thesis, Penn. State Univ., Univ. Park, PA, (1955).
55-cut/jon Cutting, C. L.; Jones, D. C.; J. Chem. Soc. (1955) 4067.
55-del/rud Deluzarche, A.; Rudloff, A.; C. R. Hebd. Seances Acad. Sci. 240 (1955) 2329.
55-gar/hal Garner, F. H.; Hall, R. T. W.; J. Inst. Pet. 41 (1955) 1.
55-gra/gre Gragson, J. T.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Org. Chem. 20 (1955)
275.
55-ham/sto Hammond, B. R.; Stokes, R. H.; Trans. Faraday Soc. 51 (1955) 1641.
55-kaz/lib Kazanskii, B. A.; Liberman, A. L.; Dokl. Akad. Nauk SSSR 101 (1955) 877.
55-kaz/luk Kazanskii, B. A.; Lukina, M. Y.; Nakhapetyan, L. A.; Dokl. Akad. Nauk SSSR 101
(1955) 683.
55-kel/gre Kelso, R. G.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am. Chem. Soc. 77 (1955)
1751.
55-kus Kuss, E.; Z. Angew. Phys. 7 (1955) 372.
55-pet Petrov, A. D.; Izv. Akad. Nauk SSSR Ser. Khim. (1955) 639.
55-pin/mar Pines, H.; Marechal, J.; J. Am. Chem. Soc. 77 (1955) 2819.
55-roc/sie Rock, H.; Sieg, L.; Z. Phys. Chem. (Munich) 3 (1955) 355.
Landolt-Brnstein
New Series IV/8D
References 431
55-tim/hen Timmermans, J.; Hennaut-Roland, M.; J. Chim. Phys. Phys.-Chim. Biol. 52 (1955) 223.
55-web Weber, J. H.; Ind. Eng. Chem. 47 (1955) 454.
56-ano Am. Pet. Inst. Res. Proj. 45, Eighteenth Annu. Rep.,Ohio State Univ., June (1956).
56-ano-5 Am. Pet. Inst. Res. Proj. 6, Carnegie-Mellon Univ., Dec. (1956).
56-ano-6 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., May (1956).
56-ano-19 Am. Pet. Inst. Res. Proj. 45, Tech. Rept. 15, No. 2 (1956).
56-baz/sok Bazhulin, P. A.; Sokolovskaya, A. I.; Belikova, N. A.; Liberman, A. L.; Plate, A. F.; Izv.
Akad. Nauk SSSR Ser. Khim. (1956) 1130.
56-bus/gre Bussert, J. F.; Greenlee, K. W.; Derfer, J. M.; Boord, C. E.; J. Am. Chem. Soc. 78 (1956)
6076.
56-goe/mcc Goering, H. L.; McCarron, F. H.; J. Am. Chem. Soc. 78 (1956) 2270.
56-goe/ree Goering, H. L.; Reeves, R. L.; Espy, H. H.; J. Am. Chem. Soc. 78 (1956) 4926.
56-gra/kos Grandberg, I. I.; Kost, A. N.; Terentev, A. P.; Zh. Obshch. Khim. 26 (1956) 3450.
56-lev/gir Levina, R. Ya.; Gir, K. D.; Shusherina, N. P.; Zh. Obshch. Khim. 25 (1956) 768.
56-lev/gir-1 Levina, R. Ya.; Gir, K. D.; Treshchova, E. G.; Zh. Obshch. Khim. 26 (1956) 920.
56-lib/lap Liberman, A. L.; Lapshina, T. V.; Kazanskii, B. A.; Dokl. Akad. Nauk SSSR 107 (1956)
93.
56-lib/pry-2 Liberman, A. L.; Pryanishnikova, M. A.; Kazanskii, B. A.; Izv. Akad. Nauk SSSR Ser.
Khim. (1956) 1142.
56-moo/sty Moore, W. R.; Styan, G. E.; Trans. Faraday Soc. 52 (1956) 1556.
56-ohl/far Ohloff, G.; Farnow, H; Chem. Ber. 89 (1956) 1549.
56-opp/day Oppenlander, G. C.; Day, A. R.; J. Org. Chem. 21 (1956) 961.
56-pet/ser Petrov, A. A.; Sergienko, S. R.; Tsedilina, A. L.; Egorov, Yu. P.; Khim. Tekhnol. Topl.
Masel 1 (1956) 26.
56-pin/esc Pines, H.; Eschinazi, H. E.; J. Am. Chem. Soc. 78 (1956) 5950.
56-pla/sta Plate, A. F.; Stanko, V. I.; Izvest. Akad. Nauk S.S.S.R. (1956) Otdel. Khim. Nauk 1148.
56-tar/tai Tarasova, G. A.; Taits, G. S.; Plate, A. F.; Izv. Akad. Nauk SSSR Ser. Khim. (1956)
1267.
56-tur/kra Turova-Pollak, M. B.; Kraits, Z. S.; Treshchova, E. G.; Zh. Obshch. Khim. 26 (1956)
2732.
57-ano-1 Patent, Ger. 1,007,772, May 9, Farbenfabriken BayerAkt.-Ges., (1957).

57-els/str Elsner, B. B.; Strauss, H. E.; Forbes, E. J.; J. Chem. Soc. (1957) 578.
57-els/str-1 Elsner, B. B.; Strauss, H. E.; J. Chem. Soc. (1957) 583.
57-els/str-2 Elsner, B. B.; Strauss, H. E.; J. Chem. Soc. (1957) 588.
57-fra Francis, A. W.; Ind. Eng. Chem. 49 (1957) 1779.
57-hol Holmes, E. O.; J. Phys. Chem. 61 (1957) 434.
57-ish/kog Ishiguro, T.; Koga, N.; Nara, K.; Yakugaku Zasshi 77 (1957) 566.
57-kaz/luk Kazanskii, B. A.; Lukina, M. Y.; Nakhapetyan; Izv. Akad. Nauk SSSR Ser. Khim. (1957)
692.
57-kaz/luk-1 Kazanskii, B. A.; Lukina, M. Y.; Salnikova, L. G.; Dokl. Akad. Nauk SSSR 115 (1957)
301.
57-khr/bal Khromov, S. I.; Balenkova, E. S.; Treshchova, E. G.; Vestnik Moskov. Univ., Ser. Mat.,
Mekh., Astron., Fiz.Khim. 12, No. 3 (1957) 121.
57-lev/kos Levina, R. Ya.; Kostin, V. N.; Tartakovskii, V. A.; Zh. Obshch. Khim. 26 (1957) 2998.
57-nov/khr Novikov, M. M.; Khromov, S. I.; Nazarova, L. M.; Izv. Akad. Nauk SSSR Ser. Khim.
(1957) 604.
57-pla/sta Plate, A. F.; Stanko, V. I.; Dokl. Akad. Nauk SSSR 114 (1957) 339.
57-shu/che Shuikin, N. I.; Cherkashin, M. I.; Izv. Akad. Nauk SSSR Ser. Khim. (1957) 1256.
Landolt-Brnstein
New Series IV/8D
432 References
58-ano-6 Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., June (1958).
58-cla/dix Clark, S. G.; Dixon, J. A.; J. Org. Chem. 23 (1958) 1628.
58-cut/mcm Cutler, W. G.; McMickle, R. H.; Webb, W.; Schiessler, R. W.; J. Chem. Phys. 29 (1958)
727.
58-rea/sag Reamer, H. H.; Sage, B. H.; Lacey, W. N.; Chem. Eng. Data Ser. 3 (1958) 240.
59-dix/cla Dixon, J. A.; Clark, S. G.; J. Chem. Eng. Data 4 (1959) 94.
59-dix-1 Dixon, J. A.; J. Chem. Eng. Data 4 (1959) 289.
59-ehr/web Ehrett, W. E.; Weber, J. H.; J. Chem. Eng. Data 4 (1959) 142.
59-ove/mul Overberger, C. G.; Mulvaney, J. E.; J. Am. Chem. Soc. 81 (1959) 4697.
59-pla/mel Plate, A. F.; Melnikov, A. A.; Zhur. Obshchei Khim. 29 (1959) 1064.
59-wu /how Wu, W. R. K.; Howard, H. C.; Fuel 38 (1959) 119.
59-yen/ree Yen, L. C.; Reed, T. M.; J. Chem. Eng. Data 4 (1959) 102.
60-ale/ste Aleksanyan, V. T.; Sterin, K. E.; Liberman, A. L.; Lukina, M. Y.; Taits, G. S.; Tarasova,
G. A.; Terenteva, E. M.; Bull. Acad. Sci. USSR Div. Chem. Sci. (Engl. Transl.) 1 (1960)
75.
60-cam Camin, D. L.; Unpublished (1960).
60-cam/ros Camin, D. L.; Rossini, F. D.; J. Chem. Eng. Data 5 (1960) 368.
60-jef Jeffreys, G. V.; J. Inst. Pet. 46 (1960) 26.
60-kac/tog Kachinskaya, O. N.; Togoeva, S. Kh.; Meshcheryarkov, H. P.; Dokl. Akad. Nauk SSSR
132 (1960) 119.
60-mat/sai Matsuura, T.; Saito, K.; Shimakawa, Y.; Bull. Chem. Soc. Jpn. 33 (1960) 1151.
60-nar/shu Naryshkina, T. I.; Shuikin, N. I.; Zhur. Obshchei Khim. 30 (1960) 3205.
60-nat Natalis, P.; Bull. Soc. Chim. Belg. 69 (1960) 519.
60-pla/sta Plate, A. F.; Stanko, V. I.; Izvest. Akad. Nauk. SSSR. Otdel. Khim. Nauk. 51 (1960)
1481.
60-qoz/van Qozati, A.; Van Winkle, M.; J. Chem. Eng. Data 5 (1960) 269.
60-shu/nar Shuikin, N. I.; Naryshkina, T. I.; Doklady Akad. Nauk S.S.S.R. 135 (1960) 105.
60-sok/she Sokolova, E. B.; Shebanova, M. P.; Izvest. Vysshikh Ucheb.,Zavedenii, Khim. I. Khim.
Tekhnol 3 (1960) 1040.
60-wir Wright, F. J.; Recl. Trav. Chim. Pays-Bas 79 (1960) 784.
60-yak/vol Yakubovich, A. Ya.; Volkova, E. V.; J. Gen. Chem. USSR (Engl. Transl.) 30 (1960)
3935.
61-ano-9 Am. Pet. Inst. Res. Proj. 58A, Semiannual Report, June (1961).
61-bel/web Belknap, R. C.; Weber, J. H.; J. Chem. Eng. Data 6 (1961) 485.
61-del Delzenne, A. O.; Bull. Soc. Chim. Fr. (1961) 295.
61-gom/liu Gomez-Ibanez, J.; Liu, C.-T.; J. Phys. Chem. 65 (1961) 2148.
61-gve/pap Gverdtsiteli, J. M.; Papava, R.; Gelashvili, E.; Tr. Tbilissk. Gos. Univ. 80 (1961) 139.
61-hue/mau Hueckel, W.; Maucher, D.; Fechtig, O.; Kurz, J.; Heinzel, M.; Hubele, A.; Justus Liebigs
Ann. Chem. 645 (1961) 115.
61-jes/sta Jessup, R. S.; Stanley, C. L.; J. Chem. Eng. Data 6 (1961) 368.
61-luk/zot Lukina, M. Y.; Zotova, S. V.; Markov, M. A.; Ovodova, V. A.; Kazanskii, B. A.; Dokl.
Akad. Nauk SSSR 139 (1961) 381.
61-mil/gre Miller, H. M.; Greenlee, K. W.; J. Org. Chem. 26 (1961) 3734.
61-pau/yuz Paushkin, Y. M.; Yuzvyak, A. G.; Neftekhimiya 1 (1961) 60.
61-shi/hil Shinoda, K.; Hildebrand, J. H.; J. Phys. Chem. 65 (1961) 183.
61-shu/tul Shuikin, N. I.; Tulupova, E. D.; Lebedev B. L.; Bull. Acad. Sci. USSR Div. Chem. Sci.
(Engl. Transl.) (1961) 1918.
61-tar/tul Tarasova, E. M.; Tulupova, V. A.; J. Gen. Chem. USSR (Ensl. Trnsl.) 31 (1961) 1812.
61-wir Wright, F. J.; J. Chem. Eng. Data 6 (1961) 454.
Landolt-Brnstein
New Series IV/8D
References 433
62-ano-3 Am. Pet. Inst. Res. Proj. 58A, Annu. Rep., June (1962).
62-has/sno Haselden, G. G.; Snowden, P.; Trans. Faraday Soc. 58 (1962) 1515.
62-kae/web Kaes, G. L.; Weber, J. H.; J. Chem. Eng. Data 7 (1962) 344.
62-kha-1 Khalilov, Kh. M.; Zh. Fiz. Khim. 36 (1962) 2474.
62-lev/sha Levina, R. Ya.; Shanazarov, K. S.; Treshchova, E. G.; Kostin, V. N.; Zh. Obshch. Khim.
32 (1962) 3935.
62-lev/sha-1 Levina, R. Ya.; Shanazarov, K. S.; Kostin, V. N.; Treshchova, E. G.; Zh. Obshch. Khim.
32 (1962) 2637.
62-mah/gre Mahmoud, B. H.; Greenlee, K. W.; J. Org. Chem. 27 (1962) 2369.
62-nag-2 Nagata, I.; J. Chem. Eng. Data 7 (1962) 461.
62-rat/rao Ratnam, A. V.; Rao, C. V.; Murti, P. S.; Chem. Eng. Sci. 17 (1962) 392.
62-sla/mag Slaugh, L. H.; Magoon, E. F.; J. Org. Chem. 27 (1962) 1037.
62-sus/lyz Susarev, M. P.; Lyzlova, R. V.; Russ. J. Phys. Chem. (Engl. Transl.) 36 (1962) 230.
63-ano-3 Am. Pet. Inst. Res. Proj. 58A, Annu. Rep., June (1963).
63-gen/pet Genusov, M. L.; Petrov, A. A.; Zh. Obshch. Khim. 33 (1963) 2589.
63-gon/sha Gonikberg, M. G.; Shakhovskoi, G. P.; Liberman, A. L.; Vasina, T. V.; Russ. J. Phys.
Chem. (Engl. Transl.) 37 (1963) 1025.
63-gud/cam Gudzinowicz, B. J.; Campbell, R. H.; Adams, J. S.; J. Chem. Eng. Data 8 (1963) 201.
63-jef Jeffreys, G. V.; J. Chem. Eng. Data 8 (1963) 320.
63-lev/sha Levina, R. Ya.; Shanazarov, K. S.; Treshchova, E. G.; Neftekhimiya 3 (1963) 3.
63-lib/bra Liberman, A. L.; Bragin, O. V.; Guryanonva, G. K.; Kazanskii, B. A.; Dokl. Akad. Nauk
SSSR 148 (1963) 591.
63-mea/sta Mears, T. W.; Stanley, C. L.; Compere, E. L.; Howard, F. L.; J. Res. Natl. Bur. Stand.,
Sect. A 67 (1963) 475.
63-mir/sob Mironov, V. A.; Sobolev, E. V.; Elizarova, A. N.; Tetrahedron 19 (1963) 1939.
63-nef/nov Nefedov, O. M.; Novitskaya, N. N.; Petrov, A. D.; Dokl. Akad. Nauk SSSR 152 (1963)
629.
63-plu/dow Plucknett, W. K.; Dowd, R. T.; J. Chem. Eng. Data 8 (1963) 207.
63-pod Podder, C.; Z. Phys. Chem. (Munich) 39 (1963) 79.
63-pra/van Prabhu, P. S.; Van Winkle, M.; J. Chem. Eng. Data 8 (1963) 14.
63-raj/ran Raju, B. N.; Ranganathan, R.; Narasinga Rao, M.; Indian Chem. Eng. 5 (1963) 82.
63-tak/yam Takahashi, H.; Yamaguchi, M.; J. Org. Chem. 28 (1963) 1409.
63-tho/sto Thomas, A. F.; Stoll M.; Chem. Ind. (London) (1963) 1491.
63-zak/zhi Zakharkin, L. I.; Zhigareva, G. G.; Izv. Akad. Nauk SSSR, Otd. Khim. Nauk (1963).386
64-bla/per Blanc, P. Y.; Perret, A.; Teppa, F.; Helv. Chim. Acta 47 (1964) 725.
64-bro/ayy Brown, H. C.; Ayyangar, N. R.; Zweifel, G.; J. Am. Chem. Soc. 86 (1964) 1071.
64-doe/hau Doering, C. E.; Hauthal, H. G.; Noglik, H.; J. Prakt. Chem. 24 (1964) 183.
64-lib/ler Liberman, A. L.; Lerman, B. M.; Zhizhin, G. N.; Sterin, K. E.; Dokl. Akad. Nauk SSSR
156 (1964) 375.
64-mar/vel Mardanov, M. A.; Veliev, K. G.; Turner, N. I.; Azerb. Khim. Zh. No. 2 (1964) 15.
64-mir/kos Mironov, V. A.; Kostina, S. N.; Sobolev, E. V.; Elizarova, A. N.; Izv. Akad. Nauk SSSR
Ser. Khim. (1964) 864.
64-mir/kos-1 Mironov, V. A.; Kostina, S. N.; Elizarova, A. N.; Izv. Akad. Nauk SSSR Ser. Khim.
(1964) 875.
64-moe/tho Moelwyn-Hughes, E. A.; Thorpe, P. L.; Proc. R. Soc. London, A 278 (1964) 574.
64-pra/van Prabhu, P. S.; Van Winkle, M.; J. Chem. Eng. Data 9 (1964) 9.
64-sca/sat Scatchard, G.; Satkiewicz, F. G.; J. Am. Chem. Soc. 86 (1964) 130.
64-shu/kho Shuikin, N. I.; Khofman, Kh.; Erivanskaya, L. A.; Izv. Akad. Nauk SSSR. Ser. Khim.
(1964) 912.
65-for/moo Fort, R. J.; Moore, W. R.; Trans. Faraday Soc. 61 (1965) 2102.
Landolt-Brnstein
New Series IV/8D
434 References
65-lev/kos Levina, R. Ya.; Kostin, V. N.; Galpern, M. G.; Treshchova, E. G.; Zh. Obshch. Khim. 35
(1965) 785.
65-lib/ler Liberman, A. L.; Lerman, B. M.; Preobrazhenskii, A. V.; Neftekhimiya 5 (1965) 3.
65-mus/bar Musaev, I. A.; Barinova, N. N.; Smirnova, I. V.; Sanin, P. I.; Neftekhimiya 5 (1965) 603.
65-ogl/pot Ogloblin, K.A.; Potekhin, A. A.; Zh. Org. Khim. 1 (1965) 865.
65-sam/ogl Samartsev, M. A.; Ogloblin, K.A.; J. Org. Chem. USSR (Engl. Transl.) 1 (1965) 29.
65-tre/mit Treboganov, A. D.; Mitsner, B. I.; Zinkevich, E. P.; Kraevskii, A. A.; Preobrazhenskii, N.
A.; Zh. Organ. Khim. 1 (1965) 1583.
65-wat/mcl Watson, A. E. P.; McLure, I. A.; Bennett, J. E.; Benson, G. C.; J. Phys. Chem. 69 (1965)
2753.
65-zak/kor Zakharkin, L. I.; Kornev, V. V.; Zh. Organ. Khim. 1 (1965) 1608.
65-zhi/ste Zhizhin, G. N.; Sterin, K. E.; Aleksanyan, V. T.; Bobrov, A. V.; Vasina, T. V.; Lerman,
B. M.; Tyunkina, N. I.; Liberman, A. L.; Neftekhimiya 5 (1965) 461.
66-bat Battino, R.; J. Phys. Chem. 70 (1966) 3408.

66-bat/all Battino, R.; Allison, G. W.; J. Phys. Chem. 70 (1966) 3417.
66-ber/rea Berty, T. E.; Reamer, H. H.; Sage, B. H.; J. Chem. Eng. Data 11 (1966) 25.
66-dya/luk Dyachenko, A. I.; Lukina, M. Y.; Izv. Akad. Nauk SSSR Ser. Khim. (1966) 2237.
66-gan/kha Ganapathy, K.; Khanehandani, K. S.; Indian J. Biochem. 3 (1966) 66.
66-kat/cha Katti, P. K.; Chaudhry, M. M.; Prakash, O.; J. Chem. Eng. Data 11 (1966) 593.
66-khr/koc Khromov, S. I.; Kochnova, G.P.; Guseva, O. I.; Balenkova, E. S.; Neftekhimiya 6 (1966)
809.
66-lut/kov Lutugina, N. V.; Kovalichev, O. F.; Vestn. Leningr. Univ., Fiz., Khim. 21 (1966) 91.
66-mek/mag Mekhtiev, S. D.; Magerramova, R. Yu.; Neftekhimiya 6 (1966) 291.
66-rob/edm Robinson, R. L.; Edmister, W. C.; Dullien, F. A. L.; Ind. Eng. Chem. Fundam. 5 (1966)
74.
66-sab/bel Sabinin, V. E.; Belousov, V. P.; Morachevskii, A. G.; Izv. Vyssh. Uchebn. Zaved., Khim.
Khim. Tekhnol. 9 (1966) 382.
66-sad/akh Sadykhov, Sh. G.; Akhmedov, S. T.; Soldatova, V. A.; Zavyalov, Yu. M.; Dokl. Akad.
Nauk Azerb. SSR 22 (1966) 35.
66-sha/bek Shakarashvili, T. S.; Bekauri, N. G.; Soobshch. Akad. Nauk Gruz. SSR 43 (1) (1966) 97.
66-stu Studt, P.; Justus Liebigs Ann. Chem. 693 (1966) 90.
67-cru/cut Cruickshank, A. J. B.; Cutler, A. J. B.; J. Chem. Eng. Data 12 (1967) 326.
67-fin/ken Findlay, T. J. V.; Keniry, J. S.; Kidman, A. D.; Pickles, V. A.; Trans. Faraday Soc. 63
(1967) 846.
67-kut/tis Kutnevich, A. M.; Tishchenko, D. V.; Zh. Org. Khim. 3 (1967) 444.
67-loi/mer Loiseleur, H.; Merlin, J. C.; Paris, R. A.; J. Chim. Phys. Phys.-Chim. Biol. 64 (1967)
634.
67-mek/mag Mekhtiev, S. D.; Magerramova, Z. Yu.; Suleimanov, G. N.; Magerramova, R. Yu.; Azerb.
Khim. Zh. 5 (1967) 61.
67-mur/sri Murti, P. S.; Sriram, M.; Narasimhamurty, G. S. R.; Br. Chem. Eng. 12 (1967) 1882.
67-nat/rao Nataraj, V.; Rao, M. R.; Indian J. Technol. 5 (1967) 212.
67-pre/fel Prengle, H. W.; Felton, E. G.; Pike, M. A.; J. Chem. Eng. Data 12 (1967) 193.
67-rid/but Ridgway, K.; Butler, P. A.; J. Chem. Eng. Data 12 (1967) 509.
67-tep/far Tepenitsyna, E. P.; Farberov, M. I.; Izv. Vyssh. Ucheb. Zaved., Khim. Khim. Tekhnol. 10
(1967) 338.
67-tep/far Tepenitsyna, E. P.; Farberov, M. I.; Izv. Vyssh. Ucheb. Zaved., Khim. Khim. Tekhnol. 10
(1967) 338.
68-akh/yas Akhmedzade, D. A.; Yasnopolskii, V. D.; Aslanova, A. A.; Kerimova, M. M.; Azerb.
Khim. Zh. 1 (1968) 45.
Landolt-Brnstein
New Series IV/8D
References 435
68-ano-1 Am. Pet. Inst. Res. Proj. 42, Penn. State Univ. (1968).
68-bar/sat Baradarajan, A.; Satyanarayana, M.; J. Chem. Eng. Data 13 (1968) 148.
68-kem/buc Kemula, W.; Buchowski, H.; Pawlowski, W.; Rocz. Chem. 42 (1968) 1951.
68-man/mue Mann, G.; Muehlstaedt, M.; Braband, J.; Tetrahedron 24 (1968) 3607.
68-pow/swi Powell, R. J.; Swinton, F. L.; J. Chem. Eng. Data 13 (1968) 260.
68-puz/eid Puzitskii, K. V.; Eidus, Y. T.; Bulanova, T. F.; Ryabova, K. G.; Sergeeva N. S.; Izv.
Akad. Nauk SSSR. Ser. Khim. (1968) 1117.
68-ver Verhoeye, L. A. J.; J. Chem. Eng. Data 13 (1968) 462.
68-wip/cle Wipf, H. K.; Clerc, J. T.; Simon, W.; Helv. Chem. Acta 51 (1968) 1162.
69-bou/lam Boublik, T.; Lam, V. T.; Murakami, S.; Benson, G. C.; J. Phys. Chem. 73 (1969) 2356.
69-bra/fre Brazier, D. W.; Freeman, G. R.; Can. J. Chem. 47 (1969) 893.
69-bru/gub Brunet, J.; Gubbins, K. E.; Trans. Faraday Soc. 65 (1969) 1255.
69-cho/nai Chowdary, M. C.; Naidu, P. R.; Krishnan, V. R.; Indian J. Chem. 7 (1969) 796.
69-par/kho Parnes, Z. N.; Khotimskaya, G. A.; Kudryavtsev, R. V.; Lukina, M. Y.; Kursanov, D. N.;
Dokl. Akad. Nauk SSSR, Ser. Khim. 184 (1969) 615.
69-rie/hoy Riemschneider, R.; Hoyer, G.-A.; Fette, Seifen, Anstrichm. 71 (1969) 128.
69-rod/hsu Rodger, A. J.; Hsu, C. C.; Furter, W. F.; J. Chem. Eng. Data 14 (1969) 362.
69-smi/kur Smirnova, N. A.; Kurtynina, L. M.; Zh. Fiz. Khim. 43 (1969) 1883.
70-ewi/lev Ewing, M. B.; Levien, B. J.; Marsh, K. N.; Stokes, R. H.; J. Chem. Thermodyn. 2 (1970)
689.
70-fin Findenegg, G. H.; Monatsh. Chem. 101 (1970) 1081.
70-goo-3 Good, W. D.; J. Chem. Thermodyn. 2 (1970) 399.
70-har/dun Harris, K. R.; Dunlop, P. J.; J. Chem. Thermodyn. 2 (1970) 813.
70-kon/lya Konobeev, B. I.; Lyapin, V. V.; Zh. Prikl. Khim. (Leningrad) 43 (1970) 803.
70-lin/sil Lin, D. C. K.; Silberberg, I. H.; McKetta, J. J.; J. Chem. Eng. Data 15 (1970) 483.
70-mar-1 Marsh, K. N.; J. Chem. Thermodyn. 2 (1970) 359.
70-pol/mur-2 Polak, J.; Murakami, S.; Lam, V. T.; Benson, G. C.; J. Chem. Eng. Data 15 (1970) 323.
70-sto/lev Stokes, R. H.; Levien, B. J.; Marsh, K. N.; J. Chem. Thermodyn. 2 (1970) 43.
70-str/svo Strubl, K.; Svoboda, V.; Holub, R.; Pick, J.; Collect. Czech. Chem. Commun. 35 (1970)
3004.
71-goo-1 Good, W. D.; J. Chem. Thermodyn. 3 (1971) 539.

71-len/hay Lenoir, J. M.; Hayworth, K. E.; Hipkin, H. G.; J. Chem. Eng. Data 16 (1971) 129.
71-nag/oht Nagata, I.; Ohta, T.; J. Chem. Eng. Data 16 (1971) 164.
71-san/fel Sanni, S. A.; Fell, C. J. D.; Hutchison, P.; J. Chem. Eng. Data 16 (1971) 424.
72-jon/wee Jones, D. E.; Weeks, I. A.; Anand, S. C.; Wetmore, R. W.; Benson, G. C.; J. Chem. Eng.
Data 17 (1972) 501.
72-kon Konakbaeva, E. G.; Vestn. Mosk. Univ., Ser. 2: Khim. 27 (1972) 250.
72-let Letcher, T. M.; J. Chem. Thermodyn. 4 (1972) 159.
72-let-1 Letcher, T. M.; J. Chem. Thermodyn. 4 (1972) 551.
72-mar/mur Martin, M. L.; Murray, R. S.; J. Chem. Thermodyn. 4 (1972) 723.
72-sad/ali Sadykhov, Sh. G.; Aliev, V, S,; Soldatova, V. A.; Guseinov, N. S.; Turlaeva, M.;
Pashaev, A. G.; Azerb. Khim. Zh. (4) (1972) 111.
72-sid/mir Sidorova, N. G.; Mirzaeva, A. K.; Karas, A. V.; Nauch. Tr. Tashkent Univ. No. 419
(1972) 169.
72-you Young, C. L.; Aust. J. Chem. 25 (1972) 1625.
73-che/cha Chew, H. A.; Chan, R. K.; Can. J. Chem. 51 (1973) 2141.

73-chi/hou Chinikamala, A.; Houth, G. N.; Taylor, Z. L.; J. Chem. Eng. Data 18 (1973) 322.
Landolt-Brnstein
New Series IV/8D
436 References
73-lev Levien, B. J.; J. Chem. Thermodyn. 5 (1973) 679.

73-li /lu Li, I. P. C.; Lu, B. C. Y.; Chen, E. C.; J. Chem. Eng. Data 18 (1973) 305.
73-min/rue Minh, D. C.; Ruel, M.; J. Chem. Eng. Data 18 (1973) 41.
73-nag/oht Nagata, I.; Ohta, T.; Uchiyama, Y.; J. Chem. Eng. Data 18 (1973) 54.
73-nay/kud Nayar, S.; Kudchadker, A. P.; J. Chem. Eng. Data 18 (1973) 356.
73-paz Paz Andrade, M. I.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 2 (1973) 98.
73-paz-1 Paz Andrade, M. I.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 2 (1973) 97.
73-san/hut Sanni, S. A.; Hutchison, P.; J. Chem. Eng. Data 18 (1973) 317.
73-svo/ves Svoboda, V.; Vesely, F.; Holub, R.; Pick, J.; Collect. Czech. Chem. Commun. 38 (1973)
3539.
73-var/bul Varushchenko, R. M.; Bulgakova, L. L.; Russ. J. Phys. Chem. (Engl. Transl.) 47 (1973)
1491.
74-aga/aly Agaev, U. Kh.; Alyev, A. T.; Azerb. Khim. Zh. 1 (1974) 112.
74-anf/bal Anfilogova, S. N.; Balenkova, E. S.; Dmitriev, A. B.; Neftekhimiya 14 (1974) 673.
74-jai/nor Jain, D. V. S.; North, A. M.; Pethrick, R. A.; J. Chem. Soc., Faraday Trans. 1 70 (1974)
1292.
74-kon/ani Konakbaeva, E. G.; Anisimova, Z. K.; Shakhparonov, M. I.; Vestn. Mosk. Univ., Ser. 2:
Khim. 29 (1974) 30.
74-let/mar Letcher, T. M.; Marsicano, F.; J. Chem. Thermodyn. 6 (1974) 509.
74-mye/cle Myers, R. S.; Clever, H. L.; J. Chem. Thermodyn. 6 (1974) 949.
74-pur/pol Puri, P. S.; Polak, J.; Ruether, J. A.; J. Chem. Eng. Data 19 (1974) 87.
74-rao/nai Rao, M. V. P.; Naidu, P. R.; Can. J. Chem. 52 (1974) 788.
74-rao/nai-1 Rao, M. V. P.; Naidu, P. R.; J. Chem. Thermodyn. 6 (1974) 1195.
75-ana/gro Anand, S. C.; Grolier, J.-P. E.; Kiyohara, O.; Halpin, C. J.; Benson, G. C.; J. Chem. Eng.
Data 20 (1975) 184.
75-hol/zie Holzhauer, J. K.; Ziegler, W. T.; J. Phys. Chem. 79 (1975) 590.
75-hsu/cle Hsu, K.-Y.; Clever, H. L.; J. Chem. Eng. Data 20 (1975) 268.
75-let Letcher, T. M.; J. Chem. Thermodyn. 7 (1975) 205.
75-mus/ver Mussche, M. J.; Verhoeye, L. A. J.; J. Chem. Eng. Data 20 (1975) 46.
75-pav/kla Pavlov, V. A.; Klabunovskii, E. I.; Vasina, T. V.; Tyunkina, N. I.; Liberman, A. L.; Russ.
J. Phys. Chem. (Engl. Transl.) 49 (1975) 1166.
76-chr/lau Christopher, P. M.; Laukhuf, W. L. S.; Plank, C. A.; J. Chem. Eng. Data 21 (1976) 443.
76-for/ben Fortier, J.-L.; Benson, G. C.; Picker, P.; J. Chem. Thermodyn. 8 (1976) 289.
76-ha /mor Ha, H.; Morrison, J. A.; Richards, E. L.; J. Chem. Soc., Faraday Trans. 1 72 (1976)
1051.
76-mey/hot Meyer, E. F.; Hotz, C. A.; J. Chem. Eng. Data 21 (1976) 274.
76-tri/kri Tripathi, R. P.; Krishna, S.; Gulati, I. B.; J. Chem. Eng. Data 21 (1976) 44.
77-bou/lu Boublik, T.; Lu, B. C. Y.; J. Chem. Eng. Data 22 (1977) 331.
77-fer/lys Fernandez Gomez, F.; Lysenkov, V. I.; Ulyanova, O. D.; Pentin, Y. A.; Bardyshev, I. I.;
Russ. J. Phys. Chem. (Engl. Transl.) 51 (1977) 1585.
77-hwa/rob Hwang, S.-C.; Robinson, R. L.; J. Chem. Eng. Data 22 (1977) 319.
77-rad/tas Radojkovic, N.; Tasic, A.; Grozdanic, D. K.; Djordjevic, B. D.; Malic, D.; J. Chem.
Thermodyn. 9 (1977) 349.
78-kiy/hal Kiyohara, O.; Halpin, C. J.; Benson, G. C.; J. Chem. Thermodyn. 10 (1978) 721.
Landolt-Brnstein
New Series IV/8D
References 437
78-nat/yad Nath, J.; Yadava, M. L.; Singh, B.; Indian J. Chem., Sect. A: Inorg., Phys., Theor. Anal.
16 (1978) 897.
79-for/dar Fortier, J.-L.; DArcy, P. J.; Benson, G. C.; Thermochim. Acta 28 (1979) 37.
79-goa/ott Goates, J. R.; Ott, J. B.; Grigg, R. B.; J. Chem. Thermodyn. 11 (1979) 497.
79-hoe/hoe Hoepfner, A.; Hoerner, C.; Abdel-Hamid, A.; Schaller, M.; Funk, U.; Ber. Bunsen-Ges.
Phys. Chem. 83 (1979) 1031.
79-jon/has Jonas, J.; Hasha, D.; Huang, S. G.; J. Chem. Phys. 71 (1979) 3996.
79-mah/sur Maheshwari, R. C.; Suri, S. K.; Tewari, U. S.; J. Chem. Eng. Data 24 (1979) 237.
79-maj/svo Majer, V.; Svoboda, V.; Hala, S.; Pick, J.; Collect. Czech. Chem. Commun. 44 (1979)
637.
79-mal/pat Malanowski, S.; Patz, R.; Raetzsch, M. T.; Wohlfarth, C.; Fluid Phase Equilib. 3 (1979)
291.
79-mur Murakami, S.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1 (1979) 36.
79-mur-1 Murakami, S.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1 (1979) 37.
79-will/far Wilhelm, E.; Faradjzadeh, A.; Grolier, J.-P. E.; J. Chem. Thermodyn. 11 (1979) 979.
80-aic/tar Aicart, E.; Tardajos, G.; Diaz Pena, M.; J. Chem. Eng. Data 25 (1980) 140.
80-aic/tar-1 Aicart, E.; Tardajos, G.; Diaz Pena, M.; J. Chem. Thermodyn. 12 (1980) 1085.
80-dia/cre Diaz Pena, M.; Crespo Colin, A.; Compostizo, A.; Escudero, I.; J. Chem. Eng. Data 25
(1980) 17.
80-fen/khu Fenby, D. V.; Khurma, J. R.; Konner, Z. S.; Block, T. E.; Knobler, C. M.; Reeder, J.;
Scott, R. L.; Aust. J. Chem. 33 (1980) 1927.
80-jon/has Jonas, J.; Hasha, D.; Huang, S. G.; J. Phys. Chem. 84 (1980) 109.
80-mar/sym Martin, M. L.; Symons, L.; Aust. J. Chem. 33 (1980) 2005.
80-mar/you Martin, M. L.; Youings, J. C.; Aust. J. Chem. 33 (1980) 2133.
80-oht/nag Ohta, T.; Nagata, I.; J. Chem. Eng. Data 25 (1980) 283.
80-sid/goe Siddiqi, M. A.; Goetze, G.; Kohler, F.; Ber. Bunsen-Ges. Phys. Chem. 84 (1980) 529.
80-sur Suri, S. K.; J. Chem. Eng. Data 25 (1980) 390.
81-aic/tar Aicart, E.; Tardajos, G.; Diaz Pena, M.; J. Chem. Eng. Data 26 (1981) 22.
81-aic/tar-2 Aicart, E.; Tardajos, G.; Diaz Pena, M.; J. Chem. Thermodyn. 13 (1981) 783.
81-dym/you Dymond, J. H.; Young, K. J.; Int. J. Thermophys. 2 (1981) 237.
81-kiy/ben Kiyohara, O.; Benson, G. C.; J. Chem. Eng. Data 26 (1981) 263.
81-mal/rae Malanowski, S.; Raetzsch, M. T.; Fluid Phase Equilib. 7 (1981) 55.
81-mar/sym Martin, M. L.; Symons, L.; J. Chem. Thermodyn. 13 (1981) 81.
81-nai/nai Naidu, G. R.; Naidu, P. R.; J. Chem. Eng. Data 26 (1981) 197.
81-sid/koh Siddiqi, M. A.; Kohler, F.; Ber. Bunsen-Ges. Phys. Chem. 85 (1981) 17.
81-tas/djo Tasic, A. Z.; Djordjevic, B. D.; Serbanovic, S. P.; Grozdanic, D. K.; J. Chem. Eng. Data
26 (1981) 118.
82-ami/pat Aminabhavi, T. M.; Patel, R. C.; Bridger, K.; Jayadevappa, E. S.; Prasad, B. R.; J. Chem.
Eng. Data 27 (1982) 125.
82-bha/tre Bhattacharyya, S. N.; Trejo Rodriguez, A.; Andreoli-Ball, L.; Patterson, D.; Int. DATA
Ser., Sel. Data Mixtures, Ser. A No. 1 (1982) 44.
82-bha/tre-1 Bhattacharyya, S. N.; Trejo Rodriguez, A.; Andreoli-Ball, L.; Patterson, D.; Int. DATA
Landolt-Brnstein
New Series IV/8D
438 References
82-chy/str Chylinski, K.; Stryjek, R.; J. Chem. Thermodyn. 14 (1982) 1115.
82-dig/jad Diguet, R.; Jadzyn, J.; J. Chem. Eng. Data 27 (1982) 86.
82-gri/goa Grigg, R. B.; Goates, J. R.; Ott, J. B.; J. Chem. Thermodyn. 14 (1982) 101.
82-gri/phi Griot, A.; Philippe, R.; Merlin, J. C.; J. Chim. Phys. Phys.-Chim. Biol. 79 (1982) 671.
82-gro/ing Grolier, J.-P. E.; Inglese, A.; Wilhelm, E.; J. Chem. Eng. Data 27 (1982) 333.
83-gri/phi Griot, A.; Philippe, R.; Merlin, J. C.; J. Chim. Phys. Phys.-Chim. Biol. 80 (1983) 507.
83-nat/tri Nath, J.; Tripathi, A. D.; J. Chem. Eng. Data 28 (1983) 263.
83-wec Weclawski, J.; Fluid Phase Equilib. 12 (1983) 155.
83-wec/byl Weclawski, J.; Bylicki, A.; Fluid Phase Equilib. 12 (1983) 143.
83-will/ing Wilhelm, E.; Inglese, A.; Grolier, J.-P. E.; J. Chem. Eng. Data 28 (1983) 202.
84-bau/mee Bauer, H.; Meerlender, G; Rheol. Acta 23 (1984) 514.

84-cre/com Crespo Colin, A.; Compostizo, A.; Diaz Pena, M.; Bol. Soc. Quim. Peru 50 (1984) 120.
84-gar/rey Garcia, M.; Rey, C.; Villar, V. P.; Rodriguez, J. R.; J. Chem. Thermodyn. 16 (1984) 603.
84-sin/nig Singh, P. P.; Nigam, R. K.; Sharma, S. P.; Aggarwal, S.; Fluid Phase Equilib. 18 (1984)
333.
84-tan/tak Tanaka, R.; Takenaka, M.; Murakami, S.; J. Chem. Eng. Data 29 (1984) 69.
85-hra/gik Hradetzky, G.; Gikas, A.; Bittrich, H.-J.; Z. Phys. Chem. (Leipzig) 266 (1985) 165.
85-mar/bha Marwein, B. L.; Bhat, S. N.; Acustica 58 (1985) 243.
85-mcl/bar McLure, I. A.; Barbarin-Castillo, J. M.; J. Chem. Eng. Data 30 (1985) 253.
85-osw/rao Oswal, S. L.; Rao, A. V.; Indian J. Chem., Sect. A: Inorg., Phys., Theor. Anal. 24 (1985)
1026.
85-sae/com Saez, C.; Compostizo, A.; Rubio, R. G.; Crespo Colin, A.; Diaz Pena, M.; Fluid Phase
Equilib. 24 (1985) 241.
85-sin/mah Singh, H. P.; Mahl, B. S.; J. Solution Chem. 14 (1985) 751.
85-sin/sha Singh, P. P.; Sharma, S. P.; J. Chem. Eng. Data 30 (1985) 477.
85-tam/mur Tamura, K.; Murakami, S.; Doi, S.; J. Chem. Thermodyn. 17 (1985) 325.
85-tan/nak Tanaka, R.; Nakamichi, T.; Murakami, S.; J. Solution Chem. 14 (1985) 795.
86-aww/sal Awwad, A. M.; Salman, M. A.; Fluid Phase Equilib. 25 (1986) 195.
86-cod/mon Codoner, A.; Monzo, I.; Tomas, F.; Valero, R.; J. Phys. Chem. 90 (1986) 2244.
86-hne/cib Hnedkovsky, L.; Cibulka, I.; J. Chem. Thermodyn. 18 (1986) 331.
86-hol/got Holzapfel, K.; Gotze, G.; Kohler, F.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1
(1986) 40.
86-hol/got-6 Holzapfel, K.; Gotze, G.; Kohler, F.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1
(1986) 44.
(1986) 45.
(1986) 52.
86-sae/com Saez, C.; Compostizo, A.; Rubio, R. G.; Crespo Colin, A.; Diaz Pena, M.; J. Chem. Soc.,
Faraday Trans. 1 82 (1986) 1839.
86-san/sha Sandhu, J. S.; Sharma, A. K.; Wadi, R. K.; J. Chem. Eng. Data 31 (1986) 152.
86-tar/dia Tardajos, G.; Diaz Pena, M.; Lainez, A.; Aicart, E.; J. Chem. Eng. Data 31 (1986) 492.
86-tar/dia-1 Tardajos, G.; Diaz Pena, M.; Aicart, E.; J. Chem. Thermodyn. 18 (1986) 683.
87-ami Aminabhavi, T. M.; J. Chem. Eng. Data 32 (1987) 406.
Landolt-Brnstein
New Series IV/8D
References 439
87-hol/goe Holzapfel, K.; Goetze, G.; Demiriz, A. M.; Kohler, F.; Int. DATA Ser., Sel. Data
Mixtures, Ser. A No. 1 (1987) 30.
87-let/bax Letcher, T. M.; Baxter, R.; J. Solution Chem. 16 (1987) 999.
87-lin Linek, J.; Collect. Czech. Chem. Commun. 52 (1987) 2839.
87-luo/ham Luo, B.; Haman, S. E. M.; Benson, G. C.; Lu, B. C. Y.; J. Chem. Eng. Data 32 (1987)
81.
87-man/ami Manjeshwar, L. S.; Aminabhavi, T. M.; J. Chem. Eng. Data 32 (1987) 409.
87-mar-1 Marsh, K. N.; Recommended Reference Materials for the Realization of Physicochemical
Properties, Blackwell Sci. Pub.: Oxford, Relative Mol. Mass (1987).
87-nag/rob Nagarajan, N.; Robinson, R. L.; J. Chem. Eng. Data 32 (1987) 369.
87-yad/yad Yadava, R. R.; Yadava, S. S.; J. Chem. Eng. Data 32 (1987) 54.
88-cha/sur Chandrasekhar, A. C. H.; Surendranath, K. N.; Krishnaiah, A.; Chem. Scr. 28 (1988)
421.
88-gar/cob-1 Garcia, I.; Cobos, J. C.; Gonzalez, J. A.; Casanova, C.; Cocero, M. J.; J. Chem. Eng. Data
33 (1988) 423.
88-jun/tar Junquera, E.; Tardajos, G.; Aicart, E.; J. Chem. Thermodyn. 20 (1988) 1461.
88-man/ami Manjeshwar, L. S.; Aminabhavi, T. M.; J. Chem. Eng. Data 33 (1988) 184.
88-nag-1 Nagata, I.; Thermochim. Acta 127 (1988) 109.
88-nag-2 Nagata, I.; Thermochim. Acta 127 (1988) 337.
88-nij/vos Nijveldt, D.; Vos, A.; Acta Cryst., Sect. B 44 (1988) 281.
88-sai/tan Saito, A.; Tanaka, R.; J. Chem. Thermodyn. 20 (1988) 859.
88-sun/sch-1 Sun, T. F.; Schouten, J. A.; Trappeniers, N. J.; Biswas, S. N.; J. Chem. Thermodyn. 20
(1988) 1089.
89-bec/ric Becker, F.; Richter, P.; Fluid Phase Equilib. 49 (1989) 157.
89-der/poi Dernini, S.; Poicaro, A. M.; Ricci, P. F.; J. Chem. Eng. Data 34 (1989) 165.
89-lai/rod Lainez, A.; Rodrigo, M. M.; Wilhelm, E.; Grolier, J.-P. E.; J. Chem. Eng. Data 34 (1989)
332.
89-mat/gon Mato, F.; Gonzalez, G.; Arroyo, F. J.; J. Chem. Eng. Data 34 (1989) 179.
89-rai/shu Rai, R. D.; Shukla, R. K.; Shukla, A. K.; Pandey, J. D.; J. Chem. Thermodyn. 21 (1989)
125.
89-ram/sur Ramanjaneyulu, K.; Surendranath, K. N.; Krishnaiah, A.; Fluid Phase Equilib. 44 (1989)
357.
90-all/bee Allred, G. C.; Beets, J. W.; Parrish, W. R.; J. Chem. Eng. Data 35 (1990) 328.
90-che/pet Chevalier, J. L. E.; Petrino, P. J.; Gaston-Bonhomme, Y. H.; J. Chem. Eng. Data 35
(1990) 206.
90-com/fra Comelli, F.; Francesconi, R.; J. Chem. Eng. Data 35 (1990) 283.
90-fer/lap Fermeglia, M.; Lapasin, R.; Torriano, G.; J. Chem. Eng. Data 35 (1990) 260.
90-jos/ami Joshi, S. S.; Aminabhavi, T. M.; Balundgi, R. H.; Shukla, S. S.; J. Chem. Eng. Data 35
(1990) 185.
90-jos/ami-2 Joshi, S. S.; Aminabhavi, T. M.; Shukla, S. S.; J. Chem. Eng. Data 35 (1990) 247.
90-kar/kar Karaseva, N. V.; Karavaeva, A. P.; Antonova, T. N.; Chabutkina, E. M.; Koshel, G. N.;
Zh. Prikl. Khim. (Leningrad) 63 (1990) 1856.
90-rib/ber Ribeiro, A.; Bernardo-Gil, G.; J. Chem. Eng. Data 35 (1990) 204.
90-sin/mal Singh, P. P.; Malik, R.; Maken, S.; Acree, W. E.; Zvaigzne, A. I.; Thermochim. Acta 165
(1990) 113.
91-aiz/kat Aizawa, K.; Kato, M.; J. Chem. Eng. Data 36 (1991) 159.
91-kann/skj Knapstad, B.; Skjolsvik, P. A.; Oye, H. A.; J. Chem. Eng. Data 36 (1991) 84.
91-kri/vis Krishnaiah, A.; Viswanath, D. S.; J. Chem. Eng. Data 36 (1991) 317.
Landolt-Brnstein
New Series IV/8D
440 References
91-luk/tim-1 Lukyanova, V. A.; Timofeeva, L. P.; Kozina, M. P.; Kirin, V. N.; Tarakanova, A. V.;
Zh. Fiz. Khim. 65 (1991) 828.
91-pap/eva Papaioannou, D.; Evangelou, T.; Panayioton, C.; J. Chem. Eng. Data 36 (1991) 43.
91-pap/zio Papanastasiou, G. E.; Ziogas, I. I.; J. Chem. Eng. Data 36 (1991) 46.
91-ric/lau Richon, D.; Laugier, S.; Renon, H.; J. Chem. Eng. Data 36 (1991) 104.
91-she/wan Shen, S.; Wang, Y.; Feng, H.; Shi, J.; Nanjing Huagong Xueyuan Xuebao 13 (1) (1991)
50.
91-tre Trejo, L. M.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1 (1991) 9.
91-tre-1 Trejo, L. M.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No, 1 (1991) 10.
91-tre-9 Trejo, L. M.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1 (1991) 18.
92-acr/ten-4 Acree, W. E.; Teng, I. L.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1 (1992) 48.
92-acr/ten-8 Acree, W. E.; Teng, I. L.; Int. DATA Ser., Sel. Data Mixtures, Ser. A No. 1 (1992) 53.
92-ano-3 Report H&D Fitzgerald Ltd. to E. Yates, Chemical Cargo Inspection Assoc., Brussels
Belgium (1992).
92-gar/cac-1 Garcia Baonza, V.; Caceres Alonso, M.; Nunez Delgado, J.; Ber. Bunsen-Ges. Phys.
Chem. 96 (1992) 1859.
92-pit/mar Pittau, B.; Marongiu, B.; Porcedda, S.; J. Chem. Eng. Data 37 (1992) 124.
92-qin/hof Qin, A.; Hoffman, D. E.; Munk, P.; J. Chem. Eng. Data 37 (1992) 61.
92-qin/hof-2 Qin, A.; Hoffman, D. E.; Munk, P.; J. Chem. Eng. Data 37 (1992) 55.
92-ste/leh Stein, A.; Lehmann, C. W.; Luger, P.; J. Am. Chem. Soc. 114 (1992) 7684.
92-wei/wil Weiguo, S.; Williamson, A. G.; Can. J. Chem. 70 (1992) 2003.
92-yos/kat Yoshikawa, H.; Kato, M.; Kagaku Kogaku Ronbunshu 18 (1992) 723.
93-beg/tuk Beg, S. A.; Tukur, N. M.; Al-Harbi, D. K.; Hamad, E. Z.; J. Chem. Eng. Data 38 (1993)
461.
93-jan/xie Jan, D. S.; Xie, Y. C.; Tsai, F. N.; J. Chem. Eng. Data 38 (1993) 383.
94-del/fer DeLorenzi, L.; Fermeglia, M.; Torriano, G.; J. Chem. Eng. Data 39 (1994) 483.
94-kri/vis Krishnaiah, A.; Viswanath, D. S.; Toghiani, H.; Experimental Results for DIPPR
1990-91 Projects on Phase Equilibria and Pure Component Properties, DIPPR Data
Series No. 2, p. 1-10 (1994).
94-toj/ram Tojo, J.; Ramallo, A. V.; Orge, B.; J. Chem. Eng. Data 39 (1994) 480.
95-art/mun-3 Artal, M.; Munoz Embid, J.; Velasco, I.; Otin, S.; J. Chem. Thermodyn. 27 (1995) 475.
95-gaw/dor Gawronska, E.; Dordain, L.; Coxam, J. -Y.; Quint, J. R.; Grolier, J.-P. E.; J. Chem. Eng.
Data 40 (1995) 1257.
95-org/igl Orge, B.; Iglesias, M.; Tojo, J.; J. Chem. Eng. Data 40 (1995) 260.
95-osw/pat Oswal, S. L.; Patel, N. B.; J. Chem. Eng. Data 40 (1995) 840.
95-pet/gas Petrino, P. J.; Gaston-Bonhomme, Y. H.; Chevalier, J. L. E.; J. Chem. Eng. Data 40
(1995) 136.
Landolt-Brnstein
New Series IV/8D

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Survey of volume IV/8

Thermodynamic Properties of Organic Compounds

1. Enthalpies of Fusion and Transition of Organic Compounds Subvolume A

2. Densities of Aliphatic Hydrocarbons: Alkanes Subvolume B

3. Densities of Aliphatic Hydrocarbons: Alkenes, Alkadienes,

4. Densities of Monocyclic Hydrocarbons Subvolume D

5. Vapor Pressure of Aliphatic Halohydrocarbons

6. Densities of Aliphatic Halohydrocarbons

7. Densities of Aromatic Hydrocarbons

R. C. Wilhoit, X. Hong, M. Frenkel, K. R. Hall

Edited by K. R. Hall and K. N. Marsh

Thermodynamics Research Center

College Station, August 1997 R. C. Wilhoit, X. Hong, M. Frenkel, K. R. Hall

71-ano Landolt-Brnstein Sechste Auflage, II Band, Eigenschaften der Materie in ihren

1.1 Basic Concepts

1.2 Scope of the Compilation

1.3 Description of Data Tables

1.4 Evaluation, Selection and Smoothing of Data

1.4.2 Quantitative Effect of Impurity on Density of Liquids

and the molar mass of the mixture:

and assuming that the xi are small for i > 1, then

Table 2. Effect of water as an impurity on density

1.4.3 Procedure for Selection and Smoothing of Density Values - Case 1

by a polynomial in temperature with coefficients a of order p,

w j = 1 / u 2j where uj is the uncertainty assigned to the j-th observed density and n , j = j

Step 7. Fit the remaining normalized values to a series of polynomials, n = a k T k , starting

are calculated from:

approximated by fitting a polynomial of order 1-3 to the estimated uncertainties as a function of

1.4.4 Procedure for Selection and Smoothing of Density Values - Case 2

The uncertainties for the smoothed values are:

1.4.5 Procedure for Selection and Smoothing of Density Values - Case 3

1.5 Calculation Procedures

1.5.2 Selection of Data Based upon Estimated Uncertainties

y = u j z11.5 z21 (1.23)

Accept point j if y d; reject it otherwise

1.5.3 Count of the Effective Number of Density Values in a Set

Step 1. Sort the values in order of increasing temperature

n, number of values in original maximum number of

1.6 Glossary of Symbols

j observed value of j-th density in a data set

The following symbols refer to components in a mixture at a fixed temperature

c number of components in the mixture

Symbols used in the tables:

A, B, C, D, E coefficients in function for density (see section 1.4.3)

exp observed value of j-th density in a data set, j

1.7 Compound Nomenclature

1.7.2 Order of Compounds in the Tables

Compounds in the tables are sorted in the following order:

2.1 Alkylcycloalkanes (CnH2n), C3 to C5

Cyclopropane [75-19-4] C3H6 MW = 42.0806 1

c,uw = 2.7685 10-1 (combined temperature ranges, unweighted).

crystal 318.15 586.40 0.39 -0.66 70-lin/sil()

Further references: [1889-hof, 00-gus, 17-jae, 20-mou/bou, 22-tra/win-1].

Methylcyclopropane [594-11-6] C4H8 MW = 56.11 2

Table 1. Coefficients of the polynomial expansion

Cyclobutane [287-23-0] C4H8 MW = 56.1075 3

Table 1. Coefficients of the polynomial expansion

crystal II 194.65 802.00 5.00 18.37 42-ben()

Ethylcyclopropane [1191-96-4] C5H10 MW = 70.13 4

Table 1. Fit with estimated B coefficient for 13

Table 3. Recommended values.

1,1-Dimethylcyclopropane [1630-94-0] C5H10 MW = 70.13 5

Table 1. Fit with estimated B coefficient for 9