Contents
Physical Properties
Temperature Dependent Properties
Datasets
Correlations
Similar Compounds
Mixtures
Sources
Physical Properties
Property
Value
Unit
Source
ω
0.1960
KDB
Tig
653.15
K
KDB
AP
289.950
K
KDB
Δc H°liquid
[-3291.40; -3290.90]
kJ/mol
Δc H°liquid
-3291.40 ± 0.60
kJ/mol
NIST
Δc H°liquid
-3291.20 ± 1.30
kJ/mol
NIST
Δc H°liquid
-3290.90 ± 0.71
kJ/mol
NIST
μ
0.00
debye
KDB
LFL
1.10
% in Air
KDB
UFL
8.70
% in Air
KDB
Tflash,oc
266.48
K
KDB
Δf G°
38.60
kJ/mol
KDB
Rg
3.1200
KDB
Δc,gross H
3290.93
kJ/mol
KDB
Δc,net H
3070.889
kJ/mol
KDB
Δf H°gas
[-77.29; -76.40]
kJ/mol
Δf H°gas
-77.29
kJ/mol
KDB
Δf H°gas
-76.40 ± 0.79
kJ/mol
NIST
Δf H°gas
-76.90
kJ/mol
NIST
Δf H°gas
-77.24 ± 0.75
kJ/mol
NIST
Δf H°liquid
[-105.90; -105.60]
kJ/mol
Δf H°liquid
-105.60 ± 1.80
kJ/mol
NIST
Δf H°liquid
-105.90 ± 0.75
kJ/mol
NIST
Δfus H°
1.57
kJ/mol
Joback Calculated Property
Δvap H°
27.29
kJ/mol
Joback Calculated Property
IE
[9.83; 11.01]
eV
IE
10.33 ± 0.15
eV
NIST
IE
Outlier 9.83 ± 0.05
eV
NIST
IE
10.35
eV
NIST
IE
10.33 ± 0.15
eV
NIST
IE
10.30 ± 0.10
eV
NIST
IE
10.55 ± 0.03
eV
NIST
IE
10.54 ± 0.05
eV
NIST
IE
10.48
eV
NIST
IE
10.40
eV
NIST
IE
10.49
eV
NIST
IE
10.91 ± 0.07
eV
NIST
IE
10.50 ± 0.01
eV
NIST
IE
10.49
eV
NIST
IE
10.53 ± 0.05
eV
NIST
IE
Outlier 11.01
eV
NIST
IE
10.70 ± 0.10
eV
NIST
IE
10.50
eV
NIST
log 10 WS
[-2.64; -2.64]
log 10 WS
-2.64
Aq. Sol...
log 10 WS
-2.64
Estimat...
log Poct/wat
1.950
Crippen Calculated Property
McVol
70.450
ml/mol
McGowan Calculated Property
NFPA Fire
3
KDB
NFPA Health
1
KDB
Pc
[4430.00; 4514.03]
kPa
Pc
4510.00
kPa
KDB
Pc
4510.00 ± 40.00
kPa
NIST
Pc
4508.00 ± 40.53
kPa
NIST
Pc
4430.00 ± 50.66
kPa
NIST
Pc
4514.03 ± 5.06
kPa
NIST
ρc
[270.01; 270.01]
kg/m3
ρc
270.01 ± 2.81
kg/m3
NIST
ρc
270.01 ± 4.21
kg/m3
NIST
ρc
270.01 ± 2.10
kg/m3
NIST
Inp
[520.00; 599.00]
Inp
572.00
NIST
Inp
587.00
NIST
Inp
587.70
NIST
Inp
558.00
NIST
Inp
572.00
NIST
Inp
573.00
NIST
Inp
574.30
NIST
Inp
582.40
NIST
Inp
Outlier 591.00
NIST
Inp
562.00
NIST
Inp
567.80
NIST
Inp
568.00
NIST
Inp
568.00
NIST
Inp
568.30
NIST
Inp
568.40
NIST
Inp
562.60
NIST
Inp
587.60
NIST
Inp
588.00
NIST
Inp
565.00
NIST
Inp
568.00
NIST
Inp
572.00
NIST
Inp
566.20
NIST
Inp
587.90
NIST
Inp
566.50
NIST
Inp
565.60
NIST
Inp
566.10
NIST
Inp
569.40
NIST
Inp
569.90
NIST
Inp
574.50
NIST
Inp
563.00
NIST
Inp
565.00
NIST
Inp
566.00
NIST
Inp
568.00
NIST
Inp
570.00
NIST
Inp
572.00
NIST
Inp
567.80
NIST
Inp
568.30
NIST
Inp
577.00
NIST
Inp
566.00
NIST
Inp
582.00
NIST
Inp
570.00
NIST
Inp
567.00
NIST
Inp
566.00
NIST
Inp
565.00
NIST
Inp
568.00
NIST
Inp
568.80
NIST
Inp
565.55
NIST
Inp
563.30
NIST
Inp
575.90
NIST
Inp
573.00
NIST
Inp
576.00
NIST
Inp
567.00
NIST
Inp
570.00
NIST
Inp
566.00
NIST
Inp
568.00
NIST
Inp
573.00
NIST
Inp
588.00
NIST
Inp
566.00
NIST
Inp
567.00
NIST
Inp
568.00
NIST
Inp
568.00
NIST
Inp
572.00
NIST
Inp
568.00
NIST
Inp
570.00
NIST
Inp
571.00
NIST
Inp
573.00
NIST
Inp
574.00
NIST
Inp
566.30
NIST
Inp
571.00
NIST
Inp
568.00
NIST
Inp
568.00
NIST
Inp
568.00
NIST
Inp
568.00
NIST
Inp
572.00
NIST
Inp
563.00
NIST
Inp
566.00
NIST
Inp
569.00
NIST
Inp
572.00
NIST
Inp
562.00
NIST
Inp
563.00
NIST
Inp
564.00
NIST
Inp
568.00
NIST
Inp
570.00
NIST
Inp
578.00
NIST
Inp
568.00
NIST
Inp
562.00
NIST
Inp
Outlier 599.00
NIST
Inp
587.00
NIST
Inp
571.00
NIST
Inp
557.00
NIST
Inp
576.00
NIST
Inp
566.50
NIST
Inp
563.00
NIST
Inp
553.70
NIST
Inp
580.29
NIST
Inp
563.20
NIST
Inp
556.60
NIST
Inp
554.33
NIST
Inp
554.33
NIST
Inp
554.13
NIST
Inp
554.24
NIST
Inp
554.00
NIST
Inp
557.00
NIST
Inp
559.00
NIST
Inp
564.00
NIST
Inp
564.00
NIST
Inp
565.00
NIST
Inp
571.00
NIST
Inp
566.00
NIST
Inp
566.00
NIST
Inp
569.00
NIST
Inp
Outlier 520.00
NIST
Inp
Outlier 524.00
NIST
Inp
560.00
NIST
Inp
560.00
NIST
Inp
564.00
NIST
Inp
562.00
NIST
Inp
554.50
NIST
Inp
564.00
NIST
Inp
554.00
NIST
Inp
Outlier 527.00
NIST
Inp
562.00
NIST
Inp
563.00
NIST
Inp
587.00
NIST
Inp
566.00
NIST
Inp
587.00
NIST
Inp
568.00
NIST
Inp
570.00
NIST
Inp
564.00
NIST
Inp
570.00
NIST
Inp
570.00
NIST
Inp
560.00
NIST
Inp
558.00
NIST
Inp
Outlier 533.00
NIST
Inp
572.00
NIST
Inp
557.00
NIST
Inp
570.00
NIST
Inp
577.00
NIST
Inp
573.00
NIST
Inp
564.00
NIST
Inp
573.00
NIST
Inp
564.00
NIST
Inp
559.00
NIST
Inp
553.70
NIST
Inp
554.33
NIST
Inp
566.50
NIST
I
[694.00; 720.00]
I
694.00
NIST
I
700.00
NIST
I
710.00
NIST
I
698.00
NIST
I
700.00
NIST
I
720.00
NIST
I
694.00
NIST
I
720.00
NIST
S°liquid
[204.14; 206.70]
J/mol×K
S°liquid
204.14
J/mol×K
NIST
S°liquid
204.47
J/mol×K
NIST
S°liquid
206.70
J/mol×K
NIST
Tboil
322.40
K
KDB
Tc
[511.60; 511.75]
K
Tc
511.70
K
KDB
Tc
511.70 ± 0.20
K
NIST
Tc
511.60
K
NIST
Tc
511.70 ± 0.20
K
NIST
Tc
511.60 ± 0.15
K
NIST
Tc
511.75 ± 0.05
K
NIST
Tfus
[176.64; 180.05]
K
Tfus
179.30
K
KDB
Tfus
179.20
K
Aq. Sol...
Tfus
Outlier 176.64 ± 0.30
K
NIST
Tfus
179.60 ± 0.30
K
NIST
Tfus
179.55 ± 0.30
K
NIST
Tfus
Outlier 177.06 ± 0.20
K
NIST
Tfus
179.25 ± 0.40
K
NIST
Tfus
179.26 ± 0.40
K
NIST
Tfus
179.69 ± 0.10
K
NIST
Tfus
179.26 ± 0.07
K
NIST
Tfus
179.38 ± 0.05
K
NIST
Tfus
179.25 ± 0.06
K
NIST
Tfus
179.26 ± 0.05
K
NIST
Tfus
179.28 ± 0.04
K
NIST
Tfus
179.35 ± 0.20
K
NIST
Tfus
179.35 ± 0.20
K
NIST
Tfus
179.23 ± 0.01
K
NIST
Tfus
179.23 ± 0.05
K
NIST
Tfus
179.25 ± 0.07
K
NIST
Tfus
179.38 ± 0.05
K
NIST
Tfus
179.23 ± 0.40
K
NIST
Tfus
179.68 ± 0.30
K
NIST
Tfus
179.31 ± 0.20
K
NIST
Tfus
178.85 ± 0.30
K
NIST
Tfus
178.85 ± 0.30
K
NIST
Tfus
178.85 ± 0.20
K
NIST
Tfus
178.85 ± 0.30
K
NIST
Tfus
178.15 ± 0.50
K
NIST
Tfus
178.35 ± 0.50
K
NIST
Tfus
180.05 ± 0.50
K
NIST
Ttriple
[179.00; 179.71]
K
Ttriple
179.71 ± 0.05
K
NIST
Ttriple
179.71 ± 0.01
K
NIST
Ttriple
179.69 ± 0.08
K
NIST
Ttriple
179.00 ± 0.20
K
NIST
Vc
[0.259; 0.259]
m3 /kmol
Vc
0.259
m3 /kmol
KDB
Vc
0.259
m3 /kmol
NIST
Zc
0.2745520
KDB
Zra
0.27
KDB
Temperature Dependent Properties
Property
Value
Unit
Temperature (K)
Source
Cp,gas
[93.96; 160.10]
J/mol×K
[329.05; 539.00]
Cp,gas
93.96 ± 0.19
J/mol×K
329.05
NIST
Cp,gas
102.01 ± 0.84
J/mol×K
353.00
NIST
Cp,gas
108.16 ± 0.84
J/mol×K
372.00
NIST
Cp,gas
117.30 ± 1.30
J/mol×K
395.00
NIST
Cp,gas
117.09 ± 0.23
J/mol×K
395.05
NIST
Cp,gas
126.30 ± 1.30
J/mol×K
424.00
NIST
Cp,gas
138.70 ± 1.30
J/mol×K
463.00
NIST
Cp,gas
139.47 ± 0.28
J/mol×K
463.10
NIST
Cp,gas
150.70 ± 1.70
J/mol×K
503.00
NIST
Cp,gas
160.10 ± 1.70
J/mol×K
539.00
NIST
Cp,liquid
[125.90; 128.83]
J/mol×K
[293.15; 300.00]
Cp,liquid
126.17
J/mol×K
293.15
NIST
Cp,liquid
125.90
J/mol×K
293.70
NIST
Cp,liquid
126.74
J/mol×K
298.15
NIST
Cp,liquid
126.87
J/mol×K
298.15
NIST
Cp,liquid
127.28
J/mol×K
298.15
NIST
Cp,liquid
126.78
J/mol×K
298.15
NIST
Cp,liquid
128.83
J/mol×K
298.15
NIST
Cp,liquid
127.44
J/mol×K
300.00
NIST
η
[0.0002502; 0.0007268]
Pa×s
[253.15; 353.15]
η
0.0007268
Pa×s
253.15
Saturat...
η
0.0006786
Pa×s
258.15
Saturat...
η
0.0006347
Pa×s
263.15
Saturat...
η
0.0005930
Pa×s
268.15
Saturat...
η
0.0005567
Pa×s
273.15
Saturat...
η
0.0005224
Pa×s
278.15
Saturat...
η
0.0005230
Pa×s
278.15
Tempera...
η
0.0004932
Pa×s
283.15
Tempera...
η
0.0004922
Pa×s
283.15
Saturat...
η
0.0004646
Pa×s
288.15
Saturat...
η
0.0004657
Pa×s
288.15
Tempera...
η
0.0004390
Pa×s
293.15
Dynamic...
η
0.0004380
Pa×s
293.15
Density...
η
0.0004390
Pa×s
293.15
Viscosi...
η
0.0004380
Pa×s
293.15
Viscosi...
η
0.0004405
Pa×s
293.15
Tempera...
η
0.0004382
Pa×s
293.15
Saturat...
η
0.0004390
Pa×s
293.15
Dynamic...
η
0.0004148
Pa×s
298.15
Saturat...
η
0.0004173
Pa×s
298.15
Tempera...
η
0.0004160
Pa×s
298.15
Dynamic...
η
0.0004160
Pa×s
298.15
Viscosi...
η
0.0004160
Pa×s
298.15
Dynamic...
η
0.0004150
Pa×s
298.15
Density...
η
0.0003940
Pa×s
303.15
Viscosi...
η
0.0003940
Pa×s
303.15
Dynamic...
η
0.0003923
Pa×s
303.15
Saturat...
η
0.0003940
Pa×s
303.15
Dynamic...
η
0.0003940
Pa×s
303.15
Density...
η
0.0003714
Pa×s
308.15
Saturat...
η
0.0003740
Pa×s
308.15
Density...
η
0.0003550
Pa×s
313.15
Density...
η
0.0003521
Pa×s
313.15
Saturat...
η
0.0003350
Pa×s
318.15
Saturat...
η
0.0003190
Pa×s
323.15
Saturat...
η
0.0003048
Pa×s
328.15
Saturat...
η
0.0002912
Pa×s
333.15
Saturat...
η
0.0002793
Pa×s
338.15
Saturat...
η
0.0002690
Pa×s
343.15
Saturat...
η
0.0002590
Pa×s
348.15
Saturat...
η
0.0002502
Pa×s
353.15
Saturat...
Δfus H
[0.34; 4.90]
kJ/mol
[122.00; 179.70]
Δfus H
4.90
kJ/mol
122.00
NIST
Δfus H
0.34
kJ/mol
138.00
NIST
Δfus H
0.60
kJ/mol
179.70
NIST
Δfus H
0.60
kJ/mol
179.70
NIST
Δsub H
42.60
kJ/mol
122.00
NIST
Δvap H
[27.20; 29.21]
kJ/mol
[298.15; 481.50]
Δvap H
29.21
kJ/mol
298.15
NIST
Δvap H
29.20
kJ/mol
305.50
NIST
Δvap H
29.00
kJ/mol
306.00
NIST
Δvap H
27.90 ± 0.10
kJ/mol
310.00
NIST
Δvap H
27.30 ± 0.10
kJ/mol
322.00
NIST
Δvap H
27.30
kJ/mol
322.40
KDB
Δvap H
27.30
kJ/mol
322.40
NIST
Δvap H
27.40
kJ/mol
323.00
NIST
Δvap H
28.00
kJ/mol
353.00
NIST
Δvap H
27.20
kJ/mol
418.00
NIST
Δvap H
27.50
kJ/mol
481.50
NIST
n 0
[1.39456; 1.40640]
[293.15; 313.15]
n 0
1.40640
293.15
Isobari...
n 0
1.40363
298.15
KDB
n 0
1.40292
298.15
Density...
n 0
1.39456
313.15
Density...
ρl
[726.57; 762.30]
kg/m3
[273.15; 308.15]
ρl
762.30
kg/m3
273.15
Phase e...
ρl
757.50
kg/m3
278.15
Phase e...
ρl
752.60
kg/m3
283.15
Phase e...
ρl
747.70
kg/m3
288.15
Phase e...
ρl
745.00
kg/m3
293.00
KDB
ρl
742.80
kg/m3
293.15
Phase e...
ρl
745.70
kg/m3
293.15
Correla...
ρl
739.74
kg/m3
298.15
Experim...
ρl
737.80
kg/m3
298.15
Phase e...
ρl
733.63
kg/m3
298.15
Densiti...
ρl
740.00
kg/m3
298.15
Density...
ρl
726.57
kg/m3
308.15
Densiti...
Δfus S
[2.49; 40.13]
J/mol×K
[122.00; 179.70]
Δfus S
40.13
J/mol×K
122.00
NIST
Δfus S
2.49
J/mol×K
138.00
NIST
Δfus S
3.35
J/mol×K
179.70
NIST
csound,fluid
[1129.90; 1283.50]
m/s
[283.15; 313.15]
csound,fluid
1283.50
m/s
283.15
Speeds ...
csound,fluid
1206.60
m/s
298.15
Speeds ...
csound,fluid
1129.90
m/s
313.15
Speeds ...
γ
[0.02; 0.02]
N/m
[283.15; 313.15]
γ
0.02
N/m
283.15
Thermop...
γ
0.02
N/m
293.20
KDB
γ
0.02
N/m
298.15
Thermop...
γ
0.02
N/m
313.15
Thermop...
Δvap S
97.98
J/mol×K
298.15
NIST
λ
[0.12; 0.14]
W/m×K
[257.08; 316.54]
λ
0.14
W/m×K
257.08
Thermal...
λ
0.14
W/m×K
257.27
Thermal...
λ
0.14
W/m×K
257.40
Thermal...
λ
0.13
W/m×K
276.13
Thermal...
λ
0.13
W/m×K
276.33
Thermal...
λ
0.13
W/m×K
276.47
Thermal...
λ
0.13
W/m×K
293.63
Thermal...
λ
0.13
W/m×K
293.83
Thermal...
λ
0.13
W/m×K
293.97
Thermal...
λ
0.13
W/m×K
300.67
Thermal...
λ
0.13
W/m×K
300.87
Thermal...
λ
0.13
W/m×K
301.01
Thermal...
λ
0.12
W/m×K
316.21
Thermal...
λ
0.12
W/m×K
316.40
Thermal...
λ
0.12
W/m×K
316.54
Thermal...
Datasets
Viscosity, Pa*s (1)
Speed of sound, m/s (1)
Viscosity, Pa*s
Fixed
Measured
Temperature, K - Liquid
Pressure, kPa - Liquid
Viscosity, Pa*s - Liquid
273.15
100.00
0.0006
273.15
10000.00
0.0006
273.15
30000.00
0.0007
273.15
40000.00
0.0008
293.15
100.00
0.0004
293.15
10000.00
0.0005
293.15
30000.00
0.0006
293.15
40000.00
0.0006
298.15
100.00
0.0004
298.15
10000.00
0.0005
298.15
30000.00
0.0005
298.15
40000.00
0.0006
313.15
10000.00
0.0004
313.15
30000.00
0.0005
313.15
45000.00
0.0005
333.15
10000.00
0.0003
333.15
30000.00
0.0004
333.15
45000.00
0.0004
353.15
15000.00
0.0003
353.15
30000.00
0.0003
353.15
45000.00
0.0004
Reference
Speed of sound, m/s
Operational condition: Frequency, MHz =
8 (Liquid)
Fixed
Measured
Temperature, K - Liquid
Pressure, kPa - Liquid
Speed of sound, m/s - Liquid
258.15
100.00
1419.058
258.15
5072.00
1446.07
258.15
10244.00
1473.008
258.15
15262.00
1498.119
258.15
20158.00
1521.653
258.15
25083.00
1544.511
258.15
30141.00
1567.131
273.15
100.00
1336.626
273.15
5169.00
1366.736
273.15
10059.00
1394.32
273.15
15219.00
1422.015
273.15
20251.00
1447.913
273.15
25184.00
1472.273
273.15
30227.00
1496.252
293.15
105.00
1230.093
293.15
5059.00
1262.962
293.15
10088.00
1294.375
293.15
15198.00
1324.591
293.15
20121.00
1352.283
293.15
25192.00
1379.573
293.15
30134.00
1404.98
313.15
107.00
1126.831
313.15
5113.00
1164.014
313.15
10058.00
1198.273
313.15
15132.00
1231.306
313.15
20097.00
1261.807
313.15
25098.00
1290.997
313.15
30162.00
1319.175
333.15
149.00
1026.636
333.15
5035.00
1067.634
333.15
10139.00
1106.967
333.15
15108.00
1142.542
333.15
20130.00
1176.238
333.15
25152.00
1207.969
333.15
30170.00
1238.041
353.15
261.00
929.399
353.15
5019.00
974.633
353.15
10069.00
1018.218
353.15
15107.00
1058.051
353.15
20063.00
1094.384
353.15
25009.00
1128.301
353.15
30157.00
1161.49
Reference
Correlations
Similar Compounds
Find more compounds similar to Cyclopentane .
Mixtures
Find more mixtures with Cyclopentane .
Sources
KDB Pure (Korean Thermophysical Properties Databank)
KDB Vapor Pressure Data
Crippen Method
Speeds of Sound and Isentropic Compressibilities for Binary Mixtures of a Cyclic Diether with a Cyclic Compound at Three Temperatures
Determination of activity coefficients at infinite dilution of organic solutes in the ionic liquid, trihexyl(tetradecyl)-phosphonium tris(pentafluoroethyl) trifluorophosphate, by gas liquid chromatography
Experimental and predicted vapour liquid equilibrium of 1,4-dioxane with cycloalkanes and benzene
Experimental liquid liquid equilibria of 1-methylimidazole with hydrocarbons and ethers
Determination of activity coefficients at infinite dilution of organic solutes in the ionic liquid, tributylmethylphosphonium methylsulphate by gas liquid chromatography
Activity coefficients at infinite dilution measurements for organic solutes in the ionic liquid N-butyl-4-methylpyridinium tosylate using GLC at T = (328.15, 333.15, 338.15, and 343.15)K
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 1-butyl-1-methylpyrrolidinium trifluoromethanesulfonate using GLC
Activity coefficients at infinite dilution measurements for organic solutes and water in the 1-hexyloxymethyl-3-methyl-imidazolium and 1,3-dihexyloxymethyl-imidazolium bis(trifluoromethylsulfonyl)-imide ionic liquids The cation influence
On the behaviour of solutions of xenon in liquid cycloalkanes: Solubility of xenon in cyclopentane
Phase equilibrium relations for binary mixed hydrate systemscomposed of carbon dioxide and cyclopentane derivatives
Activity coefficients at infinite dilution of organic solvents and water in 1-butyl-3-methylimidazolium dicyanamide. A literature review of hexane/hex-1-ene separation
High selective water/butan-1-ol separation on investigation of limiting activity coefficients with [P8,8,8,8][[NTf2] ionic liquid
Separation of binary mixtures based on limiting activity coefficients data using specific ammonium-based ionic liquid and modelling of thermodynamic functions
Measurements of activity coefficient at infinite dilution for organic solutes in tetramethylammonium chloride + ethylene glycol deep eutectic solvent using gas-liquid chromatography
Tetramethylammonium chloride + glycerol deep eutectic solvent as separation agent for organic liquid mixtures: Assessment from experimental limiting activity coefficients
New ionic liquid [P4,4,4,4][NTf2] in bio-butanol extraction on investigation of limiting activity coefficients
Measurements of activity coefficients at infinite dilution for organic solutes in two quaternary ammonium-based ionic liquids [DDA][ClO4] and [DDA][BF4]
The determination of activity coefficients at infinite dilution using g.l.c. for hydrocarbons in furfural at T = 278:15 K and T = 298:15 K
Activity coefficients at infinite dilution for hydrocarbons in furfuryl alcohol at T=(278.15 and 298.15) K, determined by g.l.c.
Activity coefficients at infinite dilution measurements for organic solutes in the ionic liquid 1-butyl-3-methyl-imidazolium 2-(2-methoxyethoxy) ethyl sulfate using g.l.c. at T = (298.15, 303.15, and 308.15) K
Activity coefficients at infinite dilution measurements for organic solutes in the ionic liquid hexyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl)-imide using g.l.c. at T = (298.15, 313.15, and 333.15) K
Systems with ionic liquids: Measurement of VLE and c1 data and prediction of their thermodynamic behavior using original UNIFAC, mod. UNIFAC(Do) and COSMO-RS(Ol)
Measurement of activity coefficients at infinite dilution using polar and non-polar solutes in the ionic liquid 1-methyl-3-octyl-imidazolium diethyleneglycolmonomethylethersulfate at T = (288.15, 298.15, and 313.15) K
Thermophysical study of 1,4-dioxane with cycloalkane mixtures
Dynamic viscosities of binary mixtures of cycloalkanes with primary alcohols at T = (293.15, 298.15, and 303.15) K: New UNIFAC-VISCO interaction parameters
Measurements of activity coefficients at infinite dilution of aromatic and aliphatic hydrocarbons, alcohols, and water in the new ionic liquid [EMIM][SCN] using GLC
Development of a Henry s constant correlation and solubility measurements of n-pentane, i-pentane, cyclopentane, n-hexane, and toluene in water
Activity coefficients at infinite dilution measurements for organic solutes in the ionic liquid trihexyltetradecylphosphonium-bis-(2,4,4-trimethylpentyl)- phosphinate using g.l.c. at T = (303.15, 308.15, 313.15, and 318.15) K
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid triethylsulphonium bis(trifluoromethylsulfonyl)imide
Measurements of activity coefficients at infinite dilution of aliphatic and aromatic hydrocarbons, alcohols, thiophene, tetrahydrofuran, MTBE, and water in ionic liquid [BMIM][SCN] using GLC
Influence of temperature on the (liquid + liquid) equilibria of {3-methyl pentane + cyclopentane + methanol} ternary system at T = (293.15, 297.15, and 299.15) K
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 4-methyl-N-butyl-pyridinium bis(trifluoromethylsulfonyl)-imide
Activity coefficients at infinite dilution of organic solutes in the ionic liquid 1-ethyl-3-methylimidazolium trifluoromethanesulfonate using gas liquid chromatography at T = (313.15, 323.15, and 333.15) K
Activity coefficients at infinite dilution for solutes in the trioctylmethylammonium bis(trifluoromethylsulfonyl)imide ionic liquid using gas liquid chromatography
Activity coefficients at infinite dilution of organic solutes in the ionic liquid 1-octyl-3-methylimidazolium hexafluorophosphate using gas liquid chromatography at T = (313.15, 323.15, and 333.15) K
Gas liquid chromatography measurements of activity coefficients at infinite dilution of various organic solutes and water in tri-iso-butylmethylphosphonium tosylate ionic liquid
Measurements of activity coefficients at infinite dilution of organic solutes and water in 1-propyl-1-methylpiperidinium bis{(trifluoromethyl)sulfonyl}imide ionic liquid using g.l.c.
Measurements of activity coefficients at infinite dilution of organic compounds and water in isoquinolinium-based ionic liquid [C8iQuin][NTf2] using GLC
Activity coefficients at infinite dilution of organic solutes in the ionic liquid trihexyl(tetradecyl)phosphonium tetrafluoroborate using gas liquid chromatography at T = (313.15, 333.15, 353.15, and 373.15) K
Activity coefficients at infinite dilution of organic solutes in the ionic liquid 1-butyl-3-methylimidazolium hexafluoroantimonate using gas liquid chromatography at T = (313.15, 323.15, and 333.15) K
Activity coefficients at infinite dilution of organic solutes in the ionic liquid, methyl(trioctyl)ammonium thiosalicylate, [N1888][TS] by gas liquid chromatography at T = (303.15, 313.15, and 323.15) K
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 1-ethyl-3-methylimidazolium tetracyanoborate
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(3-hydroxypropyl)pyridinium bis(trifluoromethylsulfonyl)-amide
Thermodynamics and activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 1-butyl-1-methylpyrrolidinium tetracyanoborate
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 4-(2-methoxyethyl)-4-methylmorpholinium bis(trifluoromethylsulfonyl)-amide
Measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-hexyl-3-methylimidazolium tetracyanoborate
Activity coefficients at infinite dilution of organic solutes in the ionic liquid trihexyltetradecylphosphonium hexafluorophosphate using gas liquid chromatography at T = (313.15, 333.15, 353.15, and 363.15) K
Determination of infinite dilution activity coefficients using HS-SPME/GC/FID for hydrocarbons in furfural at temperatures of (298.15, 308.15, and 318.15) K
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)-1-methylpiperidinium bis(trifluoromethylsulfonyl)-amide
Measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-ethyl-3-methylimidazolium methanesulfonate
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)-amide
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 4-(2-methoxyethyl)-4-methylmorpholinium trifluorotris(perfluoroethyl)phosphate
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)- 1-methylpiperidinium trifluorotris(perfluoroethyl)phosphate
Physicochemical properties and activity coefficients at infinite dilution for organic solutes and water in a novel bicyclic guanidinium superbase-derived protic ionic liquid
Experimental and theoretical study on infinite dilution activity coefficients of various solutes in piperidinium ionic liquids
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)- 1-methylpyrrolidinium trifluorotris(perfluoroethyl)phosphate
Measurements of activity coefficients at infinite dilution for organic solutes and water in N-hexylisoquinolinium thiocyanate, [HiQuin][SCN] using GLC
Activity coefficients at infinite dilution of organic solutes in N-formylmorpholine and N-methylpyrrolidone from gas-liquid chromatography
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-hydroxyethyl)- 3-methylimidazolium trifluorotris(perfluoroethyl)phosphate
Activity coefficients at infinite dilution of organic solutes in diethylene glycol and triethylene glycol from gas-liquid chromatography
Activity coefficients at infinite dilution of organic solutes in the ionic liquid trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl)imide using gas-liquid chromatography at T = (313.15, 333.15, 353.15 and 373.15) K
Measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-butyl-1-methylpyrrolidinium tricyanomethanide
Thermodynamics and activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-butyl-1-methylmorpholinium tricyanomethanide
The study of activity coefficients at infinite dilution for organic solutes and water in 1-butyl-4-methylpyridinium dicyanamide, [B4MPy][DCA] using GLC
Measurement of activity coefficients at infinite dilution of organic solutes in the ionic liquid 1-ethyl-3-methylimidazolium 2-(2-methoxyethoxy) ethylsulfate at T = (308.15, 313.15, 323.15 and 333.15) K using gas + liquid chromatography
Measurement of activity coefficients at infinite dilution of organic solutes in the ionic liquid 1-hexyl-1,4-diaza[2.2.2]bicyclooctanium bis(trifluoromethylsulfonyl)imide using gas-liquid chromatography
Thermodynamics and activity coefficients at infinite dilution for organic solutes, water and diols in the ionic liquid choline bis(trifluoromethylsulfonyl)imide
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 4-(3-hydroxypropyl)-4-methylmorpholinium bis(trifluoromethylsulfonyl)-amide
Activity coefficients at infinite dilution for organic solutes and water in 1-ethyl-1-methylpyrrolidinium lactate
Activity coefficients at infinite dilution, physicochemical and thermodynamic properties for organic solutes and water in the ionic liquid ethyl-dimethyl-(2-methoxyethyl)ammonium trifluorotris-(perfluoroethyl)phosphate
The effect of the naphthenic ring on the VLE of (carbon dioxide + alkane) mixtures
Screening of environmental friendly ionic liquid as a solvent for the different types of separations problem: Insight from activity coefficients at infinite dilution measurement using (gas + liquid) chromatography technique
A 1-alkylcyanopyridinium-based ionic liquid in the separation processes
Thermodynamics and selectivity of separation based on activity coefficients at infinite dilution of various solutes in 1-allyl-3-methylimidazolium bis{(trifluoromethyl)sulfonyl}imide ionic liquid
Separation of aliphatic from aromatic hydrocarbons and sulphur compounds from fuel based on measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid N,N-diethyl-N-methyl-N-(2-methoxy-ethyl)ammonium bis(trifluoromethylsulfonyl)imide
Thermodynamics and limiting activity coefficients measurements for organic solutes and water in the ionic liquid 1-dodecyl-3-methylimidzolium bis(trifluoromethylsulfonyl) imide
Activity coefficients at infinite dilution of hydrocarbons in glycols: Experimental data and thermodynamic modeling with the GCA-EoS
Separation of binary mixtures hexane/hex-1-ene, cyclohexane/cyclohexene and ethylbenzene/styrene based on limiting activity coefficients
Separation of water/butan-1-ol based on activity coefficients at infinite dilution in 1,3-didecyl-2-methylimidazolium dicyanamide ionic liquid
Separation of binary mixtures hexane/hex-1-ene, cyclohexane/cyclohexene and ethylbenzene/styrene based on gamma infinity data measurements
Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid trihexyl-tetradecyl-phosphonium tricyanomethanide
The use of ionic liquids for separation of binary hydrocarbons mixtures based on gamma infinity data measurements
Excess Molar Volumes for Three and Four Component Mixtures Simulating the Binary Mixture (Cyclohexane+ Hexadecane)
Activity Coefficients at Infinite Dilution of Organic Solutes and Water in Tributylethylphosphonium Diethylphosphate Using Gas Liquid Chromatography: Thermodynamic Properties of Mixtures Containing Ionic Liquids
Isobaric Vapor Liquid Equilibrium for Nine Binary Systems of Cracking C5 Fraction at 250 kPa
Correlation of Experimental Liquid Liquid Equilibrium Data for Ternary Systems Using NRTL and GMDH-Type Neural Network
Activity Coefficients at Infinite Dilution of Various Solutes in Tetrapropylammonium Bromide + 1,6-Hexanediol Deep Eutectic Solvent
Liquid-Liquid Equilibria for the Binary Systems of N-Formylmorpholine with Cycloalkanes
Solubility of 1-Alkyl-3-methylimidazolium Hexafluorophosphate in Hydrocarbons
Saturated Liquid Viscosity of Cyclopentane and Isopentane
Activity Coefficients at Infinite Dilution of Organic Solutes in 1-Hexyl-3-methylimidazolium Hexafluorophosphate from Gas-Liquid Chromatography
Determination of Activity Coefficients at Infinite Dilution of Solutes in the Ionic Liquid 1-Hexyl-3-methylimidazolium Tetrafluoroborate Using Gas-Liquid Chromatography at the Temperatures 298.15 K and 323.15 K
Temperature and Density Dependence of the Viscosity of Cyclopentane
Thermal Conductivity and Thermal Diffusivity of Twenty-Nine Liquids: Alkenes, Cyclic (Alkanes, Alkenes, Alkadienes, Aromatics), and Deuterated Hydrocarbons
Determination of Activity Coefficients at Infinite Dilution of Polar and Nonpolar Solutes in the Ionic Liquid 1-Ethyl-3-methyl- imidazolium Bis(trifluoromethylsulfonyl) Imidate Using Gas-Liquid Chromatography at the Temperature 303.15 K or 318.15 K
Density, Viscosity, and Speed of Sound of Dialkyl Carbonates with Cyclopentane and Methyl Cyclohexane at Several Temperatures
Determination of Activity Coefficients at Infinite Dilution of Solutes in the Ionic Liquid 1-Butyl-3-methylimidazolium Octyl Sulfate Using Gas-Liquid Chromatography at a Temperature of 298.15 K, 313.15 K, or 328.15 K
Dynamic Viscosities of the Binary Systems Cyclohexane and Cyclopentane with Acetone, Butanone, or 2-Pentanone at Three Temperatures T ) (293.15, 298.15, and 303.15) K
Viscosities, Densities, and Speed of Sound of the Cycloalkanes with Secondary Alcohols at T = (293.15, 298.15, and 303.15) K: New UNIFAC-VISCO Interaction Parameters
Infinite Dilution Activity Coefficients for Trihexyltetradecyl Phosphonium Ionic Liquids: Measurements and COSMO-RS Prediction
Measurement of the Viscosity of Liquid Cyclopentane Obtained with a Vibrating Wire Viscometer at Temperatures between (273 and 353) K and Pressures below 45 MPa
Activity Coefficients at Infinite Dilution Measurements for Organic Solutes and Water in the Ionic Liquid 1-Butyl-3-methyl-pyridinium Trifluoromethanesulfonate
Determination of Activity Coefficients at Infinite Dilution of 35 Solutes in the Ionic Liquid, 1-Butyl-3-methylimidazolium Tosylate, Using Gas-Liquid Chromatography
Measurements of Activity Coefficients at Infinite Dilution for Organic Solutes and Water in the Ionic Liquid 1-Butyl-1-methylpiperydinium Thiocyanate
Speed of Sound Measurements and a Fundamental Equation of State for Cyclopentane
Determination of Activity Coefficients at Infinite Dilution of Solutes in the Ionic Liquid, Trihexyltetradecylphosphonium Bis(trifluoromethylsulfonyl) Imide, Using Gas-Liquid Chromatography at T ) (303.15, 308.15, 313.15, and 318.15) K
Densities and Excess Molar Volumes of Cyclopentane (1) + 1-Alkanol (2) Systems at (298.15 and 308.15) K
Density, Speed of Sound, and Refractive Index for Binary Mixtures Containing Cycloalkanes and Aromatic Compounds at T = 313.15 K
Henry s Law Constants of Organic Compounds in Water and n-Octane at T = 293.2 K
Activity Coefficients at Infinite Dilution Measurements for Organic Solutes and Water in the Ionic Liquid 1-Hexyl-3-methylimidazolium Thiocyanate
Density, Speed of Sound, and Refractive Index for Binary Mixtures Containing Cycloalkanes with o-Xylene, m-Xylene, p-Xylene, and Mesitylene at T = (298.15 and 313.15) K
Joback Method
KDB
Aqueous Solubility Prediction Method
Estimated Solubility Method
McGowan Method
NIST Webbook
The Yaws Handbook of Vapor Pressure
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