Physical Properties
Property
Value
Unit
Source
ω
0.2330
KDB
Tig
548.15
K
KDB
AP
292.150
K
KDB
Δc H°liquid
-3349.72 ± 0.58
kJ/mol
NIST
μ
0.40
debye
KDB
LFL
1.40
% in Air
KDB
UFL
8.70
% in Air
KDB
Tflash,cc
255.37
K
KDB
Tflash,oc
222.04
K
KDB
Δf G°
79.17
kJ/mol
KDB
Δc,gross H
3350.05
kJ/mol
KDB
Δc,net H
3130.009
kJ/mol
KDB
Δf H°gas
-20.93
kJ/mol
KDB
Δfus H°
7.43
kJ/mol
Joback Calculated Property
Δvap H°
[25.50; 29.82]
kJ/mol
Δvap H°
29.82
kJ/mol
NIST
Δvap H°
25.50
kJ/mol
NIST
Δvap H°
25.50 ± 0.10
kJ/mol
NIST
IE
[9.42; 9.82]
eV
IE
9.49 ± 0.03
eV
NIST
IE
9.50
eV
NIST
IE
9.52 ± 0.05
eV
NIST
IE
9.42 ± 0.02
eV
NIST
IE
9.52 ± 0.02
eV
NIST
IE
9.52 ± 0.00
eV
NIST
IE
9.48
eV
NIST
IE
Outlier 9.82 ± 0.06
eV
NIST
IE
9.50 ± 0.02
eV
NIST
IE
9.50 ± 0.02
eV
NIST
IE
9.68 ± 0.01
eV
NIST
IE
9.54 ± 0.02
eV
NIST
log 10 WS
[-2.68; -2.68]
log 10 WS
-2.68
Aq. Sol...
log 10 WS
-2.68
Estimat...
log Poct/wat
1.973
Crippen Calculated Property
McVol
77.010
ml/mol
McGowan Calculated Property
NFPA Fire
4
KDB
NFPA Health
1
KDB
Pc
[3550.00; 3560.00]
kPa
Pc
3560.00
kPa
KDB
Pc
3560.00 ± 50.00
kPa
NIST
Pc
3550.00 ± 20.00
kPa
NIST
Pc
3551.00 ± 3.44
kPa
NIST
ρc
[232.84; 234.95]
kg/m3
ρc
234.95 ± 3.51
kg/m3
NIST
ρc
232.84 ± 2.10
kg/m3
NIST
Inp
[478.00; 500.00]
Inp
489.00
NIST
Inp
481.10
NIST
Inp
485.00
NIST
Inp
483.00
NIST
Inp
480.00
NIST
Inp
488.80
NIST
Inp
489.00
NIST
Inp
491.00
NIST
Inp
488.00
NIST
Inp
488.00
NIST
Inp
489.00
NIST
Inp
481.30
NIST
Inp
488.80
NIST
Inp
Outlier 496.00
NIST
Inp
489.00
NIST
Inp
489.00
NIST
Inp
492.00
NIST
Inp
486.00
NIST
Inp
481.60
NIST
Inp
482.00
NIST
Inp
481.50
NIST
Inp
481.60
NIST
Inp
482.00
NIST
Inp
482.00
NIST
Inp
486.80
NIST
Inp
482.50
NIST
Inp
482.00
NIST
Inp
482.00
NIST
Inp
481.07
NIST
Inp
491.00
NIST
Inp
482.00
NIST
Inp
481.00
NIST
Inp
481.00
NIST
Inp
483.00
NIST
Inp
483.00
NIST
Inp
490.00
NIST
Inp
483.00
NIST
Inp
479.00
NIST
Inp
485.00
NIST
Inp
491.00
NIST
Inp
491.00
NIST
Inp
486.50
NIST
Inp
487.00
NIST
Inp
483.39
NIST
Inp
483.67
NIST
Inp
483.00
NIST
Inp
478.00
NIST
Inp
481.30
NIST
Inp
482.00
NIST
Inp
492.00
NIST
Inp
482.00
NIST
Inp
Outlier 500.00
NIST
Inp
488.00
NIST
Inp
489.00
NIST
Inp
491.00
NIST
Inp
492.00
NIST
Inp
492.00
NIST
Inp
Outlier 495.00
NIST
Inp
488.00
NIST
Inp
483.00
NIST
Inp
483.00
NIST
Inp
487.00
NIST
Inp
483.00
NIST
Inp
486.00
NIST
Inp
483.00
NIST
Inp
483.00
NIST
Inp
483.00
NIST
Inp
491.00
NIST
Inp
479.00
NIST
Inp
489.00
NIST
Inp
484.00
NIST
Inp
488.00
NIST
Inp
488.00
NIST
Inp
483.00
NIST
Inp
488.00
NIST
Inp
488.00
NIST
Inp
483.00
NIST
Inp
485.00
NIST
Inp
492.00
NIST
Inp
492.00
NIST
Inp
492.00
NIST
Inp
479.00
NIST
Inp
483.00
NIST
Inp
484.00
NIST
Inp
488.00
NIST
Inp
492.00
NIST
I
[523.00; 534.00]
I
532.00
NIST
I
523.00
NIST
I
534.00
NIST
S°liquid
[262.55; 262.60]
J/mol×K
S°liquid
262.60
J/mol×K
NIST
S°liquid
262.60
J/mol×K
NIST
S°liquid
262.55
J/mol×K
NIST
Tboil
303.11
K
KDB
Tc
[463.77; 466.59]
K
Tc
464.80
K
KDB
Tc
Outlier 466.59
K
Vapor P...
Tc
464.80 ± 0.50
K
NIST
Tc
464.70
K
NIST
Tc
465.10 ± 0.30
K
NIST
Tc
463.77 ± 0.20
K
NIST
Tc
464.74 ± 0.03
K
NIST
Tfus
[107.75; 108.08]
K
Tfus
107.90
K
KDB
Tfus
108.08
K
Aq. Sol...
Tfus
107.75 ± 0.20
K
NIST
Tfus
107.78 ± 0.20
K
NIST
Tfus
107.88 ± 0.10
K
NIST
Ttriple
[5.80; 108.01]
K
Ttriple
108.01 ± 0.00
K
NIST
Ttriple
107.79 ± 0.00
K
NIST
Ttriple
5.80 ± 0.01
K
NIST
Ttriple
107.90 ± 0.50
K
NIST
Vc
[0.298; 0.298]
m3 /kmol
Vc
0.298
m3 /kmol
KDB
Vc
0.298
m3 /kmol
NIST
Zc
0.2748820
KDB
Zra
0.27
KDB
Temperature Dependent Properties
Property
Value
Unit
Temperature (K)
Source
Cp,gas
[112.34; 157.69]
J/mol×K
[311.09; 471.08]
Cp,gas
112.34 ± 0.33
J/mol×K
311.09
NIST
Cp,gas
126.15 ± 0.38
J/mol×K
357.51
NIST
Cp,gas
139.08 ± 0.42
J/mol×K
402.32
NIST
Cp,gas
148.41 ± 0.45
J/mol×K
436.01
NIST
Cp,gas
157.69 ± 0.47
J/mol×K
471.08
NIST
Cp,liquid
[154.00; 155.31]
J/mol×K
[294.00; 298.15]
Cp,liquid
154.30
J/mol×K
294.00
NIST
Cp,liquid
154.87
J/mol×K
298.15
NIST
Cp,liquid
154.00
J/mol×K
298.15
NIST
Cp,liquid
155.31
J/mol×K
298.15
NIST
η
[0.0001949; 0.0027701]
Pa×s
[144.35; 310.48]
η
0.0027701
Pa×s
144.35
Joback Calculated Property
η
0.0012467
Pa×s
172.04
Joback Calculated Property
η
0.0007001
Pa×s
199.73
Joback Calculated Property
η
0.0004525
Pa×s
227.42
Joback Calculated Property
η
0.0003215
Pa×s
255.10
Joback Calculated Property
η
0.0002442
Pa×s
282.79
Joback Calculated Property
η
0.0001949
Pa×s
310.48
Joback Calculated Property
Δfus H
[5.81; 5.94]
kJ/mol
[107.80; 108.02]
Δfus H
5.88
kJ/mol
107.80
NIST
Δfus H
5.81
kJ/mol
107.90
NIST
Δfus H
5.81
kJ/mol
107.90
NIST
Δfus H
5.81
kJ/mol
107.90
NIST
Δfus H
5.81
kJ/mol
107.90
NIST
Δfus H
5.94
kJ/mol
108.02
NIST
Δvap H
[25.20; 29.10]
kJ/mol
[264.50; 340.50]
Δvap H
29.10
kJ/mol
264.50
NIST
Δvap H
26.20 ± 0.10
kJ/mol
284.00
NIST
Δvap H
26.30
kJ/mol
290.50
NIST
Δvap H
26.70
kJ/mol
295.00
NIST
Δvap H
25.20 ± 0.10
kJ/mol
303.00
NIST
Δvap H
25.20
kJ/mol
303.10
NIST
Δvap H
26.90
kJ/mol
303.50
NIST
Δvap H
25.20
kJ/mol
305.80
KDB
Δvap H
25.70
kJ/mol
340.50
NIST
n 0
1.36835
298.15
KDB
ρl
640.00
kg/m3
293.00
KDB
Δfus S
[53.82; 55.00]
J/mol×K
[107.80; 108.02]
Δfus S
54.56
J/mol×K
107.80
NIST
Δfus S
53.82
J/mol×K
107.90
NIST
Δfus S
53.82
J/mol×K
107.90
NIST
Δfus S
55.00
J/mol×K
107.90
NIST
Δfus S
54.97
J/mol×K
108.02
NIST
γ
0.02
N/m
298.20
KDB
λ
[0.11; 0.13]
W/m×K
[257.36; 301.75]
λ
0.13
W/m×K
257.36
Thermal...
λ
0.13
W/m×K
257.67
Thermal...
λ
0.13
W/m×K
257.93
Thermal...
λ
0.12
W/m×K
276.47
Thermal...
λ
0.12
W/m×K
276.82
Thermal...
λ
0.12
W/m×K
277.07
Thermal...
λ
0.11
W/m×K
294.04
Thermal...
λ
0.11
W/m×K
294.42
Thermal...
λ
0.11
W/m×K
294.66
Thermal...
λ
0.11
W/m×K
301.07
Thermal...
λ
0.11
W/m×K
301.46
Thermal...
λ
0.11
W/m×K
301.75
Thermal...
Datasets
Mass density, kg/m3
Fixed
Measured
Temperature, K - Liquid
Pressure, kPa - Liquid
Mass density, kg/m3 - Liquid
283.48
100.00
650.3
283.48
500.00
650.8
283.48
1000.00
651.6
283.48
3000.00
654.0
283.49
5000.00
656.3
283.49
10000.00
661.8
283.49
15000.00
666.9
283.49
20000.00
671.7
283.49
25000.00
676.2
283.49
30000.00
680.4
283.49
35000.00
684.5
283.49
40000.00
688.4
283.49
45000.00
692.1
283.49
50000.00
695.7
283.49
55000.00
699.1
283.49
60000.00
702.5
283.48
70000.00
708.8
283.48
80000.00
714.8
283.49
90000.00
720.4
283.49
100000.00
725.7
293.42
100.00
640.1
293.42
500.00
640.7
293.42
1000.00
641.4
293.42
3000.00
644.0
293.42
5000.00
646.5
293.42
10000.00
652.4
293.43
15000.00
657.9
293.43
20000.00
663.0
293.43
25000.00
667.8
293.44
30000.00
672.3
293.43
35000.00
676.7
293.42
40000.00
680.8
293.43
45000.00
684.7
293.43
50000.00
688.4
293.42
55000.00
692.0
293.42
60000.00
695.5
293.42
70000.00
702.2
293.42
80000.00
708.3
293.42
90000.00
714.1
293.42
100000.00
719.6
303.33
100.00
629.8
303.33
1000.00
631.1
303.33
3000.00
634.0
303.34
5000.00
636.7
303.34
10000.00
643.1
303.34
15000.00
649.0
303.34
20000.00
654.5
303.34
25000.00
659.6
303.34
30000.00
664.4
303.33
35000.00
668.9
303.34
40000.00
673.2
303.34
45000.00
677.3
303.34
50000.00
681.2
303.35
55000.00
685.0
303.35
60000.00
688.6
303.35
70000.00
695.6
303.34
80000.00
702.0
303.34
90000.00
707.9
303.35
100000.00
713.6
313.27
500.00
620.4
313.28
1000.00
621.3
313.27
3000.00
624.5
313.27
5000.00
627.5
313.27
10000.00
634.4
313.28
15000.00
640.8
313.28
20000.00
646.7
313.28
25000.00
652.1
313.28
30000.00
657.2
313.29
35000.00
661.9
313.29
40000.00
666.6
313.28
45000.00
670.8
313.28
50000.00
674.9
313.29
55000.00
678.8
313.29
60000.00
682.6
313.28
70000.00
689.9
313.29
80000.00
696.4
313.29
90000.00
702.6
313.29
100000.00
708.4
323.18
500.00
608.6
323.18
1000.00
609.3
323.18
3000.00
612.8
323.18
5000.00
616.1
323.19
10000.00
623.7
323.19
15000.00
630.6
323.19
20000.00
636.9
323.19
25000.00
642.7
323.19
30000.00
648.1
323.19
35000.00
653.1
323.19
40000.00
657.9
323.19
45000.00
662.4
323.19
50000.00
666.7
323.19
55000.00
670.8
323.19
60000.00
674.7
323.19
70000.00
682.2
323.19
80000.00
689.1
323.19
90000.00
695.4
323.19
100000.00
701.5
333.04
500.00
597.2
333.04
1000.00
598.1
333.04
3000.00
601.9
333.04
5000.00
605.6
333.04
10000.00
613.9
333.05
15000.00
621.4
333.05
20000.00
628.1
333.05
25000.00
634.3
333.05
30000.00
640.0
333.05
35000.00
645.3
333.05
40000.00
650.4
333.05
45000.00
655.1
333.05
50000.00
659.6
333.05
55000.00
663.9
333.05
60000.00
668.0
333.05
70000.00
675.8
333.06
80000.00
683.0
333.06
90000.00
689.6
333.05
100000.00
695.8
342.94
500.00
585.8
342.94
1000.00
586.8
342.95
3000.00
591.2
342.95
5000.00
595.3
342.95
10000.00
604.4
342.96
15000.00
612.5
342.96
20000.00
619.8
342.96
25000.00
626.3
342.96
30000.00
632.4
342.96
35000.00
638.1
342.96
40000.00
643.4
342.96
45000.00
648.4
342.96
50000.00
653.0
342.96
55000.00
657.5
342.96
60000.00
661.8
342.95
70000.00
669.9
342.95
80000.00
677.2
342.94
90000.00
684.0
342.95
100000.00
690.4
352.82
500.00
574.2
352.82
1000.00
575.6
352.82
3000.00
580.5
352.82
5000.00
585.1
352.82
10000.00
595.2
352.83
15000.00
603.9
352.83
20000.00
611.7
352.83
25000.00
618.7
352.83
30000.00
625.2
352.83
35000.00
631.2
352.83
40000.00
636.7
352.83
45000.00
641.9
352.83
50000.00
646.9
352.83
55000.00
651.5
352.84
60000.00
655.9
352.83
70000.00
664.3
352.83
80000.00
671.9
352.83
90000.00
679.0
352.83
100000.00
685.6
362.67
500.00
560.5
362.67
1000.00
561.8
362.67
3000.00
567.4
362.68
5000.00
572.6
362.68
10000.00
583.8
362.68
15000.00
593.3
362.68
20000.00
601.7
362.68
25000.00
609.2
362.68
30000.00
616.1
362.68
35000.00
622.4
362.68
40000.00
628.2
362.68
45000.00
633.7
362.68
50000.00
638.9
362.68
55000.00
643.7
362.68
60000.00
648.3
362.68
70000.00
657.1
362.67
80000.00
664.9
362.68
90000.00
672.2
362.67
100000.00
679.0
Reference
Correlations
Similar Compounds
Find more compounds similar to 1-Pentene .
Mixtures
Sources
KDB Pure (Korean Thermophysical Properties Databank)
KDB Vapor Pressure Data
Crippen Method
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
Measurement and prediction of activity coefficients at infinite dilution ( ), vapor.liquid equilibria (VLE) and excess enthalpies (HE) of binary systems with 1,1-dialkyl-pyrrolidinium bis(trifluoromethylsulfonyl)imide using mod. UNIFAC (Dortmund)
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
Measurements of different thermodynamic properties of systems containing ionic liquids and correlation of these properties using modified UNIFAC (Dortmund)
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
New ionic liquid [P4,4,4,4][NTf2] in bio-butanol extraction on investigation of limiting activity coefficients
Ammonium ionic liquids in extraction of bio-butan-1-ol from water phase using activity coefficients at infinite dilution
Measurements of activity coefficients at infinite dilution for organic solutes in two quaternary ammonium-based ionic liquids [DDA][ClO4] and [DDA][BF4]
Application of trihexyltetradecylphosphonium dicyanamide ionic liquid for various types of separations problems: Activity coefficients at infinite dilution measurements utilizing GLC method
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)
Measurements of activity coefficients at infinite dilution of aromatic and aliphatic hydrocarbons, alcohols, and water in the new ionic liquid [EMIM][SCN] using GLC
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
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 for solutes in the trioctylmethylammonium bis(trifluoromethylsulfonyl)imide ionic liquid using gas liquid chromatography
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 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
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
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
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
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
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
Use of water in aiding olefin/paraffin (liquid + liquid) extraction via complexation with a silver bis(trifluoromethylsulfonyl)imide salt
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, physicochemical and thermodynamic properties for organic solutes and water in the ionic liquid ethyl-dimethyl-(2-methoxyethyl)ammonium trifluorotris-(perfluoroethyl)phosphate
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
Thermodynamics and limiting activity coefficients measurements for organic solutes and water in the ionic liquid 1-dodecyl-3-methylimidzolium bis(trifluoromethylsulfonyl) imide
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
Activity Coefficients at Infinite Dilution of Organic Solutes and Water in Tributylethylphosphonium Diethylphosphate Using Gas Liquid Chromatography: Thermodynamic Properties of Mixtures Containing Ionic Liquids
Vapor Pressures and Vapor Liquid Critical Properties of Four Pentene Isomers
Liquid Density of n-Pentene, n-Hexene, and n-Heptene at Temperatures from 283.15 to 363.15 K and Pressures up to 100 MPa
Assessment of Pyrrolidinium-Based Ionic Liquid for the Separation of Binary Mixtures Based on Activity Coefficients at Infinite Dilution
Thermal Conductivity and Thermal Diffusivity of Twenty-Nine Liquids: Alkenes, Cyclic (Alkanes, Alkenes, Alkadienes, Aromatics), and Deuterated Hydrocarbons
Thermodynamic Properties of Mixtures Containing Ionic Liquids. 5. Activity Coefficients at Infinite Dilution of Hydrocarbons, Alcohols, Esters, and Aldehydes in 1-Methyl-3-butyl-imidazolium Bis(trifluoromethyl-sulfonyl) Imide Using Gas-Liquid Chromatography
Thermodynamic Properties of Mixtures Containing Ionic Liquids. 6. Activity Coefficients at Infinite Dilution of Hydrocarbons, Alcohols, Esters, and Aldehydes in 1-Methyl-3-octyl-imidazolium Tetrafluoroborate Using Gas-Liquid Chromatography
Thermodynamic Properties of Mixtures Containing Ionic Liquids. 8. Activity Coefficients at Infinite Dilution of Hydrocarbons, Alcohols, Esters, and Aldehydes in 1-Hexyl-3-methylimidazolium Bis(trifluoromethylsulfonyl) Imide Using Gas-Liquid Chromatography
Thermodynamic Properties of Mixtures Containing Ionic Liquids. 9. Activity Coefficients at Infinite Dilution of Hydrocarbons, Alcohols, Esters, and Aldehydes in Trimethyl-butylammonium Bis(trifluoromethylsulfonyl) Imide Using Gas-Liquid Chromatography and Static Method
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
Activity Coefficients at Infinite Dilution for Hydrocarbons in Fatty Alcohols Determined by Gas-Liquid Chromatography
Activity Coefficients at Infinite Dilution by GLC in Alkanediamines as Stationary Phases
Enhancing liquid-phase olefin-paraffin separations using novel silver-based ionic liquids
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
Activity Coefficients at Infinite Dilution Measurements for Organic Solutes and Water in the Ionic Liquid 1-Hexyl-3-methylimidazolium Thiocyanate
Joback Method
KDB
Aqueous Solubility Prediction Method
Estimated Solubility Method
McGowan Method
NIST Webbook
The Yaws Handbook of Vapor Pressure
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