Contents
Physical Properties
Temperature Dependent Properties
Pressure Dependent Properties
Datasets
Correlations
Similar Compounds
Mixtures
Sources
Physical Properties
Property
Value
Unit
Source
ω
0.2780
KDB
Δc H°liquid
[-1246.40; -1236.40]
kJ/mol
Δc H°liquid
-1236.40
kJ/mol
NIST
Δc H°liquid
-1246.40 ± 8.40
kJ/mol
NIST
μ
1.80
debye
KDB
η
0.0008270
Pa×s
Studies...
Δf G°
-73.90
kJ/mol
KDB
Rg
2.8510
KDB
Δf H°gas
[-132.00; -125.40]
kJ/mol
Δf H°gas
-129.80
kJ/mol
KDB
Δf H°gas
-132.00 ± 3.50
kJ/mol
NIST
Δf H°gas
-125.40 ± 1.00
kJ/mol
NIST
Δf H°gas
-129.00
kJ/mol
NIST
Δf H°liquid
[-169.70; -167.20]
kJ/mol
Δf H°liquid
-167.20 ± 3.50
kJ/mol
NIST
Δf H°liquid
-169.70
kJ/mol
NIST
Δfus H°
9.33
kJ/mol
Joback Calculated Property
Δvap H°
[34.40; 35.40]
kJ/mol
Δvap H°
35.22
kJ/mol
NIST
Δvap H°
35.20 ± 0.40
kJ/mol
NIST
Δvap H°
35.21 ± 0.05
kJ/mol
NIST
Δvap H°
Outlier 34.40
kJ/mol
NIST
Δvap H°
35.10 ± 0.10
kJ/mol
NIST
Δvap H°
35.20 ± 0.10
kJ/mol
NIST
Δvap H°
35.15 ± 0.01
kJ/mol
NIST
Δvap H°
35.40 ± 0.08
kJ/mol
NIST
IE
[11.04; 11.40]
eV
IE
11.07 ± 0.04
eV
NIST
IE
11.05
eV
NIST
IE
11.04
eV
NIST
IE
11.12 ± 0.05
eV
NIST
IE
11.40 ± 0.10
eV
NIST
IE
11.22 ± 0.02
eV
NIST
IE
11.39 ± 0.03
eV
NIST
log 10 WS
[-1.07; -1.06]
log 10 WS
-1.07
Aq. Sol...
log 10 WS
-1.06
Estimat...
log Poct/wat
1.464
Crippen Calculated Property
McVol
63.520
ml/mol
McGowan Calculated Property
Pc
[5380.00; 5400.00]
kPa
Pc
5400.00
kPa
KDB
Pc
5380.00 ± 50.00
kPa
NIST
ρc
440.37 ± 14.84
kg/m3
NIST
Inp
[586.00; 673.00]
Inp
645.40
NIST
Inp
648.20
NIST
Inp
656.20
NIST
Inp
654.00
NIST
Inp
650.10
NIST
Inp
647.70
NIST
Inp
644.80
NIST
Inp
632.00
NIST
Inp
630.00
NIST
Inp
632.00
NIST
Inp
638.00
NIST
Inp
641.00
NIST
Inp
633.00
NIST
Inp
645.00
NIST
Inp
640.00
NIST
Inp
629.00
NIST
Inp
641.00
NIST
Inp
620.00
NIST
Inp
641.00
NIST
Inp
643.00
NIST
Inp
648.00
NIST
Inp
660.00
NIST
Inp
628.60
NIST
Inp
606.00
NIST
Inp
607.00
NIST
Inp
610.00
NIST
Inp
632.00
NIST
Inp
Outlier 586.00
NIST
Inp
Outlier 595.00
NIST
Inp
621.00
NIST
Inp
627.00
NIST
Inp
632.00
NIST
Inp
632.00
NIST
Inp
632.00
NIST
Inp
633.00
NIST
Inp
630.00
NIST
Inp
632.00
NIST
Inp
632.00
NIST
Inp
Outlier 673.00
NIST
Inp
630.00
NIST
Inp
631.00
NIST
Inp
649.00
NIST
Inp
632.00
NIST
Inp
631.00
NIST
Inp
623.00
NIST
Inp
649.30
NIST
Inp
635.50
NIST
Inp
620.00
NIST
Inp
628.60
NIST
Inp
606.00
NIST
Inp
Outlier 595.00
NIST
Inp
632.00
NIST
Inp
649.00
NIST
Inp
635.50
NIST
I
[1045.00; 1093.00]
I
1085.00
NIST
I
1090.00
NIST
I
1080.00
NIST
I
1084.20
NIST
I
1084.96
NIST
I
1077.64
NIST
I
1076.00
NIST
I
1072.00
NIST
I
1093.00
NIST
I
1088.00
NIST
I
1088.00
NIST
I
1065.00
NIST
I
1065.00
NIST
I
1045.00
NIST
I
1045.00
NIST
I
1051.00
NIST
I
1088.00
NIST
I
1045.00
NIST
S°liquid
208.53
J/mol×K
NIST
Tboil
[356.59; 356.95]
K
Tboil
356.60
K
KDB
Tboil
356.70
K
Excess ...
Tboil
356.95
K
Excess ...
Tboil
356.59
K
Isobari...
Tboil
356.95
K
Vapor-L...
Tboil
356.95
K
Isobari...
Tc
[561.00; 563.15]
K
Tc
561.00
K
KDB
Tc
561.60 ± 0.40
K
NIST
Tc
561.20
K
NIST
Tc
563.15 ± 3.00
K
NIST
Tfus
[176.35; 241.15]
K
Tfus
237.60
K
KDB
Tfus
237.65
K
Aq. Sol...
Tfus
241.15 ± 1.00
K
NIST
Tfus
237.45
K
NIST
Tfus
237.50 ± 0.02
K
NIST
Tfus
237.85 ± 0.40
K
NIST
Tfus
237.28 ± 0.05
K
NIST
Tfus
237.70 ± 0.20
K
NIST
Tfus
Outlier 176.35 ± 0.40
K
NIST
Tfus
237.65 ± 0.30
K
NIST
Tfus
237.85 ± 0.30
K
NIST
Tfus
237.88 ± 0.20
K
NIST
Ttriple
[237.20; 237.60]
K
Ttriple
237.60 ± 0.30
K
NIST
Ttriple
237.20 ± 0.02
K
NIST
Vc
0.225
m3 /kmol
KDB
Zc
0.2604810
KDB
Zra
0.27
KDB
Temperature Dependent Properties
Property
Value
Unit
Temperature (K)
Source
Cp,gas
[81.34; 103.15]
J/mol×K
[320.02; 502.16]
Cp,gas
81.34
J/mol×K
320.02
Joback Calculated Property
Cp,gas
85.39
J/mol×K
350.38
Joback Calculated Property
Cp,gas
89.27
J/mol×K
380.73
Joback Calculated Property
Cp,gas
92.98
J/mol×K
411.09
Joback Calculated Property
Cp,gas
96.53
J/mol×K
441.45
Joback Calculated Property
Cp,gas
99.91
J/mol×K
471.80
Joback Calculated Property
Cp,gas
103.15
J/mol×K
502.16
Joback Calculated Property
Cp,liquid
[122.20; 131.00]
J/mol×K
[293.00; 300.00]
Cp,liquid
129.20
J/mol×K
293.00
NIST
Cp,liquid
124.30
J/mol×K
293.00
NIST
Cp,liquid
123.00
J/mol×K
298.00
NIST
Cp,liquid
129.70
J/mol×K
298.00
NIST
Cp,liquid
122.20
J/mol×K
298.00
NIST
Cp,liquid
129.54
J/mol×K
298.15
NIST
Cp,liquid
128.60
J/mol×K
298.15
NIST
Cp,liquid
128.99
J/mol×K
298.15
NIST
Cp,liquid
129.00
J/mol×K
298.15
NIST
Cp,liquid
128.99
J/mol×K
298.15
NIST
Cp,liquid
128.81
J/mol×K
298.15
NIST
Cp,liquid
128.90
J/mol×K
298.15
NIST
Cp,liquid
129.40
J/mol×K
298.15
NIST
Cp,liquid
131.00
J/mol×K
300.00
NIST
η
[0.0006269; 0.0008700]
Pa×s
[288.15; 313.15]
η
0.0008700
Pa×s
288.15
Densiti...
η
0.0008112
Pa×s
293.15
Densiti...
η
0.0007902
Pa×s
298.15
Thermop...
η
0.0007597
Pa×s
298.15
Densiti...
η
0.0007291
Pa×s
303.15
Thermop...
η
0.0007112
Pa×s
303.15
Densiti...
η
0.0006739
Pa×s
308.15
Thermop...
η
0.0006747
Pa×s
308.15
Densiti...
η
0.0006441
Pa×s
313.15
Thermop...
η
0.0006269
Pa×s
313.15
Densiti...
Δfus H
[2.85; 8.84]
kJ/mol
[175.00; 237.60]
Δfus H
2.85
kJ/mol
175.00
NIST
Δfus H
8.84
kJ/mol
237.20
NIST
Δfus H
8.83
kJ/mol
237.20
NIST
Δfus H
8.83
kJ/mol
237.20
NIST
Δfus H
8.75
kJ/mol
237.60
NIST
Δvap H
[31.10; 40.80]
kJ/mol
[273.00; 542.00]
Δvap H
33.91
kJ/mol
273.00
NIST
Δvap H
37.50
kJ/mol
307.50
NIST
Δvap H
34.80
kJ/mol
326.50
NIST
Δvap H
34.70
kJ/mol
329.00
NIST
Δvap H
34.80
kJ/mol
356.50
NIST
Δvap H
31.98
kJ/mol
356.60
NIST
Δvap H
32.01
kJ/mol
357.10
KDB
Δvap H
31.10
kJ/mol
446.00
NIST
Δvap H
31.10
kJ/mol
457.00
NIST
Δvap H
40.80
kJ/mol
542.00
NIST
Pvap
[5.37; 101.30]
kPa
[284.86; 356.59]
Pvap
5.38
kPa
284.86
Isother...
Pvap
5.37
kPa
284.87
Isother...
Pvap
8.96
kPa
294.83
Isother...
Pvap
8.95
kPa
294.84
Isother...
Pvap
20.75
kPa
298.15
Excess ...
Pvap
13.28
kPa
303.15
Phase E...
Pvap
14.33
kPa
304.82
Isother...
Pvap
14.32
kPa
304.82
Isother...
Pvap
21.05
kPa
313.15
Isother...
Pvap
20.75
kPa
313.15
Excess ...
Pvap
22.18
kPa
314.81
Isother...
Pvap
22.18
kPa
314.83
Isother...
Pvap
33.28
kPa
324.82
Isother...
Pvap
33.27
kPa
324.83
Isother...
Pvap
48.45
kPa
334.79
Isother...
Pvap
48.46
kPa
334.82
Isother...
Pvap
67.97
kPa
344.81
Isother...
Pvap
67.97
kPa
344.81
Isother...
Pvap
67.98
kPa
344.82
Isother...
Pvap
67.98
kPa
344.82
Isother...
Pvap
90.90
kPa
353.15
Phase E...
Pvap
94.94
kPa
354.89
Isother...
Pvap
94.95
kPa
354.89
Isother...
Pvap
94.94
kPa
354.89
Isother...
Pvap
94.95
kPa
354.89
Isother...
Pvap
95.50
kPa
355.15
Vapor-l...
Pvap
101.30
kPa
356.59
Isobari...
n 0
[1.41960; 1.44480]
[293.15; 298.15]
n 0
1.41960
293.15
Bubble ...
n 0
1.44480
293.15
Excess ...
n 0
1.41960
293.15
Vapor-L...
n 0
1.41960
293.15
Bubble ...
n 0
1.44450
293.15
Isobari...
n 0
1.41960
293.15
Activit...
n 0
1.44210
298.15
Vapour ...
n 0
1.44200
298.15
Thermod...
n 0
1.44210
298.15
Bubble ...
n 0
1.44210
298.15
Bubble-...
n 0
1.44210
298.15
Isother...
ρl
[1193.61; 1267.39]
kg/m3
[283.15; 333.15]
ρl
1267.39
kg/m3
283.15
Volumet...
ρl
1265.95
kg/m3
284.15
Volumet...
ρl
1264.50
kg/m3
285.15
Volumet...
ρl
1263.05
kg/m3
286.15
Volumet...
ρl
1261.60
kg/m3
287.15
Volumet...
ρl
1260.33
kg/m3
288.15
Densiti...
ρl
1260.35
kg/m3
288.15
Densiti...
ρl
1259.99
kg/m3
288.15
Volumet...
ρl
1260.15
kg/m3
288.15
Volumet...
ρl
1260.01
kg/m3
288.15
Densiti...
ρl
1259.99
kg/m3
288.15
Volumet...
ρl
1250.00
kg/m3
289.00
KDB
ρl
1258.70
kg/m3
289.15
Volumet...
ρl
1257.25
kg/m3
290.15
Volumet...
ρl
1255.80
kg/m3
291.15
Volumet...
ρl
1254.35
kg/m3
292.15
Volumet...
ρl
1253.00
kg/m3
293.15
Influen...
ρl
1252.77
kg/m3
293.15
Volumet...
ρl
1252.89
kg/m3
293.15
Volumet...
ρl
1252.82
kg/m3
293.15
Theoret...
ρl
1252.74
kg/m3
293.15
Thermop...
ρl
1252.77
kg/m3
293.15
Volumet...
ρl
1252.15
kg/m3
293.20
Isobari...
ρl
1251.44
kg/m3
294.15
Volumet...
ρl
1249.98
kg/m3
295.15
Volumet...
ρl
1248.52
kg/m3
296.15
Volumet...
ρl
1247.07
kg/m3
297.15
Volumet...
ρl
1246.70
kg/m3
298.15
Excess ...
ρl
1245.68
kg/m3
298.15
Isother...
ρl
1245.48
kg/m3
298.15
Densiti...
ρl
1245.75
kg/m3
298.15
Densiti...
ρl
1245.49
kg/m3
298.15
Volumet...
ρl
1245.49
kg/m3
298.15
Volumet...
ρl
1245.76
kg/m3
298.15
Densiti...
ρl
1245.59
kg/m3
298.15
Volumet...
ρl
1246.34
kg/m3
298.15
(Vapor ...
ρl
1245.80
kg/m3
298.15
Densiti...
ρl
1246.37
kg/m3
298.15
Hydroge...
ρl
1245.61
kg/m3
298.15
Volumet...
ρl
1246.00
kg/m3
298.15
Influen...
ρl
1244.15
kg/m3
299.15
Volumet...
ρl
1242.69
kg/m3
300.15
Volumet...
ρl
1241.22
kg/m3
301.15
Volumet...
ρl
1239.76
kg/m3
302.15
Volumet...
ρl
1238.70
kg/m3
303.15
Excess ...
ρl
1238.29
kg/m3
303.15
Volumet...
ρl
1238.18
kg/m3
303.15
Volumet...
ρl
1238.00
kg/m3
303.15
Influen...
ρl
1238.18
kg/m3
303.15
Volumet...
ρl
1238.27
kg/m3
303.15
Theoret...
ρl
1236.83
kg/m3
304.15
Volumet...
ρl
1235.36
kg/m3
305.15
Volumet...
ρl
1233.89
kg/m3
306.15
Volumet...
ρl
1232.42
kg/m3
307.15
Volumet...
ρl
1230.84
kg/m3
308.15
Volumet...
ρl
1230.83
kg/m3
308.15
Densiti...
ρl
1231.16
kg/m3
308.15
Densiti...
ρl
1231.00
kg/m3
308.15
Influen...
ρl
1230.84
kg/m3
308.15
Volumet...
ρl
1230.95
kg/m3
308.15
Volumet...
ρl
1230.50
kg/m3
308.15
Excess ...
ρl
1230.96
kg/m3
308.15
Volumet...
ρl
1231.21
kg/m3
308.15
Hydroge...
ρl
1231.15
kg/m3
308.15
Densiti...
ρl
1229.47
kg/m3
309.15
Volumet...
ρl
1228.00
kg/m3
310.15
Volumet...
ρl
1226.53
kg/m3
311.15
Volumet...
ρl
1225.05
kg/m3
312.15
Volumet...
ρl
1223.46
kg/m3
313.15
Volumet...
ρl
1223.46
kg/m3
313.15
Volumet...
ρl
1223.70
kg/m3
313.15
Excess ...
ρl
1223.53
kg/m3
313.15
Theoret...
ρl
1223.57
kg/m3
313.15
Volumet...
ρl
1222.09
kg/m3
314.15
Volumet...
ρl
1220.61
kg/m3
315.15
Volumet...
ρl
1219.13
kg/m3
316.15
Volumet...
ρl
1217.64
kg/m3
317.15
Volumet...
ρl
1216.56
kg/m3
318.15
Densiti...
ρl
1216.04
kg/m3
318.15
Densiti...
ρl
1216.16
kg/m3
318.15
Volumet...
ρl
1216.16
kg/m3
318.15
Volumet...
ρl
1214.55
kg/m3
318.15
Hydroge...
ρl
1216.35
kg/m3
318.15
Densiti...
ρl
1214.67
kg/m3
319.15
Volumet...
ρl
1213.18
kg/m3
320.15
Volumet...
ρl
1211.69
kg/m3
321.15
Volumet...
ρl
1210.20
kg/m3
322.15
Volumet...
ρl
1208.70
kg/m3
323.15
Volumet...
ρl
1208.61
kg/m3
323.15
Theoret...
ρl
1207.21
kg/m3
324.15
Volumet...
ρl
1205.71
kg/m3
325.15
Volumet...
ρl
1204.21
kg/m3
326.15
Volumet...
ρl
1202.71
kg/m3
327.15
Volumet...
ρl
1201.21
kg/m3
328.15
Volumet...
ρl
1199.70
kg/m3
329.15
Volumet...
ρl
1198.19
kg/m3
330.15
Volumet...
ρl
1196.69
kg/m3
331.15
Volumet...
ρl
1195.18
kg/m3
332.15
Volumet...
ρl
1193.61
kg/m3
333.15
Theoret...
ρl
1193.66
kg/m3
333.15
Volumet...
Δfus S
[16.20; 37.25]
J/mol×K
[175.00; 237.20]
Δfus S
36.80
J/mol×K
175.00
NIST
Δfus S
37.25
J/mol×K
237.20
NIST
Δfus S
16.20
J/mol×K
237.20
NIST
csound,fluid
[1117.75; 1212.92]
m/s
[293.15; 318.15]
csound,fluid
1212.92
m/s
293.15
Densiti...
csound,fluid
1193.60
m/s
298.15
Densiti...
csound,fluid
1194.44
m/s
298.15
Speeds ...
csound,fluid
1156.06
m/s
308.15
Speeds ...
csound,fluid
1117.75
m/s
318.15
Speeds ...
γ
[0.03; 0.03]
N/m
[293.15; 313.15]
γ
0.03
N/m
293.15
The add...
γ
0.03
N/m
293.20
KDB
γ
0.03
N/m
298.15
The add...
γ
0.03
N/m
303.15
The add...
γ
0.03
N/m
308.15
The add...
γ
0.03
N/m
313.15
The add...
Pressure Dependent Properties
Datasets
Viscosity, Pa*s (1)
Mass density, kg/m3 (1)
Viscosity, Pa*s
Fixed
Measured
Temperature, K - Liquid
Pressure, kPa - Liquid
Viscosity, Pa*s - Liquid
308.15
101.00
0.0006
Reference
Mass density, kg/m3
Fixed
Measured
Temperature, K - Liquid
Pressure, kPa - Liquid
Mass density, kg/m3 - Liquid
288.15
100.00
1259.9
288.15
500.00
1260.3
288.15
1000.00
1260.8
288.15
1500.00
1261.2
288.15
2000.00
1261.6
288.15
2500.00
1262.2
288.15
3100.00
1262.7
288.15
3600.00
1263.2
288.15
4100.00
1263.6
288.15
4600.00
1264.0
288.15
5100.00
1264.5
288.15
5600.00
1264.9
288.15
6100.00
1265.4
288.15
6600.00
1265.8
288.15
7100.00
1266.2
288.15
7600.00
1266.7
288.15
8100.00
1267.2
288.15
8600.00
1267.6
288.15
9200.00
1268.2
288.15
9600.00
1268.6
288.15
10100.00
1269.0
288.15
10600.00
1269.4
288.15
11100.00
1269.8
288.15
11600.00
1270.3
288.15
12100.00
1270.7
288.15
12600.00
1271.0
288.15
13100.00
1271.5
288.15
13600.00
1271.9
288.15
14100.00
1272.4
288.15
14700.00
1272.9
288.15
15200.00
1273.3
288.15
15700.00
1273.7
288.15
16300.00
1274.2
288.15
16800.00
1274.6
288.15
17200.00
1275.0
288.15
17700.00
1275.4
288.15
18200.00
1275.8
288.15
18600.00
1276.2
288.15
19000.00
1276.5
288.15
19400.00
1276.9
288.15
20000.00
1277.3
298.15
100.00
1245.5
298.15
500.00
1246.1
298.15
1000.00
1246.4
298.15
1500.00
1246.9
298.15
2000.00
1247.4
298.15
2500.00
1247.8
298.15
3100.00
1248.5
298.15
3600.00
1248.9
298.15
4100.00
1249.4
298.15
4600.00
1249.9
298.15
5100.00
1250.4
298.15
5600.00
1250.9
298.15
6100.00
1251.4
298.15
6600.00
1251.9
298.15
7100.00
1252.3
298.15
7600.00
1252.9
298.15
8100.00
1253.2
298.15
8600.00
1253.8
298.15
9200.00
1254.4
298.15
9600.00
1254.9
298.15
10000.00
1255.1
298.15
10600.00
1255.9
298.15
11100.00
1256.4
298.15
11600.00
1256.7
298.15
12100.00
1257.3
298.15
12600.00
1257.6
298.15
13100.00
1258.0
298.15
13600.00
1258.5
298.15
14200.00
1259.0
298.15
14700.00
1259.4
298.15
15200.00
1260.0
298.15
15700.00
1260.5
298.15
16200.00
1260.8
298.15
16700.00
1261.4
298.15
17300.00
1261.9
298.15
17800.00
1262.4
298.15
18300.00
1262.8
298.15
18800.00
1263.3
298.15
19200.00
1263.7
298.15
19700.00
1264.1
298.15
20200.00
1264.5
308.15
100.00
1231.0
308.15
500.00
1231.4
308.15
1000.00
1232.0
308.15
1500.00
1232.5
308.15
2000.00
1233.0
308.15
2500.00
1233.5
308.15
3100.00
1234.2
308.15
3600.00
1234.7
308.15
4100.00
1235.2
308.15
4600.00
1235.7
308.15
5100.00
1236.2
308.15
5600.00
1236.9
308.15
6100.00
1237.3
308.15
6600.00
1237.9
308.15
7100.00
1238.4
308.15
7600.00
1238.6
308.15
8100.00
1239.3
308.15
8600.00
1239.8
308.15
9200.00
1240.4
308.15
9600.00
1240.9
308.15
10100.00
1241.3
308.15
10600.00
1241.8
308.15
11100.00
1242.3
308.15
11600.00
1242.8
308.15
12100.00
1243.4
308.15
12600.00
1243.8
308.15
13100.00
1244.2
308.15
13600.00
1244.7
308.15
14200.00
1245.3
308.15
14700.00
1245.8
308.15
15200.00
1246.4
308.15
15700.00
1246.8
308.15
16200.00
1247.2
308.15
16700.00
1247.7
308.15
17200.00
1248.2
308.15
17800.00
1248.7
308.15
18300.00
1249.2
308.15
18800.00
1249.6
308.15
19200.00
1250.1
308.15
19700.00
1250.6
308.15
20200.00
1251.0
318.15
100.00
1216.4
318.15
500.00
1216.7
318.15
1000.00
1217.4
318.15
1500.00
1218.0
318.15
2000.00
1218.5
318.15
2500.00
1219.1
318.15
3100.00
1219.8
318.15
3600.00
1220.3
318.15
4100.00
1220.9
318.15
4600.00
1221.4
318.15
5100.00
1222.0
318.15
5600.00
1222.6
318.15
6100.00
1223.1
318.15
6600.00
1223.6
318.15
7100.00
1224.1
318.15
7600.00
1224.7
318.15
8100.00
1225.2
318.15
8600.00
1225.8
318.15
9200.00
1226.3
318.15
9600.00
1226.9
318.15
10100.00
1227.5
318.15
10600.00
1227.9
318.15
11100.00
1228.4
318.15
11600.00
1229.0
318.15
12100.00
1229.5
318.15
12500.00
1230.0
318.15
13100.00
1230.6
318.15
13600.00
1231.0
318.15
14200.00
1231.6
318.15
14700.00
1232.1
318.15
15200.00
1232.7
318.15
15600.00
1233.1
318.15
16300.00
1233.8
318.15
16800.00
1234.2
318.15
17300.00
1234.8
318.15
17800.00
1235.2
318.15
18200.00
1235.5
318.15
18900.00
1236.2
318.15
19200.00
1236.5
318.15
19700.00
1237.1
318.15
20200.00
1237.5
Reference
Correlations
Similar Compounds
Find more compounds similar to Ethane, 1,2-dichloro- .
Mixtures
Ethyl Acetate + Ethane, 1,2-dichloro-
Ethane, 1,2-dichloro- + 1-Hexanol
Phenol, 2-methyl- + Ethane, 1,2-dichloro-
Ethane, 1,2-dibromo- + Ethane, 1,2-dichloro-
Formamide, N,N-dimethyl- + Ethane, 1,2-dichloro-
Cyclohexanone + Ethane, 1,2-dichloro-
Ethyl ether + Ethane, 1,2-dichloro-
Diisopropyl ether + Ethane, 1,2-dichloro-
Propane, 2-methoxy-2-methyl- + Ethane, 1,2-dichloro-
2-Propenenitrile + Ethane, 1,2-dichloro-
Ethane, 1,2-dichloro- + Methane, nitro-
Ethane, 1,2-dichloro- + Phosphoramidic acid, phenyl-, diphenyl ester
Ethane, 1,2-dichloro- + 1,4-Dioxane
1-Propanol + Ethane, 1,2-dichloro-
Butanoic acid, ethyl ester + Ethane, 1,2-dichloro-
Pentanoic acid, ethyl ester + Ethane, 1,2-dichloro-
Ethyl formate + Ethane, 1,2-dichloro-
Propanoic acid, ethyl ester + Ethane, 1,2-dichloro-
Ethane, 1,2-dichloro- + Cyclopentanone
Formic acid, butyl ester + Ethane, 1,2-dichloro-
Find more mixtures with Ethane, 1,2-dichloro- .
Sources
KDB Pure (Korean Thermophysical Properties Databank)
KDB Vapor Pressure Data
Crippen Method
Temperature and Pressure Dependence of the Volumetric Properties of Binary Liquid Mixtures Containing Dihaloalkanes
Densities, Excess Molar Volumes, Ultrasonic Speeds, and Isentropic Compressibilities of Hexan-1-ol with 1,2-Dichloroethane, 1,2-Dibromoethane, and 1,1,2,2-Tetrachloroethene at (293.15 and 298.15) K
Bubble points of some binary mixtures formed by o-cresol at 95.75 kPa
Isobaric vapour liquid equilibria for binary mixtures of 1,2-dibromoethane with 1,2-dichloroethane, trichloromethane, and 1,1,2,2-tetrachloroethane at atmospheric pressure
Excess Gibbs energies of selected binary mixtures formed by N,N-dimethyl formamide at 95.5 kPa
Co-solvent effects in LLE of 1-hydroxyethyl-3-methylimidazolium based ionic liquids + 2-propanol + dichloromethane or 1,2-dichloroethane
A simple apparatus for data solubility determination
Vapour pressure and excess Gibbs energy of binary 1,2-dichloroethane + cyclohexanone, chloroform + cyclopentanone and chloroform + cyclohexanone mixtures at temperatures from 298.15 to 318.15 K
Isothermal vapour liquid equilibria of binary systems of 1,2-dichloroethane with ethers
Vapor-liquid equilibrium and excess Gibbs energies of some binary mixtures of acrylonitrile at 95.5 kPa
Isothermal vapour liquid equilibria for 1,2-dichloroethane + nitromethane and + nitroethane binary systems at temperatures between 333.15 and 353.15K
Using binary mixtures of dicationic ionic liquids for determination ofactivity coefficients at infinite dilution by gas-liquid chromatography
Determination and correlation of solubilities of 1,2-bis(2-oxo-5,5-dimethyl-1,3,2-dioxyphosphacyclohexyl-2-imino) ethane in selected solvents
Speeds of sound, isentropic compressibilities and refractive indices for some binary mixtures of nitromethane with chloroalkane at temperatures from 298.15 to 318.15 K. Comparison with theories
Solid-liquid equilibrium of diphenyl anilinophosphonate in the different organic solvents
Hydrogen bond interactions in the blends of 1,4-dioxane with some 1, 2- disubstituted ethanes at T = (298.15, 308.15 and 318.15) K
Measurements of activity coefficients at infinite dilution for organic solutes in two quaternary ammonium-based ionic liquids [DDA][ClO4] and [DDA][BF4]
(Vapor + liquid) equilibria for the binary mixtures (1-propanol + dibromomethane, or + bromochloromethane, or + 1,2-dichloroethane or +1-bromo-2-chloroethane) at T = 313.15 K.
Excess volumes and speeds of sound of mixtures of 1,2-dibromoethane with chlorinated ethanes and ethenes at 303.15 K
Thermodynamic study of (alkyl esters + a,x-alkyl dihalides) I: HE and V E for 25 binary mixtures {xCu-1H2u-1CO2C2H5 + (1-x)a,x-ClCH2(CH2)v-2CH2Cl}, where u = 1 to 5, a = 1 and v = x = 2 to 6
Isothermal (vapour + liquid) equilibria in the binary mixtures (1,2-dichloroethane and 1,1,1-trichloroethane with cyclopentanone) within the temperature range (298.15 to 313.15) K
Thermodynamic study of (alkyl esters + a,x-alkyl dihalides)III. HE m and V E m for 20 binary mixtures {xCu-1H2u-1CO2C4H9 + (1 - x)a,x-ClCH2(CH2)v-2CH2Cl}, where u = 1 to 4, a = 1 and v = x = 2 to 6
Bubble points of the binary mixtures formed by ethylbenzene with some chloroaliphatics and substituted benzenes at p = 94.7 kPa
Densities and viscosities of binary liquid mixtures of N-methylacetamide with some chloroethanes and chloroethenes at T = 308.15 K
Thermodynamic study of (alkyl esters + a,x-alkyl dihalides) V. Hex and Vex for 25 binary mixtures {xCu-1H2u-1CO2CH3 + (1-x)a,x-ClCH2(CH2)v-2CH2Cl}, where u = 1 to 5, a = 1 and v = x = 2 to 6
Isobaric (vapour + liquid) equilibria data for the binary systems {1,2-dichloroethane (1) + toluene (2)} and {1,2-dichloroethane (1) + acetic acid (2)} at atmospheric pressure
Activity coefficients and excess Gibbs free energy of some binary mixtures formed by p-cresol at 95.23 kPa
Excess molar enthalpies and (vapour + liquid) equilibria for mixtures containing N,N-dialkylamides and a,x-dichloroalkanes
Excess enthalpies and isothermal (vapour + liquid) equilibria of (1-methyl-2-pyrrolidone + 1-chloroalkane or +,?-dichloroalkane) mixtures
Thermodynamic study of (alkyl esters + a,x-alkyl dihalides) VII. HE m and VE m for 20 binary mixtures {xCu 1H2u 1CO2C3H7 + (1 x)a,x-ClCH2(CH2)v 2CH2Cl}, where u = 1 to 4, a = 1 and v = x = 2 to 6. An analysis of behavior using the COSMO-RS methodology
Studies on thermodynamic properties of binary mixtures of hexan-1-ol with halogenated compounds at T = (308.15 and 313.15) K
Thermophysical and sonochemical behaviour of binary mixtures of decan-1-ol with halohydrocarbons at (T = 293.15 and 313.15) K
Activity coefficient at infinite dilution measurements for organic solutes (polar and non-polar) in fatty compounds: Saturated fatty acids
Activity coefficient at infinite dilution measurements for organic solutes (polar and non-polar) in fatty compounds Part II: C18 fatty acids
(Liquid + liquid) equilibria of quaternary systems containing water, phosphoric acid, dichloromethane and 1,2-dichloroethane
Activity coefficients at infinite dilution of organic solutes in 1-hexyl-3- methylimidazolium trifluoroacetate and influence of interfacial adsorption using gas liquid chromatography
Salting-out effect on the (liquid + liquid) equilibrium for the ternary systems (water + phosphoric acid + dichloromethane or 1,2-dichloroethane)
Solvation parameter model and thermodynamic parameters in a dicationic ionic liquid based on pyrrolidinium
Theoretical and experimental study on volumetric and electromagnetic properties of binary systems consisting of 1,2-dichloroethane with benzene and its derivatives at T = (293.15 to 333.15) K
Solubility of 4-methyl-2-nitroaniline in fourteen organic solvents from T = (278.15 to 313.15) K and mixing properties of solutions
Influence of chlorine atom on interactions between halo-hydrocarbons and 1-nonanol: Density and speed of sound measurements
The additivity of surface and volumetric properties of alpha,omega-dihalogenoalkanes
Excess molar enthalpies of dimethylsulfoxide with chloroethanes and chloroethenes at 298.15K
Volumetric properties of binary liquid mixtures of alcohols with 1,2-dichloroethane at different temperatures and atmospheric pressure
Volumetric properties of binary liquid mixtures of ketones with chloroalkanes at different temperatures and atmospheric pressure
Volumetric and electromagnetic properties of binary mixtures consist of benzene derivatives at different temperature and ternary mixtures with 1,2-dichloroethane at T = 293.15 K with application of the Prigogine-Flory-Patterson theory and PC-SAFT
Solubility Measurement and Correlation for e-2,4,6,8,10,12-Hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane in Five Organic Solvents at Temperatures between 283.15 and 333.15 K and Different Chloralkane + Ethyl Acetate Binary Solvents at Temperatures between 283.15 and 323.15 K
Solubility Measurement and the Correlation of 1-Naphthaleneacetic Acid in Pure and Methanol + Water Binary Solvents from T = (278.25 to 323.55) K
Solid Liquid Phase Equilibrium of N,N'-Piperazinebis(neopentylglycol)phosphoramidate in Selected Solvents from T = (293.15 to 333.15) K
Synthesis and Solubility of 5,5-Dimethyl-2-(phenyl(phenylamino)methyl)-1,3,2-dioxaphosphinane 2-oxide in Selected Solvents between 278.15 K and 347.15 K
Measurement and Correlation of Solubility of Resorcinol Bis(cyclic 2,2-dimethyl-1,3-propanediol phosphate) in Selected Solvents from T = 293.15 to 333.15 K
Solubility Measurement and Thermodynamic Modeling of N-(4-Methylphenyl-Z-3-chloro-2-(phenylthio)propenamide in 12 Pure Solvents at Temperatures Ranging from 278.15 to 318.15 K
Solution Thermodynamics of Benzotriazole in Different Pure Solvents
Isothermal Vapor-Liquid Equilibria and Excess Gibbs Energies for Binary Mixtures of Cyclic Ethers with 1,2-Dichloroethane
Densities and Excess Molar Volumes for the Binary and Ternary Systems of (1,4-Dioxane, 1-Propanol or 2-Propanol, and 1,2-Dichloroethane) at T = (288.15 to 318.15) K. Experimental Measurements and Prigogine-Flory-Patterson Modeling
Isobaric Vapor-Liquid Equilibrium for the Binary Systems of 1,2-Dichloroethane + sec-Butyl Acetate, n-Propyl Acetate, and tert-Butyl Acetate at 101.3 kPa
Physico-Chemical Properties of LiFSI Solutions I. LiFSI with Valeronitrile, Dichloromethane, 1,2-Dichloroethane, and 1,2-Dichlorobenzene
Thermodynamic Parameters of a New Synthesized Tricationic Ionic Liquid Stationary Phase by Inverse Gas Chromatography
Thermodynamic Studies of Solubility for Naphthalene in 12 Solvents from 279 to 330 K
Measurement and Correlation of Solubilities of 5,5'-Dinitramino-3,3'-bi[1,2,4-triazolate] Carbohydrazide Salt (CBNT) in Various Pure Solvents and a Binary Mixture (Dimethyl Sulfoxide + Water) from 298.15 to 343.15 K
Determination and Correlation of Solubilities of 1,3,5-Trifluoro-2,4,6-triiodobenzene in Different Solvents from 289.25 to 332.15 K
Isobaric Vapor Liquid Equilibrium Data for the 1,2-Dichloroethane-1-Butanol System
Heat Capacities of alpha,omega-Dichloroalkanes at Temperatures from 284.15 K to 353.15 K and a Group Additivity Analysis
Vapor-Liquid Equilibria and Excess Molar Enthalpies for N-Methyl-2-pyrrolidone with Chloroethanes and Chloroethenes
Bubble Temperature Measurements on the Binary Mixtures of n-Heptane or Nitrobenzene or Chlorobenzene with Some Chloroethanes and Chloroethylenes at (94.6 to 95.8) kPa
Bubble-Temperature Measurements on Some Binary Mixtures Formed by Tetrahydrofuran or Amyl Alcohol with Hydrocarbons, Chlorohydrocarbons, or Butanols at (94.6 or 95.8) kPa
Isothermal Vapor-Liquid Equilibria of ethyl acetate + dibromomethane, or + bromochloromethane or + 1,2-dichloroethane or +1-bromo-2-chloroethane at T = 313.15 K
Phase Equilibria on Four Binary Systems: 1,2-Dichloroethane + trans-1,2-Dichloroethylene, 1-Octene + 2-Methyl Thiophene, 2-Ethyl Thiophene + 2,2,4-Trimethylpentane, and Cyclopropanecarbonitrile + Water
Activity Coefficients at Infinite Dilution in 1-Alkyl-3-methylimidazolium Tetrafluoroborate Ionic Liquids
Measurement and Correlation of Griseofulvin Solubility in Different Solvents at Temperatures from (281.95 to 357.60) K
Solubilities of 2,4-Dinitro-l-phenylalanine in Monosolvents at (273.15 to 368.15) K
Thermophysical properties of the binary mixtures of 1,2-Dichloroethane with Chlorobenzene and Bromobenzene from 298.15 to 313.15 K
Solubilities of (a,Z)-2-Amino-a-(methoxyimino)-4-thiazoleethanethioic Acid S-2-Benzothiazolyl Ester in Different Pure Solvents and Binary Mixtures of Tetrahydrofuran + Dichloromethane or 1,2-Dichloroethane
Activity Coefficients at Infinite Dilution in Methylimidazolium Nitrate Ionic Liquids
Measurement and Correlation of the Solubility of Prednisone Acetate in Different Solvents
Volumetric Properties of Binary Mixtures of 1,2-Dichloroethane with Polyethers from (283.15 to 333.15) K and at Atmospheric Pressure
Solubilities of Tris(o-phenylenedioxy)cyclotriphosphazene in Selected Solvents
Determination of Gas Concentrations in Liquids by Nuclear Magnetic Resonance: Hydrogen in Organic Solvents
Solubilities of 3-Methoxy-N-phenylaniline and 3-(Methylthio)-N-phenylaniline in Five Organic Solvents (285 K to 333.75 K)
Determination of Henry's Law Constants Using Internal Standards with Benchmark Values
Volumetric Study for the Binary Nitromethane with Chloroalkane Mixtures at Temperatures in the Range (298.15 to 318.15) K
Solubilities of 1,3,2-Dioxaphosphorinane-2-methanol-a,a-5,5-tetramethyl 2-oxide in Selected Solvents at 273.15 K to 343.15 K
Solubilities of 1,3,2-Dioxaphosphorinane-2-methanol-a,5,5-trimethyl-a-phenyl-2-oxide in Selected Solvents between 278.15 K and 343.15 K
Determination and Correlation of Solubilities of 2-Isopropylthioxanthone (ITX) in Seven Different Solvents from (299.15 to 329.85) K
Densities and Isothermal Compressibilities at Pressures up to 20 MPa of the Systems N,N-Dimethylformamide or N,N-Dimethylacetamide + r,o-Dichloroalkane
Densities and Isothermal Compressibilities at Pressures up to 20 MPa of the Systems 1-Methyl-2-pyrrolidone + 1-Chloroalkane or + r,u-Dichloroalkane
Solubility of Imidacloprid in Different Solvents
Isobaric Vapor Liquid Equilibrium for Dimethylsulfoxide with Chloroethanes and Chloroethenes
Solubility of Enrofloxacin Sodium in Various Solvents at Various Temperatures
Solubility of Canthaxanthin in Pure Solvents from (293.15 to 343.15) K
Vapor-Liquid Equilibria of Binary Mixtures Formed by Hexan-1-ol with Chloroethanes and Chloroethenes at 95.6 kPa
Densities and Viscosities of (1-Propanol + 1,2-Dichloroethane), (1-Propanol + Benzaldehyde), (Benzaldehyde + 1,2-Dichloroethane), and (1-Propanol + 1,2-Dichloroethane + Benzaldehyde) Mixtures from T = 288.15 K to 313.15 K
Studies on Transport and Thermodynamic Properties of Binary Mixtures of Hexan-1-ol with Halogenated Compounds at 293.15 K
Densities and Excess Molar Volumes of the Binary Mixtures of Cyclohexanone with Chloroalkanes at Temperatures between (288.15 and 318.15) K
Excess Molar Volumes and Sound Speed in (Phenylacetonitrile + 1,2-Dichloroethane), (Phenylacetonitrile + 1,1,2-Trichloroethane), (Phenylacetonitrile + 1,1,2,2-Tetrachloroethane), (Phenylacetonitrile + Trichloroethene), and (Phenylacetonitrile + Tetrachloroethene) at Temperatures of (303.15, 308.15, and 313.15) K
Densities and Excess Molar Volumes of the Binary Mixtures of Cyclopentanone with Chloroalkanes at T = (288.15, 298.15, 308.15, and 318.15) 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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