Physical Properties
Property
Value
Unit
Source
ω
0.2690
KDB
PAff
841.60
kJ/mol
NIST
BasG
812.40
kJ/mol
NIST
Δc H°liquid
[-3368.97; -3359.70]
kJ/mol
Δc H°liquid
-3368.97
kJ/mol
NIST
Δc H°liquid
-3359.70 ± 6.50
kJ/mol
NIST
μ
1.20
debye
KDB
η
0.0003610
Pa×s
Densiti...
Δf G°
-125.50
kJ/mol
KDB
Δf H°gas
[-293.10; -282.20]
kJ/mol
Δf H°gas
-293.10
kJ/mol
KDB
Δf H°gas
-285.00
kJ/mol
NIST
Δf H°gas
-283.20 ± 1.30
kJ/mol
NIST
Δf H°gas
-282.20 ± 1.90
kJ/mol
NIST
Δf H°liquid
[-322.90; -313.60]
kJ/mol
Δf H°liquid
-315.40
kJ/mol
NIST
Δf H°liquid
-313.60 ± 1.30
kJ/mol
NIST
Δf H°liquid
-322.90 ± 5.00
kJ/mol
NIST
Δfus H°
2.48
kJ/mol
Joback Calculated Property
Δvap H°
27.84
kJ/mol
Joback Calculated Property
IE
[9.24; 9.48]
eV
IE
9.24
eV
NIST
IE
9.48
eV
NIST
IE
9.41
eV
NIST
log 10 WS
[-0.24; -0.24]
log 10 WS
-0.24
Aq. Sol...
log 10 WS
-0.24
Estimat...
log Poct/wat
1.431
Crippen Calculated Property
McVol
87.180
ml/mol
McGowan Calculated Property
Pc
[3397.00; 3430.00]
kPa
Pc
3430.00
kPa
KDB
Pc
3397.00 ± 8.00
kPa
NIST
Pc
3430.00 ± 10.00
kPa
NIST
Inp
[544.00; 570.12]
Inp
563.70
NIST
Inp
562.70
NIST
Inp
562.00
NIST
Inp
Outlier 544.00
NIST
Inp
549.00
NIST
Inp
570.12
NIST
Inp
568.00
NIST
Inp
566.00
NIST
Inp
566.00
NIST
Inp
567.00
NIST
Inp
554.50
NIST
Inp
558.00
NIST
Inp
563.00
NIST
Inp
570.00
NIST
Inp
560.00
NIST
Inp
556.00
NIST
Inp
556.00
NIST
Inp
556.00
NIST
Inp
560.00
NIST
Inp
568.00
NIST
Inp
563.00
NIST
Inp
556.00
NIST
I
[666.00; 688.00]
I
666.00
NIST
I
688.00
NIST
S°gas
357.80
J/mol×K
NIST
S°liquid
265.30
J/mol×K
NIST
Tboil
[328.25; 328.30]
K
Tboil
328.30
K
KDB
Tboil
328.25
K
Vapor-L...
Tc
[496.40; 497.10]
K
Tc
497.10
K
KDB
Tc
497.00
K
Measure...
Tc
496.40 ± 0.30
K
NIST
Tc
497.10
K
NIST
Tc
497.10 ± 0.20
K
NIST
Tfus
[164.25; 164.50]
K
Tfus
164.50
K
KDB
Tfus
164.25
K
Aq. Sol...
Tfus
164.50 ± 0.20
K
NIST
Ttriple
164.56 ± 0.07
K
NIST
Vc
0.323
m3 /kmol
KDB
Zc
0.2676350
KDB
Temperature Dependent Properties
Property
Value
Unit
Temperature (K)
Source
Cp,gas
[147.83; 203.44]
J/mol×K
[332.99; 508.60]
Cp,gas
147.83
J/mol×K
332.99
Joback Calculated Property
Cp,gas
158.08
J/mol×K
362.26
Joback Calculated Property
Cp,gas
167.93
J/mol×K
391.53
Joback Calculated Property
Cp,gas
177.38
J/mol×K
420.79
Joback Calculated Property
Cp,gas
186.44
J/mol×K
450.06
Joback Calculated Property
Cp,gas
195.13
J/mol×K
479.33
Joback Calculated Property
Cp,gas
203.44
J/mol×K
508.60
Joback Calculated Property
Cp,liquid
[187.50; 188.00]
J/mol×K
[298.00; 298.15]
Cp,liquid
188.00
J/mol×K
298.00
NIST
Cp,liquid
187.50
J/mol×K
298.15
NIST
Cp,liquid
187.80
J/mol×K
298.15
NIST
η
[0.0002780; 0.0004430]
Pa×s
[273.15; 313.15]
η
0.0003900
Pa×s
273.15
Density...
η
0.0004430
Pa×s
273.15
Densiti...
η
0.0004170
Pa×s
278.15
Densiti...
η
0.0003920
Pa×s
283.15
Densiti...
η
0.0003600
Pa×s
283.15
Density...
η
0.0003897
Pa×s
283.15
Experim...
η
0.0003640
Pa×s
288.15
Experim...
η
0.0003700
Pa×s
288.15
Densiti...
η
0.0003482
Pa×s
293.15
Experim...
η
0.0003330
Pa×s
293.15
Density...
η
0.0003327
Pa×s
298.15
Experim...
η
0.0003190
Pa×s
298.15
Density...
η
0.0003040
Pa×s
303.15
Density...
η
0.0003152
Pa×s
303.15
Experim...
η
0.0002994
Pa×s
308.15
Experim...
η
0.0002846
Pa×s
313.15
Experim...
η
0.0002780
Pa×s
313.15
Density...
Δfus H
[7.60; 7.60]
kJ/mol
[164.56; 164.60]
Δfus H
7.60
kJ/mol
164.56
NIST
Δfus H
7.60
kJ/mol
164.60
NIST
Δfus H
7.60
kJ/mol
164.60
NIST
Δvap H
[27.90; 31.20]
kJ/mol
[306.50; 355.50]
Δvap H
30.40
kJ/mol
306.50
NIST
Δvap H
30.00
kJ/mol
310.00
NIST
Δvap H
29.90
kJ/mol
314.00
NIST
Δvap H
30.20
kJ/mol
319.00
NIST
Δvap H
27.90
kJ/mol
328.00
NIST
Δvap H
27.94
kJ/mol
328.30
NIST
Δvap H
29.60
kJ/mol
340.00
NIST
Δvap H
31.20
kJ/mol
355.50
NIST
ν
[0.0000004; 0.0000005]
m2 /s
[283.15; 313.15]
ν
0.0000005
m2 /s
283.15
Kinemat...
ν
0.0000005
m2 /s
298.15
Kinemat...
ν
0.0000004
m2 /s
313.15
Kinemat...
Pvap
[6.24; 221.79]
kPa
[263.15; 354.82]
Pvap
6.24
kPa
263.15
Isother...
Pvap
6.25
kPa
263.15
Thermod...
Pvap
6.40
kPa
263.53
Isother...
Pvap
10.67
kPa
273.15
Isother...
Pvap
10.64
kPa
273.15
Thermod...
Pvap
10.80
kPa
273.34
Isother...
Pvap
11.59
kPa
274.90
Isother...
Pvap
11.59
kPa
274.91
Isother...
Pvap
17.41
kPa
283.15
Isother...
Pvap
17.31
kPa
283.15
Thermod...
Pvap
17.60
kPa
283.27
Isother...
Pvap
17.79
kPa
283.60
A milli...
Pvap
18.55
kPa
284.82
Isother...
Pvap
22.07
kPa
288.60
A milli...
Pvap
27.06
kPa
293.15
Thermod...
Pvap
27.25
kPa
293.15
Isother...
Pvap
27.40
kPa
293.25
Isother...
Pvap
27.43
kPa
293.50
A milli...
Pvap
28.78
kPa
294.80
Isother...
Pvap
28.78
kPa
294.80
Isother...
Pvap
28.78
kPa
294.81
Isother...
Pvap
33.39
kPa
298.15
Thermod...
Pvap
33.72
kPa
298.40
A milli...
Pvap
41.16
kPa
303.15
Isother...
Pvap
40.86
kPa
303.15
Thermod...
Pvap
41.20
kPa
303.22
Isother...
Pvap
41.10
kPa
303.30
A milli...
Pvap
43.26
kPa
304.79
Isother...
Pvap
43.24
kPa
304.79
Isother...
Pvap
49.80
kPa
308.20
A milli...
Pvap
59.90
kPa
313.10
A milli...
Pvap
60.22
kPa
313.15
Isother...
Pvap
59.81
kPa
313.15
Thermod...
Pvap
62.40
kPa
313.20
Isother...
Pvap
60.30
kPa
313.24
Isother...
Pvap
62.95
kPa
314.75
Isother...
Pvap
62.97
kPa
314.76
Isother...
Pvap
62.97
kPa
314.76
Isother...
Pvap
71.61
kPa
318.10
A milli...
Pvap
85.01
kPa
323.00
A milli...
Pvap
85.15
kPa
323.15
Thermod...
Pvap
85.65
kPa
323.15
Isother...
Pvap
85.80
kPa
323.21
Isother...
Pvap
89.66
kPa
324.90
Isother...
Pvap
89.69
kPa
324.90
Isother...
Pvap
100.34
kPa
327.90
A milli...
Pvap
117.70
kPa
332.90
A milli...
Pvap
118.27
kPa
333.15
Thermod...
Pvap
118.78
kPa
333.15
Isother...
Pvap
120.40
kPa
333.15
Thermod...
Pvap
119.20
kPa
333.19
Isother...
Pvap
124.02
kPa
334.85
Isother...
Pvap
137.39
kPa
337.80
A milli...
Pvap
160.66
kPa
343.15
Thermod...
Pvap
167.14
kPa
344.84
Isother...
Pvap
167.57
kPa
344.85
Isother...
Pvap
221.79
kPa
354.82
Isother...
Pvap
221.39
kPa
354.82
Isother...
n 0
[1.36594; 1.36980]
[293.15; 298.20]
n 0
1.36900
293.15
(Vapor ...
n 0
1.36890
293.15
A novel...
n 0
1.36980
293.15
Vapor-L...
n 0
1.36766
298.15
Phase e...
n 0
1.36648
298.15
Volumet...
n 0
1.36648
298.15
Volumet...
n 0
1.36610
298.15
sotherm...
n 0
1.36594
298.15
Quatern...
n 0
1.36628
298.15
Isobari...
n 0
1.36600
298.15
Solubil...
n 0
1.36764
298.15
Atmosph...
n 0
1.36766
298.15
Vapor-L...
n 0
1.36632
298.20
Vapor-L...
ρl
[713.96; 761.34]
kg/m3
[273.15; 318.15]
ρl
761.30
kg/m3
273.15
Physico...
ρl
761.34
kg/m3
273.15
Densiti...
ρl
756.14
kg/m3
278.15
Densiti...
ρl
751.02
kg/m3
283.15
Densiti...
ρl
745.90
kg/m3
288.15
Physico...
ρl
745.85
kg/m3
288.15
Densiti...
ρl
740.65
kg/m3
293.15
Densiti...
ρl
739.80
kg/m3
293.15
Measure...
ρl
739.45
kg/m3
293.20
Liquid-...
ρl
735.40
kg/m3
298.15
Phase e...
ρl
734.10
kg/m3
298.15
Solubil...
ρl
735.69
kg/m3
298.15
Excess ...
ρl
735.36
kg/m3
298.15
Densiti...
ρl
735.69
kg/m3
298.15
Excess ...
ρl
735.00
kg/m3
298.15
Physico...
ρl
735.99
kg/m3
298.15
Excess ...
ρl
735.35
kg/m3
298.15
Mixing ...
ρl
735.48
kg/m3
298.15
Excess ...
ρl
740.60
kg/m3
298.15
Vapor-L...
ρl
735.21
kg/m3
298.15
Excess ...
ρl
735.99
kg/m3
298.15
Excess ...
ρl
735.99
kg/m3
298.15
Excess ...
ρl
735.40
kg/m3
298.15
Densiti...
ρl
737.80
kg/m3
298.20
Phase e...
ρl
730.10
kg/m3
303.15
Densiti...
ρl
724.60
kg/m3
308.15
Physico...
ρl
724.85
kg/m3
308.15
Densiti...
ρl
724.82
kg/m3
308.15
Densiti...
ρl
719.42
kg/m3
313.15
Densiti...
ρl
718.08
kg/m3
313.20
Liquid-...
ρl
713.96
kg/m3
318.15
Densiti...
Δfus S
46.18
J/mol×K
164.56
NIST
csound,fluid
[103.70; 1086.92]
m/s
[288.15; 493.06]
csound,fluid
1086.92
m/s
288.15
Mixing ...
csound,fluid
1082.11
m/s
288.15
Influen...
csound,fluid
1086.62
m/s
288.15
Mixing ...
csound,fluid
1082.40
m/s
288.15
Excess ...
csound,fluid
1083.38
m/s
288.15
Influen...
csound,fluid
1083.38
m/s
288.15
Influen...
csound,fluid
1071.61
m/s
290.65
Influen...
csound,fluid
1070.62
m/s
290.65
Influen...
csound,fluid
1071.61
m/s
290.65
Influen...
csound,fluid
1060.05
m/s
293.15
Influen...
csound,fluid
1060.05
m/s
293.15
Influen...
csound,fluid
1063.43
m/s
293.15
Mixing ...
csound,fluid
1059.10
m/s
293.15
Influen...
csound,fluid
1059.40
m/s
293.15
Excess ...
csound,fluid
1047.83
m/s
295.65
Influen...
csound,fluid
1048.48
m/s
295.65
Influen...
csound,fluid
1048.48
m/s
295.65
Influen...
csound,fluid
1036.63
m/s
298.15
Influen...
csound,fluid
1036.10
m/s
298.15
Excess ...
csound,fluid
1036.94
m/s
298.15
Influen...
csound,fluid
1040.35
m/s
298.15
Mixing ...
csound,fluid
1036.94
m/s
298.15
Influen...
csound,fluid
1025.38
m/s
300.65
Influen...
csound,fluid
1025.42
m/s
300.65
Influen...
csound,fluid
1025.42
m/s
300.65
Influen...
csound,fluid
1024.33
m/s
301.65
Influen...
csound,fluid
1017.42
m/s
303.15
Mixing ...
csound,fluid
1014.04
m/s
303.15
Influen...
csound,fluid
1013.90
m/s
303.15
Influen...
csound,fluid
1013.00
m/s
303.15
Excess ...
csound,fluid
1012.81
m/s
303.15
Influen...
csound,fluid
1013.90
m/s
303.15
Influen...
csound,fluid
1024.70
m/s
303.19
Speed o...
csound,fluid
1001.35
m/s
305.65
Influen...
csound,fluid
1002.41
m/s
305.65
Influen...
csound,fluid
1002.70
m/s
305.65
Influen...
csound,fluid
1002.41
m/s
305.65
Influen...
csound,fluid
991.34
m/s
308.15
Influen...
csound,fluid
990.99
m/s
308.15
Influen...
csound,fluid
990.10
m/s
308.15
Excess ...
csound,fluid
989.90
m/s
308.15
Influen...
csound,fluid
990.99
m/s
308.15
Influen...
csound,fluid
994.68
m/s
308.15
Mixing ...
csound,fluid
988.60
m/s
308.16
Speed o...
csound,fluid
979.62
m/s
310.65
Influen...
csound,fluid
980.00
m/s
310.65
Influen...
csound,fluid
978.47
m/s
310.65
Influen...
csound,fluid
979.62
m/s
310.65
Influen...
csound,fluid
960.40
m/s
313.08
Speed o...
csound,fluid
967.03
m/s
313.15
Influen...
csound,fluid
968.16
m/s
313.15
Influen...
csound,fluid
968.63
m/s
313.15
Influen...
csound,fluid
968.16
m/s
313.15
Influen...
csound,fluid
956.80
m/s
315.65
Influen...
csound,fluid
956.80
m/s
315.65
Influen...
csound,fluid
955.73
m/s
315.65
Influen...
csound,fluid
957.31
m/s
315.65
Influen...
csound,fluid
946.03
m/s
318.15
Influen...
csound,fluid
944.34
m/s
318.15
Influen...
csound,fluid
945.54
m/s
318.15
Influen...
csound,fluid
945.54
m/s
318.15
Influen...
csound,fluid
942.70
m/s
318.19
Speed o...
csound,fluid
934.24
m/s
320.65
Influen...
csound,fluid
934.24
m/s
320.65
Influen...
csound,fluid
933.01
m/s
320.65
Influen...
csound,fluid
934.76
m/s
320.65
Influen...
csound,fluid
912.40
m/s
323.07
Speed o...
csound,fluid
922.97
m/s
323.15
Influen...
csound,fluid
922.97
m/s
323.15
Influen...
csound,fluid
923.46
m/s
323.15
Influen...
csound,fluid
921.93
m/s
323.15
Influen...
csound,fluid
904.70
m/s
328.21
Speed o...
csound,fluid
876.80
m/s
333.13
Speed o...
csound,fluid
855.10
m/s
338.07
Speed o...
csound,fluid
826.30
m/s
343.12
Speed o...
csound,fluid
797.50
m/s
348.24
Speed o...
csound,fluid
781.50
m/s
353.11
Speed o...
csound,fluid
748.60
m/s
358.22
Speed o...
csound,fluid
727.10
m/s
363.16
Speed o...
csound,fluid
707.10
m/s
368.17
Speed o...
csound,fluid
698.90
m/s
373.05
Speed o...
csound,fluid
668.30
m/s
378.05
Speed o...
csound,fluid
646.40
m/s
383.08
Speed o...
csound,fluid
627.50
m/s
388.11
Speed o...
csound,fluid
609.10
m/s
393.16
Speed o...
csound,fluid
580.10
m/s
398.11
Speed o...
csound,fluid
558.00
m/s
403.24
Speed o...
csound,fluid
537.60
m/s
408.23
Speed o...
csound,fluid
515.80
m/s
413.20
Speed o...
csound,fluid
494.40
m/s
418.24
Speed o...
csound,fluid
476.00
m/s
423.15
Speed o...
csound,fluid
453.80
m/s
428.24
Speed o...
csound,fluid
430.30
m/s
433.05
Speed o...
csound,fluid
405.80
m/s
438.19
Speed o...
csound,fluid
387.30
m/s
443.09
Speed o...
csound,fluid
360.30
m/s
448.23
Speed o...
csound,fluid
339.50
m/s
453.10
Speed o...
csound,fluid
313.60
m/s
458.19
Speed o...
csound,fluid
287.10
m/s
463.23
Speed o...
csound,fluid
265.00
m/s
468.18
Speed o...
csound,fluid
236.50
m/s
473.17
Speed o...
csound,fluid
206.10
m/s
478.08
Speed o...
csound,fluid
177.70
m/s
483.20
Speed o...
csound,fluid
142.80
m/s
488.11
Speed o...
csound,fluid
103.70
m/s
493.06
Speed o...
γ
[0.01; 0.02]
N/m
[243.08; 393.13]
γ
0.02
N/m
243.08
Surface...
γ
0.02
N/m
248.01
Surface...
γ
0.02
N/m
253.11
Surface...
γ
0.02
N/m
258.13
Surface...
γ
0.02
N/m
263.10
Surface...
γ
0.02
N/m
268.13
Surface...
γ
0.02
N/m
273.16
Surface...
γ
0.02
N/m
278.11
Surface...
γ
0.02
N/m
283.12
Surface...
γ
0.02
N/m
288.13
Surface...
γ
0.02
N/m
293.07
Surface...
γ
0.02
N/m
298.08
Surface...
γ
0.02
N/m
303.11
Surface...
γ
0.02
N/m
308.15
Surface...
γ
0.02
N/m
313.16
Surface...
γ
0.02
N/m
318.11
Surface...
γ
0.02
N/m
323.16
Surface...
γ
0.01
N/m
328.14
Surface...
γ
0.01
N/m
333.15
Surface...
γ
0.01
N/m
338.16
Surface...
γ
0.01
N/m
343.13
Surface...
γ
0.01
N/m
348.13
Surface...
γ
0.01
N/m
353.13
Surface...
γ
0.01
N/m
358.15
Surface...
γ
0.01
N/m
363.13
Surface...
γ
0.01
N/m
368.13
Surface...
γ
0.01
N/m
373.12
Surface...
γ
0.01
N/m
378.12
Surface...
γ
0.01
N/m
383.12
Surface...
γ
0.01
N/m
388.14
Surface...
γ
0.01
N/m
393.13
Surface...
αdiff
[2.73e-08; 6.40e-08]
m2 /s
[303.15; 493.15]
αdiff
6.40e-08
m2 /s
303.15
Thermal...
αdiff
6.17e-08
m2 /s
313.15
Thermal...
αdiff
5.87e-08
m2 /s
323.15
Thermal...
αdiff
5.70e-08
m2 /s
333.15
Thermal...
αdiff
5.42e-08
m2 /s
343.15
Thermal...
αdiff
5.26e-08
m2 /s
353.15
Thermal...
αdiff
5.05e-08
m2 /s
363.15
Thermal...
αdiff
4.83e-08
m2 /s
373.15
Thermal...
αdiff
4.72e-08
m2 /s
383.15
Thermal...
αdiff
4.64e-08
m2 /s
393.15
Thermal...
αdiff
4.55e-08
m2 /s
403.15
Thermal...
αdiff
4.48e-08
m2 /s
413.15
Thermal...
αdiff
4.38e-08
m2 /s
423.15
Thermal...
αdiff
4.31e-08
m2 /s
433.15
Thermal...
αdiff
4.18e-08
m2 /s
443.15
Thermal...
αdiff
4.05e-08
m2 /s
453.15
Thermal...
αdiff
3.91e-08
m2 /s
458.15
Thermal...
αdiff
3.86e-08
m2 /s
463.15
Thermal...
αdiff
3.66e-08
m2 /s
468.15
Thermal...
αdiff
3.55e-08
m2 /s
473.15
Thermal...
αdiff
3.47e-08
m2 /s
475.15
Thermal...
αdiff
3.36e-08
m2 /s
477.15
Thermal...
αdiff
3.36e-08
m2 /s
479.15
Thermal...
αdiff
3.30e-08
m2 /s
481.15
Thermal...
αdiff
3.22e-08
m2 /s
483.15
Thermal...
αdiff
3.07e-08
m2 /s
485.15
Thermal...
αdiff
3.02e-08
m2 /s
487.15
Thermal...
αdiff
2.95e-08
m2 /s
489.15
Thermal...
αdiff
2.81e-08
m2 /s
491.15
Thermal...
αdiff
2.73e-08
m2 /s
493.15
Thermal...
Datasets
Mass density, kg/m3
Fixed
Measured
Temperature, K - Liquid
Pressure, kPa - Liquid
Mass density, kg/m3 - Liquid
283.15
100.00
750.94
288.15
100.00
745.79
293.15
100.00
740.59
298.15
100.00
735.34
303.15
100.00
730.04
308.15
100.00
724.69
313.15
100.00
719.29
318.15
100.00
713.84
323.15
100.00
708.45
283.15
5000.00
756.29
288.15
5000.00
751.33
293.15
5000.00
746.34
298.15
5000.00
741.32
303.15
5000.00
736.27
308.15
5000.00
731.19
313.15
5000.00
726.07
318.15
5000.00
720.92
323.15
5000.00
715.73
283.15
10000.00
761.29
288.15
10000.00
756.52
293.15
10000.00
751.7
298.15
10000.00
746.89
303.15
10000.00
742.05
308.15
10000.00
737.18
313.15
10000.00
732.27
318.15
10000.00
727.36
323.15
10000.00
722.39
283.15
15000.00
765.93
288.15
15000.00
761.32
293.15
15000.00
756.68
298.15
15000.00
752.04
303.15
15000.00
747.37
308.15
15000.00
742.69
313.15
15000.00
737.97
318.15
15000.00
733.26
323.15
15000.00
728.51
283.15
20000.00
770.32
288.15
20000.00
765.86
293.15
20000.00
761.35
298.15
20000.00
756.85
303.15
20000.00
752.37
308.15
20000.00
747.84
313.15
20000.00
743.29
318.15
20000.00
738.74
323.15
20000.00
734.2
283.15
25000.00
774.48
288.15
25000.00
770.15
293.15
25000.00
765.77
298.15
25000.00
761.42
303.15
25000.00
757.05
308.15
25000.00
752.67
313.15
25000.00
748.27
318.15
25000.00
743.91
323.15
25000.00
739.51
283.15
30000.00
778.47
288.15
30000.00
774.24
293.15
30000.00
770.01
298.15
30000.00
765.75
303.15
30000.00
761.51
308.15
30000.00
757.26
313.15
30000.00
752.99
318.15
30000.00
748.75
323.15
30000.00
744.49
283.15
35000.00
782.29
288.15
35000.00
778.15
293.15
35000.00
774.0
298.15
35000.00
769.88
303.15
35000.00
765.74
308.15
35000.00
761.6
313.15
35000.00
757.46
318.15
35000.00
753.35
323.15
35000.00
749.2
283.15
40000.00
785.94
288.15
40000.00
781.89
293.15
40000.00
777.85
298.15
40000.00
773.81
303.15
40000.00
769.79
308.15
40000.00
765.75
313.15
40000.00
761.71
318.15
40000.00
757.7
323.15
40000.00
753.67
283.15
45000.00
789.45
288.15
45000.00
785.49
293.15
45000.00
781.54
298.15
45000.00
777.6
303.15
45000.00
773.65
308.15
45000.00
769.71
313.15
45000.00
765.77
318.15
45000.00
761.86
323.15
45000.00
757.92
283.15
50000.00
792.86
288.15
50000.00
788.97
293.15
50000.00
785.09
298.15
50000.00
781.23
303.15
50000.00
777.36
308.15
50000.00
773.49
313.15
50000.00
769.65
318.15
50000.00
765.83
323.15
50000.00
761.98
283.15
55000.00
796.13
288.15
55000.00
792.3
293.15
55000.00
788.51
298.15
55000.00
784.71
303.15
55000.00
780.95
308.15
55000.00
777.14
313.15
55000.00
773.39
318.15
55000.00
769.63
323.15
55000.00
765.85
283.15
60000.00
799.29
288.15
60000.00
795.55
293.15
60000.00
791.81
298.15
60000.00
788.1
303.15
60000.00
784.37
308.15
60000.00
780.65
313.15
60000.00
776.97
318.15
60000.00
773.29
323.15
60000.00
769.61
283.15
65000.00
802.37
288.15
65000.00
798.67
293.15
65000.00
795.0
298.15
65000.00
791.36
303.15
65000.00
787.7
308.15
65000.00
784.04
313.15
65000.00
780.41
318.15
65000.00
776.82
323.15
65000.00
773.22
Reference
Correlations
Similar Compounds
Find more compounds similar to Propane, 2-methoxy-2-methyl- .
Mixtures
Benzene + Propane, 2-methoxy-2-methyl-
Toluene + Propane, 2-methoxy-2-methyl-
Propane, 2-methoxy-2-methyl- + Ethylbenzene
Propane, 2-methoxy-2-methyl- + Pentane, 2,2,4-trimethyl-
2-Propanol, 2-methyl- + Propane, 2-methoxy-2-methyl-
Propane, 2-methoxy-2-methyl- + Pentane, 3-methyl-
n-Hexane + Propane, 2-methoxy-2-methyl-
Propane, 2-methoxy-2-methyl- + Heptane
Butane, 1-chloro- + Propane, 2-methoxy-2-methyl-
Propane, 2-methoxy-2-methyl- + Butane, 2-chloro-
Propane, 1-chloro-2-methyl- + Propane, 2-methoxy-2-methyl-
2-Pyrrolidinone, 1-methyl- + Propane, 2-methoxy-2-methyl-
Propane, 2-methoxy-2-methyl- + 1-Hexyne
Propane, 2-methoxy-2-methyl- + 2-Hexyne
Propane, 2-methoxy-2-methyl- + o-Xylene
Benzene, 1,3-dimethyl- + Propane, 2-methoxy-2-methyl-
p-Xylene + Propane, 2-methoxy-2-methyl-
Propane, 2-methoxy-2-methyl- + Ethane, 1,2-dichloro-
Propane, 2-methoxy-2-methyl- + Cyclohexane
Propane, 2-methoxy-2-methyl- + Acetone
Find more mixtures with Propane, 2-methoxy-2-methyl- .
Sources
KDB Pure (Korean Thermophysical Properties Databank)
KDB Vapor Pressure Data
Crippen Method
Influence of Temperature on Thermodynamic Properties of Methyl t-Butyl Ether (MTBE)+Gasoline Additives
Kinematic Viscosities for Ether + Alkane Mixtures: Experimental Results and UNIFAC-VISCO Parameters
Experimental and Predicted Viscosities of Binary Mixtures Containing Chlorinated and Oxygenated Compounds
(Solid + liquid) phase equilibria of binary mixtures containing N-methyl-2-pyrrolidinone and ethers at atmospheric pressure
Phase equilibria for binary systems of octane boosters with 2,2,4-trimethylpentane
Determination of excess molar enthalpies of the ternary system methyl tert-butyl ether + 1-pentanol + nonane at 298.15K Analysis and comparison with predicted values of the UNIFAC model and some empirical methods
Liquid-liquid equilibrium data of water with neohexane, methylcyclohexane, tert-butyl methyl ether, n-heptane and vapor -liquid-liquid equilibrium with methane
Thermodynamics of binary mixtures containing N-methyl-2-pyrrolidinone VLE measurements for systems with ethers Comparison with the Mod. UNIFAC (Do) and DISQUAC models Predictions for VLE, GE m, HEm and SLE?
Infinite dilution activity coefficient measurements by inert gas stripping method
Thermodynamics of isomeric hexynes +MTBE binary mixtures
(Liquid + liquid) equilibria for the quaternary system water + methyl tert-butyl ether + ethanol + benzene at 303.15K
Liquid liquid equilibria for the MTBE+water + salts systems at 298.15K
Influence of temperature on thermodynamics of ethers + xylenes
Isothermal vapour liquid equilibria of binary systems of 1,2-dichloroethane with ethers
Study of the effect of increasing the chain length of the alkane in excess molar enthalpies of mixtures containing methyl tert-butyl ether, 1-propanol, alkane
Phase equilibria and interfacial tensions in the systems methyl tert-butyl ether + acetone + cyclohexane, methyl tert-butyl ether + acetone and methyl tert-butyl ether + cyclohexane
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 1-butyl-1-methylpyrrolidinium trifluoromethanesulfonate using GLC
Isothermal vapour liquid equilibria in the binary and ternary systems composed of tert-butyl methyl ether, 3,3-dimethyl-2-butanone and 2,2-dimethyl-1-propanol
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
Study on the effect of increasing the chain length of the alkanol in excess molar enthalpies of mixtures containing 2-methoxy-2-methylpropane, 1-alkanol, decane
Activity coefficients at infinite dilution of organic solutes in the ionic liquid 1-ethyl-3-methylimidazolium methanesulfonate
Solubility of caprolactam in different organic solvents
A novel static analytical apparatus for phase equilibrium measurements
Liquid liquid equilibria at 298.15 K for ternary mixtures of methyl tert-butyl ether + methanol (or ethanol) + imidazolium-based ionic liquids at atmospheric pressure
Atmospheric densities and interfacial tensions for 1- alkanol (1-butanol to 1-octanol) + water and ether (MTBE, ETBE, DIPE, TAME and THP) + water demixed mixtures.
Phase equilibria of (water + propionic acid or butyric acid + 2-methoxy- 2-methylpropane) ternary systems at 298.2 K and 323.2 K
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
Experimental and modeled volumetric behavior of linear and branched ethers
Determination and modeling for solid-liquid phase equilibrium of ternary caprolactam + cyclohexanone oxime + methyl tert-butyl ether system
A milliliter-scale setup for the efficient characterization of isothermal vapor-liquid equilibria using Raman spectroscopy
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
Thermodynamics and activity coefficients at infinite dilution for organic solutes in the ionic liquid 1-butyl-1-methylpyrrolidinium dicyanamide
New ionic liquid [P4,4,4,4][NTf2] in bio-butanol extraction on investigation of limiting activity coefficients
Liquid-liquid equilibrium measurement and thermodynamics modeling for the systems water + thioglycolic acid + isopropyl ether/methyl tert-butyl ether at 298.15 and 308.15 K
Ammonium ionic liquids in extraction of bio-butan-1-ol from water phase using activity coefficients at infinite dilution
Liquid-liquid equilibrium data and thermophysical properties for ternary systems composed of water, acetic acid and different solvents
Excess molar enthalpies of the ternary mixtures: methyl tert-butyl ether +2-methylpentane + (n-decane or n-dodecane) at the temperature 298.15 K
Excess molar enthalpies of the ternary mixtures: (methyl tert-butyl ether or 2-methyltetrahydrofuran + cyclohexane + 2,2,4- trimethylpentane} at the temperature 298.15 K
Densities and derived thermodynamic properties of the binary systems of 1,1-dimethylethyl methyl ether with allyl methacrylate, butyl methacrylate, methacrylic acid, and vinyl acetate at T = (298.15 and 308.15) K
Excess molar enthalpies of the ternary mixtures: {tetrahydrofuran or 2-methyltetrahydrofuran + methyl tert-butyl ether + n-dodecane} at the temperature 298.15 K
Quaternary (liquid + liquid) equilibria for (water + 1,1-dimethylethyl methyl ether + diisopropyl ether + toluene) at the temperature 298.15 K
Quaternary (liquid + liquid) equilibria for (water + 2-propanol + 1,1-dimethylethyl methyl ether + diisopropyl ether) at the temperature 298.15 K
Excess molar enthalpies of the ternary mixtures: (tetrahydrofuran or 2-methyltetrahydrofuran + methyl tert-butyl ether + n-octane) at the temperature 298.15 K
(Liquid + liquid) phase equilibria of 1-alkyl-3-methylimidazolium methylsulfate with alcohols, or ethers, or ketones
Excess molar enthalpies of the ternary mixtures (1-hexene + tetrahydrofuran or 2-methyltetrahydrofuran + methyl tert-butyl ether) at the temperature 298.15K.
Excess enthalpy, density, and speed of sound determination for the ternary mixture (methyl tert-butyl ether + 1-butanol + n-hexane)
(Vapor + liquid) equilibrium of the binary mixtures formed by acetonitrile with selected compounds at 95.5 kPa
Thermodynamics of biofuels: Excess enthalpies for binary mixtures involving ethyl 1,1-dimethylethyl ether and hydrocarbons at different temperatures using a new flow calorimeter
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
Volumetric behaviour of binary liquid systems composed of toluene, isooctane, and methyl tert-butyl ether at temperatures from (298.15 to 328.15) K
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 4-methyl-N-butyl-pyridinium bis(trifluoromethylsulfonyl)-imide
Gas liquid chromatography measurements of activity coefficients at infinite dilution of various organic solutes and water in tri-iso-butylmethylphosphonium tosylate ionic liquid
Volumetric behaviour of the ternary liquid system composed of methyl tert-butyl ether, toluene, and isooctane at temperatures from (298.15 to 328.15) K: Experimental data and correlation
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 measurements for organic solutes and water in the ionic liquid 1-ethyl-3-methylimidazolium tetracyanoborate
Volumetric and viscometric properties of binary mixtures of {methyl tert-butyl ether (MTBE) + alcohol} at several temperatures and p = 0.1 MPa: Experimental results and application of the ERAS model
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
Interactions of volatile organic compounds with 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 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 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
Isothermal (vapor + liquid) equilibria and excess enthalpy data of {1-hexene + methyl butyl ether (MBE)} and {1-hexene + methyl tert-butyl ether (MTBE)} binary systems at several temperatures
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
Interactions of volatile organic compounds with the ionic liquids 1-butyl-1-methylpyrrolidinium tetracyanoborate and 1-butyl-1-methylpyrrolidinium bis(oxalato)borate
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
Measurement of critical temperatures and critical pressures for binary mixtures of methyl tert-butyl ether (MTBE) + alcohol and MTBE + alkane
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
Infinite dilution activity coefficients of volatile organic compounds in two ionic liquids composed of the tris(pentafluoroethyl) trifluorophosphate ([FAP]) anion and a functionalized cation
Experimental and theoretical excess molar enthalpies of ternary and binary mixtures containing 2-Methoxy-2-Methylpropane, 1-propanol, heptane
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
Contribution to study of the thermodynamics properties of mixtures containing 2-methoxy-2-methylpropane, alkanol, alkane
Measurement and correlation of critical properties for binary mixtures and ternary mixtures containing gasoline additives
Thermodynamics and activity coefficients at infinite dilution for organic solutes, water and diols in the ionic liquid choline bis(trifluoromethylsulfonyl)imide
Solubility and solution thermodynamics of sorbic acid in eight pure organic solvents
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
Volumetric behavior of the ternary system (methyl tert-butyl ether + methylbenzene + butan-1-ol) and its binary sub-system (methyl tert-butyl ether + butan-1-ol) within the temperature range (298.15 to 328.15) K
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
Solubility measurement and correlation of the form A of ibrutinib in organic solvents from 278.15 to 323.15 K
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
Thermodynamic study of molecular interaction-selectivity in separation processes based on limiting activity coefficients
Liquid-liquid equilibrium for ternary systems of water + 2,2,3,3-tetrafluoro-1-propanol + isopropyl ether/tert-butyl methyl ether at 298.2, 308.2 K
The use of ionic liquids for separation of binary hydrocarbons mixtures based on gamma infinity data measurements
Liquid-liquid equilibria for azeotropic mixture of methyl tert-butyl ether and methanol with ionic liquids at different temperatures
Liquid-liquid equilibrium study for ternary systems of water + propargyl alcohol + solvents at 308.2 K: Measurement and thermodynamic modelling
Excess molar enthalpies of the ternary mixtures: methyl tert-butyl ether + 3-methylpentane + (n-decane or n-dodecane) at 298.15K
Isothermal vapor-liquid equilibrium of binary and ternary systems of anisole, hexane, and toluene and ternary system of methyl tert-butyl ether, hexane, and toluene
sothermal and Isobaric Vapor-Liquid Equilibrium and Excess Molar Enthalpy of the Binary Mixtures of 2-Methoxy-2-methylpropane + 2-Methyl-2-butanol or + 2-Butanol
Solubility of Amorphous Clopidogrel Hydrogen Sulfate in Different Pure Solvents
Solubility of Agomelatine Crystal Form I and Form II in Pure Solvents and (Isopropanol + Water) Mixtures
Activity Coefficients at Infinite Dilution of Organic Solutes and Water in Tributylethylphosphonium Diethylphosphate Using Gas Liquid Chromatography: Thermodynamic Properties of Mixtures Containing Ionic Liquids
Quaternary, Ternary, and Binary LLE Measurements for 2-Methoxy-2-methylpropane + Furfural + Acetic Acid + Water at Temperatures between 298 and 307 K
Speed of Sound Measurements of 2-Methoxy-2-methylpropane in the Temperature Range of 293.15 and 673.15 K and for Pressures up to 10 MPa
Liquid-Liquid Equilibria of Ionic Liquids-Water-Acetic Acid Mixtures
Measurements and Thermodynamic Models for the Separation of 2-Methoxyethanol and Water Azeotropic Mixtures via Different Solvents
Solid-Liquid Phase Equilibrium and Thermodynamic Properties of Olaparib in Selected Organic Solvents and (Tetrahydrofuran + MTBE, Acetonitrile + Isopropyl Alcohol) Binary Solvent Mixtures
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
Physicochemical Properties of LiFSI Solutions II: LiFSI with Water, MTBE, and Anisole
Vapor-Liquid Equilibrium Measurements of Ether Alcohol Blends for Investigation on Reformulated Gas
Solubility Measurement and Correlation of Probenecid in 12 Pure Organic Solvents and Thermodynamic Properties of Mixing of Solutions
Measurement and Correlation of the Solubility of Dienogest in Twelve Pure and Water + Methanol Binary Solvents at Temperatures from 273.15 to 318.15 K
Solubility of Imidazoles in Ethers
Mixing Properties for the Ternary Mixture Methyl tert-Butyl Ether + 1-Butanol + Decane at 298.15 K
Vapor-Liquid Equilibria for the Binary Systems of Dimethoxymethane with Some Fuel Oxygenates
Oxygenated Gasoline Additives: Saturated Heat Capacities between (277 and 355) K
Excess Molar Volumes and Surface Tensions of Xylene with Isopropyl Ether or Methyl tert-Butyl Ether at 298.15 K
Solubility of a-Carotene in Binary Solvents Formed by Some Hydrocarbons with tert-Butyl Methyl Ether and with tert-Amyl Methyl Ether
Liquid-Liquid Equilibrium of MTBE + Ethanol + Water and MTBE + 1-Hexanol + Water over the Temperature Range of 288.15 to 308.15 K
Experimental and Predicted Excess Molar Enthalpies of the Ternary System tert-Butyl Methyl Ether + 1-Pentanol + Decane at 298.15 K
Vapor-Liquid Equilibrium Measurements of MTBE and TAME with Toluene
Measurement of Activity Coefficients at Infinite Dilution of Benzene, Toluene, Ethanol, Esters, Ketones, and Ethers at Various Temperatures in Water Using the Dilutor Technique
Vapor-Liquid Equilibria for the Ternary Systems of Methyl tert-Butyl Ether + Methanol + Methylcyclohexane and Methyl tert-Butyl Ether + Methanol + n-Heptane and Constituent Binary Systems at 313.15 K
Liquid-Liquid Equilibria for the Ternary Systems Water + 3-Methyl-2-cyclopentenone with Ethyl Acetate or Methyl tert-Butyl Ether at 293.2 K
Densities and Viscosities for the Ternary Systems of Methyl tert-Butyl Ether + Methanol + Benzene and Methyl tert-Butyl Ether + Methanol + Toluene and Their Sub-binary Systems at 298.15 K
Surface Tension of Dimethoxymethane and Methyl tert-Butyl Ether
Phase Equilibrium Properties of Binary and Ternary Mixtures Containing 1,1-Dimethylethyl Methyl Ether, 1-Propanol, and Hexane at T ) 313.15 K
Liquid-Liquid Equilibria of the Ternary System Water + Acetic Acid + Methyl tert-Butyl Ether
Activity Coefficients at Infinite Dilution Measurements for Organic Solutes and Water in the Ionic Liquid 1-Butyl-3-methyl-pyridinium Trifluoromethanesulfonate
Solubility of Artemisinin in Different Single and Binary Solvent Mixtures Between (284.15 and 323.15) K and NRTL Interaction Parameters
Determination of Activity Coefficients at Infinite Dilution of 35 Solutes in the Ionic Liquid, 1-Butyl-3-methylimidazolium Tosylate, Using Gas-Liquid Chromatography
Density, Viscosity, Vapor-Liquid Equilibrium, and Excess Molar Enthalpy of [Chloroform + Methyl tert-Butyl Ether]
Measurements of Activity Coefficients at Infinite Dilution for Organic Solutes and Water in the Ionic Liquid 1-Butyl-1-methylpiperydinium Thiocyanate
Interactions of Volatile Organic Compounds with the Ionic Liquid 1-Butyl-1-methylpyrrolidinium Dicyanamide
Excess Molar Enthalpies of Ternary and Binary Mixtures Containing 2-Methoxy-2-Methylpropane, Ethanol, and Nonane
Excess Volumes of Ternary Mixtures 2,2,4-Trimethylpentane + Diisopropyl Ether or Methyl tert-Butyl Ether + Methanol, Ethanol, or 1-Propanol at 298.15 K
Determination of Henry's Law Constants Using Internal Standards with Benchmark Values
Liquid Liquid Equilibria for the Ternary System 2-Methoxy-2-methylpropane + Phenol + Water
Measurements of Liquid Liquid Equilibria for the Quaternary System 2-Methoxy-2-methylpropane + Phenol + Hydroquinone + Water at 313.15 K
Thermal Diffusivity of 2-Methoxy-2-methylpropane at Temperatures from (303.15 to 493.15) K and Pressures from (1.5 to 10) MPa
Experimental Determination and Correlation of Liquid Liquid Equilibria for the Ternary System 2-Methoxy-2-methylpropane + o-Cresol + Water at 298.15 K and 313.15 K
Densities and Viscosities of MTBE + Heptane or Octane at p ) 0.1 MPa from (273.15 to 363.15) K
Densities and Viscosities of MTBE + Nonane or Decane at p = 0.1 MPa from (273.15 to 363.15) K
Phase Equilibria of (1-Ethyl-3-methylimidazolium Ethylsulfate + Hydrocarbon, + Ketone, and + Ether) Binary Systems
Excess Enthalpy, Density, and Speed of Sound for the Ternary Mixture Methyl tert-Butyl Ether (1) + Butan-1-ol (2) + Octane (3)
Measurement and Correlation of Liquid-Liquid Equilibrium Data for Water + Acetic Acid + Methyl tert-Butyl Ether + NaCl
Excess Molar Enthalpies of Ternary and Binary Mixtures Containing 2-Methoxy-2-methylpropane, 1-Propanol, and Nonane
Isobaric Vapor-Liquid Equilibria at 101.32 kPa and Densities, Speeds of Sound, and Refractive Indices at 298.15 K for MTBE or DIPE or TAME + 1-Propanol Binary Systems
Vapor-Liquid Equilibria and Interfacial Tensions of the System Ethanol + 2-Methoxy-2-methylpropane
Mixing Properties for Binary Liquid Mixtures of Methyl tert-Butyl Ether with Propylamine and Dipropylamine at Temperatures from (288.15 to 308.15) 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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