This page contains azeotrope data for various binary and ternary mixtures of solvents. Data includes composition of mixture by weight (in binary azeotropes when only one fraction is given, it is the fraction of the second component), boiling point of components, boiling point of mixture, and specific gravity of mixture. Boiling points are at 760 mm Hg unless otherwise stated. Where the mixture separates into layers, values are shown for upper (U) and lower (L) layers.
Additional recommended knowledge
Data is obtained from Lange's 10th edition[1] and CRC 44th edition[2] unless otherwise noted (see color code table).
Binary azeotropes
Data source color code
|
CRC & Lange's
| CRC only
| Lange's only
| other (see references)
|
Azeotropes of water, BP=100°C
‡ CRC 44th ed. lists azeotropes for acetic acid/water and acetone/water, Lange's 10th ed. as well as numerous web sources indicate no azeotrope for these pairs.
Azeotropes of allyl alcohol, BP=97.0°C
2nd Component | BP of comp. | BP of mixture | % by weight | spef. grav
|
with various solvents
|
methyl butyrate | 102.7°C | 93.8°C | 45 |
|
n-propyl acetate | 101.6°C | 94.2°C | 47 |
|
benzene | 80.2°C | 76.8°C | 82.6
| 0.874
|
toluene | 110.8°C | 92.4°C | 50 |
|
cyclohexane | 80.8°C | 74°C | 80 |
|
carbon tetrachloride | 76.8°C | 72.3°C | 88.5
| 1.450
|
ethylene chloride | 83.7°C | 79.9°C | 82 |
|
|
| Azeotropes of ethanol, BP=78.4°C
|
Azeotropes of methanol, BP=64.7°C
|
- Azeotropes of n-propanol, BP=97.2°C
2nd Component | BP of comp. | BP of mixture | % by weight | spef. grav
|
with various solvents
|
methyl butyrate | 102.7°C | 94.4°C | 51 |
|
n-propyl formate | 80.8°C | 80.65°C | 97 |
|
n-propyl acetate | 101.6°C | 94.7°C | 49
| 0.833
|
benzene | 80.2°C | 77.1°C | 83.1 |
|
toluene | 110.8°C | 92.4°C | 47.5
| 0.836
|
n-hexane | 68.9°C | 65.7°C | 96 |
|
carbon tetrachloride | 76.8°C | 73.1°C | 88.5
| 1.437
|
ethylene chloride | 83.7°C | 80.7°C | 81 |
|
n-propyl bromide | 71.0°C | 69.7°C | 91 |
|
- Azeotropes of acetic acid, BP=118.5°C
|
|
- Azeotropes of isopropanol, BP=82.5°C
‡ CRC and Lange's disagree on this azeotrope, but web source corroborates CRC
|
Miscellaneous azeotrope pairs
|
Ternary azeotropes
Tables of various ternary azeotropes (that is azeotropes consisting of three components). Fraction percentages are given by weight.
Data source color code
|
CRC & Lange's
| CRC only
| Lange's only
| other (see references)
|
Ternary azeotropes of water, BP=100°C
2nd component | BP 2nd comp. | 3rd component | BP 3rd comp. | | BP azeo. | % wt 1st | % wt 2nd | % wt 3rd | spec. grav
|
ethanol
| 78.4°C | ethyl acetate | 77.1°C
|
| 70.3°C | 7.8 | 9.0 | 83.2
| 0.901
|
cyclohexane | 80.8°C | 62.1°C | 7 | 17 | 76 |
|
benzene | 80.2°C | 64.9°C | 7.4 U 1.3 L 43.1 | 18.5 U 12.7 L 52.1 | 74.1 U 86.0 L 4.8
| U 0.866 L 0.892
|
chloroform | 61.2°C | 55.5°C | 3.5 U 80.8 L 0.5 | 4.0 U 18.2 L 3.7 | 92.5 U 1.0 L 95.8
| U 0.976 L 1.441
|
carbon tetrachloride
| 86.8°C
| 61.8°C
| 4.3
| 9.7
| 86.0 |
|
3.4 U 44.5 L <0.1 | 10.3 U 48.5 L 5.2 | 86.3 U 7.0 L 94.8
| U 0.935 L 1.519
|
ethylene chloride | 83.7°C | 66.7°C | 5 | 17 | 78 |
|
acetonitrile | 82.0°C | 72.9°C | 1.0 | 55.0 | 44.0 |
|
toluene | 110.6°C | 74.4°C | 12.0 U 3.1 L 20.7 | 37.0 U 15.6 L 54.8 | 51.0 U 81.3 L 24.5 | U 0.849 L 0.855
|
methyl ethyl ketone | 79.6°C | 73.2°C | 11.0 | 14.0 | 75.0 | 0.832
|
n-hexane | 69.0°C | 56.0°C | 3.0 U 0.5 L 19.0 | 12.0 U 3.0 L 75.0 | 85.0 U 96.5 L 6.0
| U 0.672 L 0.833
|
n-heptane | 98.4°C | 68.8°C | 6.1 U 0.2 L 15.0 | 33.0 U 5.0 L 75.9 | 60.9 U 94.8 L 9.1 | U 0.686 L 0.801
|
carbon disulfide | 46.2°C | 41.3°C | 1.6 | 5.0 | 93.4 |
|
n-propanol
| 97.2°C
| cyclohexane | 80.8°C | 66.6°C | 8.5 | 10.0 | 81.5 |
|
benzene | 80.2°C | 68.5°C | 8.6 | 9.0 | 82.4 |
|
carbon tetrachloride | 76.8°C | 65.4°C | 5 U 84.9 L 1.0 | 11 U 15.0 L 11.0 | 84 U 0.1 L 88.0
| U 0.979 L 1.436
|
diethyl ketone | 102.2°C | 81.2°C | 20 | 20 | 60 |
|
n-propyl acetate | 101.6°C | 82.2°C | 21.0 | 19.5 | 59.5 |
|
isopropanol
| 82.5°C
| cyclohexane
| 80.8°C
| 64.3°C
| 7.5
| 18.5
| 74.0 |
|
66.1°C
| 7.5
| 21.5
| 71.0 |
|
benzene
| 80.2°C
| 66.5°C
| 7.5
| 18.7
| 73.8 |
|
65.7°C | 8.2 U 2.3 L 85.1 | 19.8 U 20.2 L 14.4 | 72.0 U 77.5 L 0.5 | U 0.855 L 0.966
|
methyl ethyl ketone | 79.6°C | 73.4°C | 11.0 | 1.0 | 88.0 | 0.834
|
toluene | 110.6°C | 76.3°C | 13.1 U 8.5 L 61.0 | 38.2 U 38.2 L 38.0 | 48.7 U 53.3 L 1.0 | U 0.845 L 0.930
|
allyl alcohol
| 97.0°C
| n-hexane | 69.0°C | 59.7°C | 5 U 0.5 L 64.4 | 5 U 3.6 L 34.8 | 90 U 95.9 L 0.8
| U 0.668 L 0.964
|
benzene | 80.2°C | 68.2°C | 8.6 U 0.6 L 80.9 | 9.2 U 8.7 L 17.7 | 82.2 U 90.7 L 0.4
| U 0.877 L 0.985
|
cyclohexane | 80.8°C | 66.2°C | 8 | 11 | 81 |
|
carbon tetrachloride | 76.8°C | 65.2°C | 5 U 71.7 L 0.8 | 11 U 25.6 L 10.1 | 84 U 2.7 L 89.1
| U 0.777 L 1.464
|
benzene
| 80.1°C
| acetonitrile
| 82.0°C
| 66.0°C
| 8.2
| 68.5
| 23.3 |
|
methyl ethyl ketone | 79.6°C | 68.2°C | 8.8 U 0.6 L 94.7 | 65.1 U 71.3 L 0.1 | 26.1 U 28.1 L 5.2 | U 0.858 L 0.992
|
methyl ethyl ketone
| 79.6°C
| carbon tetrachloride
| 76.8°C
| 65.7°C
| 3.0 U 94.4 L 0.1
| 22.2 U 5.5 L 22.6
| 74.8 U 0.1 L 77.3
| U 0.993 L 1.313
|
cyclohexane | 81.0°C | 63.6°C | 5.0 U 0.6 L 89.9 | 60.0 U 37.0 L 10.0 | 35.0 U 62.4 L 0.1 | U 0.769 L 0.98
|
chloroform
| 61.2°C
| methanol
| 64.65°C
| 52.6°C
| 4.0 U 27.0 L 3.0
| 81.0 U 32.0 83.0
| 15.0 U 41.0 L 14.0
| U 1.022 L 1.399
|
acetone‡
| 56.5°C
| 60.4°C
| 4.0
| 57.6
| 38.4 |
|
|
‡Saddle azeotrope
|
Ternary azeotropes of methanol, BP=64.65°C
References
- ^ Lange's Handbook of Chemistry, 10th ed. pp1496-1505
- ^ CRC Handbook of Chemistry and Physics, 44th ed. pp 2143-2184
- ^ a b c d e What is an Azeotrope?. B/R Corporation. Retrieved on 24 March 2007.
- ^ a b
Hilmen, Eva-Katrine (November 2000). Separation of Azeotropic Mixtures: Tools for Anaylsis and Studies on Batch Distillation Operation. Norwegian University of Science and Technology, dept. of Chemical Engineering. Retrieved on 24 March 2007.
- ^ Merck Index of Chemicals and Drugs, 9th ed. monograph 4653
- ^ a b c d e Ponton, Jack (September 2001). Azeotrope Databank (Queriable database). The Edinburgh Collection of Open Software for Simulation and Education, Edinburgh University. Retrieved on 24 March 2007.
- ^ a b c Binary Vapor-Liquid Equilibrium Data (Queriable database). Chemical Engineering Research Information Center.
- ^ a b Tetrahydrafuran (THF) Storage and Handling. BASF. Retrieved on 24 May 2007.
- ^ 1,2-Propanediol. ChemIndustry.ru. Retrieved on 2007-12-28.
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