Cyclohexane, ethyl-
- Formula: C8H16
- Molecular weight: 112.2126
- IUPAC Standard InChI: InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3
- IUPAC Standard InChIKey: IIEWJVIFRVWJOD-UHFFFAOYSA-N
- CAS Registry Number: 1678-91-7
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Ethylcyclohexane
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Normal boiling point
Go To: Top, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
| Tboil (K) | Reference | Comment |
|---|---|---|
| 405.0 | Weast and Grasselli, 1989 | BS |
| 405. | Majer and Svoboda, 1985 | |
| 405.0 | Kawai, Jarjoui, et al., 1982 | Uncertainty assigned by TRC = 1. K; TRC |
| 405. | Olah, Prakash, et al., 1981 | Uncertainty assigned by TRC = 2. K; TRC |
| 406. | Kursanov, Parnes, et al., 1974 | Uncertainty assigned by TRC = 4. K; TRC |
| 406. | Parnes, Bolestova, et al., 1973 | Uncertainty assigned by TRC = 4. K; TRC |
| 409. | Sporka, Hanika, et al., 1973 | Uncertainty assigned by TRC = 4. K; TRC; Data excluded from overall average |
| 405.0 | Gavrilov and Trostyanskaya, 1970 | Uncertainty assigned by TRC = 1. K; TRC |
| 405. | Landa, Mrnkova, et al., 1969 | Uncertainty assigned by TRC = 3. K; TRC |
| 404. | Mekhtiev, Pashaev, et al., 1966 | Uncertainty assigned by TRC = 4. K; TRC |
| 404.9 | Prabhu and Van Winkle, 1964 | Uncertainty assigned by TRC = 0.4 K; TRC |
| 404.93 | Desty and Whyman, 1957 | Uncertainty assigned by TRC = 0.2 K; TRC |
| 404.93 | Epstein, Willingham, et al., 1956 | Uncertainty assigned by TRC = 0.2 K; TRC |
| 405.0 | Hoffman and Boord, 1956 | Uncertainty assigned by TRC = 0.4 K; TRC |
| 403.7 | Balandin, Turova-Pollyak, et al., 1955 | Uncertainty assigned by TRC = 1. K; TRC |
| 405. | Desty and Fidler, 1951 | Uncertainty assigned by TRC = 0.2 K; TRC |
| 404.85 | Fenske, Braun, et al., 1947 | Uncertainty assigned by TRC = 0.3 K; TRC |
| 404.92 | Anonymous, 1946 | Uncertainty assigned by TRC = 0.3 K; TRC |
| 404.35 | Bazhulin, Sterin, et al., 1946 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 404.93 | Forziati, Glasgow, et al., 1946 | Uncertainty assigned by TRC = 0.01 K; TRC |
| 405.1 | Smith and Pennekamp, 1945 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 405. | Anonymous, 1943 | Uncertainty assigned by TRC = 0.25 K; TRC |
| 404.93 | Forziati, 1943 | Uncertainty assigned by TRC = 0.15 K; TRC |
| 404.93 | Willingham, 1943 | Uncertainty assigned by TRC = 0.1 K; TRC |
| 403.15 | Anonymous, 1940 | Uncertainty assigned by TRC = 0.2 K; TRC |
| 403.55 | Anonymous, 1939 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 404.8 | Evans, 1938 | Uncertainty assigned by TRC = 0.8 K; TRC |
| 404.75 | Evans, 1938, 2 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 405. | Brown, Durand, et al., 1936 | Uncertainty assigned by TRC = 2. K; TRC |
| 404. | Brown, Durand, et al., 1936 | Uncertainty assigned by TRC = 2. K; TRC |
| 402.65 | Ipatieff and Komarewsky, 1936 | Uncertainty assigned by TRC = 1.5 K; TRC |
| 405.05 | Leslie and White, 1935 | Uncertainty assigned by TRC = 0.6 K; TRC |
| 403.6 | Signaigo and Cramer, 1933 | Uncertainty assigned by TRC = 1.5 K; TRC |
| 405.0 | Timmermans, 1927 | Uncertainty assigned by TRC = 0.3 K; source of data not clear; TRC |
| 403.15 | Gilman and Beaber, 1925 | Uncertainty assigned by TRC = 3. K; TRC |
| 402. | Gilman and Hoyle, 1922 | Uncertainty assigned by TRC = 4. K; TRC |
| 410. | Vavon, 1914 | Uncertainty assigned by TRC = 4. K; TRC; Data excluded from overall average |
| 403. | Sabatier and Senderens, 1901 | Uncertainty assigned by TRC = 3. K; TRC |
| 402. | Sabatier and Senderens, 1901, 2 | Uncertainty assigned by TRC = 3. K; TRC |
References
Go To: Top, Normal boiling point, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]
Majer and Svoboda, 1985
Majer, V.; Svoboda, V.,
Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]
Kawai, Jarjoui, et al., 1982
Kawai, T.; Jarjoui, M.; Burwell, R.L.,
Hydrogeration of nitroxides on Pt/SiO2,
J. Am. Chem. Soc., 1982, 104, 2951-6. [all data]
Olah, Prakash, et al., 1981
Olah, G.A.; Prakash, G.K.S.; Arvanaghi, M.; Bruce, M.R.,
Palladium - catalyzed reduction of compounds with Mg/CH3OH,
Andgew. Chem., 1981, 93, 1, 107-9. [all data]
Kursanov, Parnes, et al., 1974
Kursanov, D.N.; Parnes, Z.N.; Loim, N.M.,
Applications of ionic hydrogenation to organic synthesis,
Synthesis, 1974, 9, 633-51. [all data]
Parnes, Bolestova, et al., 1973
Parnes, Z.N.; Bolestova, G.I.; Intyakova, E.I.; Kursanov, D.N.,
Zh. Org. Khim., 1973, 9, 1704-7. [all data]
Sporka, Hanika, et al., 1973
Sporka, K.; Hanika, J.; Ruzicka, V.; Poucek, J.,
Investigation of hydrogenation in liquid phase. XXVI. Kinetics of parallel -consecutive reaction in hydrogenation of 4-vinylcyclohexane,
Collect. Czech. Chem. Commun., 1973, 38, 166-74. [all data]
Gavrilov and Trostyanskaya, 1970
Gavrilov, B.G.; Trostyanskaya, I.I.,
J. Appl. Chem. USSR (Engl. Trans.), 1970, 43, 2143-5. [all data]
Landa, Mrnkova, et al., 1969
Landa, S.; Mrnkova, A.; Bartova, N.,
Hydrogenation of some heterocyclic oxygen-containing compounds,
Sb. Vys. Sk. Chem.-Technol. Praze, Technol. Paliv, 1969, 16, 159-70. [all data]
Mekhtiev, Pashaev, et al., 1966
Mekhtiev, S.D.; Pashaev, T.A.; Iseeva, F.A.,
Alkylation of cyclohexane hydrocarbons by cyclohexane in the presence of sulfuric acid,
Azerb. Khim. Zh., 1966, 2, 91-6. [all data]
Prabhu and Van Winkle, 1964
Prabhu, P.S.; Van Winkle, M.,
Vapor-Liquid Equilibria at Subatmospheric Pressures of the Ethylcyclohexane-n-Octane System,
J. Chem. Eng. Data, 1964, 9, 9. [all data]
Desty and Whyman, 1957
Desty, D.H.; Whyman, B.H.F.,
Anal. Chem., 1957, 29, 320. [all data]
Epstein, Willingham, et al., 1956
Epstein, M.B.; Willingham, C.B.; Mair, B.J.; Rossini, F.D.,
Hydrocarbons in the 126 to 132 deg Fraction of Petroleum,
Anal. Chem., 1956, 28, 1924. [all data]
Hoffman and Boord, 1956
Hoffman, J.; Boord, C.E.,
J. Am. Chem. Soc., 1956, 78, 4973-74. [all data]
Balandin, Turova-Pollyak, et al., 1955
Balandin, A.A.; Turova-Pollyak, M.B.; Kan, S.,
Catalytic transformations of cyclohexane hydrocarbons on aluminosilicate catalyst.,
Dokl. Akad. Nauk SSSR, 1955, 105, 716-19. [all data]
Desty and Fidler, 1951
Desty, D.H.; Fidler, F.A.,
Ind. Eng. Chem., 1951, 43, 905. [all data]
Fenske, Braun, et al., 1947
Fenske, M.R.; Braun, W.G.; Wiegand, R.V.; Quiggle, D.; McCormick, R.H.; Rank, D.H.,
Raman Spectra of Hydrocarbons,
Anal. Chem., 1947, 19, 700. [all data]
Anonymous, 1946
Anonymous, R.,
, Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1946. [all data]
Bazhulin, Sterin, et al., 1946
Bazhulin, P.A.; Sterin, K.E.; Bulanova, T.F.; Solovova, O.P.; Turova-Pollyak, M.B.; Kazanskii, B.A.,
Izv. Akad. Nauk SSSR, 1946, 1946, 7. [all data]
Forziati, Glasgow, et al., 1946
Forziati, A.F.; Glasgow, A.R.; Willingham, C.B.; Rossini, F.D.,
Specification adn Properties of 29 Paraffin, 4 Alkylcyclopentanes, 10 Alkylcyclohexanes and 8 Alkylbenzene Hydrocarbons,
J. Res. Natl. Bur. Stand. (U. S.), 1946, 36, 129. [all data]
Smith and Pennekamp, 1945
Smith, H.A.; Pennekamp, E.F.H.,
The Catalytic Hydrogenation of the Benzene Nucleus II. The Hydrogenation of Benzene and Mono-alkylkbenzenes,
J. Am. Chem. Soc., 1945, 67, 276. [all data]
Anonymous, 1943
Anonymous, R.,
, Sunbury Rep. No. 2176, Anglo-Iranian Oil Co., 1943. [all data]
Forziati, 1943
Forziati, A.F.,
, Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., 1943. [all data]
Willingham, 1943
Willingham, C.B.,
, Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., 1943. [all data]
Anonymous, 1940
Anonymous, R.,
, Am. Pet. Inst. Hydrocarbon Res. Proj., Second Annu. Rep., Ohio State Univ., Aug. 31, 1940. [all data]
Anonymous, 1939
Anonymous, R.,
, Am. Pet. Inst. Hydrocarbon Res. Proj., First Annu. Rep., Ohio State Univ., Aug. 31, 1939. [all data]
Evans, 1938
Evans, E.B.,
The viscosity of hydrocarbons. Parts IV-VI,
J. Inst. Pet. Technol., 1938, 24, 321. [all data]
Evans, 1938, 2
Evans, E.B.,
The viscosity of hydrocarbons. Parts VII and VIII,
J. Inst. Pet. Technol., 1938, 24, 537. [all data]
Brown, Durand, et al., 1936
Brown, J.H.; Durand, H.W.; Marvel, C.S.,
The Reduction of Aromatic Compounds with Hydrogen and a Platinum Oxide- Platinum Black Catalysis in the Presence of Halogen Acid,
J. Am. Chem. Soc., 1936, 58, 1594. [all data]
Ipatieff and Komarewsky, 1936
Ipatieff, V.N.; Komarewsky, V.I.,
Desctructive Alkylation with a Hydrogenating Agent,
J. Am. Chem. Soc., 1936, 58, 922. [all data]
Leslie and White, 1935
Leslie, R.T.; White, J.D.,
Present Status or the Isolation and Identification of The Volatile Hydrocarbons in a Midcontinent Petroleum,
J. Res. Natl. Bur. Stand. (U. S.), 1935, 15, 211. [all data]
Signaigo and Cramer, 1933
Signaigo, F.K.; Cramer, P.L.,
The preparation of some mono- and dialkylcylohexanes,
J. Am. Chem. Soc., 1933, 55, 3326-32. [all data]
Timmermans, 1927
Timmermans, J.,
The Melting Point of Organic Substances,
Bull. Soc. Chim. Belg., 1927, 36, 502. [all data]
Gilman and Beaber, 1925
Gilman, H.; Beaber, N.J.,
The Preparation of Hydrocarbons by Reaction Between Alkyl Sulfonates and Organomagnesium Halides,
J. Am. Chem. Soc., 1925, 47, 518. [all data]
Gilman and Hoyle, 1922
Gilman, H.; Hoyle, R.E.,
A New Method for the Introduction of An Ethyl Group. The Reaction Between Organomagnesium Halides and Diethyl SUlfate,
J. Am. Chem. Soc., 1922, 44, 2621. [all data]
Vavon, 1914
Vavon, G.,
Hydrogeneration catalyst in the presence of platinum blacks. Transformation of aldehydes and ketones to alcohols,
Ann. Chim. (Paris), 1914, 1, 144-200. [all data]
Sabatier and Senderens, 1901
Sabatier, P.; Senderens, J.B.,
C. R. Hebd. Seances Acad. Sci., 1901, 132, 1254. [all data]
Sabatier and Senderens, 1901, 2
Sabatier, P.; Senderens, J.B.,
General Method of Synthesis of Naphthenes,
C. R. Hebd. Seances Acad. Sci., 1901, 132, 566-71. [all data]
Notes
Go To: Top, Normal boiling point, References
- Symbols used in this document:
Tboil Boiling point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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