1-Hexene

• Formula: C₆H₁₂
• Molecular weight: 84.1595
• IUPAC Standard InChI: InChI=1S/C6H12/c1-3-5-6-4-2/h3H,1,4-6H2,2H3 Copy

  
• IUPAC Standard InChIKey: LIKMAJRDDDTEIG-UHFFFAOYSA-N Copy
• CAS Registry Number: 592-41-6
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Hexene-1; 1-n-Hexene; 1-C6H12; Butylethylene; Hexene; Hex-1-ene; UN 2370; Hexylene; Neodene 6 XHP; NSC 74121; Dialene 6
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
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Normal boiling point

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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

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]

Humphrey and Van Winkle, 1967
Humphrey, J.L.; Van Winkle, M., Vapor-Liquid Equilibria at 60 deg C for n-Hexane-Alkyl Amines and 1-Hexene- Alkyl AMines, J. Chem. Eng. Data, 1967, 12, 526. [all data]

Suryanarayana and Van Winkle, 1966
Suryanarayana, Y.S.; Van Winkle, M., Solvent effect on relative volatility: n-hexane + 1-hexene system., J. Chem. Eng. Data, 1966, 11, 7-12. [all data]

Kaal. T.A., Ordyan, et al., 1965
Kaal. T.A.; Ordyan, M.B.; Eidus, Y.T., Synthesis of Carboxylic Acid Derivatives Uner Conditions of Acid Catalysis From Carbon Monoxide, Olefines, and Acylating Agents, Zh. Org. Khim., 1965, 1, 1187-9. [all data]

Wright, 1961
Wright, F.J., Influence of temperature on viscosity of nonassociated liquids, J. Chem. Eng. Data, 1961, 6, 454. [all data]

Wright, 1960
Wright, F.J., Latent Heat of Vaporization and Composition, Recl. Trav. Chim. Pays-Bas, 1960, 79, 784-9. [all data]

Searles, Nickerson, et al., 1959
Searles, S.; Nickerson, R.G.; Witsiepe, W.K., Oxetanes. IX. Structural and Solvent Effects in the Reaction of γ-Bromo Alcohols with Base, J. Org. Chem., 1959, 24, 1839. [all data]

Desty and Whyman, 1957
Desty, D.H.; Whyman, B.H.F., Anal. Chem., 1957, 29, 320. [all data]

Urry, Stacey, et al., 1954
Urry, W.H.; Stacey, F.W.; Huyser, E.S.; Juveland, O.O., The Peroxide- and Light-induced Additions of Alcohols to Olefins, J. Am. Chem. Soc., 1954, 76, 450. [all data]

Zafiriadis and Mastagli, 1954
Zafiriadis, Z.; Mastagli, P., C. R. Hebd. Seances Acad. Sci., 1954, 238, 821. [all data]

Schuhmacher, Wibaut, et al., 1953
Schuhmacher, J.P.; Wibaut, J.P.; Paerels, G.B., Recl. Trav. Chim. Pays-Bas, 1953, 72, 1037. [all data]

Robertson, Heyes, et al., 1952
Robertson, P.W.; Heyes, J.K.; Swedlund, B.E., The Kinetics of Halogen Addition to Unsaturated Compounds XXII. Alkyl- and Halogenoalkylethylenes, J. Chem. Soc., 1952, 1952, 1014. [all data]

Desty and Fidler, 1951
Desty, D.H.; Fidler, F.A., Ind. Eng. Chem., 1951, 43, 905. [all data]

Kharasch and Zavist, 1951
Kharasch, M.S.; Zavist, A.F., Reactions of Atoms and Free Radicals in Solution. XXIII. The Peroxide- Induced Addition of Sulfuryl Chloride to 1-Alkenes, J. Am. Chem. Soc., 1951, 73, 964. [all data]

Braun, Spooner, et al., 1950
Braun, W.G.; Spooner, D.F.; Fenske, M.R., Raman spectra hydrocarbons and oxygenated compounds, Anal. Chem., 1950, 22, 1074. [all data]

Campbell, Burney, et al., 1950
Campbell, T.W.; Burney, W.; Jacobs, T.L., THe Reaction of Gignard Reagents with D-t-butyl Peroxide, J. Am. Chem. Soc., 1950, 72, 2735. [all data]

Mears, Fookson, et al., 1950
Mears, T.W.; Fookson, A.; Pomerantz, P.; Rich, E.H.; Dussinger, C.S.; Howard, F.L., Syntheses and Properties of Two Olefins, Six Paraffins, and Their Intermediates, J. Res. Natl. Bur. Stand. (U. S.), 1950, 44, 299. [all data]

Tilicheev and Milovidova, 1949
Tilicheev, M.D.; Milovidova, N.V., Isolation of individual hydrocarbons from a paraffin cracking distillate: II isolation of n-alkanes and 1-alkenes with the carbon atom number from five to eleven, Zh. Prikl. Khim. (Leningrad), 1949, 22, 611-24. [all data]

Anonymous, 1947
Anonymous, R., , Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1947. [all data]

Kazanskii, Liberman, et al., 1947
Kazanskii, B.A.; Liberman, A.L.; Plate, A.F.; Rozengart, M.I.; Tarasova, G.A., Synthesis and Properties of Some 1-Alkenes, Zh. Obshch. Khim., 1947, 17, 1503. [all data]

Anonymous, 1946
Anonymous, R., , Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1946. [all data]

Boord, Greenlee, et al., 1946
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Weight, Am. Pet. Inst. Res. Proj. 45, Eighth Annu. Rep., Ohio State Univ., June 30, 1946. [all data]

Hay, Montgomery, et al., 1945
Hay, R.G.; Montgomery, C.W.; Coull, J., Catalytic Isomerization of 1-Hexene, Ind. Eng. Chem., 1945, 37, 335. [all data]

Boord, 1942
Boord, C.E., Oil & Gas J., 1942, 41, 27, 188. [all data]

Van Pelt and Wibaut, 1941
Van Pelt, A.J.; Wibaut, J.P., The preparation of unsaturated hydrocarbons by the thermal decomposition of acetates., Recl. Trav. Chim. Pays-Bas, 1941, 60, 55. [all data]

Goldwasser and Taylor, 1939
Goldwasser, S.; Taylor, H.S., Catalytic dehydration of c6-c8 aliphatic alcohols, J. Am. Chem. Soc., 1939, 61, 1751. [all data]

Winstein and Lucas, 1938
Winstein, S.; Lucas, H.J., J. Am. Chem. Soc., 1938, 60, 836. [all data]

Maess and von Muffling, 1937
Maess, L.; von Muffling, L., On the Vapor Pressures of Hydrocarbons and Ketones, Angew. Chem., 1937, 50, 759. [all data]

Mulliken, Wakeman, et al., 1935
Mulliken, S.P.; Wakeman, R.L.; Gerry, H.T., The preparation of certain alkenes, alkadienes and alkynes, J. Am. Chem. Soc., 1935, 57, 1605-7. [all data]

Van Risseghem, Gredy, et al., 1933
Van Risseghem, H.; Gredy, B.; Piaux, I., C. R. Hebd. Seances Acad. Sci., 1933, 196, 938. [all data]

Waterman and de Kok, 1933
Waterman, H.I.; de Kok, W.J.C., The Preparation of Pure Normal α-Hexene, Recl. Trav. Chim. Pays-Bas, 1933, 52, 251. [all data]

Schmitt and Boord, 1932
Schmitt, C.G.; Boord, C.E., Nuclear syntheses in the olefin series: III the hexenes, J. Am. Chem. Soc., 1932, 54, 751-61. [all data]

Dykstra, Lewis, et al., 1930
Dykstra, H.B.; Lewis, J.F.; Boord, C.E., A nuclear synthesis of unsaturated hydrocarbons: I alpha-olefins, J. Am. Chem. Soc., 1930, 52, 3396. [all data]

Bourguel, 1927
Bourguel, M., Bull. Soc. Chim. Fr., 1927, 41, 1475. [all data]

Brame and Hunter, 1927
Brame, J.S.S.; Hunter, T.G., Composition of Cracked Distillates, J. Inst. Pet. Technol., 1927, 13, 794. [all data]

Timmermans, 1927
Timmermans, J., The Melting Point of Organic Substances, Bull. Soc. Chim. Belg., 1927, 36, 502. [all data]

Kirrmann, 1926
Kirrmann, A., 1-ethylene hydrocarbons, Bull. Soc. Chim. Fr., 1926, 39, 988-91. [all data]

Van Risseghem, 1926
Van Risseghem, H., Bull. Soc. Chim. Belg., 1926, 35, 328. [all data]

Faragher and Garner, 1921
Faragher, W.F.; Garner, F.H., The Elimination of Hydrogen CHloride from Chlorohydrocarbons, J. Am. Chem. Soc., 1921, 43, 1715-24. [all data]

Lagerlof, 1918
Lagerlof, D., Thermodynamic research: reduced formulas for simplified calculations of latent molar heat of evaporation, J. Prakt. Chem., 1918, 98, 136. [all data]

Landolt and Jahn, 1892
Landolt, H.; Jahn, H., The Molecular Refraction of Several Simple Organic Compounds for Rays of Infinitely Great Wave Length., Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1892, 10, 289. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

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