1-Octene

• Formula: C₈H₁₆
• Molecular weight: 112.2126
• IUPAC Standard InChI: InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3 Copy

  
• IUPAC Standard InChIKey: KWKAKUADMBZCLK-UHFFFAOYSA-N Copy
• CAS Registry Number: 111-66-0
• 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: α-Octene; α-Octylene; n-1-Octene; Caprylene; 1-C8H16; Oct-1-ene; Octene-1; Neodene 8; Octylene; 1-n-Octene; NSC 8457; SHOP C8
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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.

Aldrich Chemical Company Inc., 1990
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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
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Wright, 1960
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Weber, 1956
Weber, J.H., Vapor-liquid equilibria at atmospheric pressure: systems 2,2,5,- trimethylhexane - ethylbenzene and 1-octene - ethylbenzene, Ind. Eng. Chem., 1956, 48, 134. [all data]

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Brewster, 1954
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Pomerantz, Fookson, et al., 1954
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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]

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Kharasch and Mosher, 1952
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Urry, Juveland, et al., 1952
Urry, W.H.; Juveland, O.O.; Stacey, F.W., J. Am. Chem. Soc., 1952, 74, 6155. [all data]

Anonymous, 1951
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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]

Campbell, Burney, et al., 1950
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Anonymous, 1949
Anonymous, R., , Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1949. [all data]

Boord, Henne, et al., 1949
Boord, C.E.; Henne, A.L.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M., The Grignard Reagent in hydrocarbon synthesis, Ind. Eng. Chem., 1949, 41, 609. [all data]

Foehr and Fenske, 1949
Foehr, E.G.; Fenske, M.R., Magneto-optic Rotation of Hydrocarbons, Ind. Eng. Chem., 1949, 41, 1956. [all data]

Petrov and Frost, 1949
Petrov, A.A.; Frost, A.V., Redistribution of Hydrogen in Octenes on Alumino-silicate Catalyst, Dokl. Akad. Nauk SSSR, 1949, 65, 851. [all data]

Platt, Klevens, et al., 1949
Platt, J.R.; Klevens, H.B.; Price, W.C., J. Chem. Phys., 1949, 17, 466. [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]

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]

Klevens and Platt, 1947
Klevens, H.P.; Platt, J.R., J. Am. Chem. Soc., 1947, 69, 3055. [all data]

Komarewsky and Ulick, 1947
Komarewsky, V.I.; Ulick, S.C., J. Am. Chem. Soc., 1947, 69, 492. [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]

Cleveland, 1943
Cleveland, F.F., Raman spectra of hydrocarbons: I 1-octene, cis + trans-2-octene, trans-3- octene, trans-4-octene, 4-octyne, and 1-octyne, J. Chem. Phys., 1943, 11, 1. [all data]

Henne and Greenlee, 1943
Henne, A.L.; Greenlee, K.W., Hydrogenation of the triple bond., J. Am. Chem. Soc., 1943, 65, 2020. [all data]

Boord, 1942
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Greenlee, 1942
Greenlee, K.W., , Ph.D. Thesis, Ohio State Univ., Columbus, OH, 1942. [all data]

Anonymous, 1941
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Henne, Chanan, et al., 1941
Henne, A.L.; Chanan, H.H.; Turk, A., Olefins and Diolefins from Allylic Chlorides, J. Am. Chem. Soc., 1941, 63, 3474-6. [all data]

Meshcheryakov, 1941
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Van Pelt and Wibaut, 1941
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Goldwasser and Taylor, 1939
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Jostes and Bartels, 1937
Jostes, F.; Bartels, W., Oel Kohle, 1937, 13, 44, 1166. [all data]

Gelhaar, 1935
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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]

Ward and Fulweiler, 1934
Ward, A.L.; Fulweiler, W.H., Ind. Eng. Chem., Anal. Ed., 1934, 6, 396. [all data]

Dietrich, 1933
Dietrich, M.A., Syntheses in the olefin series octenes of type I and type II, Ph.D. Thesis, Ohio State Univ., Columbus, OH, 1933. [all data]

Whitmore and Herndon, 1933
Whitmore, F.C.; Herndon, J.M., The dehydration of capryl alcohol, J. Am. Chem. Soc., 1933, 55, 3428. [all data]

Mavity, 1931
Mavity, J.M., , Ph.D. Thesis, Ohio State Univ., Columbus, OH, 1931. [all data]

Wilkinson, 1931
Wilkinson, R., J. Chem. Soc., 1931, 1931, 3057. [all data]

Baurguel, 1927
Baurguel, M., Bull. Soc. Chim. Belg., 1927, 41, 1475. [all data]

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

Senderens, 1922
Senderens, J.B., Ann. Chim. (Paris), 1922, 18, 117. [all data]

Brooks and Humphrey, 1918
Brooks, B.T.; Humphrey, I., The Action of Concentrated Sulfuric Acid on Olefins, with Particular Reference to the Refining of Petroleum Distillates, J. Am. Chem. Soc., 1918, 40, 822. [all data]

Lagerlof, 1918
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Chablay, 1914
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Senderens, 1912
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Von Braun, 1911
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Krapiwin, 1908
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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]

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Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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