2-Hexyne

• Formula: C₆H₁₀
• Molecular weight: 82.1436
• IUPAC Standard InChI: InChI=1S/C6H10/c1-3-5-6-4-2/h3,5H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: MELUCTCJOARQQG-UHFFFAOYSA-N Copy
• CAS Registry Number: 764-35-2
• 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: Methyl(propyl)acetylene; 1-Methyl-2-propylacetylene; C3H7C≡CCH3; Hex-2-yne
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Phase change data
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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

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Farchan Laboratories, 1990
Farchan Laboratories, Research Chemicals Catalog, Farchan Laboratories, Gainesville, FL, 1990, 91. [all data]

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]

Elvelt, Otsa, et al., 1981
Elvelt, A.; Otsa, E.; Kirss, H.; Eisen, O., Izv. Akad. Nauk Est. SSR, 1981, 30, 53. [all data]

Labarre, 1963
Labarre, J.F., Contribution to the Study of Magneto-Optics of Bonds Between Atoms in Aliphatic Hydrocarbons, Ann. Chim., 1963, 8, 45-83. [all data]

Gallais and Labarre, 1959
Gallais, F.; Labarre, J.F., Magnetic Rotory Power of Linear Monomacetylenic Hydrocarbons, C. R. Hebd. Seances Acad. Sci., 1959, 249, 2045. [all data]

Miller, Greenlee, et al., 1954
Miller, H.M.; Greenlee, K.W.; Derfer, J.M.; Boord, C.E., J. Org. Chem., 1954, 19, 1882. [all data]

Pomerantz, Fookson, et al., 1954
Pomerantz, P.; Fookson, A.; Mears, T.W.; Rothberg, S.; Howard, F.L., Synthesis and Physical Properties of Several Acetylenic Hydrocarbons, J. Res. Natl. Bur. Stand. (U. S.), 1954, 52, 51. [all data]

Levina and Viktorova, 1950
Levina, R.Ya.; Viktorova, E.A., Isomerization of Unsaturated Hydrocarbons on Contact with Metal Oxides IX. Isomerization of Acetylenic Hydrocarbons Over Chromium Oxide on Aluminum Oxide, Zh. Obshch. Khim., 1950, 20, 677. [all data]

Anonymous, 1948
Anonymous, R., , Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., 1948. [all data]

Boord, Greenlee, et al., 1947
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Wt., Am. Pet. Inst. Res. Proj. 45, Ninth Annu. Rep., Ohio State Univ., June 30, 1947. [all data]

Hurd and Christ, 1937
Hurd; Christ, J. Am. Chem. Soc., 1937, 59, 2161. [all data]

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

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

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

Bourguel, 1925
Bourguel, M., Ann. Chim. (Paris), 1925, 3, 191. [all data]

Welt, 1897
Welt, I., Chem. Ber., 1897, 30, 1493. [all data]

Favorskii and Debout, 1890
Favorskii, A.; Debout, J. Prakt. Chem., 1890, 42, 149. [all data]

Favorskii, 1887
Favorskii, A., Zh. Russ. Fiz.-Khim. O-va., 1887, 19, 562. [all data]

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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