2,4-Hexadiene

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

  
• IUPAC Standard InChIKey: APPOKADJQUIAHP-UHFFFAOYSA-N Copy
• CAS Registry Number: 592-46-1
• Chemical structure:
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• Stereoisomers:
  • 2,4-Hexadiene, (E,Z)-
  • 2,4-Hexadiene, (E,E)-
  • (Z),(Z)-2,4-Hexadiene
• Other names: 1,4-Dimethylbutadiene; Bipropenyl; Dipropenyl; CH3CH=CHCH=CHCH3; Hexa-2,4-diene; cis,trans-hexa-2,4-diene
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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  • Gas Phase Kinetics Database
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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
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [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]

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]

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]

Paul and Tchelitcheff, 1946
Paul, R.; Tchelitcheff, S., C. R. Hebd. Seances Acad. Sci., 1946, 223, 1136. [all data]

Henne and Chanan, 1944
Henne, A.L.; Chanan, H.H., Conjugated Diolefins by Double Bond Displacerment II., J. Am. Chem. Soc., 1944, 66, 395. [all data]

Prevost, 1944
Prevost, C., Bull. Soc. Chim. Fr., 1944, 11, 218. [all data]

Henne and Turk, 1942
Henne, A.L.; Turk, A., Conjugated diolefins by double bond displacement, J. Am. Chem. Soc., 1942, 64, 826-8. [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]

Prevost, 1941
Prevost, C., Bull. Soc. Chim. Fr., 1941, 8, 89. [all data]

Whitby and Gallay, 1932
Whitby, G.S.; Gallay, W., Studies of polymers and polymerization V. The influence of methyl and \ phenyl substitution on the polymerizability of butadiene, Can. J. Res., 1932, 6, 280. [all data]

Prevost, 1928
Prevost, C., Ann. Chim. (Paris), 1928, 10, 113. [all data]

Enklaar, 1917
Enklaar, C.J., Recl. Trav. Chim. Pays-Bas, 1917, 36, 215. [all data]

Eykman, 1892
Eykman, J.F., Refractive Measurements, Ber. Dtsch. Chem. Ges., 1892, 25, 3069. [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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