Hexane, 2,2,5-trimethyl-

• Formula: C₉H₂₀
• Molecular weight: 128.2551
• IUPAC Standard InChI: InChI=1S/C9H20/c1-8(2)6-7-9(3,4)5/h8H,6-7H2,1-5H3 Copy

  
• IUPAC Standard InChIKey: HHOSMYBYIHNXNO-UHFFFAOYSA-N Copy
• CAS Registry Number: 3522-94-9
• Chemical structure:
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• Other names: 2,2,5-Trimethylhexane
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Henry's Law 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.

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]

Maretina and Petrov, 1961
Maretina, I.A.; Petrov, A.A., Conjugated Systems CXXIX. Enyne Compounds XLIX. The Order of Addition of Tertiary Alkyl Halides to Propenyl-, Isopropenyl, and Vinylmethylacetylenes, Zh. Obshch. Khim., 1961, 31, 419. [all data]

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]

Marschner and Carmody, 1951
Marschner, R.F.; Carmody, D.R., React. of Isoalkane and Olefin Percursors Catalyzed by Sulfuric Acid, J. Am. Chem. Soc., 1951, 73, 604. [all data]

Forziati and Rossini, 1949
Forziati, A.F.; Rossini, F.D., J. Res. Natl. Bur. Stand. (U. S.), 1949, 43, 473. [all data]

Hickinbottom, Porter, et al., 1949
Hickinbottom, W.J.; Porter, C.R.; Edwards, F.; Schluchterer, E.; Spitzer, F., The synthesis of some hydrocarbons, J. Inst. Pet., 1949, 35, 621-30. [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]

Howard, Mears, et al., 1947
Howard, F.L.; Mears, T.W.; Fookson, A.; Pomerantz, P.; Brooks, D.B., Preparation and physical properties of several aliphatic hydrocarbons and intermediates, J. Res. Natl. Bur. Stand. (U. S.), 1947, 38, 365. [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]

Perilstein, 1945
Perilstein, W.L., , Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1945. [all data]

Anonymous, 1944
Anonymous, R., , Sunbury Rep., Anglo-Iranian Oil Co., March 22, 1944. [all data]

Brooks, 1943
Brooks, D.B., , Natl. Advis. Comm. Aeronaut., Rep. Natl. Bur. Stand., Was hington, D. C., 1943. [all data]

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]

Turk, 1941
Turk, A., , Ph.D. Thesis, Ohio State Univ., Columbus, OH, 1941. [all data]

Brooks, Cleaton, et al., 1937
Brooks, D.B.; Cleaton, R.B.; Carter, F.R., Paraffin Hydrocarbons Isolated from Crude Synthetic Isooctane (2,2,4-Trimethylpentane), J. Res. Natl. Bur. Stand. (U. S.), 1937, 19, 319. [all data]

Noller, 1929
Noller, C.R., The Prep. of Zinc Alkyls and Their Use in the Synthesis of Hydrocarbons, J. Am. Chem. Soc., 1929, 51, 594. [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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