Cyclohexane, 1,2,4-trimethyl-

• Formula: C₉H₁₈
• Molecular weight: 126.2392
• IUPAC Standard InChI: InChI=1S/C9H18/c1-7-4-5-8(2)9(3)6-7/h7-9H,4-6H2,1-3H3 Copy

  
• IUPAC Standard InChIKey: VCJPCEVERINRSG-UHFFFAOYSA-N Copy
• CAS Registry Number: 2234-75-5
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Species with the same structure:
  • 1,2,5-trimethylcyclohexane
• Stereoisomers:
  • Cyclohexane, 1,2,4-trimethyl-, (1α,2α,4α)-
  • Cyclohexane, 1,2,4-trimethyl-, (1α,2α,4β)-
  • Cyclohexane, 1,2,4-trimethyl-, (1α,2β,4α)-
  • Cyclohexane, 1,2,4-trimethyl-, (1α,2β,4β)-
  • cis, trans, cis-1,2,4-Trimethylcyclohexane
  • 1,2,4-Trimethylcyclohexane, cis,trans,trans
  • 1-cis-2-trans-4-Trimethylcyclohexane
• Other names: 1,2,4-Trimethylcyclohexane
• 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
• Data at other public NIST sites:
  • 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 by: 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.

Smith and Pennekamp, 1945
Smith, H.A.; Pennekamp, E.F.H., The Catalytic Hydrogenation of the Benzene Nucleus III. The Hydrogenation of Polymethylbenzenes, J. Am. Chem. Soc., 1945, 67, 279. [all data]

White and Glasgow, 1939
White, J.D.; Glasgow, A.R., Separation of 1,2,4-Trimethylcyclohexane and An Isononane From A Midcontinent Petroleum, J. Res. Natl. Bur. Stand. (U. S.), 1939, 22, 137. [all data]

Eisenlohr, 1925
Eisenlohr, F., Fortschr. Chem., Phys. Phys. Chem., 1925, 18, 521. [all data]

Von Auwers, 1920
Von Auwers, K., Relation Between Constitution and Physical Properties of Hydroaromatic Compounds, Justus Liebigs Ann. Chem., 1920, 420, 84-111. [all data]

Engler and Hofer, 1913
Engler, C.; Hofer, H., Das Erdols, Vol. 1, Hirtzel Co.: Leipzig, Ger., 1913. [all data]

Ahrens and Mozd'enski, 1908
Ahrens, F.B.; Mozd'enski, L.V., Angew. Chem., 1908, 21, 1411. [all data]

Sabatier and Senderens, 1905
Sabatier, P.; Senderens, J.B., Ann. Chim. Phys., 1905, 4, 358. [all data]

Sabatier and Senderens, 1901
Sabatier, P.; Senderens, J.B., C. R. Hebd. Seances Acad. Sci., 1901, 132, 1254. [all data]

Sabatier and Senderens, 1901, 2
Sabatier, P.; Senderens, J.B., General Method of Synthesis of Naphthenes, C. R. Hebd. Seances Acad. Sci., 1901, 132, 566-71. [all data]

Markownikov, 1898
Markownikov, W., Justus Liebigs Ann. Chem., 1898, 301, 127. [all data]

Konovalov, 1887
Konovalov, M., Zh. Russ. Fiz.-Khim. O-va., 1887, 19, 255. [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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