Cyclohexane, 1,2-dimethyl- (cis/trans)

• Formula: C₈H₁₆
• Molecular weight: 112.2126
• IUPAC Standard InChI: InChI=1S/C8H16/c1-7-5-3-4-6-8(7)2/h7-8H,3-6H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: KVZJLSYJROEPSQ-UHFFFAOYSA-N Copy
• CAS Registry Number: 583-57-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  View 3d structure (requires JavaScript / HTML 5)
• Stereoisomers:
  • Cyclohexane, 1,2-dimethyl-, cis-
  • cyclohexane, 4,5-dimethyl-, cis-
  • Cyclohexane, 1,2-dimethyl-, trans-
• Other names: Cyclohexane, 1,2-dimethyl-; 1,2-Dimethylcyclohexane; o-Dimethylcyclohexane; UN 2263
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
• Options:
  • Switch to calorie-based units

Data at NIST subscription sites:

• NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)

NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.

Normal boiling point

Go To: Top, References, Notes

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]

Krylova, Mosse, et al., 1972
Krylova, I.A.; Mosse, A.L.; Shcherbina, E.I.; Efimova, T.I., Composition of separate fractions of liquid products from the pyrolysis of petroleum in a plasma jet, Khim. Vys. Energ., 1972, 6, 156-163. [all data]

Mekhtiev, Magerramova, et al., 1967
Mekhtiev, S.D.; Magerramova, Z.Yu.; Suleimanov, G.N.; Magerramova, R.Yu., Preparation of phthalimide by the oxidative ammonolysis of 1,2-dimethylcyclohexane in a fluidized catalyst bed, Azerb. Khim. Zh., 1967, 5, 61-4. [all data]

Mekhtiev and Magerramova, 1966
Mekhtiev, S.D.; Magerramova, R.Yu., Oxidative ammonolysis of dimethylcyclohexane isomers and their mitures with a fluidized bed catalyst, Neftekhimiya, 1966, 6, 291-6. [all data]

Bazhulin, Sterin, et al., 1946
Bazhulin, P.A.; Sterin, K.E.; Bulanova, T.F.; Solovova, O.P.; Turova-Pollyak, M.B.; Kazanskii, B.A., Izv. Akad. Nauk SSSR, 1946, 1946, 7. [all data]

Greenlee and Waalkes, 1945
Greenlee, K.W.; Waalkes, T.P., , Am. Pet. Inst. Res. Proj. 45 No. 123A, Ohio State Univ., 1945. [all data]

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]

Evans, 1938
Evans, E.B., The viscosity of hydrocarbons. Parts IV-VI, J. Inst. Pet. Technol., 1938, 24, 321. [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]

Chavanne and Simon, 1919
Chavanne, G.; Simon, L.J., Preparation of Several Volatile Acyclic Saturated Hydrocarbons Found in Petroleum, C. R. Hebd. Seances Acad. Sci., 1919, 168, 1324. [all data]

Sabatier and Mailhe, 1907
Sabatier, P.; Mailhe, A., Ann. Chim. Phys., 1907, 10, 551. [all data]

Sabatier and Mailhe, 1905
Sabatier, P.; Mailhe, A., Synthesis of Three Tertiary Dimethylcyclohexanols and the Corresponding Hydrocarbons, C. R. Hebd. Seances Acad. Sci., 1905, 141, 20. [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]

Notes

Go To: Top, Normal boiling point, References

• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.