Cyclohexane, butyl-

• Formula: C₁₀H₂₀
• Molecular weight: 140.2658
• IUPAC Standard InChI: InChI=1S/C10H20/c1-2-3-7-10-8-5-4-6-9-10/h10H,2-9H2,1H3 Copy

  
• IUPAC Standard InChIKey: GGBJHURWWWLEQH-UHFFFAOYSA-N Copy
• CAS Registry Number: 1678-93-9
• 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: n-Butylcyclohexane; Butane, 1-cyclohexyl-; Butylcyclohexane; 1-Cyclohexylbutane; Cyclohexane, n-butyl-
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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
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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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]

Nazarov and Kakhniashvili, 1954
Nazarov, I.N.; Kakhniashvili, A.I., Acetylene Derivatives CLV. Action of Methylmagnesium Bromide on Allyl 1-Cyclohexenyl Ketone and Allyl Isopropenyl Ketone, Sb. Statei Obshch. Khim., 1954, 2, 892-5. [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]

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

Anonymous, 1946
Anonymous, R., , Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1946. [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]

Boord, Greenlee, et al., 1945
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L., , Am. Pet. Inst. Res. Proj. 45, Seventh Annu. Rep., Ohio State Univ., June 30, 1945. [all data]

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

Smith and Pennekamp, 1945
Smith, H.A.; Pennekamp, E.F.H., The Catalytic Hydrogenation of the Benzene Nucleus II. The Hydrogenation of Benzene and Mono-alkylkbenzenes, J. Am. Chem. Soc., 1945, 67, 276. [all data]

Anonymous, 1943
Anonymous, R., , Sunbury Rep. No. 2176, Anglo-Iranian Oil Co., 1943. [all data]

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

Signaigo and Cramer, 1933
Signaigo, F.K.; Cramer, P.L., The preparation of some mono- and dialkylcylohexanes, J. Am. Chem. Soc., 1933, 55, 3326-32. [all data]

Stratford, 1929
Stratford, R., Ann. Off. Natl. Combust. Liq. (Fr.), 1929, 4, 83. [all data]

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

Douris, 1913
Douris, R., The hydrogenation of some secondary alpha-ethylene alcohols in the presence of nickel, C. R. Hebd. Seances Acad. Sci., 1913, 157, 55. [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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