1,2-Cyclohexanediol, trans-

• Formula: C₆H₁₂O₂
• Molecular weight: 116.1583
• IUPAC Standard InChI: InChI=1S/C6H12O2/c7-5-3-1-2-4-6(5)8/h5-8H,1-4H2/t5-,6-/m1/s1 Copy

  
• IUPAC Standard InChIKey: PFURGBBHAOXLIO-PHDIDXHHSA-N Copy
• CAS Registry Number: 1460-57-7
• 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.
• Stereoisomers:
  • cis-1,2-Cyclohexanediol
  • 1,2-Cyclohexanediol
• Other names: trans-1,2-Cyclohexanediol; trans-1,2-Dihydroxycyclohexane; 1,2-trans-Cyclohexanediol; 1,2-Cyclohexanediol, (E)-; trans-cyclohexane-1,2-diol
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• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • References
  • Notes
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Condensed phase thermochemistry data

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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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Phase change data

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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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of sublimation

Enthalpy of fusion

IR Spectrum

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Gas Phase Spectrum

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Additional Data

Mass spectrum (electron ionization)

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

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.

Verkade, Coops, et al., 1928
Verkade, P.E.; Coops, J., Jr.; Maan, Chr.J., Calorimetrische Untersuchungen. XV. Thermochemische studien uber cycloparaffine und ihre derivate: 1. Experimentelle daten fur funf- und sechsgliedrige cyclische diole, Ann., 1928, 467, 217-239. [all data]

Emmons, Pagano, et al., 1954
Emmons, W.D.; Pagano, A.S.; Freeman, J.P., J. Am. Chem. Soc., 1954, 76, 3472. [all data]

Maria, Costa, et al., 1995
Maria, Teresa M.R.; Costa, Felisbela S.; Leitão, M. Luísa P.; Redinha, J.S., A calorimetric study of phase transitions for some cyclohexanediols, Thermochimica Acta, 1995, 269-270, 405-413, https://doi.org/10.1016/0040-6031(95)02704-1 . [all data]

Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw, Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2 . [all data]

Zibberman-Granovskaya, 1940
Zibberman-Granovskaya, A.A., Russ. J. Phys. Chem., 1940, 14, 759. [all data]

Maria and Eusebio, 2008
Maria, Teresa M.R.; Eusebio, M. Ermelinda S., Molar Heat Capacity of 1,2-Cyclohexanediol Isomers From (173 to 428) K, J. Chem. Eng. Data, 2008, 53, 6, 1316-1320, https://doi.org/10.1021/je800047t . [all data]

Zhou, Peng, et al., 2002
Zhou, C.-R.; Peng, G.-S.; Zhang, Y.-D.; Jiang, D.G.; Wang, F.; Li, J.-J.; Shen, X.-Q., Gaoxiao Huaxue Gongcheng Xuebao, 2002, 16, 3, 237. [all data]

Zhou, Zhang, et al., 2003
Zhou, C.; Zhang, Y.; Jiang, D., Chin. J. Chem. Eng., 2003, 11, 5, 598. [all data]

Notes

Go To: Top, Condensed phase thermochemistry data, Phase change data, IR Spectrum, Mass spectrum (electron ionization), References

• Symbols used in this document:
  

  Tfus	Fusion (melting) point
  ΔcH°solid	Enthalpy of combustion of solid at standard conditions
  ΔfusH	Enthalpy of fusion
  ΔsubH	Enthalpy of sublimation

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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