Cyclopentanol

• Formula: C₅H₁₀O
• Molecular weight: 86.1323
• IUPAC Standard InChI: InChI=1S/C5H10O/c6-5-3-1-2-4-5/h5-6H,1-4H2 Copy

  
• IUPAC Standard InChIKey: XCIXKGXIYUWCLL-UHFFFAOYSA-N Copy
• CAS Registry Number: 96-41-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Cyclopentyl alcohol; Hydroxycyclopentane; UN 2244
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
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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.

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Sellers and Sunner, 1962
Sellers, P.; Sunner, S., Heats of combustion of cyclic ketones and alcohols, Acta Chem. Scand., 1962, 16, 46-52. [all data]

Bollinger, Hayes, et al., 1953
Bollinger, F.W.; Hayes, F.N.; Siegel, S., The Base-Catalyzed Decomposition of N-Nitroso-N-cyclopentylurethan, J. Am. Chem. Soc., 1953, 75, 1729-30. [all data]

Stoll, Lindenmann, et al., 1953
Stoll, A.; Lindenmann, A.; Jucker, E., Alkaloid Syntheses II. The Synthesis of Glutaraldehyde, Helv. Chim. Acta, 1953, 36, 268-74. [all data]

Winstein, Morse, et al., 1952
Winstein, S.; Morse, B.K.; Grunwald, E.; Jones, H.W.; Corse, J.; Trifan, D.; Marshall, H., Neighboring Carbon and Hydrogen. VII. Reactivity of Some ALicyclic and Bicyclic Derivatives, J. Am. Chem. Soc., 1952, 74, 1127-32. [all data]

Lecat, 1947
Lecat, M., Orthobaric Azeotropes of Sulfides, Bull. Cl. Sci., Acad. R. Belg., 1947, 33, 160-82. [all data]

Lecat, 1947, 2
Lecat, M., Some azeotropes of which one constituant is heterocyclic nitrogen, Ann. Soc. Sci. Bruxelles, Ser. 1, 1947, 61, 73. [all data]

White and Bishop, 1940
White, A.H.; Bishop, W.S., Dielectric Evidence of Molecular Rotation in the Crystals of Certain Non-aromatic Compounds, J. Am. Chem. Soc., 1940, 62, 8-16. [all data]

Timmermans and Hennaut-Roland, 1937
Timmermans, J.; Hennaut-Roland, M., Works from International Bureau at Physical-Chemical Standards. VIII. Physical constants of 20 organic compounds, J. Chim. Phys. Phys.-Chim. Biol., 1937, 34, 693. [all data]

Von Auwers and Eisenlohr, 1910
Von Auwers, K.; Eisenlohr, F., Spectrochemical studies. I. Refraction & dispersion of hydrocarbon aldehydes, ketones, acids & esters with i pair of conjug. double bonds, J. Prakt. Chem., 1910, 82, 65. [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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