1-Pentanol, 4-methyl-

• Formula: C₆H₁₄O
• Molecular weight: 102.1748
• IUPAC Standard InChI: InChI=1S/C6H14O/c1-6(2)4-3-5-7/h6-7H,3-5H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: PCWGTDULNUVNBN-UHFFFAOYSA-N Copy
• CAS Registry Number: 626-89-1
• 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: Isohexyl alcohol; Isohexanol; 2-Methyl-5-pentanol; 4-Methyl-1-pentanol; 4-Methylpentan-1-ol; 4-Methylpentanol; Pentanol, 4-methyl-
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Reaction thermochemistry 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

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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]

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]

Majer and Svoboda, 1985
Majer, V.; Svoboda, V., Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]

Cook, 1952
Cook, N.C., , Unpublished, Final Rep. Stand. Proj. on Oxygenated Compounds, Penn. State Univ., College Park, PA, 1952. [all data]

Pichler, Ziesecke, et al., 1950
Pichler, H.; Ziesecke, K.H.; Traeger, B., The Oxygen-containing Compounds, Especially Alcohols, Formed in Isosynthesis, Brennst.-Chem., 1950, 31, 361. [all data]

Sorm and Arient, 1950
Sorm, F.; Arient, Collect. Czech. Chem. Commun., 1950, 15, 175. [all data]

Hovorka, Lankelma, et al., 1940
Hovorka, F.; Lankelma, H.P.; Schneider, I., Thermodynamic Properties of the Hexyl Alcohols IV. 3-Methyl-1-pentanol and 2-Methyl-5-pentanol, J. Am. Chem. Soc., 1940, 62, 1096-8. [all data]

Sutter, 1938
Sutter, P., Helv. Chim. Acta, 1938, 21, 1266. [all data]

Kondo and Suzuki, 1936
Kondo; Suzuki, Chem. Ber., 1936, 69, 2459. [all data]

Shonle, Waldo, et al., 1936
Shonle, H.A.; Waldo, J.H.; Keltch; Coles, J. Am. Chem. Soc., 1936, 58, 585. [all data]

Wojcik and Adkins, 1933
Wojcik, B.; Adkins, H., Hydogenolysis of Succinates and Glutarates, J. Am. Chem. Soc., 1933, 55, 4939. [all data]

Morgan, Hardy, et al., 1932
Morgan, G.T.; Hardy, D.V.N.; Proctor, R.A., J. Soc. Chem. Ind., London, Trans. Commun., 1932, 51, 1-7T. [all data]

Norris and Cortese, 1927
Norris, J.F.; Cortese, F., The reactivity of atoms and groups in organic compounds: II. second contribution on the relative reactivities of the hydroxyl-hydrogen atoms in certain alcohols, J. Am. Chem. Soc., 1927, 49, 2640-50. [all data]

Levene and Allen, 1916
Levene, P.A.; Allen, C.H., J. Biol. Chem., 1916, 27, 433. [all data]

Buelens, 1908
Buelens, A., Recl. Trav. Chim. Pays-Bas, 1908, 28, 113. [all data]

Buelens, 1908, 2
Buelens, A., Bull. Cl. Sci., 1908, 1908, 921-9. [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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