Pentadecylamine

• Formula: C₁₅H₃₃N
• Molecular weight: 227.4292
• IUPAC Standard InChI: InChI=1S/C15H33N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h2-16H2,1H3 Copy

  
• IUPAC Standard InChIKey: JPZYXGPCHFZBHO-UHFFFAOYSA-N Copy
• CAS Registry Number: 2570-26-5
• 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-Pentadecylamine; 1-Pentadecanamine; 1-Pentadecylamine; Pentadecane, 1-amino-; Pentadecanamide
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• Information on this page:
  • Phase change data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • IR Spectrum
  • Mass spectrum (electron ionization)
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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:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of vaporization

Gas Chromatography

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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

Normal alkane RI, non-polar column, temperature ramp

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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.

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]

American Tokyo Kasei, 1988
American Tokyo Kasei, TCI American Organic Chemical 88/89 Catalog, American Tokyo Kasei, Portland, OR, 1988, 1610. [all data]

Jeffreys, 1899
Jeffreys, E., On Undecylamine and Pentadecylamine and the Preparation of the Higher Amines of the Aliphatic Series, Am. Chem. J., 1899, 22, 14. [all data]

Richet, 1946
Richet, H., On the Chlorides, Amides, and AMines of the Fatty Acids, Bull. Soc. Chim. Fr., 1946, 13, 52. [all data]

Staudinger and Roessler, 1936
Staudinger, H.; Roessler, K., Highly Polymerized Compounds. CXXIII. Viscosity Measurements on Long- Chain Aliphatic Amines., Chem. Ber., 1936, 69B, 49-60. [all data]

Naegeli, Gruntuch, et al., 1929
Naegeli, C.; Gruntuch, L.; Lendorff, P., A Modified Curtius Degradation III. The Degradation of Saturated Fatty Acids and Benzoic Acid, Helv. Chim. Acta, 1929, 12, 227. [all data]

Jeffreys, 1897
Jeffreys, E., Chem. Ber., 1897, 30, 898. [all data]

Emel'yanenko, Verevkin, et al., 2005
Emel'yanenko, Vladimir N.; Verevkin, Sergey P.; Koutek, Bohumir; Doubsky, Jan, Vapour pressures and enthalpies of vapourization of a series of the linear aliphatic nitriles, The Journal of Chemical Thermodynamics, 2005, 37, 1, 73-81, https://doi.org/10.1016/j.jct.2004.08.004 . [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]

Okumura, 1991
Okumura, T., retention indices of environmental chemicals on methyl silicone capillary column, Journal of Environmental Chemistry (Japan), 1991, 1, 2, 333-358, https://doi.org/10.5985/jec.1.333 . [all data]

Notes

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• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔvapH	Enthalpy of vaporization
  ΔvapH°	Enthalpy of vaporization at standard conditions

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