Tetradecanenitrile

• Formula: C₁₄H₂₇N
• Molecular weight: 209.3709
• IUPAC Standard InChI: InChI=1S/C14H27N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-13H2,1H3 Copy

  
• IUPAC Standard InChIKey: MLRCLPRHEOPXLL-UHFFFAOYSA-N Copy
• CAS Registry Number: 629-63-0
• 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: Myristonitrile; 1-Cyanotridecane; Tetradecanonitrile; Myristyl nitrile
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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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
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DRB - Donald R. Burgess, Jr.

Reduced pressure boiling point

Enthalpy of vaporization

References

Go To: Top, Phase change data, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Dorinson and Ralston, 1944
Dorinson, A.; Ralston, A.W., Refractive Indices of the Normal Saturated Aliphatic Nitriles. ammonia, J. Am. Chem. Soc., 1944, 66, 361. [all data]

Hoerr, Binkerd, et al., 1944
Hoerr, C.W.; Binkerd, E.F.; Pool, W.O.; Ralston, A.W., Solubilities of High-Molecular-Weight Normal Aliphatic Nitriles., J. Org. Chem., 1944, 9, 68-80. [all data]

Whitmore, Sutherland, et al., 1942
Whitmore, F.C.; Sutherland, L.H.; Cosby, J.N., Higher Hydrocarbons. I. Seven Alkyl Substituted Docosanes., J. Am. Chem. Soc., 1942, 64, 1360. [all data]

Merckx, Verhulst, et al., 1933
Merckx, R.; Verhulst, J.; Bruylants, P., Refractometric Investigations of the Normal Saturated Nitriles., Bull. Soc. Chim. Belg., 1933, 42, 177. [all data]

Krafft and Stauffer, 1882
Krafft, F.; Stauffer, B., The nitriles c(n)h(2n+2)cn of the higher fatty acids, Ber. Dtsch. Chem. Ges., 1882, 15, 1728-31. [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]

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]

Stridh, Sunner, et al., 1977
Stridh, G.; Sunner, S.; Svensson, C., Enthalpies of combustion, vaporization, and formation of some alkanenitriles, and the CH₂-increment in the alkanenitrile series, J. Chem. Thermodyn., 1977, 9, 1005-1010. [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]

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]

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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