Tetradecanamide

• Formula: C₁₄H₂₉NO
• Molecular weight: 227.3862
• IUPAC Standard InChI: InChI=1S/C14H29NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3,(H2,15,16) Copy

  
• IUPAC Standard InChIKey: QEALYLRSRQDCRA-UHFFFAOYSA-N Copy
• CAS Registry Number: 638-58-4
• 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: Myristamide; Myristic acid amide; Myristic amide; Tetradecylamide
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Normal melting 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 by: 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.

Yoshino and Yoshino, 1970
Yoshino, N.; Yoshino, T., Synthesis and Reactions of Metal Alkoxides III. Formation of Nitriles from Acid Amdides and Certain Metal Alkoxides, Kogyo Kagaku Zasshi, 1970, 73, 1161-4. [all data]

Jart, 1965
Jart, A. (Aage], Infrared Spectra of Carboxylic Acid Derivatives IV. Amides and Hydrazides, Acta Polytech. Scand., Chem. Met. Ser., 1965, No. 42, 55pp. [all data]

Davies, Jones, et al., 1959
Davies, M.; Jones, A.H.; Thomas, G.H., The lattice energies of the straight-chain primary amides, Trans. Faraday Soc., 1959, 55, 1100. [all data]

Mayer and Asselineau, 1955
Mayer, B.; Asselineau, J., C. R. Hebd. Seances Acad. Sci., Ser. C., 1955, 262, 668-671. [all data]

Ralston, Hoerr, et al., 1943
Ralston, A.W.; Hoerr, C.W.; Pool, W.O., Solubilities of Some Normal Aliphatic Amides, Anilides, and N,N- Diphenylamides, J. Org. Chem., 1943, 8, 473-488. [all data]

Asano and Ohta, 1931
Asano, M.; Ohta, Z., Constitution of Icelandic Moss III. Synthesis of Lichesteric Acid, J. Pharm. Soc. Jpn., 1931, 51, 395-401. [all data]

Garner and Rushbrooke, 1927
Garner; Rushbrooke, J.E., J. Chem. Soc., 1927, 1927, 1351. [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]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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