1-Dodecanamine

• Formula: C₁₂H₂₇N
• Molecular weight: 185.3495
• IUPAC Standard InChI: InChI=1S/C12H27N/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-13H2,1H3 Copy

  
• IUPAC Standard InChIKey: JRBPAEWTRLWTQC-UHFFFAOYSA-N Copy
• CAS Registry Number: 124-22-1
• 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: Dodecylamine; n-Dodecylamine; Alamine 4; Armeen 12D; Laurinamine; Laurylamine; Nissan Amine BB; 1-Aminododecane; Amine 12; Armeen 12; Lauramine; 1-Dodecylamine; Amine BB; Farmin 20D; Kemamine P690; Monododecylamine; n-Laurylamine
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• Information on this page:
  • Normal melting 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 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.

Stephenson, 1993
Stephenson, R.M., Mutual Solubility of Water and Aliphatic Amines, J. Chem. Eng. Data, 1993, 38, 625-9. [all data]

Shulman, Formo, et al., 1961
Shulman, S.; Formo, M.W.; Rheineck, A.E., Aliphatic Urethanes. Effect of Chain Length on Some Physical Properties, J. Am. Oil Chem. SOc., 1961, 38, 205-8. [all data]

Costello and Bowden, 1959
Costello, J.M.; Bowden, S.T., The Temperature Variation of Orthobaric Density Difference in Liquid-Vapour Systems. V. Amines, Recl. Trav. Chim. Pays-Bas, 1959, 78, 391. [all data]

Zvejnieks, 1954
Zvejnieks, A., Preparation and Properties of Some Pure Fatty and Rosin Amines., Sven. Kem. Tidskr., 1954, 66, 316. [all data]

Hoffman and Smyth, 1949
Hoffman, J.D.; Smyth, C.P., Molecular Freedom and Proton Transfer in Solid Long-Chain Amines., J. Am. Chem. Soc., 1949, 71, 3591. [all data]

Ralston, Reck, et al., 1948
Ralston, A.W.; Reck, R.A.; Harwood, H.J.; Du Brow, P.L., The Solubilities of Long-Chain Dialkyldimethylammonium Chlorides in Organic Solvents., J. Org. Chem., 1948, 13, 186. [all data]

Reck, Harwood, et al., 1947
Reck, R.A.; Harwood, H.J.; Ralston, A.W., Solubilities of Dodecyl- and Octadecyltrimethylammonium Chlorides in Organic Solvents., J. Org. Chem., 1947, 12, 517. [all data]

Broome, Ralston, et al., 1946
Broome, F.K.; Ralston, A.W.; Thornton, M.H., Complex Formation with High Molecular Weight Amines., J. Am. Chem. Soc., 1946, 68, 67. [all data]

Sedgwick, Hoerr, et al., 1945
Sedgwick, R.S.; Hoerr, C.W.; Ralston, A.W., Solubilities in Ethyl Alcohol of Primary Aliphatic Amine Hydrochlorides of High Molecular Weight., J. Org. Chem., 1945, 10, 498. [all data]

Ralston, Hoerr, et al., 1944
Ralston, A.W.; Hoerr, C.W.; Pool, W.O.; Harwood, H.J., Solubilities of High-Molecular-Weight Normal Aliphatic Primary Amines., J. Org. Chem., 1944, 9, 102-12. [all data]

Ralston, Hoerr, et al., 1942
Ralston, A.W.; Hoerr, C.W.; Hoffman, E.J., Studies on High Molecular Weight ALiphatic Amines and Their Salts. VII The Systems Octylamine, Dodecylamine, and Octadecylamine-Water, J. Am. Chem. Soc., 1942, 64, 1516. [all data]

Wibaut, Heierman, et al., 1938
Wibaut, J.P.; Heierman, F.; Wagtendonk, H.M., Preparation of Dodecylamine and Didodecylamine From Dodecyl Chloride By Means of Anhydrous Liquid Ammonia., Recl. Trav. Chim. Pays-Bas, 1938, 57, 456. [all data]

Krafft, 1890
Krafft, F., Chem. Ber., 1890, 23, 2360. [all data]

Lutz, 1886
Lutz, E., The Degradation of Myristic Acid to Lauric Acid, Chem. Ber., 1886, 19, 1433. [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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