Dimantine

• Formula: C₂₀H₄₃N
• Molecular weight: 297.5621
• IUPAC Standard InChI: InChI=1S/C20H43N/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(2)3/h4-20H2,1-3H3 Copy

  
• IUPAC Standard InChIKey: NAPSCFZYZVSQHF-UHFFFAOYSA-N Copy
• CAS Registry Number: 124-28-7
• 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: 1-Octadecanamine, N,N-dimethyl-; Octadecylamine, N,N-dimethyl-; Armeen DM 18D; Armine DM18D; Dimethyl-n-octadecylamine; Dimethyloctadecylamine; Dimethylstearylamine; Dymanthine; N,N-Dimethyl-n-octadecylamine; N,N-Dimethyloctadecylamine; N,N-Dimethylstearylamine; Octadecyldimethylamine; Stearyldimethylamine; N,N-Dimethyloktadecylamin; N,N-Dimethyl-1-octadecanamine; (Hydrochloride salt) dimantine; ADMA 18; Barlene 18S; Dimanthine; Dimethyl-1-octadecanamine; Dimethyl stearamine; N,N-dimethyl octadecanamine; Kemamine T-9902; Onamine 18; Adogen 342D; DM 18D; Farmin DM 80; Kemamine 9902D; N-Octadecyl-N,N-dimethylamine; N-Stearyl-N,N-dimethylamine
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • 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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of vaporization

IR Spectrum

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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

Gas Phase Spectrum

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Additional Data

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.

Ralston, Eggenberger, et al., 1947
Ralston, A.W.; Eggenberger, D.N.; Harwood, H.J.; Du Brow, P.L., The Electrical Conductivities of Long-Chain Quaternary Ammonium Chlorides Containing Hydroxyalkyl Groups., J. Am. Chem. Soc., 1947, 69, 2095. [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]

Schmidt, 1942
Schmidt, A.W., Physical properties of aliphatic compounds, Ber. Dtsch. Chem. Ges. B, 1942, 75, 1399. [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]

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:
  

  Tfus	Fusion (melting) point
  ΔvapH	Enthalpy of vaporization

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