1,2-Ethanediamine, N-(2-aminoethyl)-

• Formula: C₄H₁₃N₃
• Molecular weight: 103.1661
• IUPAC Standard InChI: InChI=1S/C4H13N3/c5-1-3-7-4-2-6/h7H,1-6H2 Copy

  
• IUPAC Standard InChIKey: RPNUMPOLZDHAAY-UHFFFAOYSA-N Copy
• CAS Registry Number: 111-40-0
• 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: Diethylenetriamine; Barsamide 115; Bis(2-aminoethyl)amine; Bis[β-aminoethyl]amine; N,N-Bis(2-aminoethyl)amine; 2,2'-Diaminodiethylamine; 3-Azapentane-1,5-diamine; 2,2'-Iminodiethylamine; (Aminoethyl)ethanediamine; Diethylamine, 2,2'-diamino-; DETA; Ethylamine, 2,2'-iminobis-; Ethylenediamine, N-(2-aminoethyl)-; Aminoethylethandiamine; D.E.H. 20; UN 2079; 1,4,7-Triazaheptane; 1,5-Diamino-3-azapentane; N-(2-Aminoethyl)-1,2-ethanediamine; ChS-P 1; N-(2-Aminoethyl)ethylenediamine; β,β'-Diaminodiethylamine; 2,2'-Iminobisethylamine; Texacure EA-20; 1,2-Ethanediamine, N1-(2-aminoethyl)-; NSC 446; H 9506; Epon 3223; Epicure T; DEH 20; Ancamine DETA; 2,2'-Iminobis(ethanamine); 2-(2-Aminoethylamino)ethylamine
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• Information on this page:
  • Reaction thermochemistry data
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Reaction thermochemistry 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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

 +  =

By formula: C₄H₁₃N₃ + C₂H₅N = C₆H₁₈N₄

 +  =

By formula: C₂H₈N₂ + C₂H₅N = C₄H₁₃N₃

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.

Dalin, Bobylev, et al., 1988
Dalin, A.R.; Bobylev, V.A.; Suslikov, V.F.; Kamskaya, O.I.; Tereshchenko, G.F., Nucleophilic cleavage and the formation of saturated heterocycles. VII. Kinetic and thermochemical study of reactions of aziridine with ethylene amines, J. Gen. Chem. USSR, 1988, 58, 1868-1871. [all data]

Notes

Go To: Top, Reaction thermochemistry data, References

• Symbols used in this document:
  

  ΔrH°	Enthalpy of reaction at standard conditions

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