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

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Condensed phase 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 as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing

Quantity Value Units Method Reference Comment
Δfliquid-65.2 ± 0.5kJ/molCcbGutner, Lebedeva, et al., 1979ALS
Δfliquid-287.0kJ/molCcrBaroody and Carpenter, 1976ALS
Quantity Value Units Method Reference Comment
Δcliquid-3366.7 ± 0.5kJ/molCcbGutner, Lebedeva, et al., 1979ALS

Constant pressure heat capacity of liquid

Cp,liquid (J/mol*K) Temperature (K) Reference Comment
254.313.Bobylev, Kamskaya, et al., 1988T = 313 to 493 K.; DH

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

1,2-Ethanediamine, N-(2-aminoethyl)- + Ethylenimine = 1,2-Ethanediamine, N,N'-bis(2-aminoethyl)-

By formula: C4H13N3 + C2H5N = C6H18N4

Quantity Value Units Method Reference Comment
Δr83.3 ± 4.2kJ/molCmDalin, Bobylev, et al., 1988liquid phase; solvent: Aqueous HCl; Kinetic

Ethylenediamine + Ethylenimine = 1,2-Ethanediamine, N-(2-aminoethyl)-

By formula: C2H8N2 + C2H5N = C4H13N3

Quantity Value Units Method Reference Comment
Δr82.8 ± 5.0kJ/molCmDalin, Bobylev, et al., 1988liquid phase; solvent: Aqueous HCl; Kinetic

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.

Gutner, Lebedeva, et al., 1979
Gutner, N.M.; Lebedeva, N.D.; Kiseleva, N.N., Enthalpies of combustion and formation of some acyl-substituted diamines, Termodin. Org. Soedin., 1979, 97-98. [all data]

Baroody and Carpenter, 1976
Baroody, E.E.; Carpenter, G.A., Heats of formation of propellant compounds (U), Rpt. NCWC/WOL-TR-76-77 by Naval Surface Weapons Center, Silver Spring, MD, 1976, 1-20. [all data]

Bobylev, Kamskaya, et al., 1988
Bobylev, V.A.; Kamskaya, O.I.; Kossoi, A.A.; Koludarova, E.Yu., Investigation of the heat capacity of ethyleneamines by differential scanning calorimetry, Zhur. Obshch. Khim., 1988, 58, 2536-2538. [all data]

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

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