1H-1,2,3,4-Tetrazol-5-amine, 1-methyl-

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Gas 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
DRB - Donald R. Burgess, Jr.

Quantity Value Units Method Reference Comment
Δfgas302.4 ± 2.8kJ/molCcbKozyro, Simirskii, et al., 1990ALS
Δfgas313.2kJ/molN/AWilliams, McEwan, et al., 1957Value computed using ΔfHsolid° value of 193.0 kj/mol from Williams, McEwan, et al., 1957 and ΔsubH° value of 120.2 kj/mol from Kozyro, Simirskii, et al., 1990.; DRB

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

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Individual Reactions

1H-1,2,3,4-Tetrazol-5-amine, 1-methyl- = C2H5N5

By formula: C2H5N5 = C2H5N5

Quantity Value Units Method Reference Comment
Δr8.62kJ/molKinHenry, Finnegan, et al., 1955liquid phase

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.

Kozyro, Simirskii, et al., 1990
Kozyro, A.A.; Simirskii, V.V.; Krasulin, A.P.; Sevruk, V.M.; Kabo, G.Ya.; Frenkel, M.L.; Gaponik, P.N.; Grigor'ev, Yu.V., Thermodynamic properties of tetrazole derivatives in different aggregation states, Russ. J. Phys. Chem. (Engl. Transl.), 1990, 64, 348-350. [all data]

Williams, McEwan, et al., 1957
Williams, M.M.; McEwan, W.S.; Henry, R.A., The heats of combustion of substituted triazoles, tetrazoles and related high nitrogen compounds, J. Phys. Chem., 1957, 61, 261-267. [all data]

Henry, Finnegan, et al., 1955
Henry, R.A.; Finnegan, W.G.; Lieber, E., Kinetics of the isomerization of substituted 5-aminotetrazoles, J. Am. Chem. Soc., 1955, 77, 2264-2270. [all data]


Notes

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