Hydrazine

• Formula: H₄N₂
• Molecular weight: 32.0452
• IUPAC Standard InChI: InChI=1S/H4N2/c1-2/h1-2H2 Copy

  
• IUPAC Standard InChIKey: OAKJQQAXSVQMHS-UHFFFAOYSA-N Copy
• CAS Registry Number: 302-01-2
• 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: Levoxine; N2H4; Diamine; Hydrazyna; Rcra waste number U133; Hydrazine, anhydrous; Hydrazine base; Nitrogen hydride, (N2H4); Oxytreat 35
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Mass spectrum (electron ionization)
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
  • X-ray Photoelectron Spectroscopy Database, version 5.0
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Gas phase ion energetics 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 evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias

Data compiled as indicated in comments:
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

View reactions leading to H₄N₂⁺ (ion structure unspecified)

Ionization energy determinations

Appearance energy determinations

References

Go To: Top, Gas phase ion energetics data, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Hunter and Lias, 1998
Hunter, E.P.; Lias, S.G., Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update, J. Phys. Chem. Ref. Data, 1998, 27, 3, 413-656, https://doi.org/10.1063/1.556018 . [all data]

Mautner(Meot-Ner), Nelsen, et al., 1984
Mautner(Meot-Ner), M.; Nelsen, S.F.; Willi, M.R.; Frigo, T.B., Special effects of an unusually large neutral to radical cation geometry change. Adiabatic ionization energies and proton affinities of alkylhydrazines, J. Am. Chem. Soc., 1984, 106, 7384. [all data]

Wiberg, Fischer, et al., 1979
Wiberg, N.; Fischer, G.; Bachhuber, H., Diazen und andere Distickstoffhydride: Bildungswarmen, Dissoziationsenergien, Auftrittspotentiale, Protonenaffinitaten, Z. Naturforsch. B:, 1979, 34, 1385. [all data]

Bodor, Dewar, et al., 1970
Bodor, N.; Dewar, M.J.S.; Jennings, W.B.; Worley, S.D., Photoelectron spectra of molecules-IV.Ionization potentials and heats of formation of some hydrazines and amines, Tetrahedron, 1970, 26, 4109. [all data]

Melton, 1966
Melton, C.E., Study by mass spectrometry of the decomposition of ammonia by ionizing radiation in a wide-range radiolysis source, J. Chem. Phys., 1966, 45, 4414. [all data]

Akopyan and Vilesov, 1963
Akopyan, M.E.; Vilesov, F.I., Decay of the molecular ions formed in photoionization of hydrazine and some of its alkyl derivatives, Kinetika i Kataliz, 1963, 4, 39, In original 32. [all data]

Akopyan, Vilesov, et al., 1963
Akopyan, M.E.; Vilesov, F.I.; Terenin, A.N., Mass spectrometric investigation of photoionization of molecules and dissociation of excited molecular ions, Izv. Akad. Nauk SSSR, Ser. Fiz., 1963, 27, 1083, In original 1054. [all data]

Dibeler, Franklin, et al., 1959
Dibeler, V.H.; Franklin, J.L.; Reese, R.M., Electron impact studies of hydrazine and the methyl-substituted hydrazines, J. Am. Chem. Soc., 1959, 81, 68. [all data]

Vilesov and Terenin, 1957
Vilesov, F.I.; Terenin, A.N., The photoionization of the vapors of certain organic compounds, Dokl. Akad. Nauk SSSR, 1957, 115, 744, In original 539. [all data]

Vovna, Vilesov, et al., 1975
Vovna, V.I.; Vilesov, F.I.; Lopatin, S.N., Photoelectron spectra of hydrazine and some alkyl derivatives, Opt. Spectrosc., 1975, 38, 143. [all data]

Rademacher, 1975
Rademacher, P., Acyclische Hydrazine, Chem. Ber., 1975, 108, 1548. [all data]

Nelsen and Buschek, 1974
Nelsen, S.F.; Buschek, J.M., Photoelectron spectra of hydrazines. III. Evidence for similar lone pair-lone pair dihedral angles for acyclic hydrazines, J. Am. Chem. Soc., 1974, 96, 2392. [all data]

Osafune, Katsumata, et al., 1973
Osafune, K.; Katsumata, S.; Kimura, K., Photoelectron spectroscopic study of hydrazine, Chem. Phys. Lett., 1973, 19, 369. [all data]

Barz and Fritz, 1972
Barz, P.; Fritz, H.P., Untersuchungen an biochemish ligandensystemen, V. Komplexchemische und physikalisch-chemische untersuchungen am 1,2-dimethylhydrazin, Z. Naturforsch. B:, 1972, 27, 1131. [all data]

Foner and Hudson, 1958
Foner, S.N.; Hudson, R.L., Mass spectrometric detection of triazene and tetrazene and studies of the free radicals NH₂, and N₂H₃, J. Chem. Phys., 1958, 29, 442. [all data]

Foner and Hudson, 1978
Foner, S.N.; Hudson, R.L., On the heat of formation of diimide, J. Chem. Phys., 1978, 68, 3162. [all data]

Foner and Hudson, 1958, 2
Foner, S.N.; Hudson, R.L., Diimide-identification and study by mass spectrometry, J. Chem. Phys., 1958, 28, 719. [all data]

Fisher and Heath, 1965
Fisher, I.P.; Heath, G.A., Dissociation energy of the N-H bond in hydrazine, Nature, 1965, 208, 1199. [all data]

Notes

Go To: Top, Gas phase ion energetics data, References

• Symbols used in this document:
  

  AE	Appearance energy
  IE (evaluated)	Recommended ionization energy

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