Hydrazine, methyl-
- Formula: CH6N2
- Molecular weight: 46.0717
- IUPAC Standard InChIKey: HDZGCSFEDULWCS-UHFFFAOYSA-N
- CAS Registry Number: 60-34-4
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: Methylhydrazine; Monomethylhydrazine; MMH; CH3NHNH2; Hydrazomethane; 1-Methylhydrazine; Metylohydrazyna; Rcra waste number P068; UN 1244
- Permanent link for this species. Use this link for bookmarking this species for future reference.
- Information on this page:
- Other data available:
- Data at other public NIST sites:
- Options:
Data at NIST subscription sites:
NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.
Gas phase ion energetics data
Go To: Top, References, Notes
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
LL - Sharon G. Lias and Joel F. Liebman
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 7.7 ± 0.15 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 898.8 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 866.4 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
7.7 ± 0.15 | EQ | Mautner(Meot-Ner), Nelsen, et al., 1984 | LBLHLM |
8.67 | PE | Bodor, Dewar, et al., 1970 | RDSH |
8.00 ± 0.06 | PI | Akopyan and Vilesov, 1963 | RDSH |
7.67 ± 0.02 | PI | Akopyan, Vilesov, et al., 1963 | RDSH |
8.6 ± 0.1 | EI | Dibeler, Franklin, et al., 1959 | RDSH |
8.40 ± 0.05 | PE | Vovna, Vilesov, et al., 1975 | Vertical value; LLK |
9.34 | PE | Rademacher, 1975 | Vertical value; LLK |
9.36 | PE | Kimura, Katsumata, et al., 1975 | Vertical value; LLK |
9.32 | PE | Nelsen and Buschek, 1974 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
N2H?+ | 13.3 ± 0.3 | ? | EI | Dibeler, Franklin, et al., 1959 | RDSH |
N2H2?+ | 11.2 ± 0.2 | ? | EI | Dibeler, Franklin, et al., 1959 | RDSH |
N2?+ | 13.2 ± 0.3 | ? | EI | Dibeler, Franklin, et al., 1959 | RDSH |
CH2N2+ | 15.2 ± 0.2 | ? | EI | Dibeler, Franklin, et al., 1959 | RDSH |
CH3+ | 14.1 ± 0.3 | ? | EI | Dibeler, Franklin, et al., 1959 | RDSH |
CH3N2+ | 9.2 ± 0.2 | H2+H | PI | Akopyan and Vilesov, 1963 | RDSH |
CH3N2+ | 11.9 ± 0.3 | H2+H | EI | Dibeler, Franklin, et al., 1959 | RDSH |
CH4N2+ | 9.9 ± 0.1 | H2 | EI | Foner and Hudson, 1970 | RDSH |
CH4N2+ | 9.4 ± 0.1 | H2 | PI | Akopyan and Vilesov, 1963 | RDSH |
CH4N2+ | 10.4 ± 0.2 | H2 | EI | Dibeler, Franklin, et al., 1959 | RDSH |
CH5N+ | 11.3 ± 0.1 | NH | PI | Akopyan and Vilesov, 1963 | RDSH |
CH5N2+ | 10.2 ± 0.1 | H | EI | Foner and Hudson, 1970 | RDSH |
CH5N2+ | 9.2 ± 0.1 | H | PI | Akopyan and Vilesov, 1963 | RDSH |
CH5N2+ | 10.2 ± 0.1 | H | EI | Dibeler, Franklin, et al., 1959 | RDSH |
N2H3+ | 9.82 | CH3 | EI | Burgers, Drewello, et al., 1989 | LL |
N2H3+ | 9.5 ± 0.1 | CH3 | PI | Akopyan and Vilesov, 1963 | RDSH |
N2H3+ | 10.7 ± 0.3 | CH3 | EI | Dibeler, Franklin, et al., 1959 | RDSH |
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]
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]
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]
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]
Kimura, Katsumata, et al., 1975
Kimura, K.; Katsumata, S.; Osafune, K.,
Photoelectron spectroscopic study of skew compounds. Methylhydrazine and unsymmetrical dimethylhydrazine,
Bull. Chem. Soc. Jpn., 1975, 48, 2736. [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]
Foner and Hudson, 1970
Foner, S.N.; Hudson, R.L.,
Mass spectrometric studies of atom-molecule reactions using high-intensity crossed molecular beams,
J. Chem. Phys., 1970, 53, 4377. [all data]
Burgers, Drewello, et al., 1989
Burgers, P.C.; Drewello, T.; Schwarz, H.; Terlouw, J.K.,
CH5N2 hydrazyl radicals, cations and dication radicals studied by mass spectrometry. Is the N-protonated formaldehyde hydrazon cation +CH2-NH-NH2 a bridged species?,
Int. J. Mass Spectrom. Ion Processes, 1989, 95, 157. [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
- The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
- Customer support for NIST Standard Reference Data products.