Hydrazine, 1,1-dimethyl-
- Formula: C2H8N2
- Molecular weight: 60.0983
- IUPAC Standard InChIKey: RHUYHJGZWVXEHW-UHFFFAOYSA-N
- CAS Registry Number: 57-14-7
- 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. - Species with the same structure:
- Other names: as-Dimethylhydrazine; Dimazin; Dimazine; Hydrazine, N,N-dimethyl-; N,N-Dimethylhydrazine; UDMH; 1,1-Dimethylhydrazine; (CH3)2NNH2; Unsym-dimethylhydrazine; Dimethylhydrazine, unsymmetrical; Dimethylhydrazine, unsym.; 1,1-Dimethylhydrazin; asymmetric Dimethylhydrazine; uns-Dimethylhydrazine; Niesymetryczna dwu metylohydrazyna; Rcra waste number U098; UN 1163; Unsymmetrical dimethylhydrazine; u-Dimethylhydrazine; gem-Dimethylhydrazine; NSC 60517
- 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 thermochemistry data
Go To: Top, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Donald R. Burgess, Jr.
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°gas | 19.9 ± 0.86 | kcal/mol | N/A | Donovan, Shomate, et al., 1960 | Value computed using ΔfHliquid° value of 48.3±3.6 kj/mol from Donovan, Shomate, et al., 1960 and ΔvapH° value of 35±0.2 kj/mol from missing citation. |
Condensed phase thermochemistry data
Go To: Top, Gas phase thermochemistry data, Phase change data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), References, Notes
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 |
---|---|---|---|---|---|
ΔfH°liquid | 11.55 ± 0.86 | kcal/mol | Ccb | Donovan, Shomate, et al., 1960 | Reanalyzed by Cox and Pilcher, 1970, Original value = 11.90 kcal/mol; ALS |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°liquid | -472.91 ± 0.86 | kcal/mol | Ccb | Donovan, Shomate, et al., 1960 | Reanalyzed by Cox and Pilcher, 1970, Original value = -473.28 ± 0.43 kcal/mol; ALS |
ΔcH°liquid | -473.15 ± 0.70 | kcal/mol | Ccb | Aston, Rock, et al., 1952 | Reanalyzed by Cox and Pilcher, 1970, Original value = -472.65 ± 0.70 kcal/mol; ALS |
Quantity | Value | Units | Method | Reference | Comment |
S°liquid | 47.861 | cal/mol*K | N/A | Aston, Wood, et al., 1953 | DH |
Constant pressure heat capacity of liquid
Cp,liquid (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
39.209 | 298.15 | Aston, Wood, et al., 1953 | T = 13 to 300 K.; DH |
Phase change data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), References, Notes
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:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing
AC - William E. Acree, Jr., James S. Chickos
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 337.1 | K | N/A | Weast and Grasselli, 1989 | BS |
Tboil | 336.2 | K | N/A | Majer and Svoboda, 1985 | |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 216. | K | N/A | McMillan, 1967 | Uncertainty assigned by TRC = 1.5 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Ttriple | 215.95 | K | N/A | Aston, Wood, et al., 1953, 2 | Uncertainty assigned by TRC = 0.02 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ΔvapH° | 8.418 | kcal/mol | N/A | Majer and Svoboda, 1985 | |
ΔvapH° | 8.37 ± 0.04 | kcal/mol | V | Aston, Wood, et al., 1953, 3 | ALS |
Reduced pressure boiling point
Tboil (K) | Pressure (atm) | Reference | Comment |
---|---|---|---|
336.2 | 0.991 | Aldrich Chemical Company Inc., 1990 | BS |
Enthalpy of vaporization
ΔvapH (kcal/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
8.3659 | 298.15 | N/A | Aston, Wood, et al., 1953 | P = 20.90 kPa; DH |
7.780 | 336.2 | N/A | Majer and Svoboda, 1985 | |
8.15 | 284. | N/A | Bourret-Courchesne, Ye, et al., 2000 | Based on data from 267. to 303. K.; AC |
8.72 | 277. | A | Stephenson and Malanowski, 1987 | Based on data from 238. to 292. K. See also Aston, Wood, et al., 1953 and Boublik, Fried, et al., 1984.; AC |
Entropy of vaporization
ΔvapS (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
28.06 | 298.15 | Aston, Wood, et al., 1953 | P; DH |
Antoine Equation Parameters
log10(P) = A − (B / (T + C))
P = vapor pressure (atm)
T = temperature (K)
View plot Requires a JavaScript / HTML 5 canvas capable browser.
Temperature (K) | A | B | C | Reference | Comment |
---|---|---|---|---|---|
237.74 to 293.08 | 4.70745 | 1388.51 | -40.613 | Aston, Wood, et al., 1953 | Coefficents calculated by NIST from author's data. |
Enthalpy of fusion
ΔfusH (kcal/mol) | Temperature (K) | Reference | Comment |
---|---|---|---|
2.40741 | 215.95 | Aston, Wood, et al., 1953 | DH |
2.407 | 216. | Domalski and Hearing, 1996 | AC |
Entropy of fusion
ΔfusS (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
11.15 | 215.95 | Aston, Wood, et al., 1953 | DH |
Gas phase ion energetics data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, IR Spectrum, Mass spectrum (electron ionization), 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) | 7.29 ± 0.05 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 221.6 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 213.8 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
7.29 ± 0.05 | EQ | Mautner(Meot-Ner), Nelsen, et al., 1984 | LBLHLM |
8.05 ± 0.05 | PE | Vovna, Vilesov, et al., 1975 | LLK |
8.28 | PE | Bodor, Dewar, et al., 1970 | RDSH |
7.67 ± 0.05 | PI | Akopyan and Vilesov, 1963 | RDSH |
7.46 ± 0.02 | PI | Akopyan, Vilesov, et al., 1963 | RDSH |
8.1 ± 0.1 | EI | Dibeler, Franklin, et al., 1959 | RDSH |
8.82 | PE | Rademacher, 1975 | Vertical value; LLK |
8.85 | PE | Kimura, Katsumata, et al., 1975 | Vertical value; LLK |
8.88 | PE | Nelsen and Buschek, 1974 | Vertical value; LLK |
8.88 | PE | Nelsen and Buschek, 1974, 2 | Vertical value; LLK |
Appearance energy determinations
IR Spectrum
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Gas Phase Spectrum
Notice: This spectrum may be better viewed with a Javascript and HTML 5 enabled browser.
Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.
Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
View spectrum image in SVG format.
Download spectrum in JCAMP-DX format.
Owner | NIST Standard Reference Data Program Collection (C) 2018 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | Sadtler Research Labs Under US-EPA Contract |
State | gas |
Mass spectrum (electron ionization)
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, IR Spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Spectrum
Notice: This spectrum may be better viewed with a Javascript and HTML 5 enabled browser.
Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
Due to licensing restrictions, this spectrum cannot be downloaded.
Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | Japan AIST/NIMC Database- Spectrum MS-NW-1126 |
NIST MS number | 229632 |
References
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Donovan, Shomate, et al., 1960
Donovan, T.M.; Shomate, C.H.; McBride, W.R.,
The heat of combustion of tetramethyltetrazene and 1,1-dimethylhydrazine,
J. Phys. Chem., 1960, 64, 281-282. [all data]
Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G.,
Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]
Aston, Rock, et al., 1952
Aston, J.G.; Rock, E.J.; Isserow, S.,
The heats of combustion of the methyl substituted hydrazines and some observations on the burning of volatile liquids,
J. Am. Chem. Soc., 1952, 74, 2484-24. [all data]
Aston, Wood, et al., 1953
Aston, J.G.; Wood, J.L.; Zolki, T.P.,
The thermodynamic properties and configuration of unsymmetrical dimethylhydrazine,
J. Am. Chem. Soc., 1953, 75, 6202-6204. [all data]
Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]
Majer and Svoboda, 1985
Majer, V.; Svoboda, V.,
Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]
McMillan, 1967
McMillan, J.A.,
Hydrazine-1,1-Dimethylhydrazine Solid-Liquid Phase Diagram,
J. Chem. Eng. Data, 1967, 12, 39. [all data]
Aston, Wood, et al., 1953, 2
Aston, J.G.; Wood, J.L.; Zolki, T.P.,
The Thermodynamic Properties and Configuration of Unsymmetrical Dimethylhydrazine,
J. Am. Chem. Soc., 1953, 75, 6202. [all data]
Aston, Wood, et al., 1953, 3
Aston, J.G.; Wood, J.L.; Zolki, T.P.,
The thermodynamic properties and configuration of unsymmetrical dimethylhydrazine,
J. Am. Chem. Soc., 1953, 75, 6202-62. [all data]
Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc.,
Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]
Bourret-Courchesne, Ye, et al., 2000
Bourret-Courchesne, E.; Ye, Q.; Peters, D.W.; Arnold, J.; Ahmed, M.; Irvine, S.J.C.; Kanjolia, R.; Smith, L.M.; Rushworth, S.A.,
Pyrolysis of dimethylhydrazine and its co-pyrolysis with triethylgallium,
Journal of Crystal Growth, 2000, 217, 1-2, 47-54, https://doi.org/10.1016/S0022-0248(00)00398-5
. [all data]
Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw,
Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2
. [all data]
Boublik, Fried, et al., 1984
Boublik, T.; Fried, V.; Hala, E.,
The Vapour Pressures of Pure Substances: Selected Values of the Temperature Dependence of the Vapour Pressures of Some Pure Substances in the Normal and Low Pressure Region, 2nd ed., Elsevier, New York, 1984, 972. [all data]
Domalski and Hearing, 1996
Domalski, Eugene S.; Hearing, Elizabeth D.,
Heat Capacities and Entropies of Organic Compounds in the Condensed Phase. Volume III,
J. Phys. Chem. Ref. Data, 1996, 25, 1, 1, https://doi.org/10.1063/1.555985
. [all data]
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]
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]
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]
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. IV. Empirical estimation of lone pair-lone pair dihedral angles and prediction of lone pair ionization potentials for some cyclic and bicyclic hydrazines,
J. Am. Chem. Soc., 1974, 96, 6982. [all data]
Nelsen and Buschek, 1974, 2
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]
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]
Fisher and Henderson, 1967
Fisher, I.P.; Henderson, E.,
Mass spectrometry of free radicals,
J. Chem. Soc. Faraday Trans., 1967, 63, 1342. [all data]
Gowenlock, Jones, et al., 1961
Gowenlock, B.G.; Jones, P.P.; Majer, J.R.,
Bond dissociation energies in some molecules containing alkyl substituted CH3, NH2, and OH,
J. Chem. Soc. Faraday Trans., 1961, 57, 23. [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]
Foner and Hudson, 1962
Foner, S.N.; Hudson, R.L.,
Mass spectrometry of inorganic free radicals,
Advan. Chem. Ser., 1962, 36, 34. [all data]
Notes
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), References
- Symbols used in this document:
AE Appearance energy Cp,liquid Constant pressure heat capacity of liquid IE (evaluated) Recommended ionization energy S°liquid Entropy of liquid at standard conditions Tboil Boiling point Tfus Fusion (melting) point Ttriple Triple point temperature ΔcH°liquid Enthalpy of combustion of liquid at standard conditions ΔfH°gas Enthalpy of formation of gas at standard conditions ΔfH°liquid Enthalpy of formation of liquid at standard conditions ΔfusH Enthalpy of fusion ΔfusS Entropy of fusion ΔvapH Enthalpy of vaporization ΔvapH° Enthalpy of vaporization at standard conditions ΔvapS Entropy of vaporization - 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.