Oxiniacic acid
- Formula: C6H5NO3
- Molecular weight: 139.1088
- IUPAC Standard InChIKey: FJCFFCXMEXZEIM-UHFFFAOYSA-N
- CAS Registry Number: 2398-81-4
- 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: 3-Pyridinecarboxylic acid, 1-oxide; Nicotinic acid, 1-oxide; Nicotinic acid oxide; Nicotinic acid N-oxide; Pyridine-3-carboxylic acid N-oxide; 3-Carboxypyridine N-oxide; 3-Pyridinecarboxylic acid oxide; N-Hydroxynicotinic acid; NSC 93890
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Phase change data
Go To: Top, 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
AC - William E. Acree, Jr., James S. Chickos
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔsubH° | 152.3 ± 1.9 | kJ/mol | V | Acree, Tucker, et al., 1995 | ALS |
ΔsubH° | 152.3 ± 1.9 | kJ/mol | ME | Acree Jr., 1995 | See also Abboud, Jimenez, et al., 1995.; AC |
Mass spectrum (electron ionization)
Go To: Top, Phase change data, 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
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Additional Data
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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 | NIST Mass Spectrometry Data Center, 1998. |
NIST MS number | 292105 |
References
Go To: Top, Phase change data, 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.
Acree, Tucker, et al., 1995
Acree, W.E., Jr.; Tucker, S.A.; Ribeiro da Silva, M.D.M.C.; Matos, M.A.R.; Goncalves, J.M.; Ribeiro da Silva, M.A.V.; Pilcher, G.,
Enthalpies of combustion of 4-nitropyridine N-oxide and pyridine-3-carboxylic acid N-oxide: the dissociation enthalpies of the N-O bonds in pyridine N-oxide derivatives,
J. Chem. Thermodyn., 1995, 27, 391-398. [all data]
Acree Jr., 1995
Acree Jr.,
Enthalpies of combustion of 4-nitropyridineN-oxide and pyridine-3-carboxylic acidN-oxide: the dissociation enthalpies of the N---O bonds in pyridineN-oxide derivatives,
The Journal of Chemical Thermodynamics, 1995, 27, 4, 391-398, https://doi.org/10.1006/jcht.1995.0038
. [all data]
Abboud, Jimenez, et al., 1995
Abboud, J.-L.M.; Jimenez, P.; Roux, M.V.; Turrion, C.; Lopez-Mardomingo, C.; Podosenin, A.; Rogers, D.W.; Liebman, J.F.,
Interrelations of the energetics of amides and alkenes: enthalpies of formation of N,N-dimethyl dertivatives of pivalamide, 1-adamantylcarboxamide and benzamide, and of styrene and its a-, trans-β- and β,β-methylated derivates,
J. Phys. Org. Chem., 1995, 8, 15-25. [all data]
Notes
Go To: Top, Phase change data, Mass spectrum (electron ionization), References
- Symbols used in this document:
ΔsubH° Enthalpy of sublimation at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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