Uvitonic acid
 | |
| Names | |
|---|---|
| IUPAC name
6-Methyl-2,4-pyridinedicarboxylic acid | |
Other names
| |
| Identifiers | |
| 499-50-3 | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 14208829 |
| |
| |
| Properties | |
| C8H7NO4 | |
| Molar mass | 181.145480 g/mol |
| Appearance | White crystalline solid |
| Density | 1.5±0.1 g/cm3 |
| Melting point | 170 °C (dec.)(lit.) |
| Boiling point | 525.3±50.0 °C at 760 mmHg |
| Vapor pressure | 0.0±1.5 mmHg at 25°C |
| Hazards | |
| GHS pictograms |  [1] |
| GHS signal word | WARNING |
| H302, H315, H319, H335 | |
| P261, P301+312, P302+352, P304+340, P305+351+338 | |
| Flash point | 271.5±30.1 °C |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Uvitonic acid (6-methyl-2,4-pyridinedicarboxylic acid) is an organic compound with the formula CH3C5H2N(COOH)2.[2][3] The acid is a pyridine analogue of the benzene derivative uvitic acid.[4] Under normal conditions, the acid is a white crystalline substance.[5]
Preparation
Uvitonic acid is obtained by the action of ammonia on glutaric acid.[6]
See also
References
- ↑ "SAFETY DATA SHEET". oakwoodchemical.com. Oakwood Chemical. Retrieved 22 November 2016.
- ↑ "CAS No. 499-50-3 (uvitonic acid)". guidechem.com. Retrieved 22 November 2016.
- ↑ "Uvitonic acid". Chemical Book. chemicalbook.com. Retrieved 22 November 2016.
- ↑ Senning, Alexander (2006). Elsevier's Dictionary of Chemoetymology: The Whys and Whences of Chemical Nomenclature and Terminology. Elsevier. p. 410. ISBN 9780080488813. Retrieved 31 October 2016.
- ↑ "Uvitonic acid". wiktionary.org. Retrieved 22 November 2016.
- ↑ Coffey, S. (June 3, 2016). Dihydric Alcohols, Their Oxidation Products and Derivatives: A Modern Comprehensive Treatise (2 ed.). Elsevier. p. 237. ISBN 9781483221311. Retrieved 22 November 2016.
External links
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