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| Names | |||
|---|---|---|---|
| Preferred IUPAC name
Pyridine-4-carboxylic acid | |||
| Other names
Isonicotinic acid 4-Pyridinecarboxylic acid p-Pyridinecarboxylic acid 4-Picolinic acid | |||
| Identifiers | |||
3D model (JSmol) |
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| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.000.208 | ||
| KEGG | |||
PubChem CID |
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| UNII | |||
CompTox Dashboard (EPA) |
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| Properties | |||
| C6H5NO2 | |||
| Molar mass | 123.111 g·mol−1 | ||
| Appearance | White to off-white crystalline solid | ||
| Density | Solid | ||
| Melting point | 310 °C (590 °F; 583 K) (sublimes) | ||
| Hazards | |||
| NFPA 704 (fire diamond) | |||
| Safety data sheet (SDS) | http://datasheets.scbt.com/sc-250188.pdf | ||
| Related compounds | |||
Related compounds |
nicotinic acid, pyridine isoniazid | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Isonicotinic acid or pyridine-4-carboxylic acid is an organic compound with the formula C5H4N(CO2H). It is a derivative of pyridine with a carboxylic acid substituent at the 4-position. It is an isomer of picolinic acid and nicotinic acid, which have the carboxyl group at the 2- and 3-position respectively compared to the 4-position for isonicotinic acid.
Derivatives
Isonicotinic acids is a term loosely used for derivatives of isonicotinic acid. Hydrazide derivatives include isoniazid, iproniazid, and nialamide. Amide and ester derivatives include ethionamide and dexamethasone isonicotinate.
See also
References
- ↑ Isonicotinic acid at chemicalland21.com
External links
- Isonicotinic+Acids at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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