Dinicotinic acid
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Names | |
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Preferred IUPAC name
Pyridine-3,5-dicarboxylic acid | |
Other names
3,5-Pyridinedicarboxylic acid
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Identifiers | |
3D model (JSmol)
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131640 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.007.177 ![]() |
EC Number |
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279307 | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C7H5NO4 | |
Molar mass | 167.120 g·mol−1 |
Hazards | |
GHS labelling: | |
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Signal word
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H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Dinicotinic acid (pyridine-3,5-dicarboxylic acid) is an organic compound that belongs to the heterocycles (more precisely, ). It belongs to the group of pyridine dicarboxylic acids and consists of a pyridine ring, which carries two carboxy groups in the 3- and 5-position.
Upon heating, it decarboxylates and decomposes to nicotinic acid:[1]
References[]
- ^ Alam, Mahbub; Khan, M. Hafeez (1980). "Preparation of some nicotinic acid derivatives". Philippine Journal of Science. 109 (1–2): 19–21.
See also[]
- Dipicolinic acid, an isomeric dicarboxylic acid
Categories:
- Pyridines
- Dicarboxylic acids
- Aromatic acids
- Organic compound stubs