|   | |
| Names | |
|---|---|
| Preferred IUPAC name 5-Methylbenzene-1,3-dicarboxylic acid | |
| Other names 5-Methyl-1,3-benzenedicarboxylic acid; 3,5-Dicarboxytoluene; 5-Methylisophthalic acid | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.007.166 | 
| EC Number | 
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|  PubChem CID | |
| UNII | |
|  CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C9H8O4 | |
| Molar mass | 180.159 g·mol−1 | 
| Appearance | White crystalline solid | 
| Density | 1.4±0.1 g/cm3 | 
| Melting point | 298 °C | 
| Boiling point | 408.7±33.0 °C at 760 mmHg | 
| Vapor pressure | 0.0±1.0 mmHg at 25°C | 
| Hazards | |
| GHS labelling: | |
|   | |
| Warning | |
| 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 | |
| Flash point | 215.1±21.9 °C | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Uvitic acid (5-methylisophthalic acid) is an organic compound with the formula CH3C6H3(COOH)2. [1] [2] The name comes from Latin uva which means a grape. The acid is called so because it may be produced indirectly from tartaric acid, which is found in the grape. [3] [4] Under normal conditions, the acid is a white crystalline substance.
Uvitic acid is obtained by oxidizing mesitylene. [5]