Trimellitic acid
 | |
| Names | |
|---|---|
| Preferred IUPAC name Benzene-1,2,4-tricarboxylic acid | |
| Other names 1,2,4-Benzenetricarboxylic acid; 4-Carboxyphthalic acid; 1,2,4-Tricarboxybenzene | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.007.667 |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C9H6O6 | |
| Molar mass | 210.141 g·mol−1 |
| Appearance | White solid |
| Melting point | 221–222 °C (430–432 °F; 494–495 K)[1] |
| 21 g/L (0.1M) at 25 °C[citation needed] | |
| log P | 2.721 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Trimellitic acid (benzene-1,2,4-tricarboxylic acid) is a chemical compound with the molecular formula C6H3(СООН)3. Like the other isomers of benzenetricarboxylic acid, trimellitic acid is a colorless solid. It is prepared by oxidation of 1,2,4-trimethylbenzene.[2]
Isomers
[edit]- Hemimellitic acid (benzene-1,2,3-tricarboxylic acid)
- Trimesic acid (benzene-1,3,5-tricarboxylic acid)
See also
[edit]References
[edit]- ^ Fishwick, Brian (1957). "233. The analysis of mixtures of benzene-carboxylic acids by partition chromatography". Journal of the Chemical Society (Resumed): 1196. doi:10.1039/JR9570001196.
- ^ Park, Chang-Man; Sheehan, Richard J. (2000). "Phthalic Acids and Other Benzenepolycarboxylic Acids". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.1608200816011811.a01. ISBN 0471238961.
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