Chemistry:Uvitic acid
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Names | |
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Preferred IUPAC name
5-Methylbenzene-1,3-dicarboxylic acid | |
Other names
5-Methyl-1,3-benzenedicarboxylic acid; 3,5-Dicarboxytoluene; 5-Methylisophthalic acid
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
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PubChem CID
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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 pictograms | |
GHS Signal word | Warning |
H315, H319, H335 | |
P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, 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). | |
Infobox references | |
Tracking categories (test):
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] Under normal conditions, the acid is a white crystalline substance.
Preparation
Uvitic acid is obtained by oxidizing mesitylene.[4]
See also
References
- ↑ "Uvitic acid". rdchemicals.com. http://www.rdchemicals.com/chemicals.php?mode=details&mol_id=2975. Retrieved 31 October 2016.
- ↑ "Uvitic acid". chemspider.com. http://www.chemspider.com/Chemical-Structure.61445.html. Retrieved 31 October 2016.
- ↑ Senning, Alexander (2006). Elsevier's Dictionary of Chemoetymology: The Whys and Whences of Chemical Nomenclature and Terminology. Elsevier. pp. 410. ISBN 9780080488813. https://books.google.com/books?id=Fl4sdCYrq3cC&q=uvitic+acid+--+uva+a+grape&pg=PA410. Retrieved 31 October 2016.
- ↑ "Definition of uvitic acid". merriam-webster.com. http://www.merriam-webster.com/dictionary/uvitic%20acid. Retrieved 31 October 2016.
Original source: https://en.wikipedia.org/wiki/Uvitic acid.
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