Uvitic acid

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Uvitic acid
Uvitic acid.svg
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 Edit this at Wikidata
EC Number
  • 207-881-2
  • InChI=1S/C9H8O4/c1-5-2-6(8(10)11)4-7(3-5)9(12)13/h2-4H,1H3,(H,10,11)(H,12,13)
    Key: PMZBHPUNQNKBOA-UHFFFAOYSA-N
  • Cc1cc(cc(c1)C(=O)O)C(=O)O
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:
GHS07: Exclamation mark
Signal word
 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).
Infobox references

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[]

  1. ^ "Uvitic acid". rdchemicals.com. Retrieved 31 October 2016.
  2. ^ "Uvitic acid". chemspider.com. Retrieved 31 October 2016.
  3. ^ Senning, Alexander (2006). Elsevier's Dictionary of Chemoetymology: The Whys and Whences of Chemical Nomenclature and Terminology. Elsevier. p. 410. ISBN 9780080488813. Retrieved 31 October 2016.
  4. ^ "Definition of uvitic acid". merriam-webster.com. Retrieved 31 October 2016.
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