Trimellitic anhydride

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Trimellitic anhydride
Trimellitic anhydride.svg
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.008.190 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 209-008-0
KEGG
PubChem CID
RTECS number
  • DC2050000
UNII
  • InChI=1S/C9H4O5/c10-7(11)4-1-2-5-6(3-4)9(13)14-8(5)12/h1-3H,(H,10,11)
    Key: SRPWOOOHEPICQU-UHFFFAOYSA-N
  • C1=CC2=C(C=C1C(=O)O)C(=O)OC2=O
Properties
C9H4O5
Molar mass 192.126 g·mol−1
Appearancecolorless or white solid
Density 1.54 g/cm3
Melting point 168 °C (334 °F; 441 K)
Boiling point 390 °C (734 °F; 663 K)
Hazards
GHS labelling:
GHS-pictogram-acid.svg GHS-pictogram-exclam.svg GHS-pictogram-silhouette.svg
Danger
H317, H318, H334, H335
P261, P271, P272, P280, P285, P302+P352, P304+P340, P304+P341, P305+P351+P338, P310, P312, P321, P333+P313, P342+P311, P363, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Trimellitic anhydride is an organic compound with the formula HO2CC6H3(C2O3). It is the cyclic anhydride of trimellitic acid. Several thousand tons of this colorless solid are produced annually as a precursor to plasticizers for polyvinyl chloride. It is produced by air-oxidation of 1,2,4-trimethylbenzene. [1]

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References

  1. Röhrscheid, Freimund (2000). "Carboxylic Acids, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry . Weinheim: Wiley-VCH. doi:10.1002/14356007.a05_249.