Trimesic acid

Trimesic acid
Names
Preferred IUPAC name
Benzene-1,3,5-tricarboxylic acid
Identifiers
3D model (JSmol)
Abbreviations TMA
2053080
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.008.253
EC Number
  • 209-077-7
51147
UNII
  • InChI=1S/C9H6O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H,(H,10,11)(H,12,13)(H,14,15) Y
    Key: QMKYBPDZANOJGF-UHFFFAOYSA-N Y
  • InChI=1/C9H6O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H,(H,10,11)(H,12,13)(H,14,15)
    Key: QMKYBPDZANOJGF-UHFFFAOYAC
  • c1c(cc(cc1C(=O)O)C(=O)O)C(=O)O
Properties
C9H6O6
Molar mass 210.14034
Acidity (pKa) 3.12, 3.89, 4.70
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
Safety data sheet (SDS) Oxford MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Trimesic acid, also known as benzene-1,3,5-tricarboxylic acid, is an organic compound with the formula C6H3(CO2H)3. It is one of three isomers of benzenetricarboxylic acid. A colorless solid, trimesic acid has some commercial value as a precursor to some plasticizers.

Trimesic acid can be combined with para-hydroxypyridine to make a water-based gel, stable up to 95 °C.

Trimesic acid crystallizes from water to form a hydrogen-bonded hydrated network with wide unidimensional empty channels.