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 |
|
51147 | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C9H6O6 | |
Molar mass | 210.14034 |
Acidity (pKa) | 3.12, 3.89, 4.70 [1] |
Hazards [2] | |
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).
|
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. [3] A colorless solid, trimesic acid has some commercial value as a precursor to some plasticizers. [4]
Trimesic acid can be combined with para-hydroxypyridine to make a water-based gel, stable up to 95 °C. [5]
Trimesic acid crystallizes from water to form a hydrogen-bonded hydrated network with wide unidimensional empty channels. [6] [7]
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 |
|
51147 | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C9H6O6 | |
Molar mass | 210.14034 |
Acidity (pKa) | 3.12, 3.89, 4.70 [1] |
Hazards [2] | |
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).
|
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. [3] A colorless solid, trimesic acid has some commercial value as a precursor to some plasticizers. [4]
Trimesic acid can be combined with para-hydroxypyridine to make a water-based gel, stable up to 95 °C. [5]
Trimesic acid crystallizes from water to form a hydrogen-bonded hydrated network with wide unidimensional empty channels. [6] [7]