Trimesic acid

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Trimesic acid
Skeletal formula
Ball-and-stick model
Names
Preferred IUPAC name
Benzene-1,3,5-tricarboxylic acid
Identifiers
3D model (JSmol)
2053080
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.008.253 Edit this at Wikidata
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) checkY
    Key: QMKYBPDZANOJGF-UHFFFAOYSA-N checkY
  • 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[1]
Hazards[2]
Safety data sheet (SDS) Oxford MSDS
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
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY  (what is checkY☒N ?)
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.[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 in a hydrogen-bonded hydrated network with wide unidimensional empty channels.[6]

See also[]

References[]

  1. ^ Brown, H.C.; McDaniel, D.H.; Häfliger, O. (1955). "Chapter 14—Dissociation Constants". In Braude, E.A.; Nachod, F.C. (eds.). Determination of Organic Structures by Physical Methods. New York: Academic Press. doi:10.1016/B978-1-4832-3166-2.50018-4.
  2. ^ "1,3,5-Benzenetricarboxylic acid". pubchem.ncbi.nlm.nih.gov.
  3. ^ Marković, Zoran; Badjuk, Dalibor; Gutman, Ivan (2004). "Geometry and Conformations of Benzenecarboxylic Acids". J. Serb. Chem. Soc. 69 (11): 877–882. doi:10.2298/JSC0411877M.
  4. ^ Röhrscheid, Freimund (2000). "Carboxylic Acids, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a05_249.
  5. ^ Tang, Li Ming; Wang, Yu Jiang (2009). "Highly Stable Supramolecular Hydrogels Formed from 1,3,5-Benzenetricarboxylic Acid and Hydroxyl Pyridines". Chinese Chemical Letters. 20 (10): 1259–1262. doi:10.1016/j.cclet.2009.04.030.
  6. ^ Herbstein, Frank H. (1987). "Structural Parsimony and Structural Variety Among Inclusion Complexes (with Particular Reference to the Inclusion Compounds of Trimesic acid, N-(p-tolyl)-tetrachlorophthalimide, and the Heilbron "Complexes")". Top. Curr. Chem. Topics in Current Chemistry. 140. pp. 107–139. doi:10.1007/bfb0003838. ISBN 3-540-17307-2.


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