B4589
1,2,4-Benzenetricarboxylic acid
≥99%
Synonym(s):
Benzene-1,2,4-tricarboxylic acid, Trimellitic acid
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About This Item
Linear Formula:
C6H3(CO2H)3
CAS Number:
Molecular Weight:
210.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-432-3
Beilstein/REAXYS Number:
2214815
MDL number:
Assay:
≥99%
Form:
powder
InChI key
ARCGXLSVLAOJQL-UHFFFAOYSA-N
InChI
1S/C9H6O6/c10-7(11)4-1-2-5(8(12)13)6(3-4)9(14)15/h1-3H,(H,10,11)(H,12,13)(H,14,15)
SMILES string
OC(C1=C(C(O)=O)C=C(C(O)=O)C=C1)=O
assay
≥99%
form
powder
Quality Level
Related Categories
Application
1,2,4-Benzenetricarboxylic acid (trimellitic acid) is generally used as carboxylate ligand in the synthesis of a wide range of metal-organic frameworks (MOFs). It can also be used to synthesize Ln3+ encapsulated nanocrystals which exhibit white-light luminescence.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A three-dimensional metal?organic framework with a distorted Kagome related layer showing canted antiferromagnetic behaviour.
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Chemical Communications (Cambridge, England), 11, 1278-1280 (2008)
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Dental materials journal, 39(3), 435-443 (2020-01-15)
The purpose of this study was to use a new scratch test and tensile test to evaluate the bond strength between artificial erosive enamel or dentin and self-adhesive resin composites as a coating material. Coronal enamel or dentin surface was
Imparting Tunable and white-light luminescence to a nanosized metal?organic framework by controlled encapsulation of lanthanide cations.
Zhou Y and Yan B
Inorganic Chemistry, 53(7), 3456-3463 (2014)
Three-dimensional metal?organic frameworks constructed from bix and 1, 2, 4-benzenetricarboxylate.
Yao J, et al.
CrystEngComm, 10(10), 1379-1383 (2008)
Robert F Rando et al.
Antimicrobial agents and chemotherapy, 50(9), 3081-3089 (2006-08-31)
Recent studies of cellulose-based polymers substituted with carboxylic acids like cellulose acetate phthalate (CAP) have demonstrated the utility of using carboxylic acid groups instead of the more common sulfate or sulfonate moieties. However, the pK(a) of the free carboxylic acid
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