T53503
Tricarballylic acid
99%
Synonym(s):
1,2,3-Propanetricarboxylic acid
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About This Item
Linear Formula:
(HO2CCH2)2CHCO2H
CAS Number:
Molecular Weight:
176.12
Beilstein:
1783567
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
mp
156-161 °C (lit.)
SMILES string
OC(=O)CC(CC(O)=O)C(O)=O
InChI
1S/C6H8O6/c7-4(8)1-3(6(11)12)2-5(9)10/h3H,1-2H2,(H,7,8)(H,9,10)(H,11,12)
InChI key
KQTIIICEAUMSDG-UHFFFAOYSA-N
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General description
Tricarballylic acid also known as 1,2,3-Propanetricarboxylic acid is a small biomimetic ligand that is often used as building blocks in the synthesis of metal-organic frameworks. Additionally, it is used to produce high-value plasticizers.
Application
- Effect of organic acids on the solid-state polymorphic phase transformation of piracetam.: Examines the impact of tricarballylic acid and other organic acids on the polymorphic phase transformation of the drug piracetam, relevant for pharmaceutical formulations and drug stability studies (Fan F et al., 2023).
- Nanotubule inclusion in the channels formed by a six-fold interpenetrated, triperiodic framework.: Describes the synthesis of novel materials incorporating tricarballylic acid, which could have implications for polymer production and advanced material applications (Kusumoto S et al., 2023).
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The circular dichroism (CD) exciton chirality method was employed for the stereochemical assignment of the tricarballylic acid (TCA) side chains of fumonisin B(1) 1a (FB(1)). Using 2-naphthoate for chromophoric derivatization of the reduced TCA moieties, the absolute configuration was shown
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Journal of inorganic biochemistry, 103(2), 219-226 (2008-11-26)
The coordination behavior of copper(II) with tricarballylic acid (H(3)TCA) and imidazole (Imz) is described. Speciation in aqueous solution has been determined at 25 degrees C and 0.15M NaCl ionic strength by potentiometric measurements and EPR characterization of the species. Two
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The histidine protein kinase DcuS of Escherichia coli senses C(4)-dicarboxylates and citrate by a periplasmic domain. The closely related sensor kinase CitA binds citrate, but no C(4)-dicarboxylates, by a homologous periplasmic domain. CitA is known to bind the three carboxylate
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