W508306
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
EC Number:
202-733-3
UNSPSC Code:
12164502
PubChem Substance ID:
Beilstein/REAXYS Number:
1783567
MDL number:
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
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Jeffrey A Lewis et al.
Research in microbiology, 160(3), 179-186 (2009-03-17)
The tricarballylate utilization locus (tcuRABC) of Salmonella enterica serovar Typhimurium is comprised of a 3-gene operon (tcuABC) that encodes functions that allow this bacterium to use tricarballylate as a source of carbon and energy, and the tcuR gene, which encodes
Suzanne L Tobey et al.
Journal of the American Chemical Society, 125(36), 10963-10970 (2003-09-04)
The association of synthetic receptors to target guests often proceeds through the cooperative action of multiple binding forces. An investigation into the thermodynamic origin of cooperativity in ion-pairing host-guest binding in water is described. The binding affinities of 1,2,3,4-butanetetracarboxylate, tricarballate
Nicholas J S Harmat et al.
Bioorganic & medicinal chemistry letters, 12(4), 693-696 (2002-02-15)
A series of cyclic pseudopeptides were synthesized containing the sequence -Trp-Phe-(D)-PhePsiCH2NH-, the terminal ends of which were bound to 2-carboxy succinate or enantiomerically enriched tricarballylic acid to give the final cyclic structures. These two molecules and their subsequent derivatives were