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Safety Information

W508306

Sigma-Aldrich

Tricarballylic acid

≥99%

Synonym(s):

1,2,3-Propanetricarboxylic acid

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About This Item

Linear Formula:
(HO2CCH2)2CHCO2H
CAS Number:
99-14-9
Molecular Weight:
176.12
Beilstein:
1783567
EC Number:
202-733-3
MDL number:
MFCD00002723
UNSPSC Code:
12164502
PubChem Substance ID:
24902038

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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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

W508306-BULK:
W508306-VAR:
W508306-SAMPLE:

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Certificates of Analysis (COA)

Lot/Batch Number
STBC6952V
STBB2904
10827JG
S24255

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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
Nima Sharifi et al.
Medical hypotheses, 66(4), 732-735 (2005-12-21)
The discovery and characterization of the von Hippel Lindau (VHL) syndrome has brought about tremendous advances in understanding the molecular mechanisms of renal cell carcinoma. VHL mutations are known to act through hypoxia inducible factor, which has a physiologic role
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
Jeffrey A Lewis et al.
Journal of bacteriology, 186(6), 1629-1637 (2004-03-05)
The genes of Salmonella enterica serovar Typhimurium LT2 encoding functions needed for the utilization of tricarballylate as a carbon and energy source were identified and their locations in the chromosome were established. Three of the tricarballylate utilization (tcu) genes, tcuABC
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
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