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Merck
CN

W508306

丙三羧酸

≥99%

别名:

1,2,3-丙三甲酸

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关于此项目

线性分子式:
(HO2CCH2)2CHCO2H
化学文摘社编号:
分子量:
176.12
EC Number:
202-733-3
UNSPSC Code:
12164502
PubChem Substance ID:
Beilstein/REAXYS Number:
1783567
MDL number:
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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



存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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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
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