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Merck
CN

359394

巯基丙酮酸钠

≥85%, technical grade

别名:

3-巯基-2-氧丙酸 钠盐, 巯基丙酮酸 钠盐

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关于此项目

线性分子式:
HSCH2COCOONa
化学文摘社编号:
分子量:
142.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
233-594-7
Beilstein/REAXYS Number:
4018548
MDL number:
Assay:
≥85%
Form:
powder
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InChI key

CODUSAVZTZYYDD-UHFFFAOYSA-M

InChI

1S/C3H4O3S.Na/c4-2(1-7)3(5)6;/h7H,1H2,(H,5,6);/q;+1/p-1

SMILES string

[Na+].[O-]C(=O)C(=O)CS

grade

technical grade

assay

≥85%

form

powder

impurities

<5 wt. % ethanol

mp

200 °C (dec.) (lit.)

storage temp.

2-8°C

Quality Level

Application

Sodium mercaptopyruvate is suitable for use in the thiosulfate sulfurtransferase activity assay.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J Papenbrock et al.
European journal of biochemistry, 267(1), 145-154 (1999-12-22)
A database search for similarities between sequenced parts of the Arabidopsis thaliana genome with known sulfurtransferase sequences from Escherichia coli and mammals was undertaken to obtain information about plant sulfurtransferase-like proteins. One gene and several homologous EST clones were identified.
N E Labrou et al.
Journal of chromatography. A, 718(1), 35-44 (1995-12-01)
Three biomimetic dye ligands bearing as a triazine-linked terminal moiety a carboxylated structure, which mimics substrates and inhibitors of L-lactate dehydrogenase (LDH), were immobilized on cross-linked agarose Ultrogel A6R. These biomimetic dyes are purpose-designed analogues of commercial monochlorotriazine Cibacron Blue
Steven E Patterson et al.
Journal of medicinal chemistry, 56(3), 1346-1349 (2013-01-11)
Current cyanide antidotes are administered by IV infusion, which is suboptimal for mass casualties. Therefore, in a cyanide disaster, intramuscular (IM) injectable antidotes would be more appropriate. We report the discovery of the highly water-soluble sulfanegen triethanolamine as a promising
T Nakamura et al.
European journal of biochemistry, 267(17), 5621-5630 (2000-08-22)
Mercaptopyruvate sulfurtransferase (MST, EC 2.8.1.2) and thiosulfate sulfurtransferase (TST, rhodanese, EC 2.8.1.1) are evolutionarily related enzymes that catalyze the transfer of sulfur ions from mercaptopyruvate and thiosulfate, respectively, to cyanide ions. We have isolated and characterized two cDNAs, AtMST1 and
Herbert T Nagasawa et al.
Journal of medicinal chemistry, 50(26), 6462-6464 (2007-11-28)
A series of prodrugs of 3-mercaptopyruvate (3-MP), the substrate for the enzyme 3-mercaptopyruvate/cyanide sulfurtransferase (3-MPST) that converts cyanide to the nontoxic thiocyanate, which are highly effective cyanide antidotes, have been developed. These prodrugs of 3-MP are unique in being not

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