528056

Sigma-Aldrich

Thioglycolic acid

≥99%

Sinónimos:
Mercaptoacetic acid
Fórmula lineal:
HSCH2COOH
Número de CAS:
Peso molecular:
92.12
Beilstein/REAXYS Number:
506166
Número de EC:
Número MDL:
ID de la sustancia en PubChem:
NACRES:
NA.22

Nivel de calidad

100

densidad de vapor

3.2 (vs air)

presión de vapor

0.4 mmHg ( 25 °C)

ensayo

≥99%

temp. de autoignición

662 °F

availability

available only in EU

índice de refracción

n20/D 1.505 (lit.)

bp

96 °C/5 mmHg (lit.)

mp

−16 °C (lit.)

densidad

1.326 g/mL at 20 °C (lit.)

temp. de almacenamiento

2-8°C

SMILES string

OC(=O)CS

InChI

1S/C2H4O2S/c3-2(4)1-5/h5H,1H2,(H,3,4)

InChI key

CWERGRDVMFNCDR-UHFFFAOYSA-N

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Categorías relacionadas

Aplicación

Thioglycolic acid (TGA) can be used as:
  • A sulfur source and stabilizing agent to synthesize nanocrystalline metal sulfides via hydrothermal reaction. TGA also controls the morphology and particle sizes of nanocrystalline metal sulfides during the process.
  • An effective agglomeration suppressant for the agglomeration of sulfurized mineral pyrite.
  • A reactant to prepare 2,3-disubstituted-thiazolidin-4-one derivatives by one-pot cyclo-condensation reaction with various aldehydes and amines using supported protic acid catalyst.
  • A capping or stabilizing agent to synthesize CdTe quantum dots with controllable photoluminescence wavelengths.

Información legal

Product of Arkema

pictogramas

CorrosionSkull and crossbones

Palabra de señalización

Danger

hazcat

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1B

storage_class_code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK Alemania

WGK 1

Punto de inflamabilidad F

266.0 °F - closed cup

Punto de inflamabilidad C

130 °C - closed cup

Equipo de protección personal

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificado de Análisis

Certificado de origen

Baofu Han et al.
Colloids and surfaces. B, Biointerfaces, 100, 209-214 (2012-07-07)
Fluorescent carbon dots (CDs) were solvothermaly synthesized in water-glycol medium by using glucose as carbon source and then modified with polyethyleneimine (PEI) for the first time to improve fluorescence quality. The as-prepared CDs were monodispersed sphere particles with a diameter...
Gizem Ayna et al.
PloS one, 7(6), e40069-e40069 (2012-07-07)
Pathogen-activated and damage-associated molecular patterns activate the inflammasome in macrophages. We report that mouse macrophages release IL-1β while co-incubated with pro-B (Ba/F3) cells dying, as a result of IL-3 withdrawal, by apoptosis with autophagy, but not when they are co-incubated...
Heike E Friedl et al.
Biomaterials, 34(32), 7811-7818 (2013-07-28)
It was the purpose of this study to design and evaluate a chitosan derivative as mucoadhesive excipient for vaginal drug delivery systems. The chemical modification of chitosan was achieved by conjugation of thioglycolic acid (TGA) resulting in 1594 μmol thiol...
Yoshikazu Ishii et al.
Antimicrobial agents and chemotherapy, 54(9), 3625-3629 (2010-07-08)
ME1071, a maleic acid derivative, is a novel specific inhibitor for metallo-beta-lactamases (MBL). In this study, the potentiation of ME1071 in combination with several beta-lactams was evaluated using MBL-producing Pseudomonas aeruginosa isolates. The rates of susceptibility of MBL producers to...
Takashi Kohno et al.
Arteriosclerosis, thrombosis, and vascular biology, 33(4), 805-813 (2013-01-26)
Vascular smooth muscle cell (VSMC) migration is critically important for neointimal formation after vascular injury and atherosclerosis lesion formation. Copper (Cu) chelator inhibits neointimal formation, and we previously demonstrated that Cu transport protein antioxidant-1 (Atox1) is involved in Cu-induced cell...

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