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Merck
모든 사진(1)

문서

V800423

Sigma-Aldrich

Thioglycolic acid

LR, ~80%

동의어(들):

Mercaptoacetic acid

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About This Item

Linear Formula:
HSCH2COOH
CAS Number:
Molecular Weight:
92.12
Beilstein:
506166
EC Number:
MDL number:
UNSPSC 코드:
12352300
PubChem Substance ID:

Grade

LR

Quality Level

vapor density

3.2 (vs air)

vapor pressure

0.4 mmHg ( 25 °C)

제품 라인

Vetec

autoignition temp.

662 °F

농도

~80%

refractive index

n20/D 1.505 (lit.)

bp

96 °C/5 mmHg (lit.)

mp

−16 °C (lit.)

density

1.326 g/mL at 20 °C (lit.)

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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법적 정보

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

픽토그램

Skull and crossbonesCorrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - 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

WGK 3

Flash Point (°F)

266.0 °F - closed cup

Flash Point (°C)

130 °C - closed cup


시험 성적서(COA)

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문서 라이브러리 방문

Fabian Hintzen et al.
International journal of pharmaceutics, 436(1-2), 120-126 (2012-06-12)
The aim of this study was to investigate the influence of molar mass of thiolated polymers (thiomers) on their in situ gelling properties. Chitosan-thioglycolic acid (chitosan-TGA) and pectin-cysteine (pectin-Cys) of increasing molar mass were chosen to produce in situ gels
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
K Gradauer et al.
Journal of controlled release : official journal of the Controlled Release Society, 165(3), 207-215 (2012-12-12)
An ideal oral drug carrier should facilitate drug delivery to the gastrointestinal tract and its absorption into the systemic circulation. To meet these requirements, we developed a thiomer-coated liposomal delivery system composed of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and a maleimide-functionalized lipid, to
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
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

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