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Merck
CN

W421001

Sigma-Aldrich

Thioacetic acid

96%

Synonym(s):

Thiacetic acid

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About This Item

Linear Formula:
CH3COSH
CAS Number:
Molecular Weight:
76.12
FEMA Number:
4210
Beilstein:
1733298
EC Number:
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
12.199
NACRES:
NA.21
Organoleptic:
meaty; roasted
Biological source:
synthetic
Food allergen:
no known allergens
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biological source

synthetic

Quality Level

Assay

96%

refractive index

n20/D 1.465 (lit.)

bp

88-91.5 °C (lit.)

density

1.065 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

meaty; roasted

SMILES string

CC(S)=O

InChI

1S/C2H4OS/c1-2(3)4/h1H3,(H,3,4)

InChI key

DUYAAUVXQSMXQP-UHFFFAOYSA-N

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Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Sens. 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

64.4 °F - closed cup

Flash Point(C)

18 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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David Crich et al.
Angewandte Chemie (International ed. in English), 48(13), 2355-2358 (2009-02-21)
Highly activated thioesters formed by the rapid reaction of C-terminal thioacids derived from protected amino acids and peptides with the Sanger reagent and other electron-deficient aryl halides in the presence of a free amine immediately form a peptide bond with
I A Gol'dina et al.
Eksperimental'naia i klinicheskaia farmakologiia, 73(3), 25-27 (2010-04-23)
The influence of BM-7-02 compound on the production of cytokines in the culture of healthy volunteers' blood cells. This compound suppresses the production of main cytokine (gamma-IFN, IL-2 and IL-4) synthesized by CD4+ Th1 and Th2 cells, stimulates the production
Julián Valero et al.
Organic & biomolecular chemistry, 10(28), 5417-5430 (2012-06-14)
Polycationic oligo(chiral bicyclic guanidines) constitute useful non-peptidic penetrating agents for cell uptake and protein surface recognition. We report herein improved and selective procedures for the preparation of oligoguanidinium scaffolds linked through thioether bonds, with similar or different groups and functions
Francesco Cellesi et al.
Biomaterials, 25(21), 5115-5124 (2004-04-28)
We have previously described a gelation process based on the occurrence of both physical and a chemical mechanisms ('tandem process'), in which a telechelic linear poly(propylene glycol)-bl-poly(ethylene glycol)-bl-poly(propylene glycol) is first thermally gelled and subsequently covalently cross-linked by the reaction
E Pinart et al.
Journal of anatomy, 199(Pt 4), 435-448 (2001-11-06)
This study was undertaken to investigate the morphological characteristics and lectin affinity of the testicular lamina propria in healthy boars and in unilateral and bilateral abdominal cryptorchid boars. The lamina propria of scrotal testes from healthy boars and unilateral cryptorchid

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