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Merck
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Documentos

W421001

Sigma-Aldrich

Thioacetic acid

96%

Sinónimos:

Thiacetic acid

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About This Item

Fórmula lineal:
CH3COSH
Número de CAS:
507-09-5
Peso molecular:
76.12
FEMA Number:
4210
Beilstein/REAXYS Number:
1733298
EC Number:
208-063-8
MDL number:
MFCD00004853
UNSPSC Code:
12164502
PubChem Substance ID:
329830682
Flavis number:
12.199
NACRES:
NA.21

biological source

synthetic

Quality Level

400

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.

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

64.4 °F - closed cup

flash_point_c

18 °C - closed cup

ppe

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

Certificados de análisis (COA)

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Wen Yang et al.
Organic & biomolecular chemistry, 10(34), 6876-6884 (2012-08-01)
A highly enantio- and diastereoselective sulfa-Michael addition of thioacetic acid to α,β-disubstituted nitroalkenes catalysed by a chiral squaramide organocatalyst has been described. This organocatalytic reaction at an extremely low catalyst loading (0.2 mol%) furnished synthetically useful β-nitro sulfides in excellent
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
Angelo Alberti et al.
Physical chemistry chemical physics : PCCP, 7(2), 250-257 (2005-01-21)
The redox properties of ethyl diethoxyphosphoryldithioacetate (1), methyl diethoxyphosphorylfluorodithioacetate (2) and methyl diethoxyphosphoryldifluorodithioacetate (3) were measured by cyclic voltammetry. Addition of free radicals to the three dithioesters led to the detection of the ESR spectra of the spin adducts only
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
Libo Hu et al.
The Journal of organic chemistry, 72(12), 4543-4546 (2007-05-15)
Taurine and substituted taurines were synthesized efficiently from aziridines via ring-opening reaction with thioacetic acid, oxidation with performic acid, and hydrolysis in hydrochloric acid. The current method shows more benefit in purification and efficiency in the preparation of taurine and
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