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163678

Sigma-Aldrich

Thioacetamide

ACS reagent, ≥99.0%

Synonym(s):

TAA, Ethanethioamide

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About This Item

Linear Formula:
CH3CSNH2
CAS Number:
Molecular Weight:
75.13
Beilstein:
506006
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

Assay

≥99.0%

form

solid

mp

108-112 °C (lit.)

solubility

passes test 2%

SMILES string

CC(N)=S

InChI

1S/C2H5NS/c1-2(3)4/h1H3,(H2,3,4)

InChI key

YUKQRDCYNOVPGJ-UHFFFAOYSA-N

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General description

Thioacetamide (TAA) is a thiocarbonyl compound commonly used as a corrosion inhibitor. It prevents corrosion by forming a protective layer on metal surfaces. It undergoes deuterium exchange reaction with D2O to afford N-dideuterated thioacetamide. Infrared spectral investigations of thioacetamide and its deuterated derivative (N-dideuterated thioacetamide) have been reported.

Application

Hepatotoxin and carcinogen. An additive in enantioselective reduction of β-keto esters with immobilized baker′s yeast.
It may also be used as a sulfide source to prepare metal sulfides of metal ions like cadmium, nickel, zinc and copper.
Thioacetamide has been used as a source of sulfur required for the synthesis of CdS nanoparticlesand quantum dots.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Synthesis of copper sulfide nanowhisker via sonochemical way and its characterization
Xu C, et al
Chemistry Letters (Jpn), 32(2), 198-199 (2003)
Synthesis of nickel sulfide powders by thioacetamide in the presence of urea.
Grau J and Akinc M.
Journal of the American Ceramic Society. American Ceramic Society, 80(4), 941-951 (1997)
Cancer Research, 17, 954-954 (1952)
Journal of the Chemical Society. Perkin Transactions 1, 659-659 (1992)
Effect of molecular structure on the efficiency of amides and thiosemicarbazones used for corrosion inhibition of mild steel in hydrochloric acid
EE Ebenso, et al.
Materials Chemistry and Physics, 60, 79-90 (1999)

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