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Sigma-Aldrich

Thioacetamide

reagent grade, 98%

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Synonym(s):
TAA, Ethanethioamide
Linear Formula:
CH3CSNH2
CAS Number:
62-55-5
Molecular Weight:
75.13
Beilstein:
506006
EC Number:
200-541-4
MDL number:
MFCD00008070
PubChem Substance ID:
57647624
NACRES:
NA.21

grade

reagent grade

Quality Level

200

Assay

98%

form

solid

mp

108-112 °C (lit.)

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 is a thiocarboxamide used as a crosslinking agent for polymers, chemical reagents, and catalysts.

Thioacetamide is a thiocarbonyl compound. 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

Thioacetamide may be used as a source of sulfur required for the synthesis of CdS nanoparticles in PVA (poly (vinyl alcohol)) solutions. It may be used in the preparation of sulfur precursor stock solution, which was required during the synthesis of CdS quantum dots in PVA-COOH (carboxylic acid functionalized poly(vinyl alcohol)) and EPC (Enzyme-Polymer Conjugate) solutions.
Thioacetamide may be used in the preparation of Sb(TA)2Cl3, a precursor for oxide-free stibnite. The addition of TA during the synthesis of visible-light activated titanium dioxide photocatalysts led to an increase in its photocatalytic activity.

Pictograms

Exclamation markHealth hazard
GHS07,GHS08

Signal Word

Danger

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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Thioacetamide and thiourea impact on visible light activity of TiO2.
Zaleska A, et al.
Applied Catalysis. B, Environmental, 76(1), 1-8 (2007)
Solubility measurement, correlation and mixing properties of thioacetamide in fifteen pure solvents
Huang L, et al.
Journal of Molecular Liquids, 363, 119847-119847 (2022)
Oxide-free Sb2S3 sensitized solar cells fabricated by spin and heat-treatment of Sb (III)(thioacetamide)2Cl3.
You MS, et al.
Organic Electronics, 21, 155-159 (2015)
Infrared Spectra and Normal Vibrations of Thioamides. II. Thioacetamide.
Suzuki I.
Bulletin of the Chemical Society of Japan, 35(9), 1449-1456 (1962)
Alexandra Mansur et al.
Sensors (Basel, Switzerland), 11(10), 9951-9972 (2011-12-14)
In the present research, the concept of developing a novel system based on polymer-enzyme macromolecules was tested by coupling carboxylic acid functionalized poly(vinyl alcohol) (PVA-COOH) to glucose oxidase (GOx) followed by the bioconjugation with CdS quantum-dots (QD). The resulting organic-inorganic
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