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Merck

172502

Sigma-Aldrich

Thioacetamide

reagent grade, 98%

Sinónimos:

TAA, Ethanethioamide

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About This Item

Fórmula lineal:
CH3CSNH2
Número de CAS:
Peso molecular:
75.13
Beilstein/REAXYS Number:
506006
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

reagent grade

Quality Level

assay

98%

form

solid

mp

108-112 °C (lit.)

functional group

amine

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

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Los clientes también vieron

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)
Solubility measurement, correlation and mixing properties of thioacetamide in fifteen pure solvents
Huang L, et al.
Journal of Molecular Liquids, 363, 119847-119847 (2022)
Thioacetamide and thiourea impact on visible light activity of TiO2.
Zaleska A, et al.
Applied Catalysis. B, Environmental, 76(1), 1-8 (2007)
Synthesis and characterization of CdS quantum dots with carboxylic-functionalized poly (vinyl alcohol) for bioconjugation
Mansur HS, et al.
Polymer, 52(4), 1045-1054 (2011)
Infrared Spectra and Normal Vibrations of Thioamides. II. Thioacetamide.
Suzuki I.
Bulletin of the Chemical Society of Japan, 35(9), 1449-1456 (1962)

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