172502
Thioacetamide
reagent grade, 98%
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
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grade
reagent grade
Quality Level
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.
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.
Signal Word
Danger
Hazard Statements
Precautionary 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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Oxide-free Sb2S3 sensitized solar cells fabricated by spin and heat-treatment of Sb (III)(thioacetamide)2Cl3.
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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)
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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