Thioacetamide

AR,99%

Reagent Code: #112954
label
Alias Thioacetamide; Ethionamide
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CAS Number 62-55-5

science Other reagents with same CAS 62-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 75.13 g/mol
Formula C₂H₅NS
badge Registry Numbers
EC Number 200-541-4
MDL Number MFCD00008070
thermostat Physical Properties
Melting Point 108-112 °C(lit.)
inventory_2 Storage & Handling
Density 1.37g/mL
Storage room temperature

description Product Description

Thioacetamide is primarily used in laboratory settings as a source of hydrogen sulfide in chemical reactions. It is commonly employed in qualitative inorganic analysis to precipitate metal sulfides, aiding in the identification and separation of various metal ions. In the textile industry, it serves as a chemical intermediate in the production of dyes and other organic compounds. Additionally, thioacetamide is utilized in the synthesis of pharmaceuticals, where it acts as a building block for more complex molecules. Its role in research extends to studying the effects of sulfur-containing compounds in biological systems, particularly in toxicology and carcinogenicity studies.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (%) 99
Melting Point (°C) 108-115
Appearance White To Pale Reddish Yellow Powder Or Crystals
Solubility 2% in H2O

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿320.00
inventory 100g
10-20 days ฿680.00
inventory 500g
10-20 days ฿2,520.00
inventory 2.5kg
10-20 days ฿9,860.00

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Thioacetamide
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Thioacetamide is primarily used in laboratory settings as a source of hydrogen sulfide in chemical reactions. It is commonly employed in qualitative inorganic analysis to precipitate metal sulfides, aiding in the identification and separation of various metal ions. In the textile industry, it serves as a chemical intermediate in the production of dyes and other organic compounds. Additionally, thioacetamide is utilized in the synthesis of pharmaceuticals, where it acts as a building block for more complex molecules. Its role in research extends to studying the effects of sulfur-containing compounds in biological systems, particularly in toxicology and carcinogenicity studies.
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