928-47-2

Basic information

• Product Name: S-N-BUTYL THIOACETATE
• Synonyms: Acetic acid, thio-, S-butyl ester;CH3C(O)S(CH2)3CH3;Ethanethioic acid, S-butyl ester;S-Butyl ethanethioate;S-Butyl thioacetate;BUTYL THIOACETATE;S-N-BUTYL THIOACETATE;Thioacetic acid S-n-butyl ester
• CAS NO: 928-47-2
• Molecular Formula: C₆H₁₂OS
• Molecular Weight: 132.22
• Mol File: 928-47-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 162-163°C
• Flash Point: 162-163°C
• Appearance: /
• Density: 0,947 g/cm3
• Vapor Pressure: 2.67mmHg at 25°C
• Refractive Index: 1.4589
• BRN: 1742053
• CAS DataBase Reference: S-N-BUTYL THIOACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: S-N-BUTYL THIOACETATE(928-47-2)
• EPA Substance Registry System: S-N-BUTYL THIOACETATE(928-47-2)

Safety Data

• Statements: R10:Flammable.
• Safety Statements: S23:Do not inhale gas/fumes/vapour/spray.; S24/25:Avoid contact with skin and eyes.
• RIDADR: 1993
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 928-47-2(Hazardous Substances Data)

Usage

General Description

S-N-Butyl thioacetate is a chemical compound with the formula C6H12OS and is classified as an organic thioester. It is commonly used as a fragrance ingredient in the production of perfumes, cosmetics, soaps, and other scented products. The compound has a strong, fruity odor and is often described as having a pineapple-like aroma. It is known for its high stability and low levels of volatility, making it a valuable ingredient in the creation of long-lasting and complex fragrances. S-N-Butyl thioacetate is also used in the flavor industry, adding a distinct and pleasant aroma to a wide range of food products. Overall, it is an important and versatile chemical in the fragrance and flavor industries.

InChI:InChI=1/C6H12OS/c1-4-5(2)8-6(3)7/h5H,4H2,1-3H3

Upstream product

• 174501-65-6 1-butyl-3-methylimidazolium Tetrafluoroborate 
• 10387-40-3 potassium thioacetate 
• 506-96-7 Acetyl bromide 
• 106-97-8 n-butane 
• 108-05-4 vinyl acetate 
• 109-79-5 n-butanethiol 
• 17642-74-9 2-methyl-1,3-oxathiolane 
• 74-85-1 ethene 

Downstream Products

• 2307-35-9 n-Butylthiostearat 
• 109-79-5 n-butanethiol 
• 507-09-5 thioacetic acid 
• 1092977-40-6 (3-butylthiophenyl)-acetonitrile 
• 14925-97-4 n-butylsulfenyl chloride 
• 75-36-5 acetyl chloride 
• 64-19-7 acetic acid 
• 629-45-8 dibutyl disulfide 
• 2386-60-9 perfluoro-1-butanesulfonyl fluoride 

Relevant articles and documents

Unexpected microwave reaction of 1,3-disubstituted imidazolium salts: A novel synthesis of 1,3-disubstituted imidazole-2-thiones

Microwave-promoted reaction of 1,3-disubstituted imidazolium salts with potassium thioacetate or potassium thiocyanate under solvent-free conditions provided a rapid and efficient synthesis of 1,3-disubstituted imidazole-2-thiones. Copyright Taylor & Francis Group, LLC.

RADICAL REACTIONS OF BUTYL MERCAPTAN WITH VINYL AND ALLYL ACETATES

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RADICAL TELOMERIZATION OF ETHYLENE WITH 2-METHYL-1,3-OXATHIOLANE

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