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S-N-Butyl thioacetate, with the chemical formula C6H12OS, is an organic thioester known for its strong, fruity odor and pineapple-like aroma. It is characterized by high stability and low volatility, making it a valuable component in the formulation of long-lasting and complex fragrances.

928-47-2

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928-47-2 Usage

Uses

Used in Fragrance Industry:
S-N-Butyl thioacetate is used as a fragrance ingredient for its distinct and pleasant aroma, contributing to the creation of long-lasting and complex scents in perfumes, cosmetics, and soaps.
Used in Flavor Industry:
In the flavor industry, S-N-Butyl thioacetate is used as a flavoring agent to add a unique and appealing aroma to a wide range of food products, enhancing their sensory appeal.

Check Digit Verification of cas no

The CAS Registry Mumber 928-47-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 928-47:
(5*9)+(4*2)+(3*8)+(2*4)+(1*7)=92
92 % 10 = 2
So 928-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H12OS/c1-4-5(2)8-6(3)7/h5H,4H2,1-3H3

928-47-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name S-n-Butyl thioacetate, 98%

1.2 Other means of identification

Product number -
Other names S-butyl ethanethioate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:928-47-2 SDS

928-47-2Relevant academic research and scientific papers

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

Tao, Xiao-Le,Lei, Ming,Wang, Yan-Guang

, p. 399 - 408 (2007/10/03)

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.

FUNCTIONALIZATION OF SATURATED HYDROCARBONS IN THE PRESENCE OF APROTIC ORGANIC SUPERACIDS. 2. SINGLE-STAGE SYNTHESIS OF THIOESTERS R1CO-SR FROM n-ALKANES OR CYCLOALKANES (RH), ELEMENTAL SULFUR, AND COMPLEXES R1COBr*2AlBr3

Orlinkov, A. V.,Akhrem, I. S.,Afanas'eva, L. V.,Vitt, S. V.,Vol'pin, M. E.

, p. 90 - 92 (2007/10/02)

It has been found for the first time that n-alkanes and cycloalkanes (RH) can interact with elemental sulfur at ca. 20 deg C.These reactions go forward in the presence of aprotic organic superacids with the composition R1CO-SR in satisfactory yields.

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