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Butylisobutylsulfide, also known as 2-butyl-2-methylpropane-1-thiol, is an organic compound with the chemical formula C8H18S. It is a colorless liquid with a strong, pungent odor and is insoluble in water. This chemical is primarily used as a flavoring agent and fragrance component in the food and beverage industry, as well as in the production of certain pharmaceuticals. It is also known for its potential health benefits, such as its use in traditional medicine to treat digestive issues. However, it is important to note that butylisobutylsulfide can be harmful if ingested or inhaled in large quantities, and it should be handled with care.

1741-85-1

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1741-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1741-85-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1741-85:
(6*1)+(5*7)+(4*4)+(3*1)+(2*8)+(1*5)=81
81 % 10 = 1
So 1741-85-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18S/c1-4-5-6-9-7-8(2)3/h8H,4-7H2,1-3H3

1741-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylpropylsulfanyl)butane

1.2 Other means of identification

Product number -
Other names BUTYL ISOBUTYL SULFIDE

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:1741-85-1 SDS

1741-85-1Relevant academic research and scientific papers

An Efficient Synthesis of Unsymmetrical Sulfides Using Liquid-Liquid Phase-Transfer Catalysis

Takido, Toshio,Itabashi, Kunio

, p. 817 - 819 (2007/10/02)

The reaction between alkyl ethaneimidothioate hydrohalides (1-alkylthioethaniminium halides) and organic halides gives unsymmetrical sulfides in good yields under liquid-liquid phase-transfer conditions.

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