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592-65-4

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592-65-4 Usage

General Description

Diisobutyl sulfide is a chemical compound with the molecular formula C8H18S. It is a colorless liquid with a strong, unpleasant odor and is found naturally in the flavor of onions. Diisobutyl sulfide is commonly used as a flavoring agent in food products and as a fragrance in personal care products, particularly in soaps and cosmetics. It is also used as an industrial solvent and in organic synthesis as a reagent. However, it is important to note that diisobutyl sulfide must be handled with care, as it is flammable and can be harmful if inhaled or ingested. Additionally, it is considered a skin and eye irritant and can cause allergic reactions in some individuals.

Check Digit Verification of cas no

The CAS Registry Mumber 592-65-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 592-65:
(5*5)+(4*9)+(3*2)+(2*6)+(1*5)=84
84 % 10 = 4
So 592-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H18S/c1-7(2)5-9-6-8(3)4/h7-8H,5-6H2,1-4H3

592-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Isobutyl Sulfide

1.2 Other means of identification

Product number -
Other names Propane, 1,1‘-thiobis[2-methyl-

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:592-65-4 SDS

592-65-4Relevant articles and documents

Unusual Thermolysis of Diisobutyl Polysulfides

Korchevina,Sukhomazova,Deryagina

, p. 752 - 752 (2007/10/03)

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Chemical Conversions using Sheet Silicates: Novel Intermolecular Eliminations of Hydrogen Sulphide from Thiols

Ballantine, James A.,Galvin, Robert P.,O'Neil, Robert M.,Purnell, Howard,Rayanakorn, Mongkon,Thomas, John M.

, p. 695 - 696 (2007/10/02)

Aliphatic primary and secondary thiols react in the interlamellar layers of ion-exchanged montmorillonite catalysts to produce dialkyl sulphides via intermolecular elimination of hydrogen sulphide; similar processes result in the production of diphenyl sulphide from benzenethiol and poly(phenylenemethylene) from α-toluenethiol.

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