592-65-4 Usage
Uses
Used in Food Industry:
Diisobutyl sulfide is used as a flavoring agent for enhancing the taste and aroma of food products, capitalizing on its natural presence in onions to add a distinct flavor profile.
Used in Personal Care Industry:
In personal care products, Diisobutyl sulfide serves as a fragrance, particularly in soaps and cosmetics, where its strong odor is utilized to create appealing scents for consumer products.
Used in Industrial Applications:
Diisobutyl sulfide functions as an industrial solvent, leveraging its chemical properties to dissolve various substances, which is beneficial in numerous manufacturing processes.
Used in Organic Synthesis:
As a reagent in organic synthesis, Diisobutyl sulfide is instrumental in chemical reactions, facilitating the formation of desired products in research and commercial chemical production.
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
592-65-4Relevant academic research and scientific papers
Studies on the Reaction of Iron Sulphide with 2-Methylpropan-1-ol in Vapour Phase
D'Souza, Ita M.,Banerjee
, p. 185 - 187 (2007/10/03)
Sulphur elimination from synthetic and natural iron sulphide (FeS2) by reaction with 2-methylpropan-1-ol in vapour phase at 350-500° and 0.1-1.0 atm partial pressure of alcohol, is reported. Sulphur is eliminated mainly as alkyl sulphide and hydrogen sulphide. Kinetic model based on the theory of nucleation with branching and overlapping of nuclei best explains the experimental results. Kinetic parameters for the reaction have also been calculated.
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.
