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Diisobutyl sulfone, also known as 2,2-diisobutyl sulfone or 2,2-diisobane sulfone, is an organic compound characterized by its molecular formula C8H18O2S. This colorless liquid exhibits a faint odor and is recognized for its high boiling point and thermal stability, which render it suitable for a variety of high-temperature applications.

10495-45-1

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10495-45-1 Usage

Uses

Used in Organic Synthesis:
Diisobutyl sulfone is utilized as a reagent in organic synthesis, facilitating various chemical reactions due to its unique properties.
Used in Solvent Applications:
It serves as a solvent in multiple industrial processes, including the manufacturing of coatings and adhesives, where its solvent properties are essential for the proper formation and application of these products.
Used in Polymer Production:
Diisobutyl sulfone is employed as a plasticizer in the production of polymers, enhancing the flexibility and workability of the final polymeric materials.
Used in Heat Transfer Fluids:
Its thermal stability and high boiling point make it a candidate for use as a heat transfer fluid, particularly in applications requiring reliable heat exchange over a wide temperature range.
Used in Lithium-Ion Battery Solvents:
Diisobutyl sulfone has been studied for its potential as a solvent in lithium-ion batteries, where it could contribute to improved battery performance and safety.
Used in High-Temperature Applications:
Due to its thermal stability, diisobutyl sulfone is suitable for use in high-temperature applications where other solvents or compounds may degrade or evaporate.

Check Digit Verification of cas no

The CAS Registry Mumber 10495-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10495-45:
(7*1)+(6*0)+(5*4)+(4*9)+(3*5)+(2*4)+(1*5)=91
91 % 10 = 1
So 10495-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O2S/c1-7(2)5-11(9,10)6-8(3)4/h7-8H,5-6H2,1-4H3

10495-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-(2-methylpropylsulfonyl)propane

1.2 Other means of identification

Product number -
Other names Isobutyl sulfone

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:10495-45-1 SDS

10495-45-1Relevant academic research and scientific papers

Reactions of chlorine dioxide with organic compounds: Selective oxidation of sulfides to sulfoxides by chlorine dioxide

Kutchin,Rubtsova,Loginova

, p. 432 - 435 (2001)

A novel method for the selective oxidation of various types of sulfides to sulfoxides using chlorine dioxide as the oxidant is proposed.

Selective synthesis of sulfoxides and sulfones from sulfides using silica bromide as the heterogeneous promoter and hydrogen peroxide as the terminal oxidant

Maleki, Behrooz,Hemmati, Saba,Sedrpoushan, Alireza,Ashrafi, Samaneh Sedigh,Veisi, Hojat

, p. 40505 - 40510 (2015/02/03)

Silica bromide as a heterogeneous promoter and reagent is prepared from the reaction of silica gel with PBr3as a non-hydroscopic, filterable, cheap, and stable yellowish powder that can be stored for months. The results show that silica bromide is a suitable and efficient promoter for the chemoselective oxidation of sulfides to the corresponding sulfoxides or sulfones in the presence of 30% H2O2in acetonitrile. The excellent yields, heterogeneous conditions, simplicity, compatibility with a variety of functionalities, and ease of isolation of the products make our procedure a practical alternative.

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