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Dibutyl(dimethyl)silane, also known as 1,1,1,3,3,3-hexamethyldisilane, is an organosilicon compound with the chemical formula C8H22Si2. It is a colorless, flammable liquid that is insoluble in water but soluble in organic solvents. dibutyl(dimethyl)silane is primarily used as a coupling agent in the production of composite materials, as a release agent in the rubber industry, and as a silylating agent in organic synthesis. Dibutyl(dimethyl)silane is also employed as a precursor in the synthesis of other organosilicon compounds and as a stabilizer in various chemical processes. Due to its flammability and potential health risks, it is essential to handle this chemical with proper safety measures.

996-06-5

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996-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 996-06-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 996-06:
(5*9)+(4*9)+(3*6)+(2*0)+(1*6)=105
105 % 10 = 5
So 996-06-5 is a valid CAS Registry Number.

996-06-5SDS

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 dibutyl(dimethyl)silane

1.2 Other means of identification

Product number -
Other names Silane,dibutyl dimethyl

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:996-06-5 SDS

996-06-5Relevant academic research and scientific papers

Cleavage of Si-C and Ge-C bonds in heterylsilanes and -germanes by organolithium reagents

Gevorgyan, Vladimir,Borisova, Larisa,Lukevics, Edmunds

, p. 381 - 387 (2007/10/02)

Organolithium reagents RLi can cleave Si-C and Ge-C bonds in heterylsilanes and -germanes substituting furyl, dihydrofuryl and dihydropyranyl groups for the organolithium residue R.

Method for the preparation of a tert-hydrocarbyl silyl compound

-

, (2008/06/13)

A tert-hydrocarbyl, e.g. tert-butyl, silyl compound can be synthesized easily according to the method of the invention in which a tert-hydrocarbylmagnesium halide as a Grignard reagent is reacted with a silane compound having at least one silicon-bonded hydrogen atom and at least one silicon-bonded halogen atom simultaneously in a molecule in a suitable organic solvent so that the halogen atom in the latter reactant is replaced with the tert-hydrocarbyl group in the former reactant to give the desired tert-hydrocarbyl silyl compound in a high yield without the safety problem in the conventional method using a tert-alkyl lithium as the reactant.

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