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3-Phenoxypropyldimethylchlorosilane is a chlorosilane organosilicon compound with the chemical formula C11H17ClO2Si. It features a silicon atom bonded to a phenoxypropyl group and two dimethyl groups, as well as a chlorine atom. 3-Phenoxypropyldimethylchlorosilane is known for its reactivity and is commonly used in various industrial applications due to its unique properties.

69733-73-9

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69733-73-9 Usage

Uses

Used in Silicone Polymer Manufacturing:
3-Phenoxypropyldimethylchlorosilane is used as a crosslinking agent for the production of silicone polymers. Its ability to form covalent bonds with other molecules enhances the mechanical properties and stability of the resulting polymers.
Used in Surface Modification of Silica and Glass:
In the material industry, 3-Phenoxypropyldimethylchlorosilane is used as a surface modifier for silica and glass. It helps to improve the adhesion, wettability, and overall performance of these materials by altering their surface properties.
Used in Adhesives Production:
3-Phenoxypropyldimethylchlorosilane is used as a component in the formulation of adhesives. Its reactive nature allows it to form strong bonds with various substrates, contributing to the adhesive's effectiveness and durability.
Used in Coatings and Sealants Industry:
This chlorosilane compound is also utilized in the production of coatings and sealants. It enhances the adhesion, flexibility, and resistance to environmental factors, making the coatings and sealants more robust and long-lasting.
Due to the reactive and potentially hazardous nature of 3-Phenoxypropyldimethylchlorosilane, it must be handled and stored by trained professionals in a controlled environment to ensure safety and effectiveness in its applications.

Check Digit Verification of cas no

The CAS Registry Mumber 69733-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,3 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69733-73:
(7*6)+(6*9)+(5*7)+(4*3)+(3*3)+(2*7)+(1*3)=169
169 % 10 = 9
So 69733-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H17ClOSi/c1-14(2,12)10-6-9-13-11-7-4-3-5-8-11/h3-5,7-8H,6,9-10H2,1-2H3

69733-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-dimethyl-(3-phenoxypropyl)silane

1.2 Other means of identification

Product number -
Other names Chlordimethyl-(3-phenoxy)propylsilan

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:69733-73-9 SDS

69733-73-9Downstream Products

69733-73-9Relevant academic research and scientific papers

Waste-free and efficient hydrosilylation of olefins

Pandarus, Valerica,Ciriminna, Rosaria,Gingras, Geneviève,Béland, Fran?ois,Kaliaguine, Serge,Pagliaro, Mario

, p. 129 - 140 (2019/01/11)

High purity silicone precursors can now be synthesized by hydrosilylation of solvent-free olefins catalyzed by a highly stable and active glass hybrid catalyst consisting of mesoporous organosilica microspheres doped with Pt nanoparticles. These findings open the door to the sustainable manufacture of silicone and a way to further reduce the amount of platinum in silicones, which are ubiquitous advanced polymers with multiple uses and applications.

Catalytic activity of bis(dialkylamino)carbenium salts in hydrosilylation reactions

Chernyshev,Belyakova,Sheludyakov,Shevchenko

, p. 1003 - 1006 (2007/10/03)

Bis(dialkylamino)carbenium salts {[(Me2N)2CCl]+}2MCl4 2- (M = Ni, Pd) and {[Me2NC(X)NR2]+}2PtCl62- (R = Me, All; X = H, Cl, Me) are efficient catalysts for hydrosilylation of allyl phenyl ether, triallylamine, allyl chloride, allylamine, and 1-octene with various hydrosilanes. The catalytic activity is dependent on the salt composition and the nature of the metal M, the saturated compound, and the hydrosilane used. The catalysts used are usually insoluble in the reaction mixture, active, and stable. In some cases, carbenium salts are more selective than Speier's catalyst. Novel catalysts, silica-immobilized dialkylaminocarbenium salts, have been prepared. The kinetics of the reaction have been considered.

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