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(3-ACRYLOXYPROPYL)METHYLBIS(TRIMETHYLSILOXY)SILANE is a versatile chemical compound that functions as a crosslinking agent in the synthesis of silicone polymers. Characterized by its acryloxy and trimethylsiloxy functional groups, (3-ACRYLOXYPROPYL)METHYLBIS(TRIMETHYLSILOXY)SILANE is instrumental in various applications due to its capacity to enhance the mechanical properties and adhesion of silicone-based materials. It is recognized for its significant contributions to the performance and quality of products in a multitude of industries.

177617-17-3

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177617-17-3 Usage

Uses

Used in Adhesives and Sealants Industry:
(3-ACRYLOXYPROPYL)METHYLBIS(TRIMETHYLSILOXY)SILANE is used as a crosslinking agent for improving the mechanical properties and adhesion of silicone-based adhesives and sealants. Its presence ensures stronger bonds and better durability in a variety of applications, including construction and automotive industries.
Used in Coatings Industry:
In the coatings sector, (3-ACRYLOXYPROPYL)METHYLBIS(TRIMETHYLSILOXY)SILANE is utilized as an additive to enhance the adhesion and mechanical properties of silicone-based coatings. This results in improved wear resistance and durability, making the coatings suitable for a wide range of surfaces.
Used in Surface Treatment Products:
(3-ACRYLOXYPROPYL)METHYLBIS(TRIMETHYLSILOXY)SILANE is used as a component in surface treatment products to promote better adhesion between organic polymers and inorganic surfaces. This functionality is vital for applications requiring robust and long-lasting surface treatments.
Used as a Coupling Agent:
(3-ACRYLOXYPROPYL)METHYLBIS(TRIMETHYLSILOXY)SILANE serves as a coupling agent in the bonding process of organic polymers to inorganic surfaces. Its role is crucial for creating strong, stable bonds that are resistant to various environmental factors, thus broadening the scope of material applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 177617-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,6,1 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 177617-17:
(8*1)+(7*7)+(6*7)+(5*6)+(4*1)+(3*7)+(2*1)+(1*7)=163
163 % 10 = 3
So 177617-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H30O4Si3/c1-9-13(14)15-11-10-12-20(8,16-18(2,3)4)17-19(5,6)7/h9H,1,10-12H2,2-8H3

177617-17-3SDS

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 3-[methyl-bis(trimethylsilyloxy)silyl]propyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names 3-Acryloylamino-benzoesaeure

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:177617-17-3 SDS

177617-17-3Downstream Products

177617-17-3Relevant articles and documents

METHOD OF PREPARING ACRYLOXY-FUNCTIONAL ORGANOSILICON COMPOUNDS

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Paragraph 0075-0076, (2020/07/21)

A method of preparing an acryloxy-functional organosilicon compound is provided. The method comprises reacting (A) an initial organosilicon compound and (B) an acrylate compound in the presence of (C) a catalyst. The initial organosilicon compound (A) has one alcohol functional group (i.e., is monohydroxyl functional). The catalyst (C) has the formula M[RC(O)CHC(O)R]4, where M is a group IV transition metal and each R is an independently selected substituted or unsubstituted hydrocarbyl group. An acryloxy- functional organosilicon compound prepared by the method is also provided. The acryloxy-functional organosilicon compound is prepared in increased purity, without relying on toxic catalysts.

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