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ACRYLOXYMETHYL TRIMETHOXYSILANE is a chemical compound derived from a silane group, featuring a methoxysilane functional group. It is known for its ability to improve adhesion and durability in various products by promoting the bonding between organic and inorganic materials. ACRYLOXYMETHYL TRIMETHOXYSILANE also serves as a surface modifier, enhancing resistance to moisture, weathering, and chemical degradation in materials such as plastics, rubbers, and composites. Furthermore, it is utilized in the synthesis of hybrid organic-inorganic materials to boost their mechanical and thermal properties, thereby playing a vital role in enhancing the performance and longevity of a wide range of industrial products and materials.

21134-38-3

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21134-38-3 Usage

Uses

Used in Adhesives, Coatings, and Sealants Industry:
ACRYLOXYMETHYL TRIMETHOXYSILANE is used as a coupling agent for improving the adhesion and durability of final products by enhancing the bonding between organic and inorganic materials.
Used in Plastics, Rubbers, and Composites Industry:
ACRYLOXYMETHYL TRIMETHOXYSILANE is used as a surface modifier to increase the material's resistance to moisture, weathering, and chemical degradation, thereby extending the lifespan and performance of these materials.
Used in Synthesis of Hybrid Organic-Inorganic Materials:
ACRYLOXYMETHYL TRIMETHOXYSILANE is used to improve the mechanical and thermal properties of hybrid materials, contributing to the development of advanced materials with enhanced performance characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21134-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,3 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21134-38:
(7*2)+(6*1)+(5*1)+(4*3)+(3*4)+(2*3)+(1*8)=63
63 % 10 = 3
So 21134-38-3 is a valid CAS Registry Number.

21134-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethoxysilylmethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names (trimethoxysilyl)methyl acrylate

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:21134-38-3 SDS

21134-38-3Upstream product

21134-38-3Downstream Products

21134-38-3Relevant academic research and scientific papers

COSMETIC TREATMENT METHOD COMPRISING THE APPLICATION OF A COATING BASED ON AN AEROGEL COMPOSITION OF LOW BULK DENSITY

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Paragraph 0068, (2014/02/15)

The present invention relates to a cosmetic treatment method comprising the formation of a coating on keratin fibres characterized in that it comprises: 1) the preparation of an aerogel precursor composition comprising:—at least one organic solvent chosen from acetone, C1-C4 alcohols, C1-C6 alkanes, C1-C4 ethers, which may or may not be perfluorinated, and mixtures thereof and at least one precursor compound that contains:—at least one atom chosen from silicon, titanium, aluminium and zirconium,—at least one hydroxyl or alkoxy function directly attached to the atom chosen from silicon, titanium, aluminium and zirconium by an oxygen atom, and,—optionally an organic group directly attached to the atom chosen from silicon, titanium, aluminium and zirconium by a carbon atom, 2) the removal of the solvent or solvents resulting in the formation of an aerogel composition having a bulk density less than or equal to 0.35 g/cm3, 3) the application to the keratin fibres of the aerogel composition resulting from step 2) or of the aerogel precursor composition resulting from step 1). Advantageously, the molar ratio between the precursor compounds and the solvent is at most 1/20.

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