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(METHACRYLOXYMETHYL)METHYLDIETHOXYSILANE, with the molecular formula C13H26O4Si, is a silane coupling agent that plays a crucial role in the production of polymers and composite materials. It enhances the adhesion between inorganic materials, such as glass, and organic polymers. The presence of a reactive methacryloxy group enables it to participate in polymerization reactions, making it suitable for the creation of polymer coatings, adhesives, and sealants. Additionally, its two diethoxy groups can undergo hydrolysis to form silanol groups, which facilitate bonding to inorganic surfaces. This versatility makes (METHACRYLOXYMETHYL)METHYLDIETHOXYSILANE an essential chemical in materials science and manufacturing.

3978-58-3

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3978-58-3 Usage

Uses

Used in Polymer and Composite Material Production:
(METHACRYLOXYMETHYL)METHYLDIETHOXYSILANE is used as a coupling agent to improve the adhesion between inorganic materials and organic polymers, enhancing the overall performance and durability of the composite materials.
Used in Polymer Coatings:
(METHACRYLOXYMETHYL)METHYLDIETHOXYSILANE is used as a component in the production of polymer coatings, where its reactive methacryloxy group allows for polymerization reactions, resulting in high-quality coatings with improved adhesion and durability.
Used in Adhesives and Sealants:
(METHACRYLOXYMETHYL)METHYLDIETHOXYSILANE is used as a key ingredient in the formulation of adhesives and sealants, providing strong bonding capabilities and resistance to various environmental conditions.
Used in Materials Science and Manufacturing:
(METHACRYLOXYMETHYL)METHYLDIETHOXYSILANE is used as a versatile chemical in the field of materials science and manufacturing, where its ability to bond with both inorganic and organic materials makes it valuable for the development of new products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 3978-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,7 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3978-58:
(6*3)+(5*9)+(4*7)+(3*8)+(2*5)+(1*8)=133
133 % 10 = 3
So 3978-58-3 is a valid CAS Registry Number.

3978-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [diethoxy(methyl)silyl]methyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names Diaethoxy-methacryloyloxymethyl-methyl-silan

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:3978-58-3 SDS

3978-58-3Relevant academic research and scientific papers

Method for stabilizing unsaturated organo-silicon compounds

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Page 7, (2008/06/13)

Process for stabilizing organosilicon compounds (II) containing an unsaturated group of the vinyl, acrylic ester or vinyl ether type, during production, distillation and/or storage, comprises preparing (II) by reacting a haloalkylsilane with a salt of an unsaturated organic acid in the presence of alkylene-bis(dialkylphenol) compounds (I). Process for stabilizing organosilicon compounds of formula (II) containing an unsaturated group of the vinyl, acrylic ester or vinyl ether type, during production, distillation and/or storage, comprises preparing (II) by reacting a haloalkylsilane with a salt of an unsaturated organic acid in the presence of alkylene-bis(dialkylphenol) compounds of formula (I); [Image] H2C=C(R4>)[C(O)O]w(O)x-(R5>)y-Si(R6>)z(OR7>)3-z (II); R4>H or linear or branched 1-10 C hydrocarbyl; R5>linear, cyclic or branched 1-40 C hydrocarbyl, optionally containing heteroatom(s) selected from N, O, S or P; R6>, R7>linear, cyclic or branched 1-10 C hydrocarbyl; w, x : 0 or, in one case only, 1; y : 0 or 1; z : 0, 1 or 2; R1>, R2>linear or branched 1-20 C alkyl; R3>H or linear or branched 1-20 C alkyl.

Process for stabilizing unsaturated organosilicon compounds

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Page 4-5, (2008/06/13)

A process for stabilizing organosilicon compounds bearing unsaturated groups during their preparation, distillation, and/or storage, the organosilicon compounds bearing unsaturated groups having been obtained by reacting a haloalkylsilane with a salt of an unsaturated organic acid, by adding one or more compounds of the formula I wherein R1 and R2 are identical or different linear or branched C1-20 alkyl, and the radicals R3 are identical or different and are hydrogen or linear or branched alkyl radicals having 1-20 carbon atoms.

The Hydrolysis/Condensation Behaviour of Methacryloyloxyalkylfunctional Alkoxysilanes: Structure-Reactivity Relations

Altmann, Stefan,Pfeiffer, Juergen

, p. 1081 - 1092 (2007/10/03)

Various methacryloyloxymethylalkoxysilanes have been synthesized by nucleophilic substitution reactions starting from chloromethylalkoxysilanes under phase transfer catalysis conditions. The compounds thus obtained show an exceptionally high degree of reactivity with regard to hydrolysis and condensation both under acidic as well as under basic conditions compared to the established 3-methacryloyloxypropyltrimethoxysilane. A mechanistic model for this high reactivity by intramolecular activation is discussed.

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