Applications of Trimethoxy(methyl)silane

Trimethoxy(methyl)silane
CAS No.: 1185-55-3
Molecular Weight: 136.22
Boiling Point<760mmHg>: 101 Flash Point: 12
Color and appearance: colorless clear liquid Density<20/20>: 0.950
Refractive Index<20>: 1.369+0.0005
Min. Purity: 98.0%
Applications of Trimethoxy(methyl)silane
As a crosslinking agent for room temperature cured silicone rubber, coupling agent for glass fiber and SiO2, a strengthing treatment agent for plastic-layer pressing material.
The most common alkoxy crosslinkers are methoxy or ethoxy silanes due to their high reactivity. The reaction precedes by nucleophilic substitution usually in the presence of acid or base catalysts. Alkoxides react directly with silanols or with water to produce silanols. The newly formed silanols can react with other alkoxides or self-condense to produce a siloxane bond and water. When an acid catalyst is used, protonation of the alkoxysilane increases the reactivity of the leaving group. When a base catalyst is used, deprotonation of the silanol forms a reactive silonate anion. The by-product of the reaction is an alcohol. Common metal catalysts for these reactions are alkoxytitanium derivatives and dibutyltin dicarboxylates
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Specifications of Trimethoxy(methyl)silane

Trimethoxy(methyl)silane
CAS:1185-55-3
Molecular Formula:C4H12O3Si
Molecular Weight:136.22 g/mol
Description:
Trimethoxy(methyl)silane occurs as achromatic bright aqueous with its melting point -70°C and baking point 102-104 °C(lit.).It will decompose in water.It is stable, but damp sensitive. It is aswell awful flammable. It is adverse with water, able acids, able acerbic agents.This artefact should be stored amid 2-8°C.
Applications:
As a crosslinking agent for room temperature cured silicone rubber, coupling agent for glass fiber and SiO2, a strengthing treatment agent for plastic-layer pressing material.
The most common alkoxy crosslinkers are methoxy or ethoxy silanes due to their high reactivity. The reaction precedes by nucleophilic substitution usually in the presence of acid or base catalysts. Alkoxides react directly with silanols or with water to produce silanols. The newly formed silanols can react with other alkoxides or self-condense to produce a siloxane bond and water. When an acid catalyst is used, protonation of the alkoxysilane increases the reactivity of the leaving group. When a base catalyst is used, deprotonation of the silanol forms a reactive silonate anion. The by-product of the reaction is an alcohol. Common metal catalysts for these reactions are alkoxytitanium derivatives and dibutyltin dicarboxylates
More about: Trimethoxy(methyl)silane sale
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