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Usage

Uses

Used in Coatings Industry:
Chloromethyldimethylethoxysilane is used as a coupling agent for enhancing the adhesion and compatibility of coatings to various surfaces. Its ability to form bonds between organic and inorganic materials improves the overall performance and durability of the coatings.
Used in Adhesives Industry:
In the adhesives industry, chloromethyldimethylethoxysilane serves as a coupling agent, promoting stronger bonds between different materials. This results in improved adhesive performance and increased resistance to environmental factors such as moisture and temperature changes.
Used in Sealants Industry:
Chloromethyldimethylethoxysilane is used as a key component in the formulation of sealants, where it acts as a coupling agent. This enhances the sealants' ability to adhere to various substrates and provides better resistance to weathering and aging, ensuring a longer-lasting seal.

InChI:InChI=1/C5H13ClOSi/c1-4-7-8(2,3)5-6/h4-5H2,1-3H3

Upstream product

• 64-17-5 ethanol 
• 1719-57-9 Chloro(chloromethyl)dimethylsilane 
• 1825-62-3 ethyl trimethylsilyl ether 

Downstream Products

• 17887-25-1 Si,Si'-diethoxy-Si,Si,Si',Si'-tetramethyl-Si,Si'-methanediyl-bis-silane 
• 18082-47-8 2,6-diethoxy-2,4,4,6-tetramethyl-2,4,6-trisila-heptane 
• 17961-86-3 N-[(ethoxy-dimethyl-silanyl)-methyl]-aniline 
• 18057-24-4 1,4-bis-(chloromethyl-dimethyl-silanyloxy)-benzene 
• 18106-24-6 N-[(ethoxy-dimethyl-silanyl)-methyl]-2-chloro-aniline 
• 18405-80-6 Si-ethoxy-Si,Si,Si',Si'-tetramethyl-Si'-phenyl-Si,Si'-methanediyl-bis-silane 
• 2452-95-1 Dimethyl-(6-amino-hexaylaminomethyl)-ethoxysilane 
• 5577-70-8 (methacryloyloxymethyl)dimethylethoxysilane 
• 1719-57-9 Chloro(chloromethyl)dimethylsilane 
• 1825-62-3 ethyl trimethylsilyl ether 
• 54729-89-4 Di-n-butylaminomethyl-silan 
• 839-43-0 (Ethoxy-dimethyl-silylmethyl)-phenyl-phosphinsaeure-ethylester 
• 18151-92-3 Diphenyl-dithiophosphinsaeure-<(dimethyl-ethoxy-silyl)-methylester> 
• 18023-58-0 [(ethoxy-dimethyl-silanyl)-methyl]-cyclohexyl-amine 

Relevant academic research and scientific papers

NITROGEN-CONTAINING ORGANOSILICON COMPOUNDS. 150. SYNTHESIS AND CHROMATOGRAPHIC AND 1H, 13C, 15N, AND 29Si NMR SPECTROSCOPIC INVESTIGATION OF SUBSTITUTED (PIPERIDINOALKYL)SILANES

Substituted (piperidinoalkyl)silanes were synthesized and investigated by means of multinuclear NMR spectroscopy and GLC.The data obtained indicate an additional N-Si interaction in α-aminomethylsilanes that depends substantially on the properties of the substituents attached to the silicon atom.The effect of the R1R2R3Si substituent on the capacity of the nitrogen atom for intermolecular interactions is not restricted to steric effects but also has electronic character.

Process for the preparation of organoalkoxysilanes

An improvement in a process for the esterification of a organochlorosilane by feeding alcohol into a chlorosilane maintained within a reaction zone without said alcohol contacting said chlorosilane in the gas phase wherein the esterification is performed stepwise with extraction of hydrogen chloride which has developed, the improvement which comprises employing in at least a final esterification step an organochlorosilane of the formula wherein R represents an optionally halogen-substituted alkyl radical which can also contain an oxygen or sulfur atom in the chain, or a halogen or a NO2 group or a protected phenolic group containing aryl radical, a equals 0, 1, or 2, b equals 1 or 2, and a+b amounts to a maximum of 3, said final esterification step being performed with the addition of heat.