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Usage

Uses

Used in Adhesive Production:
Bis(trimethylsilyl)sebacate is used as a key component in the formulation of adhesives, contributing to their bonding properties and enhancing their performance in various applications.
Used in Sealant Production:
In the sealant industry, Bis(trimethylsilyl)sebacate is employed as an essential ingredient, improving the sealing capabilities and durability of the final products.
Used in Lubricant Production:
Bis(trimethylsilyl)sebacate is used as a lubricant additive, providing smooth operation and reducing friction in mechanical systems, thus extending the lifespan of equipment.
Used in Rubber Manufacturing:
Bis(trimethylsilyl)sebacate is used as a processing aid in the manufacture of rubber products, improving the production process and the final quality of rubber goods.
Despite its industrial significance, there is a lack of data about the environmental and human health impacts of Bis(trimethylsilyl)sebacate, which necessitates further research and assessment.

InChI:InChI=1/C16H34O4Si2/c1-21(2,3)19-15(17)13-11-9-7-8-10-12-14-16(18)20-22(4,5)6/h7-14H2,1-6H3

Upstream product

• 106-79-6 dimethyl sebacate 
• 996-50-9 N,N-diethyl-1,1,1-trimethylsilanamine 
• 111-20-6 1,10-decanedioic acid 
• 25561-30-2 N,O-Bis(trimethylsilyl)trifluoroacetamide 

Downstream Products

• 111-20-6 1,10-decanedioic acid 

Relevant academic research and scientific papers

Partition coefficients of ketones, phenols, aliphatic and aromatic acids, and esters in n-hexane/nitromethane

Liquid-liquid partition is used in sample preparation and in countercurrent and liquid-liquid chromatographic separations. Partition coefficients are widely used in toxicology, environmental, and analytical chemistry. The K hn determination procedure for the n-hexane/ nitromethane system was optimized and partition coefficients for 99 ketones, esters and trimethylsilyl derivatives of phenols, aliphatic and aromatic acids were determined. For 130 compounds, Khn values were predicted using mathematical relationships between Khn and other physicochemical and structural parameters. Versita Sp. z o.o.

Dealkylation of esters via treatment with N-(trimethylsilyl) diethylamine and methyl iodide

A method for the conversion of esters to carboxylic acids has been reported. Reaction of methyl o-methoxybenzoate with N-(trimethylsilyl)diethylamine and methyl iodide, followed by hydrolysis, afforded o-methoxybenzoic acid with a 94% yield based on 96% conversion. Methyl esters of not only aromatic acids but also aliphatic acids were converted to the corresponding acids with high yields. A combination of N-(trimethylsilyl)dimethylamine and methyl iodide was also effective to give p-methylbenzoic acid with a 85% yield based on 90% conversion from the corresponding methyl ester.