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Usage

Uses

Used in Silicone Rubber Production:
TETRAKIS(TRICHLOROSILYLETHYL)SILANE is used as a crosslinking agent for the production of silicone rubber. Its ability to form stable bonds enhances the rubber's overall strength and durability.
Used in Silicone Material Manufacturing:
In the manufacturing of other silicone materials, TETRAKIS(TRICHLOROSILYLETHYL)SILANE serves as a crucial component, improving the structural integrity and performance of the final product.
Used in Adhesives:
TETRAKIS(TRICHLOROSILYLETHYL)SILANE is used as a component in adhesive formulations, providing strong bonding capabilities and resistance to environmental factors.
Used in Sealants:
TETRAKIS(TRICHLOROSILYLETHYL)SILANE is utilized in sealant production, offering robust sealing properties and maintaining the integrity of sealed joints.
Used in Coatings:
TETRAKIS(TRICHLOROSILYLETHYL)SILANE is employed in the creation of coatings, enhancing their durability, flexibility, and resistance to various conditions.
Used in Other Silicone-based Products:
Its high reactivity and ability to form stable bonds make TETRAKIS(TRICHLOROSILYLETHYL)SILANE suitable for a range of other products that leverage the unique properties of silicone chemistry.
It is important to handle TETRAKIS(TRICHLOROSILYLETHYL)SILANE with care due to its flammable nature and potential to cause skin and eye irritation.

InChI:InChI=1/C8H16Cl12Si5/c9-22(10,11)5-1-21(2-6-23(12,13)14,3-7-24(15,16)17)4-8-25(18,19)20/h1-8H2

Upstream product

• 1112-55-6 tetravinylsilane 

Relevant academic research and scientific papers

Characterization of polyfunctional alkoxysilanes using potassium ( K+) ionization of desorbed species mass spectrometry

Potassium ionization of desorbed species (K+IDS) mass spectrometry has been used to characterize polyfunctional alkoxysilanes and the modes of reaction for 'star gel' precursors and simpler tetraalkoxysilanes. Efficient observation of molecular ions enabled by K+IDS can readily establish the purity of molecules such as Si(CH2CH2Si(OEt)3)4 and cyclo-(Me(CH2CH2Si(OEt)3)4SiO)4, and has been highly useful in determining the extent of intramolecular condensation in the star molecules. K+IDS has also established the distributions of polysilicate species and the presence of important reactive intermediates containing SiOOCH groups when Si(OMe)4 reacts with formic acid.

Preparation and characterization of nonpolar fluorinated carbosilane dendrimers by APcI mass spectrometry and small-angle X-ray scattering

The following highly fluorinated nonpolar dendrimers were obtained in high yields from multiple hydrosilylation reactions between core hydride terminated carbosilane dendrimers and allyl-1,1-dihydrotrifluoroethyl ether or allyl-1,1-dihydroheptadecafluorononyl ether through divergent synthetic routes: Si[CH2-CH2SiMe2(CH2CH 2CH2OCH2CF3)]4 (7), Si{CH2CH2SiMe[CH2CH2SiMe(CH 2CH2CH2OCH2CF3) 2]2}4 (8), Si[CH2CH2Si(CH2CH2CH 2OCH2C8F17)3]4 (9), Si[CH2CH2SiMe2(CH2CH 2CH2OCH2C8F17)] 4 (10), and Si{CH2-CH2Si[CH2CH2Si(CH 2CH2CH2OCH2C8F 17)3]3}4 (11). These compounds were characterized by elemental and spectroscopic analyses. Valuable mass spectral data were obtained by using atmospheric pressure chemical ionization (APcI). The fluorinated dendrimer molecule and the nonfluorinated core scatter X-ray light differently and present unique slopes on the Guinier Plot of data from small-angle X-ray light scattering (SAXS) in hexafluorobenzene. Glass transition temperatures (Tg) and thermogravimetric analyses (TGA) of the dendrimers were determined.