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Trimethylsiloxytriethoxysilane, with the molecular formula C11H26O4Si2, is a colorless liquid chemical compound. It is widely recognized for its role as a coupling agent and adhesion promoter, which significantly enhances the wetting and bonding properties of various materials. Its incorporation improves the durability and weather resistance of products, making it a valuable component in both industrial and construction applications.

17861-35-7

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17861-35-7 Usage

Uses

Used in Coatings, Adhesives, and Sealants Industry:
Trimethylsiloxytriethoxysilane is used as a coupling agent and adhesion promoter for improving the bonding strength and durability of coatings, adhesives, and sealants. Its presence ensures better adhesion to various substrates and enhances the overall performance and longevity of the final product.
Used in Glass Manufacturing:
In the glass industry, trimethylsiloxytriethoxysilane is used as a surface modifier to enhance the wetting and bonding properties of glass. This modification allows for better adhesion of coatings or other materials to the glass surface, improving the product's performance and resistance to environmental factors.
Used in Ceramics Production:
Trimethylsiloxytriethoxysilane is utilized in ceramics manufacturing as a surface modifier to improve the bonding and wetting characteristics of ceramic materials. This enhancement contributes to the improved mechanical properties and durability of the ceramics, making them suitable for various applications.
Used in Plastics Industry:
Trimethylsiloxytriethoxysilane is used in the plastics industry as a surface modifier to improve the wetting and bonding properties of plastics. This modification allows for better adhesion of coatings or other materials to the plastic surface, resulting in improved product performance and increased resistance to wear and environmental factors.
Used in Construction Applications:
In construction, trimethylsiloxytriethoxysilane is used to enhance the durability and weather resistance of building materials. Its incorporation into coatings, adhesives, and sealants ensures better adhesion to various substrates and contributes to the overall longevity and performance of construction materials.

Check Digit Verification of cas no

The CAS Registry Mumber 17861-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,6 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17861-35:
(7*1)+(6*7)+(5*8)+(4*6)+(3*1)+(2*3)+(1*5)=127
127 % 10 = 7
So 17861-35-7 is a valid CAS Registry Number.

17861-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl trimethylsilyl silicate

1.2 Other means of identification

Product number -
Other names 1,1,1-trimethyl-3,3,3-triethoxydisiloxane

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:17861-35-7 SDS

17861-35-7Downstream Products

17861-35-7Relevant academic research and scientific papers

Recovery of trimethylchlorosilane from its azeotropic mixture with SiCl4

Voronkov,Baryshok,Kuznetsova

, p. 2091 - 2094 (2001)

Reaction of tetraethoxysilane with the azeotropic mixture Me3SiCl-SiCl4 in the presence of certain cyclic (tetrahydrofuran, dioxane) and acyclic (diethyl ether) ethers, ethanol, or dimethylformamide was studied with the aim of SiMe3Cl recovery.

Monosodiumoxyorganoalkoxysilanes: Synthesis and properties

Rebrov,Muzafarov

, p. 514 - 541 (2007/10/03)

The reaction of organoalkoxysilanes with sodium hydroxide was studied in detail. Studies indicate that this reaction involves more than one stage and involves rather complex multistep process, which leads to the formation of both monosodiumoxyorganoalkoxysilanes (MSOAS) and several secondary products. Analysis of experimental evidence makes it possible to advance the mechanism behind this phenomenon and to define the optimum conditions for the preparation of pure MSOAS with high yields. Different MSOAS were synthesized and their basic physicochemical properties were studied. MSOAS are shown to constitute multifunctional reagents with chemically independent functional groups, and their reaction with trimethylchlorosilane selectively proceeds via - ONa groups, whereas their interaction with triethylesilanol and higher alcohols proceeds exclusively via - OAlk groups. Exchange interaction between MSOAS and organoalkoxysilanes via - ONa and - OAlk groups was found and studied in detail. Temperature corresponding to the onset of thermal degradation of MSOAS was estimated to be equal to ~ 180-190°C.

Treatment of Tetraalkoxysilanes with Amberlyst 15 Cation-Exchange Resin in Presence of Hexamethyldisiloxane

Hasegawa, Isao,Sakka, Sumio

, p. 4313 - 4316 (2007/10/02)

Tetraalkoxysilanes were treated with Amberlyst 15 cation-exchange resin in hexamethyldisiloxane at 40 deg C in order to substitute the trimethylsilyl group for the alkyl group in a tetraalkoxysilane partially.Tetramethoxy-, ethoxy-, propoxy-, and butoxysilanes were used for the experiments.After the treatment, SiO4R(4-n)Xn (1 /= n /= 4, R = CH3, C2H5, n-C3H7, and n-C4H9, X = Si(CH3)3) were detected by gas chromatography-mass spectrometry.The degree of trimethylsilylation of tetraalkoxysilane changed with the molar ratio of hexamethyldisiloxane to tetraalkoxysilane and quantities of the reaction products in the system depended mainly on the ratio.

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