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Diethoxysilane, with the chemical formula (C2H5O)2SiH2, is a clear, colorless liquid characterized by a sharp, sweet, ethereal odor. It is a versatile chemical compound used in the synthesis of silicones, silanes, and other organosilicon compounds, playing a crucial role in the production of silicone rubber, adhesives, coatings, and sealants. Diethoxysilane also serves as a crosslinking agent in organic polymers and a surface modifier for glass and metal substrates. Due to its highly flammable nature and potential for violent reactions with water, it requires careful handling and storage to prevent dangerous chemical reactions.

18165-68-9

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18165-68-9 Usage

Uses

Used in Silicone Production:
Diethoxysilane is used as a key ingredient in the production of silicone rubber, which is valued for its flexibility, durability, and resistance to extreme temperatures. It is employed in various applications, including automotive parts, medical devices, and consumer electronics.
Used in Adhesive and Sealant Manufacturing:
Diethoxysilane is utilized as a component in the formulation of adhesives and sealants, providing strong bonding and sealing properties. These products are widely used in construction, automotive, and aerospace industries for joining and sealing materials.
Used in Coating Industry:
As a component in coating formulations, diethoxysilane enhances the adhesion, durability, and water resistance of coatings. It is used in various applications, such as architectural coatings, automotive finishes, and protective coatings for metal structures.
Used as a Crosslinking Agent in Organic Polymers:
Diethoxysilane is employed as a crosslinking agent in the synthesis of organic polymers, improving their mechanical properties, thermal stability, and chemical resistance. This application is particularly relevant in the plastics, elastomers, and composites industries.
Used in Surface Modification of Glass and Metal Substrates:
Diethoxysilane is used as a surface modifier for glass and metal substrates, enhancing their adhesion, corrosion resistance, and durability. This application is crucial in industries such as automotive, aerospace, and construction, where improved surface properties are essential for performance and longevity.

Check Digit Verification of cas no

The CAS Registry Mumber 18165-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,6 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18165-68:
(7*1)+(6*8)+(5*1)+(4*6)+(3*5)+(2*6)+(1*8)=119
119 % 10 = 9
So 18165-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H10O2Si/c1-3-5-7-6-4-2/h3-4H2,1-2H3

18165-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethoxysilane

1.2 Other means of identification

Product number -
Other names Silane, diethoxy-

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:18165-68-9 SDS

18165-68-9Downstream Products

18165-68-9Relevant academic research and scientific papers

Process for the direct synthesis of trialkoxysilane

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Page/Page column 19, (2008/06/13)

This invention discloses a process to improve reaction stability in the Direct Synthesis of trialkoxysilanes. The process is particularly effective in the Direct Synthesis of triethoxysilane and its higher alkyl cognates providing improved triethoxysilane yields.

Direct synthesis of methyldimethoxysilane from metallic silicon and methanol using copper(I) chloride catalyst

Okamoto, Masaki,Abe, Hidenori,Kusama, Yukari,Suzuki, Eiichi,Ono, Yoshio

, p. 74 - 79 (2007/10/03)

When the reaction of metallic silicon with methanol in the presence of a small amount of thiophene was carried out at 653 K, methyldimethoxysilane was formed together with trimethoxysilane and tetramethoxysilane, the selectivity for methyldimethoxysilane being 22%. Further adding a small amount of trioxane, trimer of formaldehyde, to the reaction system improved the selectivity for methyldimethoxysilane. This indicates that formaldehyde formed by the dehydrogenation of methanol takes part in methyldimethoxysilane formation. The reaction of silicon with ethanol also gave a 14% selectivity of ethyldiethoxysilane with a 43% silicon conversion.

Process for the preparation of low silanes and silane esters

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, (2008/06/13)

A process for preparing monosilane and low silane esters thereof which comprises contacting a hydrogen silane ester of the formula Hx Si(OR)4-x, wherein R represents an alkyl or alkoxyalkyl moiety and x is 1, 2 or 3, with

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