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13175-88-7

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13175-88-7 Usage

Description

Diethoxy(ethyl)silane, with the chemical formula C6H16O2Si, is a clear, colorless liquid that serves as a versatile chemical compound in various industrial applications. It is primarily recognized for its role as a crosslinking agent in the synthesis of silicone polymers, enhancing their structural integrity and performance. Furthermore, diethoxy(ethyl)silane functions as a silane coupling agent, facilitating improved adhesion and compatibility between organic resins and inorganic materials. Due to its highly flammable nature and classification as a hazardous material, it necessitates careful handling, storage, and usage in well-ventilated areas with appropriate safety measures.

Uses

Used in Silicone Polymer Production:
Diethoxy(ethyl)silane is used as a crosslinking agent for enhancing the structural properties of silicone polymers. Its incorporation leads to the formation of a three-dimensional network within the polymer matrix, thereby improving the material's mechanical strength, thermal stability, and resistance to environmental factors.
Used in Adhesive and Sealant Formulation:
Diethoxy(ethyl)silane is utilized as a silane coupling agent in the formulation of adhesives and sealants. It promotes strong adhesion between organic resins and inorganic materials, such as glass, metal, and concrete surfaces. This results in the development of high-performance adhesives and sealants with excellent bonding strength, durability, and resistance to various environmental conditions.
Used in Coatings Industry:
In the coatings industry, diethoxy(ethyl)silane is employed as a silane coupling agent to improve the adhesion and compatibility of coatings with various substrates. Its use leads to the development of coatings with enhanced durability, resistance to corrosion, and improved surface properties, such as hardness and scratch resistance.
Used in Composite Materials:
Diethoxy(ethyl)silane is used in the production of composite materials to enhance the interfacial bonding between the organic matrix and inorganic fillers or reinforcements. This results in composites with improved mechanical properties, such as increased strength, stiffness, and toughness, as well as enhanced resistance to environmental degradation.
Used in Surface Treatment and Modification:
Diethoxy(ethyl)silane is utilized for surface treatment and modification of various materials, such as metals, ceramics, and polymers. Its application leads to the formation of a thin, chemically bonded layer on the material surface, which can improve properties like wettability, adhesion, and corrosion resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 13175-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,7 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13175-88:
(7*1)+(6*3)+(5*1)+(4*7)+(3*5)+(2*8)+(1*8)=97
97 % 10 = 7
So 13175-88-7 is a valid CAS Registry Number.

13175-88-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethoxy(ethyl)silane

1.2 Other means of identification

Product number -
Other names Aethyl-diaethyloxy-silan

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:13175-88-7 SDS

13175-88-7Downstream Products

13175-88-7Relevant articles and documents

Schott et al.

, p. 219,223 (1968)

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 (2000)

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.

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