1825-82-7

Basic information

• Product Name: ETHOXYTRICHLOROSILANE 97
• Synonyms: Trichloro(ethoxy)silane;trichloroethoxysilane;Trichloro-ethoxy-silane;Trichloroethoxy-silane;ETHOXYTRICHLOROSILANE 97
• CAS NO: 1825-82-7
• Molecular Formula: C₂H₅Cl₃OSi
• Molecular Weight: 183.48
• Product Categories: Protecting and Derivatizing Reagents;Protection and Derivatization;Silicon-Based
• Mol File: 1825-82-7.mol
• Article Data: 9

Chemical Properties

• Melting Point: -135°C
• Boiling Point: 35 °C60 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /liquid
• Density: 1.263 g/mL at 25 °C(lit.)
• Refractive Index: 1.4045
• CAS DataBase Reference: ETHOXYTRICHLOROSILANE 97(CAS DataBase Reference)
• NIST Chemistry Reference: ETHOXYTRICHLOROSILANE 97(1825-82-7)
• EPA Substance Registry System: ETHOXYTRICHLOROSILANE 97(1825-82-7)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-27-36/37/39-45
• RIDADR: UN 1760 8/PG 2
• WGK Germany: 3
• Hazardous Substances Data: 1825-82-7(Hazardous Substances Data)

Usage

General Description

Ethoxytrichlorosilane 97 is a chemical compound used as a coupling agent in the production of silicone resins, as well as an intermediate in the synthesis of other organosilicon compounds. It contains trichlorosilane functional groups that can react with various organic and inorganic materials, making it useful in a variety of industrial processes. ETHOXYTRICHLOROSILANE 97 is highly reactive and must be handled with caution due to its potential to release corrosive hydrogen chloride gas when it comes into contact with water or moisture. Additionally, it is important to store and handle ethoxytrichlorosilane 97 in a well-ventilated area and use appropriate personal protective equipment to minimize exposure and potential health hazards.

InChI:InChI=1/C2H5Cl3OS/c1-2-6-7(3,4)5/h2H2,1H3

Upstream product

• 4667-38-3 dichlorodiethoxysilane 
• 10026-04-7 tetrachlorosilane 
• 78-62-6 diethoxy dimethylsilane 
• 4667-99-6 chlorotriethoxysilane 
• 1825-62-3 ethyl trimethylsilyl ether 
• 78-10-4 tetraethoxy orthosilicate 
• 60-29-7 diethyl ether 
• 75-77-4 chloro-trimethyl-silane 
• 98-13-5 Phenyltrichlorosilane 
• 75-94-5 trichlorovinylsilane 
• 75-79-6 Methyltrichlorosilane 
• 75-36-5 acetyl chloride 
• 75-07-0 acetaldehyde 
• 64-17-5 ethanol 

Downstream Products

• 18339-84-9 ethoxy-dichloro-cyclohexyloxy-silane 
• 138769-02-5 2,6-Dichloro-2,6-diethoxy-4,4,8,8-tetraphenyl-[1,3,5,7,2,4,6,8]tetroxatetrasilocane 
• 75-00-3 chloroethane 
• 4667-38-3 dichlorodiethoxysilane 
• 631-36-7 triethylsilane 
• 1825-62-3 ethyl trimethylsilyl ether 
• 10026-04-7 tetrachlorosilane 
• 20160-43-4 tri-(pentafluoro phenyl) ethoxy silane 
• 3555-47-3 1,1,1,5,5,5-hexamethyl-3,3-bis(trimethylsiloxy)trisiloxane 

Relevant articles and documents

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The gas-phase reactions of SiCl4 and Si2Cl 6 with CH3OH and C2H5OH: An investigation by mass spectrometry and matrix-isolation infrared spectroscopy

The gas phase reactions of SiCl4 and Si2Cl 6 with CH3OH and C2H5OH have been investigated using both mass spectrometry and matrix isolation techniques. SiCl4 reacts with both CH

Method of producing arylhalosilane alkoxyphthalocyanine (by machine translation)

PROBLEM TO BE SOLVED: alkoxyphthalocyanine arylhalosilane compd. alkoxy halo silane can be efficiently manufactured to provide a novel method of producing and purpose. SOLUTION: arylhalosilane compd. alkylalkoxysilane compound having a functional group and in exchange reaction, by utilizing a bismuth halide (III), alkoxyphthalocyanine arylhalosilane compd. can be efficiently manufactured. Selected drawing: no (by machine translation)

Exchange reactions in alkoxy derivatives of silicon and germanium

Reaction SiCl4+ Ge(OR)4 → GeCl4+ Si(OR)4 was carried out for the first time. Triethoxysilane reduces tetraethoxygermane via intermediate formation of unstable GeH(OEt)3 that transforms into GeO·Et2O or Ge(OH)2.