17945-05-0

Basic information

• Product Name: TRIETHOXYSILYLPROPYLETHYLCARBAMATE
• Synonyms: TRIETHOXYSILYLPROPYLETHYLCARBAMATE;[3-(triethoxysilyl)propyl]-carbamicaciethylester;Carbamicacid,[3-(triethoxysilyl)propyl]-,ethylester;ETHYL 3-(TRIETHOXYSILYL)PROPYLCARBAMATE;(3-(TRIETHOXYSILYL)PROPYL)-CARBAMICACID,ETHYLESTER;N-[3-(Triethoxysilyl)propyl]carbamic acid ethyl ester;triethoxysilylpropylethylcarbaMe
• CAS NO: 17945-05-0
• Molecular Formula: C12H27NO5Si
• Molecular Weight: 293.43
• EINECS: 241-872-4
• Mol File: 17945-05-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: <0°C
• Boiling Point: 124 °C
• Flash Point: 95°C
• Appearance: /
• Density: 1.015
• Vapor Pressure: 0.000148mmHg at 25°C
• Refractive Index: 1.437
• CAS DataBase Reference: TRIETHOXYSILYLPROPYLETHYLCARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIETHOXYSILYLPROPYLETHYLCARBAMATE(17945-05-0)
• EPA Substance Registry System: TRIETHOXYSILYLPROPYLETHYLCARBAMATE(17945-05-0)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• TSCA: Yes
• Hazardous Substances Data: 17945-05-0(Hazardous Substances Data)

Usage

General Description

Triethoxysilylpropylethylcarbamate is a chemical compound used as a coupling agent and adhesion promoter in various industries, including coatings, adhesives, and sealants. It is a silane-based molecule that contains a carbamate functional group, which allows it to bond and crosslink with a variety of substrates, such as glass, metals, and plastics. This chemical helps improve the durability and weather resistance of coatings and adhesives by enhancing their adhesion to different surfaces. Additionally, it can also be used as a surface treatment agent to improve the performance of materials in moisture-sensitive applications. Overall, triethoxysilylpropylethylcarbamate plays a vital role in improving the adhesion, durability, and performance of various products across different industries.

InChI:InChI=1/C12H27NO5Si/c1-5-15-12(14)13-10-9-11-19(16-6-2,17-7-3)18-8-4/h5-11H2,1-4H3,(H,13,14)

Upstream product

• 998-30-1 Triethoxysilane 
• 5325-60-0 ethyl N-allylcarbamate 
• 919-30-2 3-aminopropyltriethoxysilane 
• 13822-56-5 3-(trimethoxysilyl)propan-1-amine 
• 105-58-8 Diethyl carbonate 

Downstream Products

• 24801-88-5 3-(triethoxypropyl) isocyanate 

Relevant articles and documents

SILICON DIOXIDE COMPOSITE PARTICLE WITH FAR-INFRARED RADIOACTIVITY; PRECURSOR OF THE SAME AND APPLICATION THEREOF

The present invention relates to a silicon dioxide composite particle with far-infrared radioactivity, which is formed by the hydrolysis, condensation and polymerization of an organic silane precursor having the structure of the formula (I) with a tetra-alkoxysilane. The high stability of organic silane precursor compounds and the low biotoxicity of silicon dioxide composite particles make the present far-infrared radioactive silicon dioxide composite particles of great potential for extensive use in related bio-products. [in-line-formulae]A-R1—Si(OR2)3?? Formula (I)[/in-line-formulae]

MANUFACTURING METHOD OF CARBAMATE ALKYLSILANE

PROBLEM TO BE SOLVED: To provide a manufacturing method capable of providing carbamate alkylsilane effectively from a reaction mixture obtained from a reaction of aminoalkylsilane and a carbonic ester compound at high purity and high yield. SOLUTION: There is provided a manufacturing method of carbamate alkylsilane of the formula (3) by distilling a reaction mixture obtained by reacting an organic silicate compound represented by the formula (1) and a carbonic ester compound represented by the formula (2) in a presence of a metal catalyst containing one or more kinds of metal selected from Mn and Zn. R1 is a substituted/unsubstituted bifunctional hydrocarbon group with 3 to 6 carbon atoms, R2 and R3 are each independently a substituted/unsubstituted C1 to 10 monovalent hydrocarbon group and n is an integer of 0 to 2. R4 is each independently a substituted/unsubstituted C1 to 10 monovalent hydrocarbon group. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

Process for the preparation of N-silylorganocarbamates

A process is provided for preparing an N-silylorganocarbamate, which comprises: providing a mixture of aminoorganosilane and a catalytically effective amount of basic catalyst and; combining the mixture of aminoorganosilane and basic catalyst with an organocarbonate ester the mixture of aminoorganosilane and basic catalyst, the organocarbonate ester or both being at elevated temperature at the time of their being combined.