17945-05-0

Usage

Uses

Used in Coatings Industry:
Triethoxysilylpropylethylcarbamate is used as an adhesion promoter and coupling agent for improving the bond strength between coatings and various surfaces. Its presence in coatings helps to increase their durability and resistance to weathering conditions.
Used in Adhesives Industry:
In the adhesives industry, triethoxysilylpropylethylcarbamate serves as a coupling agent to enhance the adhesive's bonding capabilities with different materials, thereby improving the overall performance and longevity of the adhesive in various applications.
Used in Sealants Industry:
Triethoxysilylpropylethylcarbamate is used as a component in sealants to boost their adhesion to substrates and to improve their resistance to environmental factors, ensuring a more reliable and long-lasting seal.
Used in Surface Treatment Agent:
As a surface treatment agent, triethoxysilylpropylethylcarbamate is applied to improve the performance of materials in moisture-sensitive applications, providing an additional layer of protection and enhancing the material's resistance to moisture-related degradation.

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 academic research and scientific papers

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]

The isocyanate group-containing alkoxysilane method (by machine translation)

[Problem] an isocyanate group-containing alkoxysilane isocyanate group-containing alkoxysilane having high purity can be efficiently produced. [Solution] The amino group-containing alkoxysilane is reacted with dialkyl carbonate, carbamate alcohol mixture is obtained. Then, the mixture was heated to obtain an isocyanate group-containing alkoxysilanes. In this case, alcohol-containing fractions of 1 second, isocyanate group-containing alkoxysilane containing 2 fractions of a second, annular byproducts including 3 a fraction is obtained. The, the first fraction of the heated mixture before mixing 3, annular reaction byproduct alcohol, cyclic carbamate returned products. Figure 1 [drawing] (by machine translation)

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

METHOD FOR PRODUCING CARBAMATOORGANOSILANES

Carbamatoorganosilanes are produced in exceptionally high yield with a high degree of purity, by reacting an aminoorganosilane with a dialkylcarbonate in the presence of a basic catalyst, wherein a first reaction period proceeds at a temperature in the range of 35-65° C., followed by a later reaction period at a temperature at least 10° C. higher. A low level of catalyst allows its removal by simple exit filtration, without a separate filtration step.

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.