137376-38-6

Basic information

• Product Name: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE
• Synonyms: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE;Triethoxysilylpropyltbutylcarbamate;N-(3-TRIETHOXYSILYLPROPYL) O-t-BUTYLCARBAMATE;tert-butyl (3-(triethoxysilyl)propyl)carbamate
• CAS NO: 137376-38-6
• Molecular Formula: C14H31NO5Si
• Molecular Weight: 321.49
• Mol File: 137376-38-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 355.422 °C at 760 mmHg
• Flash Point: >65°C
• Appearance: /
• Density: 0,99 g/cm3
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.4334
• CAS DataBase Reference: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE(137376-38-6)
• EPA Substance Registry System: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE(137376-38-6)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• TSCA: No
• Hazardous Substances Data: 137376-38-6(Hazardous Substances Data)

Usage

General Description

(3-Triethoxysilylpropyl)-t-butylcarbamate is a chemical compound that falls under the category of organosilicon compounds. It is used as a coupling agent and surface modifier in various industrial applications. This chemical is known for its ability to improve the adhesion and compatibility of materials such as coatings, adhesives, and sealants. It contains a t-butylcarbamate group, which provides the compound with specific chemical properties and reactivity. (3-Triethoxysilylpropyl)-t-butylcarbamate is commonly used in the production of composites, plastics, and rubber products due to its ability to enhance the mechanical and physical properties of these materials. Additionally, it is used as a cross-linking agent to improve the durability and strength of various products. Overall, this chemical plays a crucial role in improving the performance and quality of a wide range of industrial products.

InChI:InChI=1/C14H31NO5Si/c1-7-17-21(18-8-2,19-9-3)12-10-11-15-13(16)20-14(4,5)6/h7-12H2,1-6H3,(H,15,16)

Upstream product

• 919-30-2 3-aminopropyltriethoxysilane 
• 24424-99-5 di-tert-butyl dicarbonate 

Relevant articles and documents

Functionalised mesoporous silica: A good opportunity for controlled peptide oligomerisation

In this paper, mesoporous organosilicas functionalised with aminopropyl groups have been successfully used for peptide oligomerisation. For this purpose, three mesoporous silica SBA-15 type containing different amounts of aminopropyl groups were prepared

A reliable method to create adjacent acid-base pair sites on silica through hydrolysis of pre-anchored amide

A method to create adjacent acid-base pair sites, which are carboxyl and amino groups, respectively, on silica through hydrolysis of pre-anchored amide is proposed. This method can produce an adjacent acid-base pair site. The catalyst showed excellent catalytic performance for aldol condensation of 4-nitrobenzaldehyde with acetone, overwhelming the catalyst having only amino group and an acid-base catalyst prepared in a conventional manner.

A yolk-shell nanoreactor with a basic core and an acidic shell for cascade reactions

Smart yolk-shell nanoparticles (hollow nanoparticles with a movable core) with an acidic shell and a basic core were fabricated through an organosilane-assisted selective etching method and acted as efficient nanoreactors for catalyzing a deacetalization-Henry cascade reaction with high activity and high selectivity. This strategy is very promising for the design of multifunctional nanoreactors for cascade reactions. Copyright