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(3-Triethoxysilylpropyl)-t-butylcarbamate is an organosilicon compound characterized by its t-butylcarbamate group, which imparts unique chemical properties and reactivity. It is recognized for its ability to enhance the adhesion and compatibility of materials, making it a valuable coupling agent and surface modifier in various industries.

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  • 137376-38-6 Structure
  • Basic information

    1. Product Name: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE
    2. Synonyms: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE;Triethoxysilylpropyltbutylcarbamate;N-(3-TRIETHOXYSILYLPROPYL) O-t-BUTYLCARBAMATE;tert-butyl (3-(triethoxysilyl)propyl)carbamate
    3. CAS NO:137376-38-6
    4. Molecular Formula: C14H31NO5Si
    5. Molecular Weight: 321.49
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137376-38-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 355.422 °C at 760 mmHg
    3. Flash Point: >65°C
    4. Appearance: /
    5. Density: 0,99 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.4334
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE(137376-38-6)
    12. EPA Substance Registry System: (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE(137376-38-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. TSCA: No
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 137376-38-6(Hazardous Substances Data)

137376-38-6 Usage

Uses

Used in Composites, Plastics, and Rubber Production:
(3-Triethoxysilylpropyl)-t-butylcarbamate is used as a coupling agent and surface modifier to improve the mechanical and physical properties of composites, plastics, and rubber products. Its presence enhances the durability and strength of these materials, contributing to their overall performance and quality.
Used in Coatings, Adhesives, and Sealants:
(3-Triethoxysilylpropyl)-t-butylcarbamate is used as a cross-linking agent in the production of coatings, adhesives, and sealants. It improves the adhesion and compatibility of these materials, ensuring a stronger bond and increased resistance to environmental factors.
Used in Various Industrial Applications:
(3-Triethoxysilylpropyl)-t-butylcarbamate is utilized across different industries due to its ability to enhance the performance and quality of a wide range of products. Its versatility as a coupling agent and surface modifier makes it an essential component in the formulation of various materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 137376-38-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,3,7 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 137376-38:
(8*1)+(7*3)+(6*7)+(5*3)+(4*7)+(3*6)+(2*3)+(1*8)=146
146 % 10 = 6
So 137376-38-6 is a valid CAS Registry Number.
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)

137376-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butyl-N-(3-triethoxysilylpropyl)carbamate

1.2 Other means of identification

Product number -
Other names (3-TRIETHOXYSILYLPROPYL)-T-BUTYLCARBAMATE

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:137376-38-6 SDS

137376-38-6Downstream Products

137376-38-6Relevant articles and documents

Functionalised mesoporous silica: A good opportunity for controlled peptide oligomerisation

Subra, Gilles,Mehdi, Ahmad,Enjalbal, Christine,Amblard, Muriel,Brunel, Luc,Corriu, Robert,Martinez, Jean

, p. 6321 - 6326 (2011)

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

Synthesis of large-pore ordered mesoporous silicas containing aminopropyl groups

Mehdi, Ahmad,Reye, Catherine,Brandes, Stephane,Guilard, Roger,Corriu, Robert J. P.

, p. 965 - 968 (2005)

Ordered mesoporous silicas with large-pore diameters incorporating aminopropyl groups in variable quantity have been synthesized via the co-condensation of tetraethyl orthosilicate (TEOS) and 3-tert- butyloxycarbonylaminopropyltriethoxysilane templated wi

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

Kim, Wontae,Casalme, Loida O.,Umezawa, Taiki,Matsuda, Fuyuhiko,Otomo, Ryoichi,Kamiya, Yuichi

, p. 71 - 74 (2020)

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.

Synthesis of hexagonal mesoporous silicates functionalized with amino groups in the pore channels by a co-condensation approach

Li, Yunping,Xiong, Wei,Wang, Chun,Song, Bo,Zhang, Guolin

, p. 53991 - 54000 (2016)

Mesoporous silicates functionalized with amino groups in the pore channels have been made by the co-condensation of tetraethoxyl siloxide (TEOS) with precursors of P-Si through a triblock copolymer-templated sol-gel process under acidic conditions. Poly(alkylene oxide) block copolymer (P123) was eluted by ethanol extraction and template molecules were removed by refluxing the materials in a mixture of DMSO and water. The resulting materials were characterized in detail by FT-IR, XRD, TEM and N2 adsorption, in order to study the effect of the precursors on the mesoscopic order and pore structure. Evidence of amino groups located in the pore channels was shown through variation of pore size and BET surface area after the amino groups were coupled with benzaldehyde, and TEM images of materials after staining with RuO4. Finally, a comparative study of the catalytic performance of materials SBA-Am-10 and SBA-T-10, obtained by two methods, revealed that the catalyst synthesized by our method gave rapid reaction speed and high yields of flavanone by the Claisen-Schmidt condensation of benzaldehyde and 2′-hydroxyacetophenone.

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

Yang, Yan,Liu, Xiao,Li, Xiaobo,Zhao, Jiao,Bai, Shiyang,Liu, Jian,Yang, Qihua

supporting information, p. 9164 - 9168 (2012/11/07)

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

Carbamate silicon compounds as latent coupling agents and process for preparation and use

-

, (2008/06/13)

Novel tert-alkyl carbamate silicon compounds are provided which are useful as coupling agents. The compounds have the formulas: STR1 wherein the R groups can represent various hydrocarbon and other groups, n has a value of 1 to 10, b has a valueof from 2 to 5 and a has a value of 1, 2 or 3. Processes are also provided for the preparation of the carbamate compounds and their use as coupling agents.

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