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3179-76-8

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  • 3-Aminopropylmethyldiethoxysilane CAS 3179-76-8 In stock 3-Aminopropyl(diethoxy)methylsilane

    Cas No: 3179-76-8

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3179-76-8 Usage

Chemical Properties

Colorless transparent liquid

Uses

(3-Aminopropyl)diethoxymethylsilane is used as silane coupling agent. The aromatic imine monolayers were prepared by reacting (3-aminopropyl)diethoxymethylsilane.

Flammability and Explosibility

Nonflammable

Safety Profile

Poison by intraperitoneal route.Moderately toxic by ingestion and skin contact. A skinirritant. When heated to decomposition it emits toxicfumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 3179-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3179-76:
(6*3)+(5*1)+(4*7)+(3*9)+(2*7)+(1*6)=98
98 % 10 = 8
So 3179-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H21NO2Si/c1-4-10-12(3,11-5-2)8-6-7-9/h4-9H2,1-3H3

3179-76-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L16401)  (3-Aminopropyl)diethoxymethylsilane, 97%   

  • 3179-76-8

  • 25g

  • 223.0CNY

  • Detail
  • Alfa Aesar

  • (L16401)  (3-Aminopropyl)diethoxymethylsilane, 97%   

  • 3179-76-8

  • 100g

  • 721.0CNY

  • Detail
  • Aldrich

  • (371890)  3-Aminopropyl(diethoxy)methylsilane  97%

  • 3179-76-8

  • 371890-50ML

  • 466.83CNY

  • Detail
  • Aldrich

  • (371890)  3-Aminopropyl(diethoxy)methylsilane  97%

  • 3179-76-8

  • 371890-250ML

  • 1,722.24CNY

  • Detail

3179-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Aminopropyl-methyl-diethoxysilane

1.2 Other means of identification

Product number -
Other names CA0742

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:3179-76-8 SDS

3179-76-8Related news

Reinforcement properties of 3-Aminopropylmethyldiethoxysilane (cas 3179-76-8) and N-(2-Aminoethyl)-3-aminopropylmethyldimethoxysilane on polyurethane ester foam07/11/2019

Museum artifacts made of polyurethane foam are frequently affected by conservation issues mainly related to the loss of their mechanical properties. While effective polyurethane ether foam treatments already exist, no convenient consolidation treatment exists for polyurethane ester foams. The po...detailed

3179-76-8Relevant articles and documents

ORGANOSILICON COMPOUND AND ITS PRODUCTION METHOD, COMPOUNDING AGENT FOR RUBBER, RUBBER COMPOSITION, AND TIRE

-

, (2012/12/13)

A method for producing a sulfur-containing organosilicon compound capable of dramatically reducing hysteresis loss of the cured rubber composition and improving abrasion resistance and its production method are provided. A compounding agent for rubber containing the sulfur-containing organosilicon compound, a rubber composition prepared by blending such compounding agent for rubber, and a tire produced by using the cured rubber composition are also provided. The sulfur-containing organosilicon compound has a hydrolyzable silyl group, amino group, and mercapto group.

Platinum oxide (PtO2): A potent hydrosilylation catalyst

Sabourault, Nicolas,Mignani, Gerard,Wagner, Alain,Mioskowski, Charles

, p. 2117 - 2119 (2007/10/03)

(matrix presented) Platinum oxide was found to be a versatile and powerful hydrosilylation catalyst upon a wide variety of functionalized alkenes and especially aminated alkenes. Moreover, highly reproducible results and easy removal make this new catalys

Process for making a silylisocyanurate

-

, (2008/06/13)

This invention provides a process for making a silylorganocarbamate or a silylisocyanurate which process comprises reacting an aminosilane with a dialkyl carbonate, diaryl carbonate or a mixture thereof in the presence of a basic catalyst to obtain the silylorganocarbamate; optionally, neutralizing the basic catalyst and residual aminosilane with a neutralizing agent; and adding a cracking catalyst and heating at subatmospheric pressure to obtain the silylisocyanurate; or heating a silylorganocarbamate at a temperature sufficient for dissociation of the carbamate at subatmospheric pressure in the presence of a cracking catalyst and a timerization catalyst to obtain a silylisocyanurate.

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