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Triisocyanato-methyl-silane, also known as isocyanatomethyltrimethoxysilane, is an organosilicon compound belonging to the isocyanate family, with the chemical formula C7H15N3O3Si. It is recognized for its excellent adhesion properties and high strength, making it a valuable component in various industrial applications.

5587-61-1

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5587-61-1 Usage

Uses

Used in Polyurethane Production:
Triisocyanato-methyl-silane is used as a crosslinking agent for the production of polyurethane materials, such as adhesives, elastomers, and coatings. It enhances the durability and performance of these materials by forming strong chemical bonds between polymer chains.
Used in Silane-Modified Polymers:
In the formulation of silane-modified polymers, triisocyanato-methyl-silane is used as a reactive component to improve the material's adhesion, mechanical properties, and chemical resistance. Its incorporation into polymers results in materials with enhanced performance characteristics.
Used as an Adhesion Promoter:
Triisocyanato-methyl-silane is used as an adhesion promoter for various substrates, including glass, metals, and plastics. It forms strong covalent bonds with these substrates, improving the adhesion of coatings, adhesives, and other materials, leading to better performance and durability.
It is important to handle triisocyanato-methyl-silane with caution due to its potential hazards as a reactive and sensitizing substance. Proper safety measures should be taken during its use to ensure the well-being of workers and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 5587-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5587-61:
(6*5)+(5*5)+(4*8)+(3*7)+(2*6)+(1*1)=121
121 % 10 = 1
So 5587-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H3N3O3Si/c1-11(5-2-8,6-3-9)7-4-10/h1H3

5587-61-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name triisocyanato(methyl)silane

1.2 Other means of identification

Product number -
Other names Methyltriisocyanatosilane

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:5587-61-1 SDS

5587-61-1Relevant academic research and scientific papers

Neue Wege zu Polysilanen

Hengge, Edwin,Kalchauer, Wilfried

, p. 793 - 802 (2007/10/02)

Disilane dervatives undergo disproportionation reactions to polysilanes.Investigated were 1,2-dimethyldisilane and 1,2-dimethyltetrachlorodisilane with catalysts like NH4Cl, AgCN, and Na-cyanamide.In case of 1,2-dimethylsilane, with more than catalytic amounts of NH4Cl, a nitrogen containing polysilane is formed.Two new compounds MeSiH(NCO)2 and Me2Si2(NCO)4 were synthesized and characterized.The last one leads to a polymer at heating.Additionally an electrochemical formation of polydimethylsilane is described.

ULTRAVIOLET SPECTROSCOPIC INVESTIGATION OF ISOCYANATO- AND ISOTHIOCYANATO SILANES CONTAINING PHENYL- AND METHYL GROUPS

Veszpremi, Tamas,Barta, Istvan,Nagy, Jozsef

, p. 243 - 250 (2007/10/02)

The members of the series R(n)Si(NCO)(4-n) and R(n)Si(NCS)(4-n), where R = -CH3 and -C6H5, were prepared, their ultraviolet spectra recorded and the observed bands assigned.The spectra were compared to those of halogeno derivatives.The similarity of halogen- and pseudohalogeno-groups and difference between the effect of methyl- and phenyl-groups were studied.

Chemical process

-

, (2008/06/13)

Optionally substituted silicon isocyanates are prepared by reacting a corresponding silicon halide with an alkali metal cyanate or an alkaline earth metal cyanate in an inert solvent having a dielectric constant below about 10, in the presence of a crown ether as a catalyst.

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