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(10-CARBOMETHOXYDECYL)DIMETHYLCHLOROSILANE, with the molecular formula C14H29ClO3Si, is a chlorosilane compound characterized by a 10-carbomethoxydecyl group, two dimethyl groups, and a chlorosilane group. It is renowned for its capacity to form stable bonds with a variety of surfaces such as metals, glass, and polymers, which makes it a versatile surface modifier in numerous industrial applications, especially in the creation of silicone-based materials. Its role as a coupling agent further enhances the adhesion and compatibility of different materials in composite and polymer formulations.

53749-38-5

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53749-38-5 Usage

Uses

Used in Silicone-based Material Production:
(10-CARBOMETHOXYDECYL)DIMETHYLCHLOROSILANE is used as a surface modifier for its ability to form stable bonds with various surfaces, which is crucial in the production of silicone-based materials. This enhances the material's performance characteristics, such as adhesion, durability, and resistance to environmental factors.
Used in Coating Industry:
In the coating industry, (10-CARBOMETHOXYDECYL)DIMETHYLCHLOROSILANE is used as an additive to improve the adhesion of coatings to different substrates, thereby increasing the coatings' effectiveness and longevity.
Used in Adhesive Formulation:
(10-CARBOMETHOXYDECYL)DIMETHYLCHLOROSILANE is utilized as a coupling agent in adhesive formulations to enhance the compatibility and adhesion between different materials, ensuring stronger and more durable bonds.
Used in Sealant Production:
In sealant production, (10-CARBOMETHOXYDECYL)DIMETHYLCHLOROSILANE is employed to improve the sealant's bonding capabilities with various surfaces, contributing to a more robust and reliable seal.
Used in Composite Material Industry:
(10-CARBOMETHOXYDECYL)DIMETHYLCHLOROSILANE is used as a coupling agent in the composite material industry to improve the interfacial adhesion between the matrix and the reinforcement, leading to enhanced mechanical properties of the composite.

Check Digit Verification of cas no

The CAS Registry Mumber 53749-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,4 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53749-38:
(7*5)+(6*3)+(5*7)+(4*4)+(3*9)+(2*3)+(1*8)=145
145 % 10 = 5
So 53749-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H29ClO2Si/c1-17-14(16)12-10-8-6-4-5-7-9-11-13-18(2,3)15/h4-13H2,1-3H3

53749-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 11-[chloro(dimethyl)silyl]undecanoate

1.2 Other means of identification

Product number -
Other names -

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:53749-38-5 SDS

53749-38-5Downstream Products

53749-38-5Relevant academic research and scientific papers

Synthesis of Poly(silyl ethers) via Iridium-Catalyzed Dehydrocoupling Polymerization

Zhai, Xiao-Yong,Hu, Shu-Bo,Shi, Lei,Zhou, Yong-Gui

, p. 2342 - 2347 (2018)

Poly(silyl ethers) (PSEs) are promising degradable materials, and the development of an efficient method to produce them from readily available materials is highly desirable. Herein, we present a dehydrocoupling polymerization of AB-type silyl alcohol monomers catalyzed by homogeneous iridium(I) complexes bearing a bisphosphine ligand. A series of PSEs containing aliphatic or aromatic linkers have been synthesized. The PDI of PSEs could be tuned by varying the ligand of iridium/bisphosphine complexes. Moderate to high yields of polymers with number-average molecular weights (Mn) up to 9.27 × 104 were obtained. The PSEs possess good thermal stability and low glass-transition temperature (Tg = -42 to -83 °C).

Polysilylether: A Degradable Polymer from Biorenewable Feedstocks

Cheng, Chen,Watts, Annabelle,Hillmyer, Marc A.,Hartwig, John F.

supporting information, p. 11872 - 11876 (2016/11/16)

The synthesis of polysilylethers (PSEs) using a monomer derived from a biorenewable feedstock is reported. The AB-type monomer was synthesized from undecenoic acid through hydrosilylation and reduction, and the polymerization was catalyzed by earth-abundant metal salts. High-molar-mass products were achieved, and the degree of polymerization was controlled by varying the amount of an AA-type monomer in the reaction. The PSEs possess good thermal stability and a low glass-transition temperature (Tg≈?67 °C). To demonstrate the utility of the PSEs, polyurethanes were synthesized from low-molar-mass hydroxy-telechelic PSEs.

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