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CAS

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652159-43-8

(10-broModecyl)triethoxysilane, with the chemical formula C16H36BrNO3Si, is a silane coupling agent that serves as a versatile surface modifier. It is a colorless to pale yellow liquid, soluble in organic solvents like ethanol and acetone, and is instrumental in enhancing the adhesion between organic and inorganic materials.

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  • 652159-43-8 Structure

  • Basic information

    1. Product Name: (10-broModecyl)triethoxysilane
    2. Synonyms: (10-broModecyl)triethoxysilane
    3. CAS NO:652159-43-8
    4. Molecular Formula: C16H35BrO3Si
    5. Molecular Weight: 383.4368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 652159-43-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (10-broModecyl)triethoxysilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (10-broModecyl)triethoxysilane(652159-43-8)
    11. EPA Substance Registry System: (10-broModecyl)triethoxysilane(652159-43-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 652159-43-8(Hazardous Substances Data)

652159-43-8 Usage

Uses

Used in Adhesives and Sealants Industry:
(10-broModecyl)triethoxysilane is used as a surface modifier to improve the adhesion and performance of adhesives and sealants. Its ability to bond organic and inorganic materials contributes to the enhanced durability and reliability of these products.
Used in Coatings Industry:
In the coatings industry, (10-broModecyl)triethoxysilane is used as an additive to improve the adhesion of coatings to various substrates, ensuring a strong bond and long-lasting protection.
Used in Construction Industry:
(10-broModecyl)triethoxysilane is used as a component in construction materials to enhance their water repellency and corrosion resistance, thereby increasing the longevity and durability of structures.
Used in Automotive Industry:
In the automotive sector, (10-broModecyl)triethoxysilane is utilized to improve the adhesion of coatings and sealants, ensuring better protection for vehicle components and enhancing their resistance to environmental factors.
Used in Electronics Industry:
(10-broModecyl)triethoxysilane is employed in the electronics industry to improve the adhesion of materials used in the manufacturing of electronic devices, ensuring better performance and reliability of the products.

Check Digit Verification of cas no

The CAS Registry Mumber 652159-43-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,1,5 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 652159-43:
(8*6)+(7*5)+(6*2)+(5*1)+(4*5)+(3*9)+(2*4)+(1*3)=158
158 % 10 = 8
So 652159-43-8 is a valid CAS Registry Number.

652159-43-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-bromodecyl(triethoxy)silane

1.2 Other means of identification

Product number -
Other names Silane,(10-bromodecyl)triethoxy

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:652159-43-8 SDS

652159-43-8Downstream Products

652159-43-8Relevant articles and documents

Synthesis and lead(II) sorption of silica gel-immobilized, di-ionizable calix[4]arenes

Zhang, Dongmei,Wang, Jing,Lawson, Thomas R.,Bartsch, Richard A.

, p. 5076 - 5082 (2008/02/01)

Di-ionizable calix[4]arenes with two lower-rim N-(X)sulfonyl carboxamide groups were covalently linked to silica gel via a single attachment on the upper rim. Both the acidity of the ionizable groups (X group variation) and the length of the spacer that joins the ligands to the silica gel matrix were varied. Preliminary evaluation of these new ion-exchange resins for sorption of lead(II) from aqueous solutions was conducted.

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