Welcome to LookChem.com Sign In|Join Free

CAS

  • or
3-Acetoxypropyl methyl dichlorosilane, with the molecular formula C6H13Cl2O2Si, is a chemical compound that serves as a silane coupling agent. It is synthesized by reacting methyltrichlorosilane with acetoxypropyl chloride and is known for its role as a reactive adhesion promoter and surface modifier. 3-ACETOXYPROPYL METHYL DICHLOROSILANE enhances the adhesion between certain substrates and organic resins or polymers, thereby improving the mechanical and thermal properties of materials in various industrial applications.

5290-24-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 5290-24-4 Structure
  • Basic information

    1. Product Name: 3-ACETOXYPROPYL METHYL DICHLOROSILANE
    2. Synonyms: 3-(dichloromethylsilyl)-1-propanoacetate;ACETOXYPROPYLMETHYLDICHLOROSILANE;3-ACETOXYPROPYL METHYL DICHLOROSILANE;3-(dichloromethylsilyl)propyl acetate;3-[Dichloro(methyl)silyl]-1-propanol acetate;3-Acetoxypropyldichloro(methyl)silane;gamma-Acetoxypropylmethyldichlorosilane
    3. CAS NO:5290-24-4
    4. Molecular Formula: C6H12Cl2O2Si
    5. Molecular Weight: 215.15
    6. EINECS: 226-126-8
    7. Product Categories: N/A
    8. Mol File: 5290-24-4.mol
  • Chemical Properties

    1. Melting Point: <0°C
    2. Boiling Point: 98 °C
    3. Flash Point: 85°C
    4. Appearance: /
    5. Density: 1.289
    6. Vapor Pressure: 0.13mmHg at 25°C
    7. Refractive Index: 1.4434
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-ACETOXYPROPYL METHYL DICHLOROSILANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-ACETOXYPROPYL METHYL DICHLOROSILANE(5290-24-4)
    12. EPA Substance Registry System: 3-ACETOXYPROPYL METHYL DICHLOROSILANE(5290-24-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 34
    3. Safety Statements: 26-36/37/39
    4. RIDADR: 2987
    5. WGK Germany:
    6. RTECS:
    7. TSCA: Yes
    8. HazardClass: N/A
    9. PackingGroup: N/A
    10. Hazardous Substances Data: 5290-24-4(Hazardous Substances Data)

5290-24-4 Usage

Uses

Used in Adhesives Industry:
3-Acetoxypropyl methyl dichlorosilane is used as an adhesion promoter for improving the bonding strength between substrates and organic resins or polymers in the adhesives industry. Its ability to enhance the interfacial adhesion contributes to the development of high-performance adhesives with increased durability and reliability.
Used in Coatings Industry:
In the coatings industry, 3-Acetoxypropyl methyl dichlorosilane is used as a surface modifier to improve the adhesion and durability of coatings on various substrates. Its incorporation into coating formulations results in coatings with enhanced mechanical properties, such as scratch resistance and abrasion resistance, as well as improved resistance to environmental factors like moisture and chemicals.
Used in Sealants Industry:
3-Acetoxypropyl methyl dichlorosilane is used as a reactive component in the formulation of sealants, where it enhances the adhesion between the sealant and the substrate. This leads to improved sealing performance, increased resistance to environmental stress, and longer-lasting sealant joints in various applications, such as construction, automotive, and aerospace industries.
Used in Polysilanes Manufacturing:
3-Acetoxypropyl methyl dichlorosilane is utilized in the manufacturing process of polysilanes, a class of polymers with potential applications in optoelectronics, photovoltaics, and other high-tech fields. Its presence in the synthesis process contributes to the formation of polysilane polymers with desired properties, such as high thermal stability and unique electronic characteristics.
Used as a Crosslinking Agent in Silicone Elastomers:
In the production of silicone elastomers, 3-Acetoxypropyl methyl dichlorosilane is used as a crosslinking agent. It facilitates the formation of a three-dimensional network within the elastomer matrix, resulting in improved mechanical properties, such as tensile strength, tear resistance, and elasticity. This makes the silicone elastomers suitable for a wide range of applications, including automotive, medical, and consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 5290-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5290-24:
(6*5)+(5*2)+(4*9)+(3*0)+(2*2)+(1*4)=84
84 % 10 = 4
So 5290-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9Cl3O2Si/c1-5(9)10-3-2-4-11(6,7)8/h2-4H2,1H3

5290-24-4SDS

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 3-[dichloro(methyl)silyl]propyl acetate

1.2 Other means of identification

Product number -
Other names Dichlor-methyl-(3-acetoxy-propyl)-silan

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:5290-24-4 SDS

5290-24-4Downstream Products

5290-24-4Relevant articles and documents

Mechanistic insights into the hydrosilylation of allyl compounds - Evidence for different coexisting reaction pathways

Gigler, Peter,Drees, Markus,Riener, Korbinian,Bechlars, Bettina,Herrmann, Wolfgang A.,Kuehn, Fritz E.

, p. 1 - 14 (2013/01/14)

The hydrosilylation of allyl compounds is often accompanied by the formation of high amounts of byproducts. The formation processes have not been fully understood so far. In this work, the allyl hydrosilylation mechanism is investigated in detail and experimental and theoretical evidence for multiple, coexisting reaction pathways is provided. Based on earlier reports and the observations during an extensive catalytic study, different pathways, leading to the observed byproducts, were identified and proven by labeling experiments and DFT calculations. Oxidative addition of the silane and the insertion of the allyl compound into the Pt-H bond turned out to be the crucial, selectivity-determining steps within the catalytic cycle. Based on these findings, it should be possible to systematically influence these steps and pave the way to a rational and straightforward design of more selective catalysts.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 5290-24-4