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1,3-BIS(4-BENZOYL-3-HYDROXYPHENOXY)-2-PROPYL ACRYLATE is a chemical compound characterized by the molecular formula C35H28O7. It is an acrylate compound that features benzoyl and hydroxyphenoxy groups, which contribute to its unique properties and applications in various industries.

103637-50-9

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  • Factory Price OLED 99% 103637-50-9 1,3-Bis(4-benzoyl-3-hydroxyphenoxy)propan-2-yl acrylate Manufacturer

    Cas No: 103637-50-9

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103637-50-9 Usage

Uses

Used in Polymer Production:
1,3-BIS(4-BENZOYL-3-HYDROXYPHENOXY)-2-PROPYL ACRYLATE is used as a crosslinking agent for enhancing the thermal, mechanical, and chemical properties of polymers. Its incorporation into polymers results in materials with improved performance and durability.
Used in Coatings Industry:
In the coatings industry, 1,3-BIS(4-BENZOYL-3-HYDROXYPHENOXY)-2-PROPYL ACRYLATE is used as a crosslinking agent to improve the durability and performance of coatings. It helps in developing coatings with enhanced resistance to environmental factors, such as UV radiation, moisture, and chemicals.
Used in Adhesives Industry:
1,3-BIS(4-BENZOYL-3-HYDROXYPHENOXY)-2-PROPYL ACRYLATE is utilized as a crosslinking agent in the formulation of adhesives. Its presence in adhesives contributes to better adhesion strength, thermal stability, and resistance to chemicals, making the adhesives suitable for various applications.
Used in Advanced Material Development:
1,3-BIS(4-BENZOYL-3-HYDROXYPHENOXY)-2-PROPYL ACRYLATE is employed in the development of high-performance materials with specific properties tailored for specialized applications. Its unique structure allows for the creation of materials with enhanced mechanical, thermal, and chemical resistance, making them suitable for use in demanding environments.
It is crucial to handle 1,3-BIS(4-BENZOYL-3-HYDROXYPHENOXY)-2-PROPYL ACRYLATE with care, as it may pose health and environmental risks if not managed properly. Proper safety measures and disposal methods should be followed to minimize any potential hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 103637-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,3 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103637-50:
(8*1)+(7*0)+(6*3)+(5*6)+(4*3)+(3*7)+(2*5)+(1*0)=99
99 % 10 = 9
So 103637-50-9 is a valid CAS Registry Number.

103637-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(4-benzoyl-3-hydroxyphenoxy)propan-2-yl prop-2-enoate

1.2 Other means of identification

Product number -
Other names 1,3-BIS(4-BENZOYL-3-HYDROXYPHENOXY)-2-PROPYL ACRYLATE

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:103637-50-9 SDS

103637-50-9Downstream Products

103637-50-9Relevant articles and documents

UV light stabilizer based on benzophenone

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, (2008/06/13)

Benzophenone derivatives having at least one hydroxyl group in the ortho-position relative to the carbonyl group are used for stabilizing numerous substrates against the action of UV light. 1,3-bis-(4-Benzoyl-3-hydroxyphenoxy)-2-propanol is a photo-absorber containing two benzophenone groups. Particularly suitable stabilizers are esters of this substituted propanol with unsaturated carboxylic acids, for example esters of acrylic acid and methacrylic acid. These compounds are prepared by esterifying the substituted propanol with an unsaturated acid or by esterifying the substituted propanol with a saturated acid containing a reactive methylene group and subjecting the product to subsequent condensation with a keto compound. They can be polymerized and are suitable for the preparation of homopolymers and copolymers.

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