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13675-34-8

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13675-34-8 Usage

Description

1,5-PENTANEDIOL DIMETHACRYLATE is a versatile chemical compound that is widely used in the production of polymers, adhesives, and coatings. As a dimethacrylate ester, it contains two methacrylate groups which enable it to undergo polymerization reactions, resulting in the formation of strong and durable materials. Its ability to crosslink with other polymers makes it an important chemical in the fields of materials science and polymer chemistry.

Uses

Used in Dental Adhesives:
1,5-PENTANEDIOL DIMETHACRYLATE is used as a key component in dental adhesives for its ability to form strong and durable bonds with dental materials. Its polymerization properties ensure a long-lasting and stable adhesive effect, contributing to the overall success of dental procedures.
Used in Polymer Production:
1,5-PENTANEDIOL DIMETHACRYLATE is used as a crosslinking agent in the production of various polymers. Its ability to react with other monomers and polymers allows for the creation of materials with enhanced mechanical properties, such as increased strength, flexibility, and durability.
Used in Adhesives and Coatings Industry:
1,5-PENTANEDIOL DIMETHACRYLATE is used as a critical ingredient in the formulation of adhesives and coatings. Its polymerization capabilities enable the development of high-performance adhesives and coatings with excellent adhesion, resistance to environmental factors, and long-term stability.
Used in Material Science Research:
1,5-PENTANEDIOL DIMETHACRYLATE is utilized as a model compound in material science research to study the properties and behavior of polymers and their potential applications. Its unique structure and reactivity provide valuable insights into the development of new materials and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 13675-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13675-34:
(7*1)+(6*3)+(5*6)+(4*7)+(3*5)+(2*3)+(1*4)=108
108 % 10 = 8
So 13675-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O4/c1-10(2)12(14)16-8-6-5-7-9-17-13(15)11(3)4/h1,3,5-9H2,2,4H3

13675-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-PENTANEDIOL DIMETHACRYLATE

1.2 Other means of identification

Product number -
Other names Bismethacrylic acid pentane-1,5-diyl ester

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:13675-34-8 SDS

13675-34-8Downstream Products

13675-34-8Relevant articles and documents

Runge-Kutta analysis for optimizing the Zn-catalyzed transesterification conditions of MA and MMA with diols to maximize monoesterified products

Kato, Taito,Akebi, Shin-Ya,Nagae, Haruki,Yonehara, Koji,Oku, Tomoharu,Mashima, Kazushi

, p. 6975 - 6986 (2021/11/17)

Terminal hydroxylated acrylates and methacrylates were prepared by catalytic transesterification of acrylates and methacrylates with diols catalyzed by a system of a tetranuclear zinc alkoxide, [Zn(tmhd)(OMe)(MeOH)]4 (1a), with 4 equiv. of 2,2′-bipyridine (L1). The reaction time to reach the equilibrium state was analyzed by kinetic studies and a curve-fitting analysis based on the Runge-Kutta method for optimizing the best reaction conditions for mono-esterification. In addition to these kinetic analyses, DFT calculations estimated a proposed mechanism of the catalytic transesterification. This journal is

DI(METH)ACRYLATES

-

, (2008/06/13)

The present invention relates to di(meth)acrylate which is useful as a UV light or electron ray curing coating agent, etc., represented by the following general formula (I). (wherein, R1and R2are the same or different and represent a hydrogen atom or CH3, and R3and R4are the same or different and represent lower alkyl of 1~6 carbon atoms). The di(meth)acrylate of the present invention is easily cured to provide a cured product having superior toughness and flexibility.

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