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2425-01-6

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2425-01-6 Usage

Description

1,4-BIS(GLYCIDYLOXY)BENZENE, also known as 2,2''-[1,4-Phenylenebis(oxymethylene)]dioxirane, is an organic compound characterized by its epoxide structure. It possesses unique chemical properties due to the presence of the epoxide group, which allows it to participate in various chemical reactions and form different derivatives. 1,4-BIS(GLYCIDYLOXY)BENZENE has been found to have potential applications in various industries, particularly due to its fungicidal activity.

Uses

Used in Agricultural Industry:
1,4-BIS(GLYCIDYLOXY)BENZENE is used as a fungicide for its fungicidal activity against Phytophthora infestans, a pathogen responsible for causing significant damage to crops. The compound's ability to inhibit the growth and development of this pathogen makes it a valuable tool in protecting agricultural produce and maintaining crop yields.
Used in Chemical Synthesis:
1,4-BIS(GLYCIDYLOXY)BENZENE can be used as a building block or intermediate in the synthesis of various chemical compounds, including polymers, resins, and other specialty chemicals. Its epoxide functionality allows for a wide range of reactions, such as ring-opening reactions with amines, thiols, and alcohols, which can lead to the formation of new products with diverse applications.
Used in Composite Materials:
The compound's ability to form covalent bonds with other molecules makes it a potential candidate for use in the development of composite materials. These materials can exhibit enhanced mechanical, thermal, and chemical properties compared to their individual components, making them suitable for various applications, such as in the automotive, aerospace, and construction industries.
Used in Adhesives and Sealants:
Due to its reactive epoxide group, 1,4-BIS(GLYCIDYLOXY)BENZENE can be used as a component in the formulation of adhesives and sealants. These products can provide strong, durable bonds between different materials, making them useful in various applications, such as in construction, automotive, and electronics industries.
Used in Coatings:
The compound's chemical reactivity and ability to form cross-linked structures can make it a valuable component in the development of coatings with improved properties, such as increased durability, chemical resistance, and adhesion. These coatings can be applied in various industries, including automotive, aerospace, and marine, to protect surfaces from environmental factors and wear.

Check Digit Verification of cas no

The CAS Registry Mumber 2425-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2425-01:
(6*2)+(5*4)+(4*2)+(3*5)+(2*0)+(1*1)=56
56 % 10 = 6
So 2425-01-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4/c1-2-10(14-6-12-8-16-12)4-3-9(1)13-5-11-7-15-11/h1-4,11-12H,5-8H2/t11-,12-/m1/s1

2425-01-6 Well-known Company Product Price

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  • Alfa Aesar

  • (B20628)  1,4-Bis(glycidyloxy)benzene, 97%   

  • 2425-01-6

  • 1g

  • 296.0CNY

  • Detail
  • Alfa Aesar

  • (B20628)  1,4-Bis(glycidyloxy)benzene, 97%   

  • 2425-01-6

  • 5g

  • 1177.0CNY

  • Detail
  • Alfa Aesar

  • (B20628)  1,4-Bis(glycidyloxy)benzene, 97%   

  • 2425-01-6

  • 25g

  • 4721.0CNY

  • Detail

2425-01-6SDS

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 2-[[4-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane

1.2 Other means of identification

Product number -
Other names 2,2'-p-phenylenedioxydimethyl-bis-oxirane

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:2425-01-6 SDS

2425-01-6Relevant articles and documents

Epoxy thermosets from model mixtures of the lignin-to-vanillin process

Fache,Boutevin,Caillol

, p. 712 - 725 (2016/02/12)

Epoxy thermosets were prepared from mixtures of phenolics modelling the product stream of the lignin-to-vanillin process. Vanillin is one of the only mono-aromatic compounds produced on an industrial scale from lignin. This process leads to mixtures of phenolic compounds. Isolation of pure vanillin is costly both economically and environmentally. The present work demonstrates that these purification steps are not necessary in order to prepare high-performance epoxy thermosets from biomass. Model mixtures of depolymerization products of lignins from both softwood and hardwood were prepared. These mixtures were subjected in a first step to a Dakin oxidation in order to increase their phenolic functionality. In the second step, they were glycidylated to obtain mixtures of epoxy monomers. Each of the components of the mixtures was individually subjected to the same reactions to provide further insights on their reactivity. Epoxy thermosets were conveniently prepared from these epoxy monomer mixtures. These potentially bio-based epoxy thermosets displayed outstanding thermo-mechanical properties while avoiding environmentally damaging purification steps. Thus, their production could advantageously be integrated in a biorefinery as a high value added product from lignin processing.

Synthesis of novel poly(hydroxyether terephthalate) via polyaddition of 2,5-difluoroterephthalic acid with aromatic bis(epoxide)s

Huang, Xiao-Song,Qing, Feng-Ling

experimental part, p. 1076 - 1082 (2009/04/07)

A novel and more reliable synthetic route to 2,5-difluoroterephthalic acid was developed. A series of new poly(hydroxyether terephthalate) were prepared by the polyaddition of 2,5-difluoroterephthalic acid with various aromatic bis(epoxide)s catalyzed by tetrabutyl ammonium bromide.

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