2425-01-6

Usage

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.

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

Upstream product

• 123-31-9 hydroquinone 
• 106-89-8 epichlorohydrin 
• 93-59-4 Perbenzoic acid 
• 67-66-3 chloroform 
• 37592-20-4 1,4-bis(allyloxy)benzene 

Downstream Products

• 34972-11-7 3,3'-di-morpholin-4-yl-1,1'-p-phenylenedioxy-bis-propan-2-ol 
• 34972-12-8 p-Bis(3-tert-butylthio-2-hydroxypropoxy)benzol 
• 34972-13-9 1-[4-(2-Hydroxy-3-phenylsulfanyl-propoxy)-phenoxy]-3-phenylsulfanyl-propan-2-ol 
• 7734-54-5 3,3'-(1,4-phenylenebis(oxy))bis(propane-1,2-diol) 
• 15129-28-9 1,4-bis-(3-chloro-2-hydroxy-propoxy)-benzene 

Relevant academic research and scientific papers

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

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.

TACN-based oligomers with aromatic backbones for efficient nucleic acid delivery

Cationic oligomers with a rigid aromatic backbone were first applied as non-viral gene delivery vectors. These materials showed better DNA condensation ability than their flexible analogues. In vitro transfection experiments revealed that the materials with more rigid backbone exhibited considerably higher TE and lower cytotoxicity than 25 kDa PEI. This journal is the Partner Organisations 2014.

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

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.