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Usage

Uses

Used in Coatings Industry:
Bisphenol A diacrylate is used as a key ingredient in the production of coatings for its high reactivity and ability to form strong crosslinked polymers, which contribute to the durability and performance of the coatings.
Used in Adhesives Industry:
In the adhesives industry, Bisphenol A diacrylate serves as a critical component due to its capacity to create robust crosslinked structures, enhancing the adhesive's bonding strength and stability.
Used in Polymer Materials:
Bisphenol A diacrylate is utilized in the creation of various polymer materials, leveraging its reactivity to produce polymers with specific properties tailored for different applications.
Used in Paints and Inks Industry:
Bisphenol A diacrylate is employed as a vital component in the formulation of paints and inks, where its reactivity and crosslinking ability contribute to the quality and performance of these products, including their color stability, drying time, and resistance to wear.
Used in Dental Materials:
In the dental industry, Bisphenol A diacrylate is used in the development of dental materials such as fillings and restorative resins, capitalizing on its properties to create strong, durable, and long-lasting dental restorations.
Despite its widespread use, the potential health and environmental risks associated with Bisphenol A diacrylate have prompted the exploration of alternative chemicals that can offer similar functionality without the associated concerns.

Upstream product

• 80-05-7 BPA 
• 814-68-6 acryloyl chloride 

Relevant academic research and scientific papers

Effective biobased phosphorus flame retardants from starch-derived bis-2,5-(hydroxymethyl)furan

A series of biobased phosphorus flame retardants has been prepared by converting starch-derived bis-2,5-(hydroxymethyl)furan to the corresponding diacrylate followed by Michael addition of phosphite to generate derivatives with phosphorus moieties attache

METHOD FOR PRODUCING AROMATIC ESTER

PROBLEM TO BE SOLVED: To provide a method for producing a high-purity aromatic ester in a high yield without using an aqueous medium as a reaction solvent. SOLUTION: This method for producing the aromatic ester comprises reacting an organic carboxylic acid halide with a phenol in the presence of a Lewis acid in an organic solvent. The concrete example of a preferable Lewis acid is a zinc compound such as zinc chloride, zinc bromide, zinc acetate, an aluminum compound such as aluminum chloride, aluminum bromide, diethylaluminum chloride, a boron compound such as boron trifluoride, boron trichloride, a titanium compound such as titanium tetrachloride, a zirconium compound such as zirconium chloride, and a tin compound such as tin tetrachloride, tin trichloride. A (meth)acrylic acid halide is preferable as the organic carboxylic acid halide.

Fungicidal use of diphenyl esters of alkylenes

The alkylene diphenyl ester compounds having the formula STR1 wherein halo is fluorine, chlorine or bromine; R is a radical having not more than 4 carbon atoms, selected from the group consisting of alkenyl, haloalkenyl and haloalkyl; R1 and R2 are each independently hydrogen or methyl; X is hydroxy or the radical RCOO--; m has a value of from 0 to 2; n has a value of from 0 to 6; w and p have values of 0 or 1, except that w is 1 when n is zero; the application of said compounds to plant in amounts sufficient to control fungi infestation and application of mixtures of said compounds to plants.