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Addition of further Bisphenol A and a catalyst and heat can produce Bisphenol A glycidyl ether epoxy resins of higher molecular weight that are solid. [8] Structure of bisphenol-A diglycidyl ether epoxy resin: n denotes the number of polymerized subunits and is typically in the range from 0 to 25
Tetrabromobisphenol A diglycidyl ether is an epoxy resin consisting of tetrabromobisphenol A with ether linkages to two epichlorohydrin groups. An alernative structural comparison is as brominated form of bisphenol A diglycidyl ether. It is a brominated aromatic chemical used principally for giving flame retardant properties to materials. [1]
Hexion offers resins for a wide range of applications like Abrasives, Adhesives, Chemical Intermediates, Civil Engineering, Coatings, Composites, Crop Protection, Electrical/Electronics, Engineered Wood, Fertilizers and Pesticides, Fibers and Textiles, Foams, Friction Materials, Furniture, Molding Compounds, Oilfield, Oriented Strand Board ...
Exceptions include bisphenol S, P, and M. "Bisphenol" is a common name; the letter following denotes the variant, which depends on the additional substituents. Bisphenol A is the most popular representative of the group, with millions of metric tons produced globally in the past decade, often simply called "bisphenol".
About 25–30% of all BPA is used in the manufacture of epoxy resins and vinyl ester resins. [9] [10] For epoxy resin, it is first converted to its diglycidyl ether (usually abbreviated BADGE or DGEBA). [44] [45] This is achieved by a reaction with epichlorohydrin under basic conditions. Some of this is further reacted with methacrylic acid to ...
Bis-GMA (bisphenol A-glycidyl methacrylate) is a resin commonly used in dental composite, dental sealants. [1] [2] and dental cement. It is the diester derived from methacrylic acid and the bisphenol A diglycidyl ether. Bearing two polymerizable groups, it is prone to form a crosslinked polymer that is used in dental restorations. [3]
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