Bisphenol

The bisphenols are a group of chemical compounds with two hydroxyphenyl functionalities. Most of them are based on diphenylmethane. The exceptions are Bisphenol S, P, and M . "Bisphenol" is a common name, the following letter refers to one of the reactants. Bisphenol A is the most popular representative of this group, often called only "bisphenol".

Structural formula Name CAS Reactants Systematic name
Bisphenol A 80-05-7 Phenol Acetone 2,2-Bis(4-hydroxyphenyl)propane
Bisphenol AP 1571-75-1 Phenol Acetophenone 1,1-Bis(4-hydroxyphenyl)-1-phenyl-ethane
Bisphenol AF 1478-61-1 Phenol Hexafluoroacetone 2,2-Bis(4-hydroxyphenyl)hexafluoropropane
Bisphenol B 77-40-7 Phenol Butanone 2,2-Bis(4-hydroxyphenyl)butane
Bisphenol BP 1844-01-5 Phenol Benzophenone Bis-(4-hydroxyphenyl)diphenylmethane
Bisphenol C 79-97-0 Cresol Acetone 2,2-Bis(3-methyl-4-hydroxyphenyl)propane
Bisphenol C 14868-03-2 Phenol Dichloroketene Bis(4-hydroxyphenyl)-2,2-dichlorethylene
Bisphenol E Phenol Acetaldehyde 1,1-Bis(4-hydroxyphenyl)ethane
Bisphenol F 87139-40-0 Phenol Formaldehyde Bis(4-hydroxydiphenyl)methane
Bisphenol G 127-54-8 2-Isopropylphenol Acetone 2,2-Bis(4-hydroxy-3-isopropyl-phenyl)propane
Bisphenol M 13595-25-0 1,3-Bis(2-(4-hydroxyphenyl)-2-propyl)benzene
Bisphenol S 80-09-1 Phenol Sulfur trioxide Bis(4-hydroxyphenyl)sulfone
Bisphenol P 2167-51-3 1,4-Bis(2-(4-hydroxyphenyl)-2-propyl)benzene
Bisphenol PH 24038-68-4 2-Phenylphenol Acetone 5,5’ -(1-Methylethyliden)-bispropane
Bisphenol TMC 129188-99-4 Phenol 3,3,5-Trimethylcyclohexanone 1,1-Bis(4-hydroyphenyl)-3,3,5-trimethyl-cyclohexane
Bisphenol Z 843-55-0 Phenol Cyclohexanone 1,1-Bis(4-hydroxyphenyl)-cyclohexane

Other articles related to "bisphenol":

Bisphenol S - Occurrence and Toxicity
... Bisphenol S has become commonly used as a plasticizing agent following the widespread bans on the use of the related compound bisphenol A due to its estrogen-mimicking properties, and ... However, bisphenol S has been shown to have similar estrogenic activity to bisphenol A, and so its main advantage in these applications is merely that it ...
Weinberg Group - BPA Congressional Investigation
... Bart Stupak (D-MI) announced that their ongoing investigation into Bisphenol A (BPA) had broadened to include The Weinberg Group ... which Dingell chairs, asked the firm for records of its work on Bisphenol A and other chemicals ... Some studies indicate that Bisphenol A, which is present in a wide range of plastics, is an endocrine disruptor and "can disrupt hormone systems in ...
Epoxy Resin Chemistry - Bisphenol A Epoxy Resin
... most common and important class of epoxy resins is formed from reacting epichlorhydrin with bisphenol A to form diglycidyl ethers of bisphenol A ... two moles of epichlorhydrin with one mole of bisphenol A to form the bisphenol A diglycidyl ether (commonly abbreviated to DGEBA or BADGE) ... Increasing the ratio of bisphenol A to epichlorhydrin during manufacture produces higher molecular weight linear polyethers with glycidyl end groups, which are semi-solid to ...
Cyanate Ester
... Cyanate esters are chemical substances generally based on a bisphenol or novolac derivative, in which the hydrogen atom of the phenolic OH group is ... Bisphenol-A and novolac based cyanate esters are the major products, bisphenol-F and bisphenol-E are also used ... The aromatic ring of the bisphenol can be substituted with an allylic group for improved toughness of the material ...