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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
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