| Identification | Back Directory | [Name]
Propoxylated Bisphenol A | [CAS]
37353-75-6 | [Synonyms]
BISPHENOL A PROPOXYLATE
propoxylated bisphenol a
nylene]bis[omega-hydroxy-
bisphenolapropoxylate(1po/phenol)
poly[oxy(methyl-1,2-ethanediyl)],alpha,alpha’-[(1-methylethylidene)di-4,1-phe
Polyoxy(methyl-1,2-ethanediyl), .alpha.,.alpha.-(1-methylethylidene)di-4,1-phenylenebis.omega.-hydroxy-
2-ethanediyl)],.alpha.,.alpha.’-[(1-methylethylidene)di-4,1-phenylene]bis[.omega.-hydroxy-Poly[oxy(methyl-1 | [EINECS(EC#)]
500-097-4 | [Molecular Formula]
C21H28O4 | [MDL Number]
MFCD00191826 | [MOL File]
37353-75-6.mol | [Molecular Weight]
344.44 |
| Hazard Information | Back Directory | [Uses]
Propoxylated Bisphenol A is used as bisphenol A polyether polyols, including bisphenol A polyoxypropylene ether, account for a significant proportion in the field of synthetic resins. In resin synthesis, it serves not only as a monomer but also as an additive and modifier for epoxy resins, pigments, coatings, and other polymer chains. Because bisphenol A polyether polyol molecules contain aromatic rings, differences in chemical bond energies lead to more stable resin structures and superior performance. In surfactant synthesis, it is frequently used as a skeletal intermediate to prepare surfactants with specific properties. | [Definition]
ChEBI: Bisphenol A bis(2-hydroxypropyl) ether is a diarylmethane. | [Flammability and Explosibility]
Nonflammable |
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