37353-75-6

Name	Bisphenol A bis(2-hydroxypropyl) ether
Synonyms	BISPHENOL A PROPOXYLATE propoxylated bisphenol a nylene]bis[omega-hydroxy- Bisphenol A bis(2-hydroxypropyl) ether 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
CAS	37353-75-6

Risk Codes	R36/38 - Irritating to eyes and skin. R51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. R38 - Irritating to the skin
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets.
UN IDs	UN 3082 9 / PGIII
WGK Germany	3

LogP	3.62
EPA chemical information	Information provided by: ofmpub.epa.gov (external link)
application	bisphenol A polyether polyol including bisphenol A polyoxypropylene ether accounts for a large proportion in the field of synthetic resins. In resin synthesis, it can be used not only as a monomer for resin synthesis, but also as an additive and modifier for epoxy resins, pigment coatings and other polymer chains. Because bisphenol A polyether polyol molecules contain aromatic rings, the difference in chemical bond energy will lead to more stable structure and better performance of the synthesized resin. In the synthesis of surfactants, surfactants with specific properties are often prepared as matrix intermediates.
Effect	The aromatic ring and carbon-oxygen chain structure in the bisphenol A polyether polyol molecule give the material specific rigidity and toughness, thereby effectively improving the polymer The structure and properties of the resin can make the synthesized resin structure more stable and better in performance. It can be made into seismic materials, photosensitive materials, adhesive materials, etc., and has broad application prospects. Bisphenol A terminal hydroxyl group is replaced by an epoxy compound and initiates a chain reaction. The chain reaction group can be one or more of ethylene oxide, propylene oxide, epichlorohydrin, and ethylene carbonate.

Last Update：2024-04-09 20:52:54

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37353-75-6

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