Informação sobre produto
- Phenol
- 4,4'-(1-methylpropylidene)bis-
- Phenol
- 4,4'-sec-butylidenedi- (6CI,7CI,8CI)
- 4,4'-(1-Methylpropylidene)bis[phenol]
- 2,2-Bis(4-hydroxyphenyl)butane
- 2,2-Bis(p-hydroxyphenyl)butane
- 4,4'-Dihydroxy-2,2-diphenylbutane
- 4,4'-sec-Butylidenediphenol
- Bis(4-hydroxyphenyl)methylethylmethane
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- Butane
- 2,2-bis(4-hydroxyphenyl)-
- NSC 1775
- p,p'-Dihydroxy-2,2-diphenylbutane
- p,p'-sec-Butylidenediphenol
- 2,2-Bis(4-Hydroxy phenyl)butane
- 2,2-Bis(4-Hydroxy phenyl)butane (Bisphenol B)
- 2,2-Bis(4-Hydroxyphenyl)Butane
- 2,2-Bis(P-Hydroxyphenyl)Butane
- 4,4'-(1-Methylpropylidene)Bisphenol
- 4,4'-Butane-2,2-Diyldiphenol
- 4,4′-(1-Methylpropylidene)bis[phenol]
- 4,4′-Dihydroxy-2,2-diphenylbutane
- 4,4′-sec-Butylidenediphenol
- Butane, 2,2-bis(4-hydroxyphenyl)-
- P,P'-Sec-Butylidenediphenol
- Phenol, 4,4′-(1-methylpropylidene)bis-
- Phenol, 4,4′-sec-butylidenedi-
Applications Bisphenol B is the analogue of Bisphenol A (B519495), which is used to make certain plastic an epoxy resins. BPA and its analogs, are also shown to activate human pregnane X receptor (PXR), a nuclear receptor that functions as a master regulator of xenobiotic metabolism.
References Yipeng, S., et al.: Env Hea. Pers., 120, 399 (2012); Krishnan, A.V., et al.: Endocrinology, 132, 2279 (1993); Steinmetz, R., et al.: Trends Endocrinol. Metab., 9, 124 (1998); Petersen, H., et al.: Eur. Food Res. Technol., 216, 355 (2003);
Propriedades químicas
Consulta técnica sobre: TR-B519565 Bisphenol B
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