Bisphenol A

• CAT Number: R011123
• CAS Number: 80-05-7
• Molecular Formula: C15H16O2
• Molecular Weight: 228.29
• Purity: ≥95%
• Synonyms: 4,4’-(1-Methylethylidene)bisphenol; 2,2-Bis(4-hydroxyphenyl)propane; BPA; (4,4’-Dihydroxydiphenyl)dimethylmethane; 4,4’-Isopropylidenediphenol; 4,4’-Methylethylidenebisphenol; Dian; Diano; Diphenylolpropane; HT 3082; Parabis; p,p’-Bisphenol A
• Target: Endogenous Metabolite
• Storage: 2°C to 8°C
• IUPAC Name: 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol
• InChI: InChI=1S/C15H16O2/c1-15(2,11-3-7-13(16)8-4-11)12-5-9-14(17)10-6-12/h3-10,16-17H,1-2H3
• InChIKey: IISBACLAFKSPIT-UHFFFAOYSA-N
• SMILES: CC(C)(C1=CC=C(C=C1)O)C2=CC=C(C=C2)O

Bisphenol A (Cat No.:R011123) is an industrial chemical used primarily in the production of polycarbonate plastics and epoxy resins. Structurally, it features two phenol groups connected by a propane bridge, providing strength and durability to plastic materials. BPA is commonly found in consumer products such as water bottles, food containers, and the inner linings of metal cans. Due to its estrogen-mimicking properties, BPA has raised health concerns related to endocrine disruption, prompting regulatory scrutiny. It typically appears as a white solid, soluble in organic solvents, and requires controlled use in sensitive applications.

Reference

1.Krishnan, Aruna V., et al. "Bisphenol-A: an estrogenic substance is released from polycarbonate flasks during autoclaving." Endocrinology 132.6 (1993): 2279-2286.
2.Ben-Jonathan, Nira, and Rosemary Steinmetz. "Xenoestrogens: the emerging story of bisphenol A." Trends in Endocrinology & Metabolism 9.3 (1998): 124-128.
3.Petersen, H., et al. "Determination of bisphenol A diglycidyl ether (BADGE) and its derivatives in food: identification and quantification by internal standard." European Food Research and Technology 216.4 (2003): 355-364.