CAS 13080-86-9
:2,2-Bis[4-(4-aminophenoxy)phenyl]propane
Description:
2,2-Bis[4-(4-aminophenoxy)phenyl]propane, commonly known as BPAF (Bisphenol A F), is an organic compound characterized by its structure, which features two phenolic groups linked by a propane bridge. This compound is a type of bisphenol and is primarily used in the production of polycarbonate plastics and epoxy resins. BPAF exhibits properties such as high thermal stability and resistance to chemical degradation, making it suitable for various industrial applications. It is also known for its potential endocrine-disrupting effects, similar to its more widely known counterpart, Bisphenol A (BPA). BPAF can interact with estrogen receptors, raising concerns regarding its safety and environmental impact. In terms of physical properties, it is typically a solid at room temperature and may have varying solubility in organic solvents. Due to its structural similarities to other bisphenols, BPAF is often studied for its toxicological effects and regulatory implications in consumer products. As awareness of chemical safety increases, the use and regulation of BPAF are under scrutiny in many regions.
Formula:C27H26N2O2
InChI:InChI=1S/C27H26N2O2/c1-27(2,19-3-11-23(12-4-19)30-25-15-7-21(28)8-16-25)20-5-13-24(14-6-20)31-26-17-9-22(29)10-18-26/h3-18H,28-29H2,1-2H3
InChI key:InChIKey=KMKWGXGSGPYISJ-UHFFFAOYSA-N
SMILES:C(C)(C)(C1=CC=C(OC2=CC=C(N)C=C2)C=C1)C3=CC=C(OC4=CC=C(N)C=C4)C=C3
Synonyms:- 2,2'-Bis(4-aminophenoxyphenyl)propane
- 2,2-Bis[4-(4-aminophenoxy)phenyl]propane
- 2,2-Bis[p-(4-aminophenoxy)phenyl]propane
- 4,4'-(4,4'-Isopropylidenediphenyl-1,1'-diyldioxy)
- 4,4′-Propane-2,2-diylbis(4,1-phenyleneoxy)dianiline
- 4,4′-[(1-Methylethylidene)bis(4,1-phenyleneoxy)]bis[benzenamine]
- 4,4′-[Isopropylidenebis(1,4-phenylene)dioxy]dianiline
- 4-[4-[2-[4-(4-Aminophenoxy)phenyl]propan-2-yl]phenoxy]benzenamine
- Aniline, 4,4′-[isopropylidenebis(p-phenyleneoxy)]di-
- Bapp
- Benzenamine, 4,4′-[(1-methylethylidene)bis(4,1-phenyleneoxy)]bis-
- Bisphenol A bis(4-aminophenyl) ether
- Cheminox CLP 5250
- Clp 5250
- Norcure 1313-50
- See more synonyms
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Found 7 products.
2,2-Bis[4-(4-aminophenoxy)phenyl]propane
CAS:Formula:C27H26N2O2Purity:>98.0%(T)(HPLC)Color and Shape:White - Yellow Solid FormMolecular weight:410.522,2-Bis[4-(4-aminophenoxy)phenyl]propane, 98%
CAS:<p>It is applied in pharmaceutical industry. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a </p>Formula:C27H26N2O2Purity:98%Molecular weight:410.52Benzenamine, 4,4'-[(1-methylethylidene)bis(4,1-phenyleneoxy)]bis-
CAS:Formula:C27H26N2O2Purity:97%Color and Shape:SolidMolecular weight:410.50754,4'-(4,4'-Isopropylidenediphenyl-1,1'-Diyldioxy)Dianiline
CAS:4,4'-(4,4'-Isopropylidenediphenyl-1,1'-Diyldioxy)DianilinePurity:98%Molecular weight:410.51g/mol2,2-Bis[4-(4-aminophenoxy)phenyl]propane
CAS:Purity:>98.0%Color and Shape:SolidMolecular weight:410.51699829101562,2-Bis[4-(4-aminophenoxy)phenyl]propane
CAS:<p>2,2-Bis[4-(4-aminophenoxy)phenyl]propane is a monomer that is used in the production of polyurethanes. It has a number of alkyl substituents, including chloride, which are removed during the process. 2,2-Bis[4-(4-aminophenoxy)phenyl]propane reacts with chlorides to form hydrochloric acid and 2,2-bis(4-hydroxyphenyl)propane. The reaction time depends on the concentration of chloride and can be determined by gel permeation chromatography. This monomer has been shown to have a kinetic data that is dependent on temperature, as well as magnetic resonance spectroscopy and proton NMR data. The product also exhibits an increase in thermal expansion when compared to other monomers.</p>Formula:C27H26N2O2Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:410.51 g/mol






