2,2-Bis(3-amino-4-hydroxylphenyl)propane(BAP) - ≥97%(HPLC)(T) , CAS No.1220-78-6

CAS: 1220-78-6 Cat. No.: B152476 Peso molecular: 258.32 Número EC: 807-962-8

GRADE & PURITY ≥97%(HPLC)(T)

Synonyms

4,4'-Isopropylidenebis(2-aminophenol) | 2,2-bis(3-amino-4-hydroxylphenyl)propane | FT-0651584 | 2,2-Bis(3-amino-4-hydroxylphenyl)propane (BAP) | SR-01000197740 | AC-9177 | 2,2-Bis-(3-amino-4-hydroxyphenyl)propane | 2,2-bis(3-amino-4-hydroxyphenyl)propane

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

4, 4'-Isopropylidenebis(2-aminophenol) | 2, 2-bis(3-amino-4-hydroxylphenyl)propane | FT-0651584 | 2, 2-Bis(3-amino-4-hydroxylphenyl)propane (BAP) | SR-01000197740 | AC-9177 | 2, 2-Bis-(3-amino-4-hydroxyphenyl)propane | 2, 2-bis(3-amino-4-hydroxyphenyl)propane

Especificaciones y pureza

≥97%(HPLC)(T)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥97%(HPLC)(T)

Nombres e identificadores

• Pubchem Sid: 488188727
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188727
• Sonrisas canónicas: CC(C)(C1=CC(=C(C=C1)O)N)C2=CC(=C(C=C2)O)N
• IUPAC Name: 2-amino-4-[2-(3-amino-4-hydroxyphenyl)propan-2-yl]phenol
• InChIKey: UHIDYCYNRPVZCK-UHFFFAOYSA-N
• INCHI: 1S/C15H18N2O2/c1-15(2,9-3-5-13(18)11(16)7-9)10-4-6-14(19)12(17)8-10/h3-8,18-19H,16-17H2,1-2H3
• Isómeros SMILES: CC(C)(C1=CC(=C(C=C1)O)N)C2=CC(=C(C=C2)O)N
• Peso molecular: 258.32
• Reaxy-Rn: 1983742
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1983742&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Diphenylmethanes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Diphenylmethanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Bisphenols
• Alternative Parents: Phenylpropanes o-Aminophenols Aniline and substituted anilines 1-hydroxy-2-unsubstituted benzenoids Primary amines Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Bisphenol - Phenylpropane - Aminophenol - O-aminophenol - Aniline or substituted anilines - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Amine - Primary amine - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as bisphenols. These are methylenediphenols, HOC6H4CH2C6H4OH, commonly p,p-methylenediphenol, and their substitution products (generally derived from condensation of two equivalent amounts of a phenol with an aldehyde or ketone).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in Dimethylformamide
• Punto de ebullición (°C): 471°C at 760 mmHg
• Punto de fusión (°C): 250℃
• Peso molecular: 258.320 g/mol
• XLogP3: 2.600
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 258.137 Da
• Monoisotopic Mass: 258.137 Da
• Topological Polar Surface Area: 92.500 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 281.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Siyao Wang, Jingfa Zhang, Yongchao Sun, Fangxu Fan, Qizheng Zhao, Gaohong He, Canghai Ma.  (2025)  Thermally rearranged polyimide membranes incorporating triptycenes for improved CO2 capture and hydrogen separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.132302]

2. Shuxin Wang, Hui Li, Gen Zhou, Jingmei Xu, Baoju Li, Xiangzi Wei, Zhe Wang.  (2025)  Bifunctional Sulfonatocalix[4]arene-MOF Fillers Enhance Proton Conductivity of Sulfonated Poly(Arylene Ether Ketone Sulfone) Membranes for Fuel Cells.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.5c07035]