63948-92-5

Basic information

• Product Name: 4,4-BIS(3-AMINOPHENOXY)BENZOPHENONE(3BABP)
• Synonyms: 4,4-BIS(3-AMINOPHENOXY)BENZOPHENONE(3BABP);4,4-BIS(3-AMINOPHENOXY)BENZOPHENONE;BABP;4,4-BIS(3-AMINOPHENO;Bis[4-(3-aMinophenoxy)phenyl] ketone;4,4'-Bis(3-aMinophenoxy)benzophenone(BABP);3-α-HSD3;AK1C2
• CAS NO: 63948-92-5
• Molecular Formula: C25H20N2O3
• Molecular Weight: 396.44
• EINECS: 1312995-182-4
• Product Categories: fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis
• Mol File: 63948-92-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 138-140 °C(Solv: ethanol (64-17-5))
• Boiling Point: 606 °C at 760 mmHg
• Flash Point: 241.1 °C
• Appearance: /
• Density: 1.265
• Storage Temp.: -20°C
• PKA: 4.11±0.10(Predicted)
• CAS DataBase Reference: 4,4-BIS(3-AMINOPHENOXY)BENZOPHENONE(3BABP)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-BIS(3-AMINOPHENOXY)BENZOPHENONE(3BABP)(63948-92-5)
• EPA Substance Registry System: 4,4-BIS(3-AMINOPHENOXY)BENZOPHENONE(3BABP)(63948-92-5)

Safety Data

• Hazardous Substances Data: 63948-92-5(Hazardous Substances Data)

Usage

General Description

4,4-Bis(3-aminophenoxy)benzophenone (3BABP) is a chemical compound that is used in the manufacturing of plastics, adhesives, and coatings. It is also used as a UV stabilizer in various plastic materials, helping to protect them from degradation caused by exposure to sunlight. 3BABP has been found to have potential health hazards, as it is considered a possible endocrine disruptor and has been associated with reproductive and developmental toxicity. It is important to handle and dispose of 3BABP and products containing it with caution to minimize exposure and potential health risks.

Upstream product

• 591-27-5 m-Hydroxyaniline 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 7440-44-0 pyrographite 

Relevant articles and documents

1,3,6-trialkylhexahydro-1,3,6-triazocine-2-on and preparation process thereof

The present invention relates to 1,3,6-Trialkylhexahydro-1,3,6-triazocine-2-on represented by the formula (1): STR1 wherein R is a C1 ?C8 alkyl group and a preparation process of the compound comprising reacting N,N',N"-trialkyldieth

Bis(3-aminophenoxy) aromatics and method of preparing the same

Bis(3-nitrophenoxy) derivatives of aromatic or bridged aromatic hydrocarbons are derived from m-dinitrobenzene and dihydroxy derivatives of said hydrocarbons and certain substituted derivatives thereof by a condensation reaction in dipolar aprotic solvents in the presence of bases. The bis(3-nitrophenoxy) derivatives and derivatives obtained are successively reduced to afford bis-(3-aminophenoxy)derivatives. This is a new method for reacting the dihydroxy-derivatives with m-dinitrobenzene, and hence can prepare novel bis(3-aminophenoxy) derivatives such as 4,4'-bis(3-amino-phenoxy)biphenyl, 1-[4-(3-aminophenoxy)phenyl]-1,3,3-trimethyl-6-(3-aminophenoxy)indan, 6,6'-bis(3-aminophenoxy)3,3,3',3'-tetramethyl-1,1'spirobiindan, and methyl substituted 2,2'-bis[4-(3-aminophenoxy)phenyl]propane.