3708-39-2

Basic information

• Product Name: 4,4'-BIS(METHYLAMINO)BENZOPHENONE
• Synonyms: 4,4'-BIS(METHYLAMINO)BENZOPHENONE;Bismethylaminobenzophenone;4,4''-BIS(METHYLAMINO)BENZOPHENONE 98+%
• CAS NO: 3708-39-2
• Molecular Formula: C₁₅H₁₆N₂O
• Molecular Weight: 240.3
• Product Categories: Benzophenones (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer Research
• Mol File: 3708-39-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: 133 °C
• Appearance: /
• CAS DataBase Reference: 4,4'-BIS(METHYLAMINO)BENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-BIS(METHYLAMINO)BENZOPHENONE(3708-39-2)
• EPA Substance Registry System: 4,4'-BIS(METHYLAMINO)BENZOPHENONE(3708-39-2)

Safety Data

• Hazardous Substances Data: 3708-39-2(Hazardous Substances Data)

Usage

General Description

4,4'-BIS(METHYLAMINO)BENZOPHENONE is a chemical compound commonly used as a UV stabilizer in various applications, such as in plastics, adhesives, and coatings. It is also used as a photoinitiator in the production of inks and photoresist formulations. 4,4'-BIS(METHYLAMINO)BENZOPHENONE is known for its ability to absorb and dissipate UV radiation, thereby protecting materials from degradation and extending their lifespan. Additionally, 4,4'-BIS(METHYLAMINO)BENZOPHENONE has been found to have potential photoprotective and antioxidant properties, making it a valuable ingredient in skincare products for protecting the skin from UV damage. However, it is important to handle this chemical with care, as it may pose health risks if not used appropriately.

Upstream product

• 90-94-8 bis(p-dimethylaminophenyl)methanone 
• 548-62-9 crystal violet 
• 57469-36-0 4,4'-bis-(cyano-methyl-amino)-benzophenone 

Downstream Products

• 57469-36-0 4,4'-bis-(cyano-methyl-amino)-benzophenone 

Relevant articles and documents

Acetic Acid Accelerated Visible-Light Photoredox Catalyzed N-Demethylation of N,N-Dimethylaminophenyl Derivatives

N,N-Dimethylaminophenyl moiety is a common fragment in medicinal chemistry as several pharmaceuticals bearing this privileged motif are on the market and under clinical evaluation. Oxidative N-demethylation is generally regarded as the major metabolic pathway. However, pharmacokinetics, metabolites studies as well as the further structural modification are precluded by the impracticality of chemical synthesis. Here we report that acetic acid can significantly accelerate visible-light photoredox catalyzed N-demethylation of N,N-dimethylaminophenyl derivatives. This approach is easy for large scale reaction and even for potential industrial manufacture. (Figure presented.).

Photocatalytic degradation of michler's ketone in water by Uv light illumination using TiO2 photocatalyst: Identification of intermediates and the reaction pathway

The TiO2/UV photocatalytic degradation ofMichler's Ketone (MK) has been investigated in aqueous heterogeneous suspensions. Results obtained show rapid and complete oxidation of MK after 24-h, and more than 97.5% of MK was mineralized after a 32-h exposure