964-68-1

Basic information

• Product Name: BENZOPHENONE-4,4'-DICARBOXYLIC ACID
• Synonyms: 4,4'-CARBONYLDIBENZOIC ACID;4,4'-DICARBOXYBENZOPHENONE;BENZOPHENONE-4,4'-DICARBOXYLIC ACID;4,4'-Carbonylbis(benzoic acid);4,4'-Carbonylbisbenzoic acid
• CAS NO: 964-68-1
• Molecular Formula: C₁₅H₁₀O₅
• Molecular Weight: 270.24
• EINECS: 1312995-182-4
• Product Categories: Aromatic Benzophenones & Derivatives (substituted);Benzophenones (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer Research
• Mol File: 964-68-1.mol
• Article Data: 7

Chemical Properties

• Melting Point: 365°C
• Boiling Point: 373.35°C (rough estimate)
• Flash Point: 291.1 °C
• Appearance: /
• Density: 1.3280 (rough estimate)
• Vapor Pressure: 2.97E-12mmHg at 25°C
• Refractive Index: 1.5000 (estimate)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.37±0.10(Predicted)
• CAS DataBase Reference: BENZOPHENONE-4,4'-DICARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: BENZOPHENONE-4,4'-DICARBOXYLIC ACID(964-68-1)
• EPA Substance Registry System: BENZOPHENONE-4,4'-DICARBOXYLIC ACID(964-68-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 964-68-1(Hazardous Substances Data)

Usage

General Description

Benzophenone-4,4'-dicarboxylic acid is an organic compound that belongs to the class of benzophenones, which are widely used in various industrial applications. It is commonly utilized as a chemical intermediate in the production of UV absorbers, as well as in the synthesis of pharmaceuticals, agrochemicals, and pigments. Benzophenone-4,4'-dicarboxylic acid is known for its ability to absorb ultraviolet radiation, making it a valuable ingredient in sunscreen and other sun protection products. It also serves as an effective photoinitiator in the polymerization of various materials, including plastics and coatings. Additionally, it is a key ingredient in the development of light-stable and weather-resistant materials used in the automotive and construction industries.

InChI:InChI=1/C15H10O5/c16-13(9-1-5-11(6-2-9)14(17)18)10-3-7-12(8-4-10)15(19)20/h1-8H,(H,17,18)(H,19,20)

Upstream product

• 4957-14-6 4,4'-dimethyldiphenylmethane 
• 58539-00-7 2,2-bis(4-methylphenyl)propionic acid 
• 106-42-3 para-xylene 
• 101-81-5 Diphenylmethane 
• 3988-03-2 bis(4-bromophenyl)methanone 
• 28537-93-1 1,1-di-p-tolyl-1-deoxy-D-glucitol 
• 14568-86-6 bis<4-(hydroxymethyl)phenyl>methane 
• 64-19-7 acetic acid 
• 790-82-9 bis(4-acetylphenyl)methane 
• 611-97-2 bis(p-methylphenyl)-methanone 
• 32446-66-5 4,4'-dicyanobenzophenone 
• 2919-20-2 1,1-di(p-tolyl)ethylene 
• 108-88-3 toluene 

Downstream Products

• 1211530-67-4 4,4'-carbonylbis(N-(2-(piperidin-1-yl)ethyl)benzamide) 
• 1176170-19-6 C₄₁H₄₀N₁₀O₅ 
• 1176170-21-0 C₃₇H₄₄N₁₀O₅ 
• 1176170-23-2 C₃₉H₄₈N₁₀O₅ 
• 1176170-25-4 C₃₇H₄₄N₁₀O₇ 
• 1797-82-6 diethyl 4,4'-benzophenonedicarboxylate 
• 500798-07-2 4,4'-dichloromethanediyl-di-benzoyl chloride 
• 145531-11-9 bis(4-tert-butoxycarbonylphenyl)methanone 
• 1233-73-4 Benzophenone-4,4'-dicarboxylic acid dimethyl ester 

Relevant articles and documents

Effect of functional group polarity on the antimalarial activity of spiro and dispiro-1,2,4-trioxolanes

Based on the structures of several lipophilic trioxolane antimalarial prototypes, we set out to determine which functional groups were associated with good antimalarial profiles and identify more polar (lower Log P/Log D) lead compounds with good physicoc

Optimized liquid-phase oxidation

Disclosed is an optimized process and apparatus for more efficiently and economically carrying out the liquid-phase oxidation of an oxidizable compound. Such liquid-phase oxidation is carried out in a bubble column reactor that provides for a highly effic

Synthesis and solubility properties of C60 fullerene derivatives bearing carboxy groups

Bis(4-tert-butoxycarbonylphenyl)diazomethanes have been prepared and treated with fullerene (C60) to give the corresponding 1,2-methano derivatives which upon hydrolysis with CF3CO2H gave the title compounds. The solubility of the latter in aqueous THF has been measured.