4131-03-7

Basic information

• Product Name: 3,3',4,4'-Tetramethoxybenzophenone
• Synonyms: 3,3',4,4'-Tetramethoxybenzophenone;bis(3,4-diMethoxyphenyl)Methanone
• CAS NO: 4131-03-7
• Molecular Formula: C₁₇H₁₈O₅
• Molecular Weight: 302.3218
• Mol File: 4131-03-7.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 456.4°Cat760mmHg
• Flash Point: 202°C
• Appearance: /
• Density: 1.147g/cm³
• Vapor Pressure: 1.62E-08mmHg at 25°C
• Refractive Index: 1.54
• CAS DataBase Reference: 3,3',4,4'-Tetramethoxybenzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3',4,4'-Tetramethoxybenzophenone(4131-03-7)
• EPA Substance Registry System: 3,3',4,4'-Tetramethoxybenzophenone(4131-03-7)

Safety Data

• Hazardous Substances Data: 4131-03-7(Hazardous Substances Data)

Usage

General Description

3,3',4,4'-Tetramethoxybenzophenone is a type of benzophenone derivative that is commonly used as a photoinitiator in the production of photopolymers and UV-curable coatings. It is a clear, colorless solid that is insoluble in water but soluble in organic solvents such as ethanol and acetone. This chemical is known for its ability to absorb UV light and initiate the polymerization process in UV-curable materials, making it an important component in the manufacture of adhesives, inks, and coatings. Its photoinitiating properties also make it useful in the production of dental composites and optical materials. Additionally, it has antioxidant and UV-absorbing properties, making it valuable in sunscreens and other cosmetic formulations. Overall, 3,3',4,4'-Tetramethoxybenzophenone is a versatile chemical with a wide range of industrial and commercial applications.

InChI:InChI=1/C17H18O5/c1-19-13-7-5-11(9-15(13)21-3)17(18)12-6-8-14(20-2)16(10-12)22-4/h5-10H,1-4H3

Upstream product

• 79-37-8 oxalyl dichloride 
• 91-16-7 1,2-dimethoxybenzene 
• 7249-36-7 2-(3,4-Dimethoxy-benzoyl)-4,5-dimethoxy-benzoic acid 
• 20153-24-6 2,2-bis(3,4-dimethoxyphenyl)acetic acid 
• 10547-58-7 4-hydroxy-3,3',4'-trimethoxy-benzophenone 
• 554-34-7 1,2-bis(3,4-dimethoxyphenyl)ethane-1,2-dione 
• 855287-22-8 tetrakis-(3,4-dimethoxy-phenyl)-ethane-1,2-diol 
• 3535-37-3 3,4-dimethoxybenzoic acid chloride 
• 93-07-2 Veratric acid 
• 7446-70-0 aluminium trichloride 
• 75-15-0 carbon disulfide 
• 7647-01-0 hydrogenchloride 
• 74084-26-7 3,3',4,4'-tetramethoxybenzhydrole 
• 64-19-7 acetic acid 

Downstream Products

• 854872-31-4 1,1-bis-(3,4-dimethoxy-phenyl)-propene 
• 5385-61-5 4,4'-(ethene-1,1-diyl)bis(1,2-dimethoxybenzene) 
• 102172-38-3 3,3-bis-(3,4-dimethoxy-phenyl)-acrylic acid 
• 102159-36-4 3-(3,4-dimethoxyphenyl)-5,6-dimethoxy-2-methyl-1H-inden-1-one 
• 856062-48-1 (3,4,3',4'-tetramethoxy-benzhydrylidene)-succinic acid-anhydride 
• 856065-30-0 (3,4,3',4'-tetramethoxy-benzhydrylidene)-succinic acid 
• 120553-10-8 3,3-bis(3,4-dimethoxyphenyl)propenal 
• 102520-61-6 1,1-bis(3,4-dimethoxyphenyl)-2-phenylbut-1-ene 
• 855287-22-8 tetrakis-(3,4-dimethoxy-phenyl)-ethane-1,2-diol 
• 241488-03-9 bis-(3,4-dimethoxy-phenyl)-[2-(2-methyl-[1,3]dioxolan-2-yl)-phenyl]-methanol 
• 1130428-28-2 2-bromo-3',4,4',5'-tetrahydroxydiphenylmethane 
• 1130428-30-6 2,2'-dibromo-4,4',5,5'-tetrahydroxydiphenylmethane 
• 1130428-33-9 2,2',3,3',6-pentabromo-4,4',5,5'-tetrahydroxydiphenylmethane 
• 1260233-95-1 2',5',6',5,6-pentabromo-3',4',3,4-tetramethoxybenzo-phenone 

Relevant articles and documents

New Dopa-AIE Compound Used as Fluorescence Sensor Material: Specificity and Quantification for Cu(II)

As a paramagnetic metal ion, Cu(II) is challenging to be detected by conventional fluorescence sensor because of its unselective paramagnetic quenching effects on common fluorophores. By combining catechol with tetraphenylethene, a typical aggregation-ind

A kind of LSD1 inhibitors and use thereof

The invention relates to novel LSD1 inhibitors and application of the LSD1 inhibitors in drugs, in particular to application of the LSD1 inhibitors in preparing LSD1-resistant inhibitor drugs, drugs for treating tumor, virus infectious diseases, hematolog

Process for producing ethylene/α-olefin copolymer

A process capable of producing an ethylene/α-olefin copolymer having a high molecular weight even under the conditions of a high polymerization temperature is provided. The process for producing an ethylene/α-olefin copolymer includes copolymerizing ethyl