2944-29-8

Basic information

• Product Name: 1,4-bis((4-aminophenyl)amino)anthrancene-9,10-dione
• Synonyms: 1,4-bis((4-aminophenyl)amino)anthrancene-9,10-dione
• CAS NO: 2944-29-8
• Molecular Weight: 420.47
• Mol File: 2944-29-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,4-bis((4-aminophenyl)amino)anthrancene-9,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-bis((4-aminophenyl)amino)anthrancene-9,10-dione(2944-29-8)
• EPA Substance Registry System: 1,4-bis((4-aminophenyl)amino)anthrancene-9,10-dione(2944-29-8)

Safety Data

• Hazardous Substances Data: 2944-29-8(Hazardous Substances Data)

Upstream product

• 81-64-1 1,4-dihydroxy-9,10-anthracenedione 
• 75508-31-5 N,N'-(((9,10-dioxo-9,10-dihydroanthracene-1,4-diyl)bis(azanediyl))bis(4,1-phenylene))diacetamide 
• 17648-03-2 9,10-Dihydroxy-2,3-dihydro-anthracene-1,4-dione 

Relevant articles and documents

A new kind of H-acid monoazo-anthraquinone reactive dyes with surprising colour

A new kind of reactive dyes containing both monoazo and anthraquinone chromophores was obtained by using 1,4-bis((4-aminophenyl)amino)anthrancene- 9,10-dione as diazo component and 1-amino-8-naphthol-3,6-disulfonicacid (H-acid) derivatives as coupling components. The dyes were characterized by UV-Vis, IR, MS, 1H NMR and 13C NMR. The results showed that the maximum absorption wavelengths of the dyes were all about 590 nm, which indicated that they were a kind of blue dyes. 1H NMR and 13C NMR results revealed that there were two kinds of tautomerisms in dye structure and a new conjugated system formed between the anthraquinone ring and the phenyl azo linkage. Density functional theory (DFT) calculations also proved the formation of the new larger conjugated system from which the blue colour was generated. The fixations of the dyes on cotton were over 88% and the light fastness reached 5 grade.