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58557-51-0

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58557-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58557-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58557-51:
(7*5)+(6*8)+(5*5)+(4*5)+(3*7)+(2*5)+(1*1)=160
160 % 10 = 0
So 58557-51-0 is a valid CAS Registry Number.

58557-51-0Downstream Products

58557-51-0Relevant academic research and scientific papers

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

Shan, Bin,Tong, Xing,Xiong, Wei,Qiu, Wenzhu,Tang, Bingtao,Lu, Rongwen,Ma, Wei,Luo, Yi,Zhang, Shufen

, p. 44 - 54 (2015/09/01)

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.

Synthesis and evaluation of technical properties of novel cationic mono-s-chloro triazinyl (MCT) reactive dyes on cotton

Javadi, Marzieh S.,Mokhtari, Javad

experimental part, p. 793 - 801 (2012/08/28)

Two novel cationic mono-s-chloro triazinyl (MCT) reactive dyes together with their analogues were synthesized via reacting an N,N-dimethyl dodecylamine with p-nitrobenzyl bromide. The resultant was reduced using stannous chloride and hydrochloric acid to produce the primary amine. The quaternary ammonium salt containing primary amine was then diazotized and coupled to H-acid/J-acid reacted with cyanuric chloride and sulfanilic acid. The analogue dyes were prepared via the same route without quaternary ammonium salt making stage. The dyes were characterized using FTIR, 1H NMR, UV-Vis spectroscopy and elemental analysis. The substantivity, exhaustion and fixation of the dyes were investigated on cotton fabric. It was found that these functional dyes could be effectively introduced to cotton for achieving simultaneous coloration and functional finishing effects. All the dyed fabrics exhibited softening efficacy. The washing and light fastness of the dyed samples were further studied.

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