Anthraquinone allergenic dispersed dye as well as extraction method and application thereof
A purification method and technology for disperse dyes, applied in the field of anthraquinone sensitizing disperse dyes, can solve the problems of low purity and the like
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Embodiment 1
[0024] Take Waters Xterra C 18 (5μm, 19×100mm) chromatographic column; mobile phase is methanol: water (70:30) and linearly changes to methanol: water (95:5) in 8 minutes; detection wavelength is 570nm; flow rate is 12ml / min.
[0025] Dissolve 50ml with methanol: water (70:30) and dissolve 5g of Disperse Blue 1 commercial dye, filter, inject 5ml each time, collect the effluent of 4.5min-5.9min, evaporate the collected solution to dryness, and obtain 100mg of solid, after analysis, The purity is 98.9%.
Embodiment 2
[0027] Take Waters Xterra C 18 (5μm, 19×100mm) chromatographic column; the mobile phase is methanol: water (80:20) and linearly changes to methanol: water (95:5) in 8 minutes; the detection wavelength is 570nm; the flow rate is 28ml / min.
[0028] Dissolve 5g of Disperse Red 11 commercial dye with 50ml of methanol: water (80:20), filter, inject 5ml each time, collect the effluent of 4.0min-4.9min, evaporate the collected solution to dryness, and obtain 90mg of solid. After analysis, the purity 99.3%.
Embodiment 3
[0030] Take Agilent Eclipse XDB C 18 (5 μm, 21.2 × 100mm) chromatographic column; mobile phase is methanol: water (85: 15) and linearly changes to methanol: water (95: 5) in 8 minutes; detection wavelength is 570nm; flow rate is 24ml / min.
[0031] Use methanol: water (85: 15) 60ml to dissolve 5g of disperse blue 35 commercial dye, filter, inject 5ml each time, collect the effluent at 3.5min-4.5min, evaporate the collected solution to dryness, and obtain 70mg of solid. After analysis, The purity is 99.9%.
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