Trisazo compound, ink composition, and colored object
A compound, triazo technology, applied in the direction of triazo dyes, etc., can solve the problem of not fully meeting the requirements of ozone gas resistance, ozone gas resistance can not fully meet market requirements, can not fully meet market requirements and other problems , to achieve the effect of excellent discharge stability, good storage stability and good filterability
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Embodiment 1-1
[0110] After reacting 20.1 parts of 2-amino-5-naphthol-1,7-disulfonic acid and 12.6 parts of p-toluenesulfonyl chloride at pH 8.0 to 8.5 at 70° C. for 1 hour, the obtained product was salted out under acidity and filtered. 28.4 parts of the compound of formula (4) was dissolved in 300 parts of water with sodium carbonate at pH 6.0 to 8.0, 18.7 parts of 35% hydrochloric acid was added, and then 0 to 5°C was added, 10.7 parts of 40% nitrous acid was added Aqueous sodium solution for diazotization.
[0111]
[0112] To this diazotized suspension was added a liquid obtained by suspending 19.1 parts of 4-amino-5-hydroxynaphthalene-1,7-disulfonic acid in 200 parts of water, and then the pH of the solution was adjusted to carbonic acid at 10 to 20°C. The sodium was stirred at 2.4-2.8 for 12 hours. After stirring, the pH was adjusted to 7.0 to 8.5 with sodium carbonate and dissolved to obtain a solution containing the monoazo compound of the formula (6).
[0113]
[0114] 14.4...
Embodiment 1-2
[0121] Except having changed 11.0 parts of 4-methoxyaniline-2-sulfonic acid of Example 1-1 to 11.7 parts of 5-sulfoanthranilic acid, 36.2 parts of the present invention were obtained in the same manner as in Example 1-1. A compound of formula (12) (Compound No. 2 in Table 2). The maximum absorption wavelength of this compound in water is 591 nm, and the solubility in water is 100 g / l or more.
[0122]
Embodiment 1-3
[0124] Except having changed 11.0 parts of 4-methoxyaniline-2-sulfonic acid in Example 1-1 to 9.8 parts of 2-aminoterephthalic acid, 30.4 parts of the formula of the present invention were obtained in the same manner as in Example 1-1 (13) The compound of (Compound No. 3 in Table 2). The maximum absorption wavelength of this compound in water is 590 nm, and the solubility in water is 100 g / l or more.
[0125]
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