Bis-azo colorants for use as bluing agents
a technology of bisazo colorants and bluing agents, which is applied in the direction of detergent compositions, organic dyes, chemistry apparatuses and processes, etc., can solve the problems of affecting the color of the treated situs, difficult to reverse yellowing by normal laundering procedures, and undesirable stains of the fabri
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example 1
[0119]To a cold (0-5° C.) solution of p-polyalkyleneoxyphenylamine (27.45 grams in 100 ml of water), containing sufficient hydrochloric acid to give a pH of 1, are added 3.58 grams of sodium nitrite. The mixture is stirred for 2 hours. The mixture is then added to a cold solution of 7.65 grams of 2,5-dimethoxyaniline in dilute hydrochloric acid to give an orange colored product. This product is further diazotized by adding sufficient hydrochloric acid to keep the pH at 1 followed by 3.58 grams of sodium nitrite. After stirring 2 hours at 0-5° C., the mixture is added to an aqueous solution of 13,96 grams of N-acetyl J acid along with sufficient sodium hydroxide to dissolve the N-acetyl J acid. During the addition of the diazonium salt, the pH is kept at 10-12 by the addition of aqueous sodium hydroxide solution. This resulted in a violet colored product represented as Formula BA 1 herein.
B. Test Methods
[0120]I. Method for Determining Hueing Deposition (HD) for Dye from a Wash Soluti...
performance example
[0127]The performance of nine different bis-azo bluing agents, three comparative and six inventive, are tested and Hueing Deposition, and Selectivity Ratio are assessed according to the equations disclosed above in the methods. The results are given in the Table immediately below.
[0128]Test Results
Selectivity RatioDyeΔE*CottonΔE*Nylon(ΔE*Cotton / ΔE*Nylon)29.2419.36 1.5119.2614.91 1.2912.0321.15 0.5719.81 5.32 3.7224.57 6.58 3.7324.57 4.33 5.6723.07 3.79 6.09 7.26 0.4914.8 6.82 1.66 4.10
[0129]All the dyes show some level of deposition on cotton and nylon, The Selectivity Ratio (SR) for the comparative bis-azo bluing agents lie within a range of 0.5 to about 1.5. Substituting an acetyl or H for the phenyl ring in N-phenyl J-acid increases the SR to above 3.5 and above 5.5, respectively. Moreover, replacing the J-acid moiety with an H-acid or chromotropic acid group also leads to improved SR values.
[0130]Thus the compositions and methods of the invention provide good deposition on cell...
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