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| 1H-Indolesulfonic acid, 3,3'-[carbonylbis(imino-4,1-phenyleneazo)]bis[2-methyl-, disodium salt Basic information |
| 1H-Indolesulfonic acid, 3,3'-[carbonylbis(imino-4,1-phenyleneazo)]bis[2-methyl-, disodium salt Chemical Properties |
| 1H-Indolesulfonic acid, 3,3'-[carbonylbis(imino-4,1-phenyleneazo)]bis[2-methyl-, disodium salt Usage And Synthesis |
Preparation | N-(4-aminophenyl)acetamide diazo, and 2-Methyl-1H-indole-5-sulfonic acid?coupling, and then will the hydrolysis of amino acylation, again will get the amino nitrogen compounds for light accidentally gasification. | Properties and Applications | dark yellow. Soluble in water for golden brown, and adequate soluble in ethanol olive yellow. The strong sulfuric acid for yellow brown, after dilution is purple. Dye with strong hydrochloric acid solution for the red light brown, have precipitation; Add thick sodium hydroxide solution for gold orange.
Standard
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Acid Resistance
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Alkali Resistance
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Light Fastness
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Soaping
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Water
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Fading
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Stain
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Fading
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Stain
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ISO
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1
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5
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1
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1-2
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2
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| 1H-Indolesulfonic acid, 3,3'-[carbonylbis(imino-4,1-phenyleneazo)]bis[2-methyl-, disodium salt Preparation Products And Raw materials |
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