Dye|Dye intermediates|Fluorescent Brightener|pigment dye

2,4-Diaminobenzenesulfonic acid

Name: 2,4-Diaminobenzenesulfonic acid

CA Name: Benzenesulfonic acid,2,4-diamino-

Molecular Structure:

2,4-Diaminobenzenesulfonic acid,Benzenesulfonic acid,2,4-diamino-,CAS 88-63-1,188.20,C6H8N2O3S

Molecular Formula:C₆H₈N₂O₃S

Molecular Weight: 188.20

CAS Registry Number: 88-63-1

List of synthetic dyes :

C.I.Reactive Orange 2

C.I.Reactive Black 39

C.I.Reactive Black 42

C.I.Reactive Red 220

C.I.Reactive Red 223

C.I.Reactive Red 4

C.I.Reactive Red 79

C.I.Reactive Yellow 1

C.I.Reactive Yellow 105

C.I.Reactive Yellow 135

C.I.Reactive Yellow 179

C.I.Reactive Yellow 160

C.I.Reactive Yellow 167

C.I.Reactive Yellow 18

C.I.Reactive Yellow 193

C.I.Reactive Yellow 2

C.I.Reactive Yellow 201

C.I.Reactive Yellow 202

C.I.Reactive Yellow 25

C.I.Reactive Yellow 35

C.I.Reactive Yellow 81

C.I.Reactive Blue 1

C.I.Reactive Blue 109

C.I.Reactive Blue 15

C.I.Reactive Blue 171

C.I.Reactive Blue 194

C.I.Reactive Blue 213

C.I.Reactive Blue 214

C.I.Reactive Blue 222

C.I.Reactive Blue 225

C.I.Reactive Blue 4

C.I.Reactive Blue 5

C.I.Reactive Blue 63

C.I.Reactive Blue 7

C.I.Reactive Green 8

C.I.Mordant Brown 33

C.I.Mordant Brown 49

C.I.Mordant Brown 97

C.I.Mordant Brown 98

C.I.Acid Yellow 127

C.I.Acid Yellow 158

C.I.Acid Brown 119

C.I.Acid Brown 120

C.I.Acid Brown 123

C.I.Acid Brown 138

C.I.Acid Brown 265

C.I.Acid Brown 395

C.I.Direct Orange 24

C.I.Direct Orange 6

C.I.Direct Black 164

C.I.Direct Brown 119

C.I.Direct Brown 123

C.I.Direct Brown 132

C.I.Direct Brown 138

C.I.Direct Brown 146

C.I.Direct Brown 147

C.I.Direct Brown 148

C.I.Direct Brown 166

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This entry was posted on Friday, January 25th, 2013 at 6:07 AM and is filed under Dye intermediates. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.

16 Responses to “2,4-Diaminobenzenesulfonic acid”

1. Reactive Yellow 25 on August 28th, 2013 at 7:34 AM

   […] Methods : 2,4-Diaminobenzenesulfonic acid diazo, and 1-(2-methyl-4-sulfophenyl)-5-oxo-4,5-dihydro-1H-pyrazole-3-carboxylic acid coupling, […]

2. Reactive Yellow 35 on August 28th, 2013 at 7:43 AM

   […] Methods :  2,4-Diaminobenzenesulfonic acid and 2,4,6-Trichloro-1,3,5-triazine condensation, its product diazo, and […]

3. Reactive Yellow 105 on August 29th, 2013 at 3:50 AM

   […] Methods : 2,4-Diaminobenzenesulfonic acid and 2,4,6-Trichloro-1,3,5-triazine condensation chlorine, product diazo, and […]

4. Reactive Yellow 160 on August 29th, 2013 at 5:05 AM

   […] Methods : 2,4-Diaminobenzenesulfonic acid diazo, and 6-hydroxy-1,4-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxamide coupling, and […]

5. Reactive Yellow 179 on August 29th, 2013 at 5:39 AM

   […] Methods : 2,4-Diaminobenzenesulfonic acid and 2,4,6-Trichloro-1,3,5-triazine condensation, its product (2 Moore) diazo, […]

6. Reactive Red 223 on September 3rd, 2013 at 1:25 AM

   […] Methods : 2,4-Diaminobenzenesulfonic acid diazo, and 4-Aminonaphthalene-1-sulfonic acid coupling, respectively with the […]

7. Reactive Blue 15 on September 3rd, 2013 at 3:23 AM

   […] : Copper phthalocyanine use chlorosulfonic and chlorinated and sulfones chlorosulfonated, and 2,4-Diaminobenzenesulfonic acid first condensation, and 2,4,6-Trichloro-1,3,5-triazine second condensation, and then four and […]

8. Reactive Blue 109 on September 3rd, 2013 at 6:17 AM

   […] acid conditions and 4-Amino-5-hydroxynaphthalene-2,7-disulfonic acidcoupling, and the other will be 2,4-Diaminobenzenesulfonic acid and 2,4,6-Trichloro-1,3,5-triazine condensation , product diazo, and the single accidentally […]

9. Reactive Blue 225 on September 3rd, 2013 at 7:26 AM

   […] Methods : 2,4-Diaminobenzenesulfonic acid and 5-Chloro-2,4,6-trifluoropyrimidine condensation, diazotization, and […]

10. Reactive Black 39 on September 4th, 2013 at 3:35 AM

    […] Methods : 2,4-Diaminobenzenesulfonic acid and 2-Aminobenzene-1,4-disulfonic acid diazo, then respectively with the […]

11. Acid Yellow 127 on September 9th, 2013 at 3:25 AM

    […] Methods :  2,4-Diaminobenzenesulfonic acid first and 2,4,6-Trichloro-1,3,5-triazine condensation, again with N-methylbenzenamine condensation, […]

12. Acid Yellow 158 on September 9th, 2013 at 4:10 AM

    […] Methods : 2,4-Diaminobenzenesulfonic acid and 2,4,6-Trichloro-1,3,5-triazine condensation, and again 3-Aminobenzenesulfonic acid […]

13. Acid Brown 138 on September 25th, 2013 at 2:10 AM

    […] Methods :   2,4-Diaminobenzenesulfonic acid diazo, Coupled with resorcinol, diazotization, Coupled with the Benzene-1,3-diamine, its products […]

14. Direct Orange 24 on September 27th, 2013 at 6:04 AM

    […] Methods : 3-Aminobenzenesulfonic acid diazo, and 2,4-Diaminobenzenesulfonic acid coupled; C.I. Direct Yellow 59 (C.I. 49000) diazo, and the generation of single accidentally […]

15. Direct Brown 132 on October 12th, 2013 at 5:56 AM

    […] hydrolysis amino acylation, product double nitriding, and 90% Benzene-1,3-diamine and  10% 2,4-Diaminobenzenesulfonic acid (2 Moore) […]

16. Direct Brown 166 on October 12th, 2013 at 6:25 AM

    […] product to double nitriding, and 0.8 Moore 2-(3-Aminophenylamino)acetic acid and 0.2 Moore 2,4-Diaminobenzenesulfonic acid (2 Moore) […]

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