Dye|Dye intermediates|Fluorescent Brightener|pigment dye

2,5-Dichlorobenzenamine

Name:2,5-Dichlorobenzenamine

CA Name: Benzenamine,2,5-dichloro-

Molecular Structure:

2,5-Dichlorobenzenamine,Benzenamine,2,5-dichloro-,CAS 95-82-9,162.02,C6H5Cl2N

Molecular Formula:C₆H₅Cl₂N

Molecular Weight: 162.02

CAS Registry Number: 95-82-9

List of synthetic dyes :

C.I.Azoic Diazo Component 3

C.I.Disperse Yellow 134

C.I.Mordant Green 11

Acid Blue 128

C.I.Acid Green 19

C.I.Pigment orange 22

C.I.Pigment red 10

C.I.Pigment red 144

C.I.Pigment red 166

C.I.Pigment red 2

C.I.Pigment red 214

C.I.Pigment red 9

C.I.Pigment Yellow 10

C.I.Pigment Yellow 156

C.I.Pigment brown 1

C.I.Pigment brown 25

C.I.Direct Blue 11

C.I.Direct Blue 51

C.I.Direct Green 12

C.I.Direct Green 7

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This entry was posted on Monday, January 14th, 2013 at 6:53 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 “2,5-Dichlorobenzenamine”

1. Disperse Yellow 134 on July 12th, 2013 at 5:00 AM

   […] Methods : 2,5-Dichlorobenzenamine diazo, cyanogen ethyl amide and ethyl allylacetoacetate condensation closed loop, with potassium […]

2. Acid Blue 128 on September 23rd, 2013 at 3:24 AM

   […] Methods :  2,5-Dichlorobenzenamine diazo, and 4-Amino-5-hydroxynaphthalene-2,7-disulfonic acid in acid conditions coupled, then and […]

3. Direct Blue 11 on October 9th, 2013 at 3:39 AM

   […] Methods :  2,5-Dichlorobenzenamine diazo, in acid conditions and 4-Amino-5-hydroxynaphthalene-2,7-disulfonic acid coupling, […]

4. Direct Blue 51 on October 9th, 2013 at 7:34 AM

   […] Methods : 2,5-Dichlorobenzenamine diazo, in acid conditions and 4-Amino-5-hydroxynaphthalene-2,7-disulfonic acid coupling, […]

5. Mordant Green 11 on November 1st, 2013 at 5:54 AM

   […] Methods : 2,5-Dichlorobenzenamine diazotization, under acid condition and 4-Amino-5-hydroxynaphthalene-2,7-disulfonic acid coupling, […]

6. Azoic Diazo Component 3 on November 12th, 2013 at 3:14 AM

   […] Methods : 2,5-Dichlorobenzenamine […]

7. Pigment Yellow 10 on November 26th, 2013 at 1:17 AM

   […] Methods : 2,5-Dichlorobenzenamine diazotization, with 3-Methyl-1-phenyl-1H-pyrazol-5(4H)-one […]

8. Pigment Yellow 156 on November 27th, 2013 at 7:22 AM

   […] Methods :2,5-Dichlorobenzenamine diazotization, and 33-Oxo-N-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)butanamide […]

9. Pigment Red 2 on November 28th, 2013 at 5:45 AM

   […] Methods : 2,5-Dichlorobenzenamine diazotization, and 3-Hydroxy-N-phenyl-2-naphthamide […]

10. Pigment Red 9 on November 28th, 2013 at 6:19 AM

    […] Methods :2,5-Dichlorobenzenamine diazotization, and 2′-Methoxy-3-hydroxy-2-naphthanilide […]

11. Pigment Red 10 on November 28th, 2013 at 6:21 AM

    […] Methods : 2,5-Dichlorobenzenamine diazotization, and 3-Hydroxy-N-p-tolyl-2-naphthamide […]

12. Pigment Red 144 on November 29th, 2013 at 6:21 AM

    […] Methods : 2,5-Dichlorobenzenamine diazotization, and 3-Hydroxy-2-naphthoyl chloride coupling, and its product (2 Moore) and […]

13. Pigment Red 166 on November 29th, 2013 at 6:48 AM

    […] Methods :2,5-Dichlorobenzenamine diazotization, and 3-Hydroxy-2-naphthoyl chloride coupling, and its product (2 Moore) and […]

14. Pigment Red 214 on December 2nd, 2013 at 6:52 AM

    […] Methods :2,5-Dichlorobenzenamine diazotization, and 3-Hydroxy-2-naphthoyl chloride coupling, and its product (2 Moore) and […]

15. Pigment Brown 1 on December 4th, 2013 at 3:20 AM

    […] Methods :2,5-Dichlorobenzenamine diazotization, and […]

16. Pigment Brown 25 on December 4th, 2013 at 3:50 AM

    […] Methods :2,5-Dichlorobenzenamine diazotization, and 3-Hydroxy-N-(2-oxo-5-benzimidazolinyl)-2-naphthamide […]

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