Dye|Dye intermediates|Fluorescent Brightener|pigment dye

M-nitroaniline

Name: M-nitroaniline

CA Name: Benzenamine,3-nitro-

Molecular Structure:

M-nitroaniline,Benzenamine,3-nitro-,CAS 99-09-2,138.12,C6H6N2O2

Molecular Formula:C₆H₆N₂O₂

Molecular Weight: 138.12

CAS Registry Number: 99-09-2

List of synthetic dyes :

C.I.Azoic Coupling Component 17

C.I.Azoic Diazo Component 7

C.I.Disperse Yellow 5

C.I.Sulphur Brown 19

C.I.Mordant Yellow 1

C.I.Mordant Blue 82

C.I.Acid Orange 18

Acid Blue 29

C.I.Acid Brown 92

C.I.Direct Red 169

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This entry was posted on Thursday, January 17th, 2013 at 1:57 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.

9 Responses to “M-nitroaniline”

1. Disperse Yellow 5 on July 8th, 2013 at 6:08 AM

   […] Methods : M-nitroaniline diazo, and […]

2. AJAY on July 8th, 2013 at 8:44 AM

   i want 2,5dichloro 3-nitroaniline

3. Azoic Coupling Component 17 on August 12th, 2013 at 6:30 AM

   […] Methods : M-nitroaniline and 3-Hydroxy-2-naphthoic […]

4. Acid Orange 18 on September 10th, 2013 at 7:03 AM

   […] Methods : M-nitroaniline diazo, coupled with 3-Hydroxynaphthalene-2,7-disulfonic […]

5. Acid Blue 29 on September 22nd, 2013 at 3:17 AM

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

6. Direct Red 148 on September 30th, 2013 at 3:56 AM

   […] Methods : (a), M-nitroaniline diazo, in alkaline conditions and 7-Amino-4-hydroxynaphthalene-2-sulfonic acid coupling, then use […]

7. Direct Red 169 on September 30th, 2013 at 6:40 AM

   […] Methods :  (a) M-nitroaniline diazo, in acid conditions and 7-Amino-4-hydroxynaphthalene-2-sulfonic acid coupling, then use […]

8. Mordant Blue 82 on November 1st, 2013 at 5:41 AM

   […] Methods : M-nitroaniline diazotization, in alkaline condition and 4-Amino-5-hydroxynaphthalene-2,7-disulfonic acid coupling, […]

9. Mordant Yellow 1 on November 19th, 2013 at 6:40 AM

   […] Methods : M-nitroaniline diazotization, and 2-Hydroxybenzoic acid […]

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