Dye|Dye intermediates|Fluorescent Brightener|pigment dye

m-Toluidine

Name: m-Toluidine

CA Name: Benzenamine,3-methyl-

Molecular Structure:

m-Toluidine,Benzenamine,3-methyl-,CAS 108-44-1,107.15,C7H9N

Molecular Formula:C₇H₉N

Molecular Weight: 107.15

CAS Registry Number: 108-44-1

List of synthetic dyes :

C.I.Azoic Diazo Component 27

C.I.Disperse Orange 66

C.I.Vat Red 40

C.I.Reactive Orange 91

C.I.Reactive Yellow 4

C.I.Reactive Brown 35

C.I.Reactive Brown 45

C.I.Basic Orange 25

C.I.Basic Violet 22

C.I.Solvent Red 207

C.I.Solvent Blue 63

C.I.Acid Orange 16

C.I.Acid Red 108

Acid Blue 352

C.I.Acid Brown 105

C.I.Pigment red 66

C.I.Pigment Blue 56

C.I.Direct Orange 34

C.I.Direct Orange 74

C.I.Direct Red 110

C.I.Direct Red 121

C.I.Direct Red 130

C.I.Direct Red 194

C.I.Direct Red 8

C.I.Direct Red 85

C.I.Direct Yellow 118

C.I.Direct Yellow 33

C.I.Direct Yellow 50

C.I.Direct Yellow 86

C.I.Direct Violet 78

C.I.Direct Brown 100

C.I.Direct Brown 106

C.I.Direct Brown 32

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This entry was posted on Thursday, March 21st, 2013 at 6:22 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.

12 Responses to “m-Toluidine”

1. Azoic Diazo Component 27 on August 13th, 2013 at 5:45 AM

   […] Methods : Diazotization of m-Toluidine coupled with […]

2. Reactive Yellow 4 on August 28th, 2013 at 2:05 AM

   […] Methods : 3-Aminonaphthalene-1,5-disulfonic acid diazo, and a m-Toluidinec oupling 2,4,6-Trichloro-1,3,5-triazine (1 Moore) […]

3. Acid Red 108 on September 13th, 2013 at 7:05 AM

   […] Methods : m-Toluidine diazo, and  4-Benzamido-5-hydroxynaphthalene-1,7-disulfonic […]

4. Basic Violet 22 on November 12th, 2013 at 6:47 AM

   […] Methods : N-methyl-2 – benzothiazolyl hydrazone and m-Toluidine and hydrogen peroxide oxidation […]

5. Acid Orange 16 on November 13th, 2013 at 7:32 AM

   […] Methods : m-Toluidine , p-Methylaniline,O-Methylaniline mixed diazotization, and 6-Hydroxynaphthalene-2-sulfonic acid […]

6. Direct Yellow 33 on November 15th, 2013 at 1:59 AM

   […] Methods : 2-Hydroxy-3-(4-aminobenzamido)-5-sulfobenzoic acid diazo, and a coupling m-Toluidine, then the light […]

7. Direct Yellow 50 on November 15th, 2013 at 2:18 AM

   […] Methods : 3-Aminonaphthalene-1,5-disulfonic acid diazo, and a coupling m-Toluidine, then the light […]

8. Direct Red 85 on November 15th, 2013 at 7:22 AM

   […] Methods :  4-Amino-3-methylbenzenesulfonic acid diazo, coupled with m-Toluidine, its product to diazo, and 7-Benzamido-4-hydroxynaphthalene-2-sulfonic acid […]

9. Direct Red 121 on November 15th, 2013 at 7:39 AM

   […] Methods : 3-Aminobenzenesulfonic acid diazo, and a coupling m-Toluidine , its product to diazo, and 7-(4-Aminobenzamido)-4-hydroxynaphthalene-2-sulfonic acid […]

10. Direct Red 130 on November 15th, 2013 at 7:41 AM

    […] Methods : 3-Aminonaphthalene-1,5-disulfonic acid diazo, and a coupling m-Toluidine , its product to diazo, and 7-(4-Amino-3-methylbenzamido)-4-hydroxynaphthalene-2-sulfonic […]

11. Direct Red 194 on November 15th, 2013 at 8:11 AM

    […] Methods : 2-Amino-3,5-dichlorobenzenesulfonic acid diazo, and m-Toluidine coupling, and then a sulfonic acid hydrolysis off base, its product (2 Moore) diazo, coupled with […]

12. Pigment Red 66 on November 28th, 2013 at 8:01 AM

    […] Methods :m-Toluidine diazotization, and 4-Benzamido-5-hydroxynaphthalene-1,7-disulfonic acid coupling, and then […]

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