Dye|Dye intermediates|Fluorescent Brightener|pigment dye

Naphthalen-1-amine

Name: Naphthalen-1-amine

CA Name: 1-Naphthalenamine

Molecular Structure:

Naphthalen-1-amine,1-Naphthalenamine,CAS 134-32-7,143.19,C10H9N

Molecular Formula:C₁₀H₉N

Molecular Weight: 143.19

CAS Registry Number: 134-32-7

List of synthetic dyes :

C.I.Azoic Coupling Component 4

C.I.Azoic Diazo Component 23

C.I.Disperse Black 1

C.I.Basic Red 6

C.I.Mordant Black 5

C.I.Mordant Green 11

C.I.Solvent Orange 39

C.I.Solvent Black 4

C.I.Solvent Yellow 4

C.I.Solvent Brown 2

C.I.Solvent Brown 5

C.I.Acid Black 17

C.I.Acid Black 21

C.I.Acid Black 26

C.I.Acid Black 27

C.I.Acid Black 5

C.I.Acid Red 119

C.I.Acid Red 299

Acid Blue 113

Acid Blue 26

C.I.Acid Violet 13

C.I.Pigment red 134

C.I.Pigment Violet 8

C.I.Direct Black 40

C.I.Direct Black 51

C.I.Direct Black 77

C.I.Direct Red 111

C.I.Direct Blue 126

C.I.Direct Blue 133

C.I.Direct Blue 186

C.I.Direct Blue 308

C.I.Direct Blue 69

C.I.Direct Blue 78

C.I.Direct Blue 83

C.I.Direct Brown 37

C.I.Direct Brown 75

C.I.Azoic Coupling Component 37

C.I.Azoic Diazo Component 112

C.I.Disperse Orange 13

C.I.Disperse Black 30

C.I.Mordant Black 18

C.I.Mordant Black 68

C.I.Solvent Orange 14

C.I.Solvent Black 3

C.I.Solvent Red 4

C.I.Solvent Brown 1

C.I.Solvent Brown 39

C.I.Acid Orange 127

C.I.Acid Black 230

C.I.Acid Black 24

C.I.Acid Black 26:2

C.I.Acid Black 35

C.I.Acid Red 11

C.I.Acid Red 20

C.I.Acid Red 44

Acid Blue 120

C.I.Acid Green 34

C.I.Acid Brown 8

C.I.Pigment red 54

C.I.Direct Black 3

C.I.Direct Black 49

C.I.Direct Black 76

C.I.Direct Red 103

C.I.Direct Blue 110

C.I.Direct Blue 132

C.I.Direct Blue 148

C.I.Direct Blue 30

C.I.Direct Blue 63

C.I.Direct Blue 71

C.I.Direct Blue 82

C.I.Direct Brown 208

C.I.Direct Brown 67

C.I.Direct Brown 99

C.I.Disperse Black 28

C.I.Basic Blue 12

C.I.Mordant Black 62

C.I.Mordant Green 12

C.I.Solvent Orange 52

C.I.Solvent Red 29

C.I.Solvent Yellow 8

C.I.Solvent Brown 3

C.I.Acid Orange 116

C.I.Acid Black 18

C.I.Acid Black 23

C.I.Acid Black 26:1

C.I.Acid Black 3

C.I.Acid Black 7

C.I.Acid Red 17

C.I.Acid Red 3

C.I.Acid Blue 114

C.I.Acid Green 19

C.I.Acid Violet 67

C.I.Pigment red 40

C.I.Direct Black 103

C.I.Direct Black 48

C.I.Direct Black 75

C.I.Direct Black 83

C.I.Direct Red 112

C.I.Direct Blue 129

C.I.Direct Blue 140

C.I.Direct Blue 258

C.I.Direct Blue 55

C.I.Direct Blue 70

C.I.Direct Blue 81

C.I.Direct Green 19

C.I.Direct Brown 50

C.I.Direct Brown 78

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This entry was posted on Tuesday, May 28th, 2013 at 5:15 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.

17 Responses to “Naphthalen-1-amine”

1. Disperse Black 30 on August 8th, 2013 at 7:45 AM

   […] Methods : Naphthalen-1-amine diazo, and […]

2. Azoic Coupling Component 4 on August 12th, 2013 at 3:17 AM

   […] Methods : Naphthalen-1-amine and 3-Hydroxy-2-naphthoic acid […]

3. Acid Red 3 on September 11th, 2013 at 8:10 AM

   […] Methods : Naphthalen-1-amine diazo, coupled with 4-Hydroxynaphthalene-2,7-disulfonic […]

4. Acid Red 11 on September 12th, 2013 at 1:51 AM

   […] Methods : Naphthalen-1-amine diazo, and 6-Hydroxynaphthalene-2-sulfonic acid […]

5. Acid Red 20 on September 12th, 2013 at 2:20 AM

   […] Methods : Naphthalen-1-amine diazo, and 5-Hydroxynaphthalene-1-sulfonic acid […]

6. Acid Violet 13 on September 18th, 2013 at 5:25 AM

   […] Methods : Naphthalen-1-amine diazo, and 4,5-Dihydroxynaphthalene-2,7-disulfonic […]

7. Acid Violet 67 on September 18th, 2013 at 8:19 AM

   […] Methods : Naphthalen-1-amine diazo, and  4-Amino-5-hydroxynaphthalene-1,7-disulfonic acid […]

8. Acid Blue 114 on September 23rd, 2013 at 3:01 AM

   […] Methods : 5-Amino-2-chlorobenzenesulfonic acid diazo, and Naphthalen-1-amine coupling, its product to diazo, and 8-(Phenylamino)naphthalen-1-ol […]

9. Acid Black 7 on September 25th, 2013 at 6:58 AM

   […] : 4-Amino-2,6-naphthalenedisulfonic acid and 4-Aminonaphthalene-2,7-disulfonic acid diazo, and Naphthalen-1-amine coupling, its product to diazo, and Naphthalen-1-amine […]

10. Direct Blue 69 on October 10th, 2013 at 2:55 AM

    […] Methods : 3-Aminonaphthalene-1,5-disulfonic acid diazo, and Naphthalen-1-amine coupling, its product to diazo, and 8-Aminonaphthalene-2-sulfonic acid coupling, again diazo, in […]

11. Acid Orange 127 on November 13th, 2013 at 7:53 AM

    […] Methods : 3-Aminobenzenesulfonic acid diazo, and Naphthalen-1-amine coupling, product to diazo, coupled with phenol, then will the phenol hydroxyl into b oxygen […]

12. Direct Blue 71 on November 18th, 2013 at 1:37 AM

    […] Methods : 3-Aminonaphthalene-1,5-disulfonic acid diazo, and Naphthalen-1-amine first coupling, its product to diazo, and 8-Aminonaphthalene-2-sulfonic acid second coupling, again […]

13. Direct Black 48 on November 19th, 2013 at 1:46 AM

    […] Methods : 5-Amino-2-hydroxybenzoic acid diazo, and Naphthalen-1-amine coupling, again diazo, in alkaline conditions and 6-Amino-4-hydroxynaphthalene-2-sulfonic acid  […]

14. Direct Black 49 on November 19th, 2013 at 1:47 AM

    […] Methods : 5-Amino-2-hydroxybenzoic acid diazo, and Naphthalen-1-amine coupling, again diazo, in alkaline conditions and 6-Amino-4-hydroxynaphthalene-2-sulfonic […]

15. Pigment Red 40 on November 28th, 2013 at 7:03 AM

    […] Methods :Naphthalen-1-amine diazotization and Naphthalen-2-ol […]

16. Pigment Red 54 on November 28th, 2013 at 7:32 AM

    […] Methods :Naphthalen-1-amine diazotization, with 5-Hydroxynaphthalene-1-sulfonic acid coupling, and then translate into calcium […]

17. Pigment Violet 8 on December 3rd, 2013 at 2:21 AM

    […] Methods : Naphthalen-1-amine diazotization, and 4-Benzamido-5-hydroxynaphthalene-1,7-disulfonic acid coupling and changed into […]

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