Dye|Dye intermediates|Fluorescent Brightener|pigment dye

Naphthalen-2-ol

Name: Naphthalen-2-ol

CA Name: 2-Naphthalenol

Molecular Structure:

Naphthalen-2-ol,2-Naphthalenol,CAS 135-19-3,144.17,C10H8O

Molecular Formula:C₁₀H₈O

Molecular Weight: 144.17

CAS Registry Number: 135-19-3

List of synthetic dyes :

C.I.Azoic Coupling Component 1

C.I.Disperse Yellow 97

C.I.Basic Blue 10

C.I.Basic Blue 6

C.I.Sulphur Brown 31

C.I.Mordant Black 15

C.I.Mordant Black 19

C.I.Mordant Blue 6

C.I.Mordant Green 4

C.I.Disperse Red 141

C.I.Basic Blue 16

C.I.Solubilised Sulphur Brown 31

C.I.Mordant Black 1

C.I.Mordant Black 17

C.I.Mordant Black 25

C.I.Mordant Green 10

C.I.Mordant Violet 30

C.I.Mordant Black 10

C.I.Mordant Black 18

C.I.Mordant Blue 4

C.I.Mordant Green 15

C.I.Mordant Violet 5

C.I.Solvent Orange 2

C.I.Solvent Orange 8

C.I.Solvent Red 1

C.I.Solvent red 17

C.I.Solvent Red 23

C.I.Solvent Red 25

C.I.Solvent Red 4

C.I.Solvent Violet 1|

C.I.Food green 4:1

C.I.Acid Orange 7

C.I.Acid Black 117

C.I.Acid Black 172

C.I.Acid Black 34

C.I.Acid Black 13

C.I.Acid Red 151

C.I.Acid Red 184

C.I.Acid Red 296

C.I.Acid Red 66

C.I.Acid Red 89

C.I.Acid Yellow 241

Acid Blue 328

C.I.Acid Yellow 59

C.I.Acid Violet 78

C.I.Acid Violet 92

C.I.Acid Brown 50

C.I.Pigment Orange 2

C.I.Pigment orange 5

C.I.Pigment red 117

C.I.Pigment red 40

C.I.Pigment red 49:2

C.I.Pigment red 50:1

C.I.Pigment Red 51:1

C.I.Pigment red 53:2

C.I.Pigment Red 68

C.I.Pigment red 93

C.I.Leuco Sulphur Brown 31

C.I.Direct Blue 22

C.I.Solvent Orange 49

C.I.Solvent Black 34

C.I.Solvent Red 102

C.I.Solvent Red 18

C.I.Solvent Red 24

C.I.Solvent Red 26

C.I.Solvent Red 80

C.I.Solvent Violet 58

C.I.Acid Orange 23

C.I.Acid Orange 8

C.I.Acid Black 168

C.I.Acid Black 243

C.I.Acid Black 43

C.I.Acid Red 10

C.I.Solvent Orange 7

C.I.Solvent Black 35

C.I.Solvent Red 13

C.I.Solvent Red 22

C.I.Solvent Red 243

C.I.Solvent Red 27

C.I.Solvent Yellow 14

C.I.Food green 4

C.I.Acid Orange 56

C.I.Acid Black 107

C.I.Acid Black 170

C.I.Acid Black 32

C.I.Acid Black 52

C.I.Acid Red 141

C.I.Acid Red 151:1

C.I.Acid Red 182

C.I.Acid Red 213

C.I.Acid Red 308

C.I.Acid Red 86

C.I.Acid Red 97

Acid Blue 161

Acid Blue 356

C.I.Acid Green 50

C.I.Acid Violet 87

C.I.Acid Brown 29

C.I.Pigment orange 17

C.I.Pigment orange 3

C.I.Pigment Orange 7

C.I.Pigment red 3

C.I.Pigment red 49

C.I.Pigment red 49:3

C.I.Pigment red 50:2

C.I.Pigment red 53

C.I.Pigment red 53:3

C.I.Pigment Red 69

C.I.Pigment Red 99

C.I.Direct Black 100

C.I.Direct Blue 27

C.I.Acid Red 442

C.I.Acid Red 88

C.I.Acid Red 99

Acid Blue 193

C.I.Acid Green 122

C.I.Acid Violet 68

C.I.Acid Violet 91

C.I.Acid Brown 355

C.I.Pigment orange 17:1

C.I.Pigment Orange 46

C.I.Pigment red 1

C.I.Pigment red 4

C.I.Pigment red 49:1

C.I.Pigment red 50

C.I.Pigment Red 51

C.I.Pigment red 53:1

C.I.Pigment red 6

C.I.Pigment Red 70

C.I.Pigment Brown 2

C.I.Direct Blue 19

C.I.Direct Violet 22

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This entry was posted on Friday, May 24th, 2013 at 4:05 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.

13 Responses to “Naphthalen-2-ol”

1. Basic Blue 6 on August 27th, 2013 at 3:52 AM

   […] Methods : commonly known as Meldola ‘s Blue. Naphthalen-2-ol with excess N,N-dimethyl-4-nitrosobenzenamine hydrochloride in hot ethanol in response, then will […]

2. Basic Blue 16 on August 27th, 2013 at 6:09 AM

   […] Methods : (C.I.Basic Red 2, C.I. 50240) diazo, and Naphthalen-2-ol […]

3. Acid Red 66 on September 13th, 2013 at 2:01 AM

   […] Methods : 3,4′-Disulfo-4-aininoazobenzene diazo, and Naphthalen-2-ol […]

4. Acid Red 89 on September 13th, 2013 at 3:02 AM

   […] Methods : 5-Amino-2-(4-amino-5-methyl-2-sulfophenyl)-4-methylbenzenesulfonic double nitriding, and Naphthalen-2-ol (2 Moore) […]

5. Acid Red 442 on September 18th, 2013 at 3:16 AM

   […] coupling, a single accidentally nitrogen compounds; 2-Aminobenzoic acid diazo, and Naphthalen-2-ol coupling, another single accidentally nitrogen compounds, and then turn it into 1:2 chromium […]

6. Sulphur Brown 31 on October 29th, 2013 at 7:08 AM

   […] Methods :  Naphthalen-2-ol sodium salt and sodium polysulfide in 270 ~ 280 ℃ calcination, product used for synthesis of […]

7. Leuco Sulphur Brown 31 on October 29th, 2013 at 7:10 AM

   […] Methods : Naphthalen-2-ol sodium salt and sodium polysulfide in 270 ~ 280 ℃ calcination, product used for synthesis of […]

8. Mordant Green 4 on November 1st, 2013 at 5:46 AM

   […] Methods : Naphthalen-2-ol and nitrous acid reaction, then the product into Desoxycholate hydrogen sulfide lactose AGAR […]

9. Disperse Red 141 on November 11th, 2013 at 5:13 AM

   […] Manufacturing Methods : 2-Methyl-4-(o-tolyldiazenyl)benzenamine diazo, and Naphthalen-2-ol coupling. […]

10. Acid Black 63 on November 14th, 2013 at 6:49 AM

    […] Methods :  2-Amino-5-nitrophenol diazo, and Naphthalen-2-ol coupling, and then into a chrome complex (1 to 2 Moore single atoms chromium azo […]

11. Pigment Orange 17:1 on November 28th, 2013 at 2:50 AM

    […] Methods :4-Aminobenzenesulfonic acid diazotization, and Naphthalen-2-ol coupling, and then into aluminum salt […]

12. Pigment Red 53:2 on November 28th, 2013 at 7:33 AM

    […] Methods :2-Amino-5-chloro-4-methylbenzenesulfonic acid diazotization, and Naphthalen-2-ol coupling, and then into calcium […]

13. Pigment Red 68 on November 28th, 2013 at 8:04 AM

    […] Methods :5-Amino-2-chloro-4-sulfobenzoic acid diazotization, and Naphthalen-2-ol coupling, and then into calcium […]

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