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Phenol

Name: Phenol

CA Name: Phenol

Molecular Structure:

Phenol,CAS 108-95-2,94.11,C6H6O

Phenol,CAS 108-95-2,94.11,C6H6O

Molecular Formula:C6H6O

Molecular Weight: 94.11

CAS Registry Number: 108-95-2

List of synthetic dyes :

C.I.Azoic Coupling Component 26

C.I.Disperse Orange 13

C.I.Disperse Orange 20

C.I.Disperse Orange 29

C.I.Disperse Red 71

C.I.Disperse Yellow 23

C.I.Disperse Violet 26

C.I.Reactive Violet 2

C.I.Basic Yellow 38

C.I.Sulphur Black 11

C.I.Disperse Orange 38

C.I.Disperse Yellow 68

C.I.Disperse Violet 31

C.I.Basic Black 2

C.I.Disperse Orange 121

C.I.Disperse Orange 21

C.I.Disperse Orange 66

C.I.Disperse yellow 104

C.I.Disperse Blue 73

C.I.Disperse Violet 38

C.I.Basic Black 3

C.I.Solubilised Sulphur Black 11

C.I.Solvent Orange 13

C.I.Solvent Orange 52

C.I.Solvent Yellow 7

C.I.Solvent Yellow 8

C.I.Solvent Violet 59

C.I.Acid Orange 127

C.I.Acid Orange 128

C.I.Acid Orange 156

C.I.Acid Orange 33

C.I.Acid Orange 45

C.I.Acid Orange 49

C.I.Acid Orange 63

C.I.Acid Orange 95

C.I.Acid Red 111

C.I.Acid Red 114

C.I.Acid Red 126

C.I.Acid Red 128

C.I.Acid Red 145

C.I.Acid Red 323

C.I.Acid Red 85

C.I.Acid Yellow 219

C.I.Acid Yellow 228

C.I.Acid Yellow 228

C.I.Acid Yellow 38

C.I.Acid Violet 41

C.I.Acid Violet 42

C.I.Pigment Violet 20

C.I.Leuco Sulphur Black 11

C.I.Fluorescent Brightener 234

C.I.Direct Orange 13

C.I.Direct Orange 63

C.I.Direct Red 39

C.I.Direct Green 1

C.I.Direct Green 19

C.I.Direct Green 57

C.I.Direct Green 85

C.I.Direct Yellow 12

C.I.Direct Green 10

C.I.Direct Green 23

C.I.Direct Green 58

C.I.Direct Violet 89

C.I.Direct Brown 202

C.I.Direct Brown 33

C.I.Direct Brown 54

C.I.Direct Brown 74

C.I.Direct Orange 101

C.I.Direct Red 37

C.I.Direct Yellow 4

C.I.Direct Green 12

C.I.Direct Green 36

C.I.Direct Green 6

C.I.Direct Brown 147

C.I.Direct Brown 43

C.I.Direct Brown 93


11 Responses to “Phenol”

  1. […] Methods : N-(4-aminophenyl)acetamide diazo, first with phenol coupling, and then hydrolysis acetyl groups, product to diazo, coupled […]

  2. […] Methods : In alkaline medium 1-Amino-2-bromo-4-hydroxyanthracene-9,10-dione and phenol […]

  3. […] Manufacturing Methods : N, N-diethyl-phenosafranine diazo, coupled with phenol. […]

  4. […] Manufacturing Methods : N, N-diethyl-phenosafranine diazo, coupled with phenol. […]

  5. […] coupled with 3-Amino-5-hydroxynaphthalene-2,7-disulfonic acid, product to diazo, coupled with phenol, next reoccupy 4-Methylbenzene-1-sulfonyl chloride will on the esterification of hydroxyl […]

  6. […] Methods : 4-(4-Aminophenyl)benzenamine double nitriding, respectively with phenol and 4-Hydroxynaphthalene-2,7-disulfonic acid coupling, then use 4-Methylbenzene-1-sulfonyl chloride […]

  7. […] Manufacturing Methods :  4-(4-Aminophenyl)benzenamine double nitriding, 2-Hydroxybenzoic acid coupled with first, then with 5-Aminonaphthalene-2-sulfonic acid and 8-Aminonaphthalene-2-sulfonic acid coupling, its product to diazo, coupled with phenol. […]

  8. […] Methods :With or without with a phenol and 4-(4-Hydroxyphenylamino)phenol  4-(Naphthaleti-2-ylamino)phenol in Sodium polysulfide of tert […]

  9. […] Manufacturing Methods : N-(4-aminophenyl)acetamide diazo, and m-Toluidine or  O-Methylaniline coupling, product to diazo, coupled with phenol. […]

  10. […] Methods : In alkaline medium 1-Amino-2-bromo-4-hydroxyanthracene-9,10-dione and phenol […]

  11. […] fuming sulfuric acid, nitric acid, sulfuric acid nitration, with sodium sulfide, and boric acid, phenol, Benzaldehyde , the addition of sulfuric acid translocation, with hydrosulfite […]

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