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Benzaldehyde

Name: Benzaldehyde

CA Name: Benzaldehyde

Molecular Structure:

Benzaldehyde,Benzaldehyde,CAS 100-52-7,106.12,C7H6O

Benzaldehyde,Benzaldehyde,CAS 100-52-7,106.12,C7H6O

Molecular Formula:C7H6O

Molecular Weight: 106.12

CAS Registry Number: 100-52-7

List of synthetic dyes :

C.I.Disperse Blue 73

C.I.Vat Yellow 2

C.I.Reactive Blue 104

C.I.Basic Orange 18

C.I.Basic Green 1

C.I.Basic Green 4

C.I.Solubilised Vat Yellow 2

C.I.Mordant Violet 10

C.I.Mordant Violet 11

C.I.Mordant Violet 19

C.I.Mordant Violet 36

C.I.Solvent Green 1

C.I.Food green 1

C.I.Food green 2

Acid Blue 109

Acid Blue 269

Acid Blue 90

Acid Blue 91

C.I.Acid Green 3

C.I.Acid Green 5

C.I.Acid Green 6

C.I.Pigment Green 1

C.I.Pigment Green 4

C.I.Fluorescent Brightener 41


18 Responses to “Benzaldehyde”

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

  2. […] Methods : benzaldehyde (1 Moore) and N-benzyl-N-ethylbenzenamine (2 Moore) condensation, and then three stlfonation, and […]

  3. […] Note: the market many similar Basic dye, they are through the Basic dye C.I. 46025 or 46065 (from benzaldehyde and diazo, and 4-Methylbenzene-1,3-diamine, cyclization, and then by oxidation with ferric chloride […]

  4. […] Methods : benzaldehyde and N1,N1,6-trimethylbenzene-1,3-diamine condensation, cyclization, and ferric chloride […]

  5. […] Methods : in the presence of sulfuric acid hydrochloric acid or, benzaldehyde and N,N-diethylbenzenamine condensation, and then will product oxidation, and translated into […]

  6. […] : commonly known as Malachite Green. (a) in the presence of hydrochloric acid or sulfuric acid, benzaldehyde (1 Moore) and N,N-dimethylaniline(2 Moore) condensation, and then used lamps and acid oxidation its […]

  7. […] Methods :  benzaldehyde with sulfuric acid and nitric acid nitrification, use the method reduction, with vinegar anhydride […]

  8. […] Methods : benzaldehyde (1 Moore) and N-ethyl-N-benzyl-3-methylaniline (2 Moore) condensation, The product was then […]

  9. […] Methods : Benzaldehyde  (1 Moore) and N-ethyl-N-benzyl-3-methylaniline (2 Moore) condensation, and heavy chromate […]

  10. […] Methods : Benzaldehyde (1 Moore) and 2-Hydroxy-3-methylbenzoic acid (2 Moore) condensation, the product with concentrated […]

  11. […] Methods : (a) Benzaldehyde (1 Moore) and 2-Hydroxy-3-methylbenzoic acid (2 Moore) in sulfuric acid solution condensation, […]

  12. […] Methods : (a) Benzaldehyde (1 Moore) and 2-Hydroxy-3-methylbenzoic acid (2 Moore) in sulfuric acid solution condensation, […]

  13. […] Methods : Benzaldehyde  (1 Moore) and N-ethyl-N-benzyl-3-methylaniline (2 Moore) condensation, And then sulfonating the […]

  14. […] Methods :Benzaldehyde (1 Moore) and 3-(Ethyl(phenyl)amino)methyl)benzenesulfonic acid (2 Moore) condensation, will […]

  15. […] Methods :  Benzaldehyde (1 Moore) and N-methyl-N-3-sulfobenzylaniline (2 Moore) condensation, and will be preparing […]

  16. […] Methods : (a) Benzaldehyde (1 Moore) and 2-Hydroxy-3-methylbenzoic acid (2 Moore) condensation, oxidation, its product again […]

  17. […] Methods : in the presence of sulfuric acid or hydrochloric acid and Benzaldehyde and N,N-diethylbenzenamine condensation, then product oxidation, reoccupy phosphorus molybdenum […]

  18. […] Methods :(a) in the presence of sulfuric acid or hydrochloric acid Benzaldehyde (1 mol) and N,N-dimethylaniline (2 Moore) condensation, then use Lead dioxide and acid oxidation […]

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