Dye|Dye intermediates|Fluorescent Brightener|pigment dye

N-benzyl-N-ethylbenzenamine

Name: N-benzyl-N-ethylbenzenamine

CA Name: Benzenemethanamine,N-ethyl-N-phenyl-

Molecular Structure:

N-benzyl-N-ethylbenzenamine,Benzenemethanamine,N-ethyl-N-phenyl-,CAS 92-59-1,211.30,C15H17N

Molecular Formula:C₁₅H₁₇N

Molecular Weight: 211.30

CAS Registry Number: 92-59-1

List of synthetic dyes :

C.I.Basic Red 94
C.I.Food green 2
C.I.Food green 3
C.I.Acid Orange 50
Acid Blue 5
Acid Blue 1
C.I.Acid Green 15
C.I.Acid Green 5

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This entry was posted on Tuesday, June 25th, 2013 at 7:28 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.

3 Responses to “N-benzyl-N-ethylbenzenamine”

1. Acid Blue 5 on November 14th, 2013 at 1:51 AM

   […] Methods : 3-Hydroxybenzaldehyde (1 Moore) and N-benzyl-N-ethylbenzenamine (2 Moore) condensation, its product two stlfonation, oxidation, and finally as calcium salting […]

2. Acid Green 5 on November 14th, 2013 at 3:03 AM

   […] Methods : Benzaldehyde (1 Moore) and N-benzyl-N-ethylbenzenamine (2 Moore) condensation, and then three stlfonation, and will product oxidation and will last them […]

3. Acid Green 15 on November 14th, 2013 at 3:10 AM

   […] Methods : 2,5-Dichlorobenzaldehyde (1 Moore) and N-benzyl-N-ethylbenzenamine (2 Moore) condensation, and then the product was disulfonated, final […]

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