Benzenemethanol,4-(diethylamino)-a-[4-(diethylamino)phenyl]-a-phenyl-

Base Information

• Chemical Name: Benzenemethanol,4-(diethylamino)-a-[4-(diethylamino)phenyl]-a-phenyl-
• CAS No.: 630-98-8
• Molecular Formula: C27H34 N2 O
• Molecular Weight: 402.58
• Mol file: 630-98-8.mol

Synonyms:Methanol,bis[p-(diethylamino)phenyl]phenyl- (6CI,7CI,8CI); Brilliant Green base; BrilliantGreen carbinol; C.I. Basic Green 1, carbinol

Chemical Property of Benzenemethanol,4-(diethylamino)-a-[4-(diethylamino)phenyl]-a-phenyl-

Chemical Property:

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Benzenemethanol,4-(diethylamino)-a-[4-(diethylamino)phenyl]-a-phenyl-

There total 11 articles about Benzenemethanol,4-(diethylamino)-a-[4-(diethylamino)phenyl]-a-phenyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

Bis-(4-diethylamino-phenyl)-phenyl-methanol; compound with sulfuric acid → brilliant green (630-98-8) + brilliant green (633-03-4) + Bis-(4-diethylamino-phenyl)-phenyl-methanol; compound with sulfuric acid

Guidance literature:

With aq. buffer; at 25 ℃; Rate constant; Equilibrium constant;

DOI:10.1246/bcsj.67.390

Reference yield:

brilliant green carbocation (25044-17-1,18198-35-1) → brilliant green (630-98-8)

Guidance literature:

With Tris buffer; cetyltrimethylammonim bromide; at 25 ℃; under 750060 Torr; Product distribution; various pressures, and different cationic micelles; kinetic parameters of the alkaline fading reactions, volume changes accompanyning the formation MD complexes, and activation volumes in the process product formation; reaction in nonmicellar systems;

DOI:10.1021/ja00361a002

Reference yield:

chlorobenzene (108-90-7) + bis(p-dimethylaminophenyl)methanone (90-94-8) → brilliant green (630-98-8)

Guidance literature:

With sodium; toluene; at 85 - 90 ℃;

upstream raw materials:

chlorobenzene

bis(p-dimethylaminophenyl)methanone

brilliant green carbocation

brilliant green

Downstream raw materials:

(4-(diethylamino)phenyl)(phenyl)methanone

N,N-diethylaniline

brilliant green

4,4'-(phenylmethylene)bis(N,N-diethylaniline)

Refernces

• 1、 Sen Gupta,Mishra,Radha Rani. "A study on equilibrium and kinetics of carbocation-to-carbinol conversion for di- and tri- arylmethane dye cations in aqueous solutions: Relative stabilities of dye carbocations and mechanism of dye carbinol formation". . p. 703 - 708. Retrieved 2007/10/03.
• 2、 Gupta, Susanta K. Sen,Arvind, Udai. "Carbenium ion-carbinol equilibration for basic triarylmethane dyes: Relative reactivities of dyes in aq. solutions". . p. 998 - 1000. Retrieved 2007/10/02.