Brimonidine Tartrate

Base Information

Chemical Name:Brimonidine Tartrate
CAS No.:79570-19-7
Molecular Formula:(x)C₄H₆O₆*C₁₁H₁₀BrN₅
Molecular Weight:442.22144
Hs Code.:
Mol file:79570-19-7.mol

Synonyms:BRIMONIDINE TARTRATE

Suppliers and Price of Brimonidine Tartrate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
BRIMONIDINE-D- TARTRATE 95.00%
1G
$ 945.95

American Custom Chemicals Corporation
BRIMONIDINE-D- TARTRATE 95.00%
25MG
$ 225.75

Total 70 raw suppliers

Chemical Property of Brimonidine Tartrate

Chemical Property:

PSA：182.92000
LogP:-3.19120

Purity/Quality:

98%, ^*data from raw suppliers

BRIMONIDINE-D- TARTRATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Brimonidine Tartrate

There total 2 articles about Brimonidine Tartrate 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:

: 147-71-7,138508-61-9
D-tartaric acid

: 59803-98-4
5-bromo-6-(imidazolin-2-ylamino)-quinoxaline

: 1400635-36-0,79570-19-7
(5-bromoquinoxalin-6-yl)-(4,5-dihydro-1H-imidazol-2-yl)-amine L-tartrate

Guidance literature:: In methanol; water;

Reference yield:

: 134892-45-8
6-amino-5-bromoquinoxaline hydrobromide

: 1400635-36-0,79570-19-7
(5-bromoquinoxalin-6-yl)-(4,5-dihydro-1H-imidazol-2-yl)-amine L-tartrate

Guidance literature:: Multi-step reaction with 3 steps

1.1: water / 2 h / 20 °C

2.1: benzene

2.2: Reflux

3.1: water; methanol

In methanol; water; benzene;

Reference yield:

: 1400635-36-0,79570-19-7
5-bromo-6-(2-imidazolylamino)quinoxaline L-tartrate

: (S)-2-(tert-butyldiphenylsilanyloxy)propionic acid (S)-2-[2-(5-bromoquinoxalin-6-ylamino)-4,5-dihydroimidazol-1-yl]-1-methyl-2-oxoethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / water / 0.25 h / 0 - 5 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dimethyl sulfoxide / 2 h / 0 - 30 °C / Inert atmosphere

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In water; dimethyl sulfoxide;