Racephedrine

Base Information

Chemical Name:Racephedrine
CAS No.:90-83-5
Molecular Formula:C₁₀H₁₅NO
Molecular Weight:165.235
Hs Code.:

Synonyms:(R*,S*)-(+-)-alpha-(1-(Methylamino)ethyl)benzyl alcohol;Benzenemethanol, alpha-(1-(methylamino)ethyl)-, (R*,S*)-(+-)- (9CI);(+-)-Ephedrine;Benzenemethanol, alpha-((1R)-1-(methylamino)ethyl)-, (alphaS)-rel-;4-13-00-01881 (Beilstein Handbook Reference);2-methylamino-1-phenyl-propan-1-ol;Ephedrine dl-;

Suppliers and Price of Racephedrine

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

Total 54 raw suppliers

Chemical Property of Racephedrine

Chemical Property:

Melting Point:38.1oC
Boiling Point:255 °C at 760 mmHg
Flash Point:85.6 °C
PSA：96.82000
Density:1.015 g/cm³
LogP:0.58650

Purity/Quality:: 99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Racephedrine

There total 346 articles about Racephedrine 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: 91.0%

: 552-79-4,1201-56-5,14222-20-9,17605-71-9,39263-91-7,42151-56-4,51018-28-1,62560-55-8,87040-40-2
(+/-)-erythro-methylephedrine

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 90-81-3,90-82-4,299-42-3,321-97-1,321-98-2,4125-58-0,34783-90-9,38732-95-5,53214-57-6,7009-81-6,90-83-5,6912-63-6
ephedrine

: 100-52-7
benzaldehyde

: 75-07-0,9002-91-9
acetaldehyde

: 124-40-3
dimethyl amine

Guidance literature:: With water; at 25 ℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;