CAS 6452-57-9
:3-Isopropylamino-1,2-propandiol
- 1,2-Dihydroxy-3-isopropylaminopropane
- 1,2-Propanediol, 3-(isopropylamino)-
- 1,2-Propanediol, 3-[(1-methylethyl)amino]-
- 3-(Isopropylamino)-1,2-Propanediol
- 3-(Propan-2-Ylamino)Propane-1,2-Diol
- 3-[(1-Methylethyl)amino]-1,2-propanediol
- 3-[(Propan-2-yl)amino]propane-1,2-diol
- 3-(Isopropylamino)propane-1,2-diol
1,2-Dihydroxy-3-isopropylaminopropane
CAS:Formel:C6H15NO2Reinheit:98%Farbe und Form:LiquidMolekulargewicht:133.18883-(Isopropylamino)-1,2-Propanediol
CAS:3-(Isopropylamino)-1,2-PropanediolReinheit:98%Molekulargewicht:133.19g/mol(2RS)-3-[(1-Methylethyl)amino]propane-1,2-diol
CAS:Kontrolliertes ProduktFormel:C6H15NO2Farbe und Form:NeatMolekulargewicht:133.193-Isopropylamino-1,2-propanediol
CAS:Impurity Metoprolol EP Impurity N
Applications 3-Isopropylamino-1,2-propanediol (Metoprolol EP Impurity N) is a versatile organic building block, used in different chemical synthesis. It is used in the preparation of heterocyclic propanolamines, which are shown to have β-adrenergic antagonist activity.
References Dean, V. et al.: Drug Design and Discovery,10, 89 (1993);Formel:C6H15NO2Farbe und Form:ColourlessMolekulargewicht:133.193-Isopropylamino-1,2-propanediol
CAS:Metoprolol tartrate impurity N is an impurity of metoprolol succinate and has been shown to have photocatalytic activity. Metoprolol tartrate impurity N has been found in commercially available pharmaceutical products. It has been validated by both phase chromatography and hydrophilic interaction chromatography, with the latter providing a more detailed separation of the compound's various reaction intermediates. Impurities such as metoprolol tartrate impurity N may be present in commercial products due to the use of pyridinium salt as a solvent in the manufacturing process. The enantiomeric purity of metoprolol tartrate impurity N was determined to be 99%.
Formel:C6H15NO2Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:133.19 g/mol







