3D-FM25981 - r-metoprolol
(R)-Metoprolol
CAS:Controlled ProductApplications (R)-Enantiomer of Metoprolol. Antihypertensive; antianginal; antiarrhythmic (class II).
References Johansson, et al.: Eur. J. Pharmacol., 24, 194 (1973), Luch, J.R., et al.: Anal. Profiles Drug Subs., 12, 325 (1983), Benfield, P., et al.: Drugs, 31, 376 (1986),Formula:C15H25NO3Color and Shape:NeatMolecular weight:267.36(R)-Metoprolol-d7
CAS:Controlled ProductApplications Labelled (R)-enantiomer of Metoprolol. An antihypertensive, though up to 380 times less potent than the (S)-enantiomer.
References Toda, N., et al.: J. Pharm. Exp. Ther., 207, 311 (1978),Formula:C15H18D7NO3Color and Shape:Light Yellow Solid With A Low Melting PointMolecular weight:274.411,2-Dihydroxy-3-isopropylaminopropane
CAS:Formula:C6H15NO2Purity:98%Color and Shape:LiquidMolecular weight:133.1888(2R)-1-[4-(2-methoxyethyl)phenoxy]-3-[(propan-2-yl)amino]propan-2-ol
CAS:Formula:C15H25NO3Purity:95%Color and Shape:LiquidMolecular weight:267.3639Metoprolol tartrate
CAS:Controlled ProductFormula:C15H25NO3·C4H6O6Color and Shape:NeatMolecular weight:684.81Metoprolol Tartrate
CAS:Controlled ProductFormula:C15H25NO3·C4H6O6Color and Shape:NeatMolecular weight:684.81alpha-Hydroxy Metoprolol (Mixture of Diastereomers)
CAS:Controlled ProductApplications A metabolite of Metoprolol.
References Lennard, M.S., et al.: Br. J. Clin. Pharmacol., 14, 713 (1982), Gengo, F.M., et al.: Clin. Pharmacol. Ther., 36, 320 (1984),Formula:C15H25NO4Color and Shape:Off-White To BeigeMolecular weight:283.36rac Metoprolol Hemi (+)-Tartrate
CAS:Controlled ProductApplications A β1 selective aryloxypropanolamine andrenergic antagonist which is used in the treatment of a variety of cardiovascular disorder (1,2).Antihypertensive; antianginal; antiarrhythmic (class II).
References 1. Johansson, B. et al.: Eur J Pharmacol. 1973 Nov;24(2):194-204.2. Benfield, P. et al.: Drugs. 1986 May;31(5):376-429.Formula:C15H25NO3·C4H6O6Color and Shape:NeatMolecular weight:684.811,3-Bis[4-(2-methoxyethyl)phenoxy]-2-propanol
CAS:Controlled ProductApplications Metoprolol (M338790) impurity.
References Ruane, R., et al.: J. Pharm. Biomed. Anal., 8, 1091 (1990), Berger, T., et al.: J. Chromatogr. Sci., 29, 310 (1991),Formula:C21H28O5Color and Shape:NeatMolecular weight:360.44rac 1-Chloro-3-[4-(2-methoxyethyl)phenoxy]-2-propanol
CAS:Controlled ProductImpurity Metoprolol USP Related Compound B
Applications An intermediate for the synthesis of β-chlorohydrins and β-chloroamines. An impurity found in metoprolol. Metroprolol USP Related Compound B.
References Moore, R., et al.: Marine Natural Products, 1, 43 (1978),Formula:C12H17ClO3Color and Shape:ColourlessMolecular weight:244.713-[4-(2-Methoxyethyl)phenoxy]-1,2-epoxypropane
CAS:Applications Impurity of Metoprolol.
References Lis, R., et al.: J. Med. Chem., 33(10), 2883 (1990)Formula:C12H16O3Color and Shape:NeatMolecular weight:208.25(R)-3-[4-(2-Methoxyethyl)phenoxy]-1,2-epoxypropane
CAS:Controlled ProductApplications Impurity of (R)-Metoprolol.
References Murthy, S., et al.: J. Labelled Comp. Radiopharm., 28, 1410 (1990),Formula:C12H16O3Color and Shape:YellowMolecular weight:208.25(R)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride
CAS:(R)-(-)-alpha-Methoxy-alpha-trifluoromethyl-phenylacetyl chloride is an enantiomer that has a chiral center. It is used in the synthesis of metoprolol and bisoprolol, which are drugs that are prescribed to treat hypertension and angina pectoris. The racemate is used in the separation of amines by high performance liquid chromatography (Hplc). This compound also has a hydroxyl group and two fatty acids, which can be identified using a chromatographic method. The compound contains a chloride as well as a transfer group.Formula:C10H8ClF3O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:252.62 g/mol
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