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Metoprolol Fumarate
(C15H25NO3)2·C4H4O4
2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-, (±)-, (E)-2-butanedioate (2:1) (salt). (±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl)-phenoxy]-2-propanol fumarate (2:1) (salt) » Metoprolol Fumarate contains not less than 99.0 percent and not more than 100.5 percent of (C15H25NO3)2·C4H4O4, calculated on the dried basis.
Packaging and storage
Preserve in tight, light-resistant containers.
Identification
B:
Prepare a test solution in methanol containing 10 mg per mL. Separately apply 20 µL of the test solution and 20 µL of a Standard solution of USP Metoprolol Fumarate RS containing 10 mg per mL to a thin-layer chromatographic plate (see Chromatography
pH
Loss on drying
Residue on ignition
Heavy metals, Method I
Chromatographic purity
Diluent
Prepare a mixture of methanol and water (10:1).
Standard dilutions
Dissolve a suitable quantity of USP Metoprolol Fumarate RS, accurately weighed, in Diluent, and dilute quantitatively with Diluent to obtain solutions having known concentrations of 1.0, 0.5, 0.2, and 0.1 mg per mL, respectively.
Test solution
Dissolve a quantity of Metoprolol Fumarate in Diluent to obtain a solution containing 100 mg per mL.
Chromatographic chamber
and Detecting reagentPrepare as directed in the test for Chromatographic purity under Metoprolol Tartrate.
Procedure
Proceed as directed for Procedure in the test for Chromatographic purity under Metoprolol Tartrate: the specified results are obtained.
Assay
Dissolve about 325 mg of Metoprolol Fumarate, accurately weighed, in 20 mL of glacial acetic acid, and titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically, using a glass electrode and a calomel electrode containing glacial acetic acid saturated with lithium chloride (see Titrimetry
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP32NF27 Page 2963
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