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Metronidazole Benzoate
» Metronidazole Benzoate contains not less than 98.5 percent and not more than 101.0 percent of C13H13N3O4, calculated on the dried basis.
Packaging and storage
Preserve in well-closed, light-resistant containers. Store at 25
USP Reference standards
USP Metronidazole RS. USP Metronidazole Benzoate RS .
USP Tinidazole Related Compound A RS .
Identification
B:
The principal spot in the chromatogram of the Test solution corresponds to that in the chromatogram of Standard solution A, as obtained in the test for Related compounds.
Acidity
Neutralize 40 mL of a mixture of dimethylformamide and water (1:1) with hydrochloric acid or 0.02 M sodium hydroxide, add 0.2 mL of methyl red TS and 2.0 g of Metronidazole Benzoate, mix to dissolve, and titrate with 0.02 M sodium hydroxide: not more than 0.25 mL is required to produce a color change.
Loss on drying
Residue on ignition
Heavy metals, Method II
Related compounds
Adsorbent:
0.2-mm layer of chromatographic silica gel mixture.
Test solution
Transfer about 200 mg of Metronidazole Benzoate, accurately weighed, to a 10-mL volumetric flask, dissolve in and dilute with acetone to volume, and mix.
Standard solution A
Dissolve an accurately weighed quantity of USP Metronidazole Benzoate RS in acetone, and dilute quantitatively, and stepwise if necessary, with acetone to obtain a solution having a known concentration of about 0.1 mg per mL.
Standard solution B
Transfer 4.0 mL of Standard solution A to a 10-mL volumetric flask, dilute with acetone to volume, and mix.
Standard solution C
Transfer about 10 mg each of USP Metronidazole RS and USP Tinidazole Related Compound A RS, accurately weighed, to a 50-mL volumetric flask, dissolve in and dilute with acetone to volume, and mix. [noteUSP Tinidazole Related Compound A RS is 2-methyl-5-nitroimidazole.]
Application volume:
10 µL.
Developing solvent system:
ethyl acetate.
Procedure
Proceed as directed for Thin-Layer Chromatography under Chromatography
Assay
Transfer about 250 mg of Metronidazole Benzoate, accurately weighed, to a suitable container, and dissolve with stirring in 50.0 mL of glacial acetic acid. Titrate with 0.1 N perchloric acid, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction (see Titrimetry
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP32NF27 Page 2972
Pharmacopeial Forum: Volume No. 31(3) Page 781
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