» Pyrimethamine contains not less than 99.0 percent and not more than 101.0 percent of C12H13ClN4, calculated on the dried basis.
Packaging and storage Preserve in tight, light-resistant containers.
B: Mix about 100 mg with 500 mg of anhydrous sodium carbonate, and ignite the mixture. Cool, add 5 mL of hot water, heat for 5 minutes on a steam bath, filter, and neutralize the filtrate with nitric acid: the solution meets the requirements of the test for Chloride 191.
C: The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay.
Melting range 741: between 238 and 242.
Loss on drying 731 Dry it at 105 for 4 hours: it loses not more than 0.5% of its weight.
Residue on ignition 281: not more than 0.1%.
Ordinary impurities 466
Test solution: a mixture of methanol and chloroform (1:1).
Standard solution: a mixture of methanol and chloroform (1:1).
Eluant: a mixture of n-propyl alcohol, glacial acetic acid, and water (8:1:1).
0.1% Phosphoric acid solution Add 1 mL of phosphoric acid to water, and dilute to 1000 mL.
Mobile phase Prepare a suitable degassed and filtered mixture of 0.1% Phosphoric acid solution and acetonitrile (83:17). Make adjustments if necessary (see System Suitability under Chromatography 621).
Standard preparation Transfer an accurately weighed quantity of USP Pyrimethamine RS to a suitable volumetric flask, and dilute with 0.1% Phosphoric acid solution to volume to obtain a solution having a known concentration of about 0.02 mg per mL.
Assay preparation Transfer an accurately weighed quantity of Pyrimethamine to a suitable volumetric flask, and dilute with 0.1% Phosphoric acid solution to volume to obtain a solution having a known concentration of about 0.02 mg per mL.
Chromatographic system (see Chromatography 621) The liquid chromatograph is equipped with a 210-nm detector and a 2.0-mm × 10-cm column that contains 3-µm packing L11. The flow rate is about 0.3 mL per minute. Chromatograph replicate injections of the Standard preparation, and record the peak responses as directed for Procedure: the capacity factor, k ¢, is not less than 2.5; the tailing factor is not more than 1.8; and the relative standard deviation is not more than 1.0%.
Procedure Separately inject equal volumes (about 5 µL) of the Standard preparation and the Assay preparation into the chromatograph, record the chromatograms, and measure the responses for the major peaks. Calculate the quantity, in percentage, of C12H13ClN4 in the portion of Pyrimethamine taken by the formula:
100(CS / CU)(rU / rS)in which CS is the concentration, in mg per mL, of USP Pyrimethamine RS in the Standard preparation; CU is the concentration, in mg per mL, of Pyrimethamine in the Assay preparation based on the weighed amount; rU and rS are the peak responses obtained from the Assay preparation and the Standard preparation, respectively; and 100 is the percent conversion factor.
Auxiliary Information Please check for your question in the FAQs before contacting USP.Chromatographic Column
USP32NF27 Page 3454Pharmacopeial Forum: Volume No. 33(5) Page 939
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.