Calcium Ascorbate (kal' see um a skor' bate). C12H14CaO12·2H2O426.34 DEFINITION Calcium Ascorbate contains NLT 98.0% and NMT 101.0% of calcium ascorbate dihydrate (C12H14CaO12·2H2O), calculated on the as-is basis. IDENTIFICATION • A. Identification TestsGeneral, Calcium 191: A 100 mg/mL solution meets the requirements. • B. A 100 mg/mL solution decolorizes a 100 mg/mL solution of dichlorophenolindophenol. ASSAY • Procedure Sample: 300 mg of Calcium Ascorbate Blank: 50 mL of water Titrimetric system (See Titrimetry 541.) Mode: Direct titration Titrant: 0.1 N iodine VS Endpoint detection: Visual Analysis: Transfer the Sample into a 250-mL conical flask, add 50 mL of water, and mix to dissolve. Immediately titrate with the Titrant, adding 3 mL of starch TS as the endpoint is approached. Perform a Blank determination. Calculate the percentage of calcium ascorbate dihydrate (C12H14CaO12·2H2O) in the Sample taken: Result = {[(VS VB) × N × F]/W} × 100
Acceptance criteria: 98.0%101.0% on the as-is basis IMPURITIES • Arsenic, Method I 211: NMT 3 µg/g • Heavy Metals, Method II 231: NMT 10 ppm • Limit of Fluoride [NotePrepare and store all solutions in plastic containers. ] Buffer solution: 294 mg/mL of sodium citrate dihydrate in water Standard stock solution: 1.1052 mg/mL of USP Sodium Fluoride RS in water Standard solution: Transfer 20.0 mL of Standard stock solution to a 100-mL volumetric flask containing 50.0 mL of Buffer solution, dilute with water to volume, and mix. Each mL of Standard solution contains 100 µg of fluoride ion. Sample solution: Transfer 2.0 g of Calcium Ascorbate to a beaker containing a plastic-coated stirring bar. Add 20 mL of water and 2.0 mL of hydrochloric acid, and stir until dissolved. Add 50.0 mL of Buffer solution and sufficient water to make 100 mL. Electrode system: Use a fluoride-specific ion-indicating electrode and a silversilver chloride reference electrode connected to a pH meter capable of measuring potentials with a minimum reproducibility of ± 0.2 mV (see pH 791). Analysis Samples: Standard solution and Sample solution Standard response line: Transfer 50.0 mL of Buffer solution and 2.0 mL of hydrochloric acid to a beaker, and add water to make 100 mL. Add a plastic-coated stirring bar, insert the electrodes into the solution, stir for 15 min, and read the potential, in mV. Continue stirring, and at 5-min intervals add 100, 100, 300, and 500 µL of Standard solution, reading the potential 5 min after each addition. Plot the logarithms of the cumulative fluoride ion concentrations (0.1, 0.2, 0.5, and 1.0 µg/mL) versus potential, in mV. Rinse and dry the electrodes, insert them into the Sample solution, stir for 5 min, and read the potential, in mV. From the measured potential and the Standard response line determine the concentration, C (in µg/mL), of fluoride ion in the Sample solution. Calculate the content of fluoride in the portion of Calcium Ascorbate taken: Result = (C × V)/W
Acceptance criteria: NMT 10 ppm SPECIFIC TESTS • Optical Rotation, Specific Rotation 781S Sample solution: 50 mg/mL in carbon dioxide-free water [NotePerform measurements immediately after preparation. ] Acceptance criteria: +95 to +97 • Loss on Drying 731: Dry 3 g at 105 for 2 h: it loses NMT 0.1% of its weight. ADDITIONAL REQUIREMENTS • Packaging and Storage: Preserve in tight, light-resistant containers. Auxiliary Information Please check for your question in the FAQs before contacting USP.
USP35NF30 Page 2441 Pharmacopeial Forum: Volume No. 27(6) Page 3255 |