Monographs: Pharmaceutical substances: Phenytoin sodium (Phenytoinum natricum)Molecular formula. C15H11N2NaO2 Relative molecular mass. 274.3 Graphic formula.
Chemical name. 5,5-Diphenylhydantoin monosodium salt; 5,5-diphenyl-2,4-imidazolidinedione monosodium salt; CAS Reg. No. 630-93-3. Description. A white powder; odourless. Solubility. Soluble in water, giving a slightly turbid solution owing to partial hydrolysis; soluble in ethanol (~750 g/l) TS; practically insoluble in ether R. Category. Anticonvulsant. Storage. Phenytoin sodium should be kept in a tightly closed container. Additional information. Phenytoin sodium is somewhat hygroscopic and on exposure to air gradually absorbs carbon dioxide. Requirements Definition. Phenytoin sodium contains not less than 98.5% and not more than 101.0% of C15H11N2NaO2, calculated with reference to the dried substance. Identity tests • Either tests A and D or tests B, C, D, and E may be applied.
Heavy metals. To 1.0 g add 24 mL of water and 6 mL of hydrochloric acid (~70 g/l) TS; heat the mixture until boiling begins. Filter, cool, and filter again through a suitable sintered glass filter. Dilute to 40 mL with water, mix, and determine the content of heavy metals as described under 2.2.3 Limit test for heavy metals, according to Method A; not more than 10 μg/g. Solution in alkali. To 20 mg add 8.0 mL of carbon-dioxide-free water R and then add gradually 2.0 mL of carbonate-free sodium hydroxide (0.1 mol/L) VS; the solution is clear and not more intensely coloured than standard colour solution Yw2 when compared as described under 1.11.1 Colour of liquids. Loss on drying. Dry to constant weight at 105°C; it loses not more than 30 mg/g. Assay. Dissolve about 0.55 g, accurately weighed, in 30 mL of glacial acetic acid R1, add 3 drops of 1-naphtholbenzein/acetic acid TS as indicator and titrate with perchloric acid (0.1 mol/l) VS, as described under 2.6 Non-aqueous titration, Method A. Each mL of perchloric acid (0.1 mol/l) VS is equivalent to 27.43 mg of C15H11N2NaO2. Additional requirements for Phenytoin sodium for parenteral use Complies with the monograph for "Parenteral preparations". Bacterial endotoxins. Carry out the test as described under 3.4 Test for bacterial endotoxins; contains not more than 0.3 IU of endotoxin RS per mg. |