Cysteine Hydrochloride (sis' te een hye'' droe klor' ide). C3H7NO2S·HCl157.62 l-Cysteine hydrochloride monohydrate ![]() ![]() ![]() Anhydrous ![]() ![]() ![]() DEFINITION Cysteine Hydrochloride is l-cysteine hydrochloride monohydrate and contains NLT 98.5% and NMT 101.5% of l-cysteine hydrochloride (C3H7NO2S·HCl), calculated on the dried basis. IDENTIFICATION ASSAY • Procedure Sample: 250 mg of Cysteine Hydrochloride Blank: Proceed as directed in the Analysis without the Sample. Titrimetric system (See Titrimetry ![]() ![]() Mode: Residual titration Titrant: 0.1 N iodine VS Back titrant: 0.1 N sodium thiosulfate VS Endpoint detection: Visual Analysis: Transfer the Sample to an iodine flask. Add 20.0 mL of water and 4 g of potassium iodide, and mix. Cool the solution in an ice bath, and add 5 mL of 3 N hydrochloric acid and 25.0 mL of 0.1 N iodine VS. Insert the stopper, and allow to stand in the dark for 20 min. Titrate the excess iodine with the Back titrant. Add 3 mL of starch TS as the endpoint is approached. Perform the Blank determination. Calculate the percentage of cysteine hydrochloride (C3H7NO2S·HCl) in the Sample taken: Result = {[(VB ![]()
Acceptance criteria: 98.5%–101.5% on the dried basis IMPURITIES • Residue on Ignition ![]() ![]() • Chloride and Sulfate, Sulfate ![]() ![]() Standard solution: 0.10 mL of 0.020 N sulfuric acid Sample: 0.33 g of Cysteine Hydrochloride Acceptance criteria: NMT 0.03%. • Iron ![]() ![]() • Heavy Metals, Method I ![]() ![]() • Related Compounds N-Ethylmaleimide solution: 40 mg/mL of N-ethylmaleimide in alcohol Standard stock solution: Dissolve 20 mg of USP l-Cysteine Hydrochloride RS in 10.0 mL of water. Add 10.0 mL of N-Ethylmaleimide solution, and mix. Allow the solution to stand for 5 min before using. Standard solution: 0.05 mg/mL from Standard stock solution in water. [Note—This solution has a concentration equivalent to 0.5% of that of the Sample solution. ] System suitability solution: Transfer 10 mg of USP l-Tyrosine RS and 10 mL of the Standard stock solution to a 25-mL volumetric flask. Dilute with water to volume. Sample stock solution: Transfer 0.2 g of Cysteine Hydrochloride to a 10-mL volumetric flask, dissolve, and dilute with water to volume. Sample solution: To 5.0 mL of the Sample stock solution add 5.0 mL of N-Ethylmaleimide solution, and mix. Allow the solution to stand for 5 min before using. Chromatographic system Mode: TLC Adsorbent: 0.25-mm layer of chromatographic silica gel mixture Application volume: 5 µL Developing solvent system: Butyl alcohol, glacial acetic acid, and water (3:1:1) Spray reagent: 2 mg/mL of ninhydrin in a mixture of butyl alcohol and 2 N acetic acid (95:5) System suitability Suitability requirements: The chromatogram of the System suitability solution exhibits two clearly separated spots. Analysis Samples: Standard solution, System suitability solution, and Sample solution. After air-drying the plate, spray with Spray reagent, and heat between 100 ![]() ![]() Acceptance criteria: Any secondary spot of the Sample solution is not larger or more intense than the principal spot of the Standard solution. Individual impurities: NMT 0.5% Total impurities: NMT 2.0% SPECIFIC TESTS • Optical Rotation, Specific Rotation ![]() ![]() Sample solution: 80 mg/mL in 6 N hydrochloric acid Acceptance criteria: +5.7 ![]() ![]() • Loss on Drying ![]() ![]() ADDITIONAL REQUIREMENTS • Packaging and Storage: Preserve in well-closed containers. Auxiliary Information— Please check for your question in the FAQs before contacting USP.
USP35–NF30 Page 2798 Pharmacopeial Forum: Volume No. 30(5) Page 1598Chromatographic Column— Chromatographic columns text is not derived from, and not part of, USP 35 or NF 30. |