1,1'-(disulfanediylbis(ethane-2,1-diyl))bis(4-phenylimidazolidin-2-one); Bis(2-(2-oxo-4-phenylimidazolidin-1-yl)ethyl) disulfide; Levamisole hydrochloride specified impurity E [EP]; 2-Imidazolidinone, 1,1'-(dithiodi-2,1-ethanediyl)bis(4-phenyl-; Bis(2-(2-oxo-4-phenylimidazolidin-1-yl)ethyl) disulfide, (+/-)-; 1,1'-((Disulfane-1,2-diyl)bis(ethylene))bis((4RS)-4-phenylimidazolidin-2-one)
Levamisole EP Impurity E (Mixture of Diastereomers) is a fully characterized chemical compound used as a reference standard of API Levamisole. The standard offered is compliant with regulatory guidelines. Levamisole EP Impurity E (Mixture of Diastereomers) is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 32190-36-6
