(2RS,6RS)-2,6-dimethyl-4-[(2R)-2-methyl-3-[4-(2-methylbutan-2-yl) phenyl]propyl]morpholine and (2RS,6RS)-2,6-dimethyl-4-[(2S)-2-methyl-3-[4-(2-methylbutan-2-yl)phenyl]propyl]morpholine, hydrochloride (1:1)
Amorolfine EP Impurity E HCl (trans-Amorolfine HCl) (Mixture of Diastereomers) is a fully characterized chemical compound used as a reference standard of API Amorolfine. The standard offered is compliant with regulatory guidelines. Amorolfine EP Impurity E HCl (trans-Amorolfine HCl) (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 - NA
