(4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl)((5S)-5-methyltetrahydrofuran-2-yl)methanone
Terazosin EP Impurity I is a fully characterized chemical compound used as a reference standard of API Lumacaftor. The standard offered is compliant with regulatory guidelines. Terazosin EP Impurity I 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
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