(S)-2-chloro-N1,N3-bis(1,3-dihydroxypropan-2-yl)-5-(2-hydroxypropanamido)-4,6-diiodoisophthalamide
Iopamidol EP Impurity I is a fully characterized chemical compound used as a reference standard of API Iopamidol. The standard offered is compliant with regulatory guidelines. Iopamidol 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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