5-O,12-Didemethyl-12-ethyl-22,23-dihydroavermectin A1a (as per EP); 12-demethyl-12-ethyl-H2B1a
Ivermectin EP Impurity E is a fully characterized chemical compound used as a reference standard of API Ivermectin. The standard offered is compliant with regulatory guidelines. Ivermectin EP Impurity E 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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Ivermectin EP Impurity A (Avermectin B1a) Mixture of avermectins, >85% B1
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M.W. 873.1
CAT# AR-I02948
CAS# 65195-55-3
