Hydrolysis 12-37 Liraglutide Impurity
Liraglutide Hydrolysis 12-37 Impurity is a fully characterized chemical compound used as a reference standard of API Liraglutide. The standard offered is compliant with regulatory guidelines. Liraglutide Hydrolysis 12-37 Impurity 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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Liraglutide Impurity 2 TFA (Kyn25-Liraglutide TFA)
M.F.
M.W. 3755.25 4*114.02
CAT# AR-L07491
CAS# NA
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