Fragment-[10-31]-Liraglutide, Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys(γ-Glu-palmitoyl)-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-Gly-OH; Liraglutide Impurity 6
Liraglutide Hydrolysis 16-37 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 16-37 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)
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CAT# AR-L07491
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