N1-Losartanyl-losartan; 2-Butyl-1-[[2'-[1-[[2-butyl-4-chloro-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-imidazol-5-yl]methyl]-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-4-chloro-1H-imidazole-5-methanol; Losartan Impurity L; Losartan EP Impurity L; Losartan USP-D
Losartan EP Impurity L is a fully characterized chemical compound used as a reference standard of API Losartan. The standard offered is compliant with regulatory guidelines. Losartan EP Impurity L 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 - 230971-71-8
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