(((2S,5R,6R)-3,3-dimethyl-7-oxo-6-((R)-2-((E)-(5-oxohexan-2-ylidene)amino)-2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl)oxy)methyl 3,3-dimethyl-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate
Sultamicillin EP Impurity E is a fully characterized chemical compound used as a reference standard of API Sultamicillin. The standard offered is compliant with regulatory guidelines. Sultamicillin 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 -
