(6R,7R)-3-methyl-8-oxo-7-pivalamido-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; 7-ADCA Pivalamide; (6R,7R)-7-[(2,2-dimethyl-1-oxopropyl)amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Cephalexin Impurity E; (6R-trans)-7-[(2,2-dimethyl-1-oxopropyl)amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; 7-Aminodeacetoxycephalosporanic Acid Pivalamide; Cefradine EP Impurity G (Cefalexin EP Impurity E)
Cephalexin Impurity E (Cefradine EP Impurity G) is a fully characterized chemical compound used as a reference standard of API Cephalexin (Cefalexin. The standard offered is compliant with regulatory guidelines. Cephalexin Impurity E (Cefradine EP Impurity G) 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 - 146794-70-9
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