(E)-7-(((R)-2-amino-2-carboxyethyl)thio)-2-((S)-2,2-dimethylcyclopropanecarboxamido)hept-3-enoic acid; (E)-(2RS)-7-[[(2R)-2-amino-2-carboxyethyl]sulfanyl]-2-[[[(1S)-2,2-dimethylcyclopropyl]carbonyl]amino]hept-3-enoic acid
Cilastatin Impurity G is a fully characterized chemical compound used as a reference standard of API Cilastatin. The standard offered is compliant with regulatory guidelines. Cilastatin 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 -
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Cilastatin EP Impurity A HCl (Mixture Of Diastereomers)
M.F.
M.W. 374.46 36.46
CAT# AR-C02762
CAS# NA
