(S,Z)-7-((2-aminoethyl)thio)-2-(2,2-dimethylcyclopropanecarboxamido)hept-2-enoic acid;(Z)-7-[(2-aminoethyl)sulfanyl]-2-[[[(1S)-2,2-dimethylcyclopropyl]carbonyl]amino]hept-2-enoic acid
Cilastatin EP Impurity H is a fully characterized chemical compound used as a reference standard of API Cilastatin. The standard offered is compliant with regulatory guidelines. Cilastatin EP Impurity H 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
