Micafungin Epimer Impurity (USP)

Micafungin Epimer Impurity (USP) is chemically Sodium 5-[(1S,2S)-2-{(2R,6S,9S,11R,12S,14aS,15S,16S,20S,23S,25aS)-20-[(R)-3-amino1-hydroxy-3-oxopropyl]-2,11,12,15-tetrahydroxy-6-[(R)-1-hydroxyethyl]-16-methyl5,8,14,19,22,25-hexaoxo-9-(4-{5-[4-(pentyloxy)phenyl]isoxazol-3-yl}benzamido)tetracosahydro-1H-dipyrrolo[2,1-c:2',1'-l][1,4,7,10,13,16]hexaazacyclohenicosin-23-yl}-1,2-dihydroxyethyl]-2-hydroxyphenyl sulfate. It is also known as Micafungin Impurity H. Micafungin Epimer Impurity (USP) is supplied with detailed characterization data compliant with regulatory guideline. Micafungin Epimer Impurity (USP) can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Micafungin .

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.