(1S,3R,4R,7R,9R,11R,15S,16R,17R,18S,19E,21E,25E,27E,29E,31E,33R,35S,36R,37S)-33-(((2R,3S,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-(6-(methyl(7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)amino)hexanamido)tetrahydro-2H-pyran-2-yl)oxy)-1,3,4,7,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,25,27,29,31-hexaene-36-carboxylic acid
Nystatin Impurity 2 is a fully characterized chemical compound used as a reference standard of API Nystatin. The standard offered is compliant with regulatory guidelines. Nystatin Impurity 2 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 - NA
