2-((2R,3R,5S)-6-((1S,3S,5Z,7R,10S,11R,12S,13E)-7-allyl-10-hydroxy-14-((1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl)-1-methoxy-3,5,11,13-tetramethyl-12-(((S)-1-nitrosopiperidine-2-carbonyl)oxy)-8-oxotetradeca-5,13-dien-1-yl)-2-hydroxy-5-methoxy-3-methyltetrahydro-2H-pyran-2-yl)-2-oxoacetic acid
Tacrolimus 21-Carboxylic Acid Nitroso Impurity is a fully characterized chemical compound used as a reference standard of API Tacrolimus. The standard offered is compliant with regulatory guidelines. Tacrolimus 21-Carboxylic Acid Nitroso Impurity 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
