thiazol-5-ylmethyl ((2S,3S,5S)-3-hydroxy-5-((S)-4-isopropyl-2,5-dioxoimidazolidin-1-yl)-1,6-diphenylhexan-2-yl)carbamate;N-[(1S,2S,4S)-2-Hydroxy-4-[(4S)-4-(1-methylethyl)-2,5-dioxo-1-imidazolidinyl]-5-phenyl-1-(phenylmethyl)pentyl]carbamic Acid 5-Thiazolylmethyl Ester; 1,3-Thiazol-5-ylmethyl N-[(1S,2S,4S)-1-benzyl-2-hydroxy-4-((4S)-4-isopropyl-2,5-dioxoimidazolidin-1-yl)-5-phenylpentyl]carbamate; Thiazol-5-ylmethyl (2S,3S,5S)-3-hydroxy-5-[(S)-4-isorpopyl-2,5-dioxoimidazolidin-1-yl]-1,6-diphenylhexan-2-ylcarbamate; Ritonavir EP Impurity F;Des(isopropylthiazolyl) Hydantoin Ritonavir (>90%)
Ritonavir EP Impurity F is a fully characterized chemical compound used as a reference standard of API Ritonavir. The standard offered is compliant with regulatory guidelines. Ritonavir EP Impurity F 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 - 1010809-61-6
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