Thiazol-5-yl-methyl (1S,2S,4S)-1-benzyl-2-hydroxy-4-[[(2-methylpropoxy) carbonyl] amino]-5-phenylpentyl]carbamate (as per EP); thiazol-5-ylmethyl (2S,3S,5S)-(5-isobutoxycarbonylamino)-3-hydroxy-1,6-diphenylhexan-2-ylcarbamate (as per USP); Ritonavir Isobutoxycarbonyl Aminoalcohol (USP)
Ritonavir EP Impurity K 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 K 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 - 1010809-39-8
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