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Ritonavir EP Impurity E
Ritonavir EP Impurity E

Ritonavir EP Impurity E

Catalog No. KMR006020
CAS No. 176655-56-4
Alt. name Hydroxy Ritonavir (USP)
Formula C37H48N6O6S2
FW 736.9
Unit Price Stock
100 mg Enquire Enquire
Chemical Name: Thiazol-5-yl-methyl [(1S,2S,4S)-1-benzyl-2-hydroxy-4-[[(2S)-2-[[[[2-(1-hydroxy-1-methylethyl)thiazol-4-yl]methyl]methylcarbamoyl]amino]-3-methylbutanoyl]amino]-5-phenylpentyl]carbamate (as per EP); Thiazol-5-ylmethyl (2S,3S,5S)-3-hydroxy-5-[(S)-2-(3-{[2-(2-hydroxypropan-2-yl)thiazol-4-yl]methyl}-3-methylureido)-3-methylbutanamido]-1,6-diphenylhexan-2-ylcarbamate (as per USP)
Purity: >95%
Storage: Store at 2-8 deg. C for long term storage
Shipping: Product is stable to be Shipped at Room Temperature
Ritonavir EP Impurity E is chemically Thiazol-5-yl-methyl [(1S,2S,4S)-1-benzyl-2-hydroxy-4-[[(2S)-2-[[[[2-(1-hydroxy-1-methylethyl)thiazol-4-yl]methyl]methylcarbamoyl]amino]-3-methylbutanoyl]amino]-5-phenylpentyl]carbamate (as per EP); Thiazol-5-ylmethyl (2S,3S,5S)-3-hydroxy-5-[(S)-2-(3-{[2-(2-hydroxypropan-2-yl)thiazol-4-yl]methyl}-3-methylureido)-3-methylbutanamido]-1,6-diphenylhexan-2-ylcarbamate (as per USP) . Ritonavir EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Ritonavir EP Impurity E 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 Ritonavir EP Impurity E.

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

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