Search Results for " Lopinavir "
Lopinavir EP Impurity A
| SZ目录编号: | SZ-L008002 |
| CAS 号 | 192726-05-9 |
| 分子式 | C27H38N4O3 |
| 分子量 | 466.6 |
| 投资状态 | In Stock |
化学名称: (2S)-N-[(1S,3S,4S)-1-Benzyl-4-amino-3-hydroxy-5-phenylpentyl]-3-methyl-2-[2-oxotetrahydropyrimidin1(2H)-yl]butanamide (as per EP); (S)-N-[(2S,4S,5S)-5-Amino-4-hydroxy-1,6-diphenylhexan-2-yl]-3-methyl-2-[2-oxotetrahydropyrimidin-1(2H)-yl]butanamide (as per USP)
异名: Lopinavir Free Amine (USP)
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: CC(C)[C@H](N1CCCNC1=O)C(N[C@@H](CC2=CC=CC=C2)C[C@H](O)[C@@H](N)CC3=CC=CC=C3)=O
Lopinavir EP Impurity A is chemically (2S)-N-[(1S,3S,4S)-1-Benzyl-4-amino-3-hydroxy-5-phenylpentyl]-3-methyl-2-[2-oxotetrahydropyrimidin1(2H)-yl]butanamide (as per EP); (S)-N-[(2S,4S,5S)-5-Amino-4-hydroxy-1,6-diphenylhexan-2-yl]-3-methyl-2-[2-oxotetrahydropyrimidin-1(2H)-yl]butanamide (as per USP). It is also known as Lopinavir Free Amine (USP). Lopinavir EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Lopinavir EP Impurity A 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 Lopinavir.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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