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Lovastatin Hydroxy Impurity
| SZ CAT No: | SZ-L074024 |
| CAS No | NA |
| Mol.F. | C24H36O6 |
| Mol.Wt. | 420.5 |
| Inv. Status | Synthesis on demand |
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Usage Note:
Lovastatin Hydroxy Impurity is chemically (3R,7S,8aR)-8-(2-((2R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl)-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl 3-hydroxy-2-methylbutanoate. Lovastatin Hydroxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Lovastatin Hydroxy Impurity 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 Lovastatin.
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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