Lovastatin EP Impurity A | CAS 73573-88-3 - Request Quote
Lovastatin EP Impurity A
| SZ CAT No: | SZ-L074002 |
| CAS No | 73573-88-3 |
| Mol.F. | C23H34O5 |
| Mol.Wt. | 390.5 |
| Inv. Status | Synthesis on demand |
| Shipping Condition | Room Temperature |
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Usage Note:
Lovastatin EP Impurity A is chemically (1S,7S,8S,8aR)-8-[2-[(2R,4R)-4-Hydroxy-6-oxooxan-2-yl]ethyl]-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl (2S)-2-methylbutanoate (as per EP). It is also known as Mevastatin (EP) ; Compactin ; Pravastatin Deshydroxy Impurity. Lovastatin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Lovastatin 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 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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Lovastatin Reference Standard
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Lovastatin EP Impurity A for DMF Filing
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