Search Results for " Lovastatin "
Lovastatin EP Impurity A
| SZ目录编号: | SZ-L074002 |
| CAS 号 | 73573-88-3 |
| 分子式 | C23H34O5 |
| 分子量 | 390.5 |
| 投资状态 | In Stock |
| Shipping Condition | Ambient Temperature |
化学名称: (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)
异名: Mevastatin (EP) ; Compactin ; Pravastatin Deshydroxy Impurity
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: O=C(O1)C[C@@](O)([H])C[C@@]1([H])CC[C@]2([H])[C@]3([H])C(C=C[C@]2([H])C)=CCC[C@]3([H])OC([C@@](CC)([H])C)=O
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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