Levonorgestrel EP Impurity P | CAS 100021-05-4 - Request Quote
Levonorgestrel EP Impurity P
| SZ CAT No: | SZ-L021015 |
| CAS No | 100021-05-4 |
| Mol.F. | C21H28O2 |
| Mol.Wt. | 312.5 |
| Inv. Status | In Stock |
| Shipping Condition | Room Temperature |
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Usage Note:
Levonorgestrel EP Impurity P is chemically 13-Ethyl-17-hydroxy-18,19-dinor-17α-pregn-5-en-20-yn-3-one (as per EP). It is also known as Δ5-levonorgestrel (EP). Levonorgestrel EP Impurity P is supplied with detailed characterization data compliant with regulatory guideline. Levonorgestrel EP Impurity P 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 Levonorgestrel.
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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Levonorgestrel Reference Standard
Levonorgestrel EP Impurity P for ANDA Filing
Levonorgestrel EP Impurity P for Forced Degradation Studies
Levonorgestrel EP Impurity P Identification Standards
Levonorgestrel EP Impurity P for DMF Filing
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