Desogestrel EP Impurity E | CAS 70805-85-5 - Request Quote
Desogestrel EP Impurity E
| SZ CAT No: | SZ-D056006 |
| CAS No | 70805-85-5 |
| Mol.F. | C22H30O2 |
| Mol.Wt. | 326.5 |
| Inv. Status | In Stock |
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Usage Note:
Desogestrel EP Impurity E is chemically 13-Ethyl-11-methylidene-18,19-dinor-17α-pregn-4-en-20-yne-3β,17-diol (as per EP);13-Ethyl-3-hydroxy-11-methylene-18,19-dinor-17α-pregn-4-en-20-yn-17-ol (as per USP). Desogestrel EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Desogestrel EP Impurity E 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 Desogestrel.
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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Desogestrel EP Impurity E for Method Validation
Desogestrel Reference Standard
Desogestrel EP Impurity E for ANDA Filing
Desogestrel EP Impurity E for Forced Degradation Studies
Desogestrel EP Impurity E Identification Standards
Desogestrel EP Impurity E for DMF Filing
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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.
SynZeal will update these details as per new developments or findings in product specifications without further notice.


