Oxytetracycline EP Impurity F | CAS 4660-26-8 - Request Quote
Oxytetracycline EP Impurity F
| SZ CAT No: | SZ-O012007 |
| CAS No | 4660-26-8 |
| Mol.F. | C22H22N2O8 |
| Mol.Wt. |
442.4 |
| Inv. Status |
Out of Stock |
| Rel. CAS No | 51596-09-9 (HCl salt) |
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Usage Note:
Oxytetracycline EP Impurity F is chemically (4S,4aR,5R,12aS)-4-(Dimethylamino)-3,5,10,11,12a-pentahydroxy-6-methyl-1,12-dioxo-1,4,4a,5,12,12a-hexahydrotetracene-2-carboxamide (as per E). Oxytetracycline EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Oxytetracycline EP Impurity F 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 Oxytetracycline.
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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Oxytetracycline EP Impurity F for Method Validation
Oxytetracycline Reference Standard
Oxytetracycline EP Impurity F for ANDA Filing
Oxytetracycline EP Impurity F for Forced Degradation Studies
Oxytetracycline EP Impurity F Identification Standards
Oxytetracycline EP Impurity F for DMF Filing
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SynZeal will update these details as per new developments or findings in product specifications without further notice.


