Deferoxamine EP Impurity E | CAS 804456-12-0 - Request Quote
Deferoxamine EP Impurity E
| SZ CAT No: | SZ-D131005 |
| CAS No | 804456-12-0 |
| Mol.F. | C19H36N4O7 |
| Mol.Wt. |
432.5 |
| Inv. Status |
Synthesis on demand |
| Rel. CAS No | 100105-69-9 (HCl salt) |
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Usage Note:
Deferoxamine EP Impurity E is chemically Methyl 4-[[5-[[4-[(5-aminopentyl)(hydroxy)amino]-4-oxobutanamido]pentyl](hydroxy)amino]-4-oxobutanoate (as per EP). Deferoxamine EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Deferoxamine 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 Deferoxamine.
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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Deferoxamine EP Impurity E for Method Validation
Deferoxamine Reference Standard
Deferoxamine EP Impurity E for ANDA Filing
Deferoxamine EP Impurity E for Forced Degradation Studies
Deferoxamine EP Impurity E Identification Standards
Deferoxamine EP Impurity E for DMF Filing
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