| CAS No. | CATO-C4X-20014 |
| Molecular Formula | C12H24Cl6N3OP |
| Molecular Weight | 470.03 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Ifosfamide Impurity 4 is closely related to an amide group, organophosphorus functionality, a hydroxyl group, an ether linkage, chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
Ifosfamide Impurity 4 (CAS CATO-C4X-20014) is a certified pharmaceutical impurity reference standard with the molecular formula C12H24Cl6N3OP and a molecular weight of 470.03 g/mol.
Structurally, Ifosfamide Impurity 4 (C12H24Cl6N3OP) contains an amide group, organophosphorus functionality, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of -0.5, corresponding to approximately 0 ring(s) or double-bond equivalent(s). With a molecular weight of 470.03 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.
This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.
CATO manufactures Ifosfamide Impurity 4 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.
| Molecular Formula | C12H24Cl6N3OP |
| Molecular Weight | 470.03 g/mol |
| Purity | >95% |
| Storage | Store at room temperature, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | -0.5 |
| Halogen Content | Cl-containing |
| Nitrogen Atoms | 3 |