| CAS No. | 757-06-2 |
| Molecular Formula | C5H6F5IO |
| Molecular Weight | 304.00 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Fulvestrant Impurity 11.
Fulvestrant Impurity 11 (CAS 757-06-2) is a certified pharmaceutical impurity reference standard with the molecular formula C5H6F5IO and a molecular weight of 304.00 g/mol.
Based on its molecular formula C5H6F5IO, Fulvestrant Impurity 11 contains a hydroxyl group, an ether linkage, fluorine/iodine substitution; these features give the compound characteristic functional-group stretching vibrations in infrared spectroscopy. The molecular weight of 304.00 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 Fulvestrant Impurity 11 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 | C5H6F5IO |
| Molecular Weight | 304.00 g/mol |
| Purity | >90% |
| Storage | Store at room temperature |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO, water (slightly soluble) |
| Stability | Stable under recommended storage conditions |
| Degree of Unsaturation (DBE) | 0.0 |
| CAS Registry Year (est.) | 1957 |
| Halogen Content | F/I-containing |