| CAS No. | 1474-78-8 |
| Molecular Formula | C7H15O5P |
| Molecular Weight | 210.16 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Foscarnet Sodium EP Impurity D is closely related to a phosphate ester group, a carboxylic acid group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
As a process- or degradation-related impurity, Foscarnet Sodium EP Impurity D (CAS 1474-78-8, C7H15O5P) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Owing to a phosphate ester group, a carboxylic acid group, a hydroxyl group, an ether linkage, Foscarnet Sodium EP Impurity D is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 210.16 g/mol — guide the selection of appropriate sample preparation and analytical techniques.
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.
The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.
| Molecular Formula | C7H15O5P |
| Molecular Weight | 210.16 g/mol |
| Purity | >95% |
| Storage | Store in a cool place (≤25°C), keep sealed and dry |
| Solubility (reference) | Soluble in methanol, ethanol, DMSO, water |
| Stability | Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 0.5 |
| CAS Registry Year (est.) | 1957 |