| CAS No. | 3031-98-9 |
| Molecular Formula | C7H12O7 |
| Molecular Weight | 208.17 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Ascorbic Acid EP Impurity D is closely related to a carbohydrate-derived structure in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
As a process- or degradation-related impurity, Ascorbic Acid EP Impurity D (CAS 3031-98-9, C7H12O7) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Based on its molecular formula C7H12O7, Ascorbic Acid EP Impurity D contains a carbohydrate-derived structure; these features give the compound characteristic functional-group stretching vibrations in infrared spectroscopy. The molecular weight of 208.17 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry.
Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.
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 | C7H12O7 |
| Molecular Weight | 208.17 g/mol |
| Purity | >90% |
| 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) | 2.0 |
| CAS Registry Year (est.) | 1957 |