| CAS No. | 2256-06-6 |
| Molecular Formula | C26H30ClFN2O2 |
| Molecular Weight | N/A |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
CATO supplies 4-(4-(3-Chlorophenyl)-4-(pyrrolidine-1-carbonyl)piperidin-1-yl)-1-(4-fluorophenyl)butan-1-one oxalate (CAS 2256-06-6), a certified reference material (molecular formula C26H30ClFN2O2C2H2O4, MW 547.02 g/mol) for analytical method development and quality control.
The molecular framework of 4-(4-(3-Chlorophenyl)-4-(pyrrolidine-1-carbonyl)piperidin-1-yl)-1-(4-fluorophenyl)butan-1-one oxalate (C26H30ClFN2O2C2H2O4) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
As a certified reference material (CRM), 4-(4-(3-Chlorophenyl)-4-(pyrrolidine-1-carbonyl)piperidin-1-yl)-1-(4-fluorophenyl)butan-1-one oxalate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
| Molecular Formula | C26H30ClFN2O2 C2H2O4 |
| Molecular Weight | 547.02 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor, low volatility) |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 13.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1957 |
| Halogen Content | F/Cl-containing |
| Nitrogen Atoms | 2 |