| CAS No. | 905371-34-8 |
| Molecular Formula | C16H13F3N4O5 |
| Molecular Weight | 398.29 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
2-(2-(4-Nitrophenoxy)acetyl)-N-(3-(trifluoromethyl)phenyl)hydrazine-1-carboxamide (CAS 905371-34-8), molecular formula C16H13F3N4O5 and molecular weight 398.29 g/mol, is a CATO reference standard with documented purity and traceability.
2-(2-(4-Nitrophenoxy)acetyl)-N-(3-(trifluoromethyl)phenyl)hydrazine-1-carboxamide (C16H13F3N4O5) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.
CATO manufactures 2-(2-(4-Nitrophenoxy)acetyl)-N-(3-(trifluoromethyl)phenyl)hydrazine-1-carboxamide 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 | C16H13F3N4O5 |
| Molecular Weight | 398.29 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor, low volatility) |
| Purity | 97%+ |
| Storage | Store at 2-8°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) | 11.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1987 |
| Halogen Content | F-containing |
| Nitrogen Atoms | 4 |