| CAS No. | 853333-68-3 |
| Molecular Formula | C22H22ClNO3 |
| Molecular Weight | 383.87 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 383.87 g/mol gives N-(4-Butylphenyl)-5-(3-chloro-4-methoxyphenyl)furan-2-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
N-(4-Butylphenyl)-5-(3-chloro-4-methoxyphenyl)furan-2-carboxamide (CAS 853333-68-3), molecular formula C22H22ClNO3 and molecular weight 383.87 g/mol, is a CATO reference standard with documented purity and traceability.
The molecular framework of N-(4-Butylphenyl)-5-(3-chloro-4-methoxyphenyl)furan-2-carboxamide (C22H22ClNO3) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
CATO manufactures N-(4-Butylphenyl)-5-(3-chloro-4-methoxyphenyl)furan-2-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 | C22H22ClNO3 |
| Molecular Weight | 383.87 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 12.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1987 |
| Halogen Content | Cl-containing |
| Nitrogen Atoms | 1 |