| CAS No. | 428847-21-6 |
| Molecular Formula | C15H12FIO3 |
| Molecular Weight | 386.16 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 386.16 g/mol gives 4-((2-Fluorobenzyl)oxy)-3-iodo-5-methoxybenzaldehyde distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies 4-((2-Fluorobenzyl)oxy)-3-iodo-5-methoxybenzaldehyde (CAS 428847-21-6), a certified reference material (molecular formula C15H12FIO3, MW 386.16 g/mol) for analytical method development and quality control.
The molecular framework of 4-((2-Fluorobenzyl)oxy)-3-iodo-5-methoxybenzaldehyde (C15H12FIO3) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, a polycyclic aromatic system. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
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 4-((2-Fluorobenzyl)oxy)-3-iodo-5-methoxybenzaldehyde 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 | C15H12FIO3 |
| Molecular Weight | 386.16 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 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) | 9.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 2025 |
| Halogen Content | F/I-containing |