| CAS No. | 875050-49-0 |
| Molecular Formula | C17H15IO4 |
| Molecular Weight | 410.20 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 410.20 g/mol gives Methyl 2-(3-formyl-4-((2-iodobenzyl)oxy)phenyl)acetate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
Methyl 2-(3-formyl-4-((2-iodobenzyl)oxy)phenyl)acetate (CAS 875050-49-0), molecular formula C17H15IO4 and molecular weight 410.20 g/mol, is a CATO reference standard with documented purity and traceability.
Based on its molecular formula C17H15IO4, Methyl 2-(3-formyl-4-((2-iodobenzyl)oxy)phenyl)acetate contains a flavonoid core, a hydroxyl group, an ether linkage, iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 410.20 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.
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.
As a certified reference material (CRM), Methyl 2-(3-formyl-4-((2-iodobenzyl)oxy)phenyl)acetate 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 | C17H15IO4 |
| Molecular Weight | 410.20 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at room temperature, 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) | 10.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1987 |
| Halogen Content | I-containing |