| CAS No. | 372983-17-0 |
| Molecular Formula | C26H32O |
| Molecular Weight | 360.53 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
The occurrence of 1-Methoxy-4-((4-(4-pentylcyclohexyl)phenyl)ethynyl)benzene is closely related to a steroid core, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies 1-Methoxy-4-((4-(4-pentylcyclohexyl)phenyl)ethynyl)benzene (CAS 372983-17-0), a certified reference material (molecular formula C26H32O, MW 360.53 g/mol) for analytical method development and quality control.
Structurally, 1-Methoxy-4-((4-(4-pentylcyclohexyl)phenyl)ethynyl)benzene (C26H32O) contains a steroid core, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 360.53 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
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), 1-Methoxy-4-((4-(4-pentylcyclohexyl)phenyl)ethynyl)benzene 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 | C26H32O |
| Molecular Weight | 360.53 g/mol |
| Appearance | Pale yellow to yellow crystalline powder |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 11.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 2025 |