| CAS No. | 68610-82-2 |
| Molecular Formula | C20H30O4 |
| Molecular Weight | 334.45 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 334.45 g/mol gives di-N-Hexyl phthalate(mixture of isomers) distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies di-N-Hexyl phthalate(mixture of isomers) (CAS 68610-82-2), a certified reference material (molecular formula C20H30O4, MW 334.45 g/mol) for analytical method development and quality control.
di-N-Hexyl phthalate(mixture of isomers) (C20H30O4) contains a steroid core, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.
CATO manufactures di-N-Hexyl phthalate(mixture of isomers) 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 | C20H30O4 |
| Molecular Weight | 334.45 g/mol |
| Appearance | Off-white to pale yellow crystalline powder |
| Purity | 1000 μg/mL in Hexane |
| 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 |
| Degree of Unsaturation (DBE) | 6.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1976 |