| CAS No. | 97232-24-1 |
| Molecular Formula | C22H26O5 |
| Molecular Weight | 370.44 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 370.44 g/mol gives 3,16-Diacetoxy-estra-1,3,5(10) tren-17-one distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies 3,16-Diacetoxy-estra-1,3,5(10) tren-17-one (CAS 97232-24-1), a certified reference material (molecular formula C22H26O5, MW 370.44 g/mol) for analytical method development and quality control.
The molecular framework of 3,16-Diacetoxy-estra-1,3,5(10) tren-17-one (C22H26O5) is characterized by a flavonoid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 3,16-Diacetoxy-estra-1,3,5(10) tren-17-one 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 | C22H26O5 |
| Molecular Weight | 370.44 g/mol |
| Appearance | Pale yellow to yellow crystalline powder |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO, water (slightly soluble) |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 10.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1984 |