| CAS No. | 2241747-15-7 |
| Molecular Formula | C39H53N5O10S |
| Molecular Weight | 783.93 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
CATO supplies 1-(9H-Fluoren-9-ylmethyl) (3S)-3-carboxy-25-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-5,21-dioxo-10,13,16-trioxa-2,6,20-triazapentacosanoate (CAS 2241747-15-7), a certified reference material (molecular formula C39H53N5O10S, MW 783.93 g/mol) for analytical method development and quality control.
The molecular framework of 1-(9H-Fluoren-9-ylmethyl) (3S)-3-carboxy-25-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-5,21-dioxo-10,13,16-trioxa-2,6,20-triazapentacosanoate (C39H53N5O10S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing 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 1-(9H-Fluoren-9-ylmethyl) (3S)-3-carboxy-25-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-5,21-dioxo-10,13,16-trioxa-2,6,20-triazapentacosanoate 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 | C39H53N5O10S |
| Molecular Weight | 783.93 g/mol |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 16.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1998 |
| Nitrogen Atoms | 5 |
| Sulfur Atoms | 1 |