| CAS No. | 39024-75-4 |
| Molecular Formula | C140H262O19 |
| Molecular Weight | 2249.57 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 2249.57 g/mol gives 1,3,4,6-Tetrakis-O-(1-oxohexadecyl)- β-D-fructofuranosyl-α-D-glucopyranoside tetrapalmitate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies 1,3,4,6-Tetrakis-O-(1-oxohexadecyl)- β-D-fructofuranosyl-α-D-glucopyranoside tetrapalmitate (CAS 39024-75-4), a certified reference material (molecular formula C140H262O19, MW 2249.57 g/mol) for analytical method development and quality control.
1,3,4,6-Tetrakis-O-(1-oxohexadecyl)- β-D-fructofuranosyl-α-D-glucopyranoside tetrapalmitate (C140H262O19) contains a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system. 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.
The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.
| Molecular Formula | C140H262O19 |
| Molecular Weight | 2249.57 g/mol |
| Purity | 97%+ |
| Storage | Store at room temperature, 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.) | 1968 |