| CAS No. | 1609400-90-9 |
| Molecular Formula | C10H10O4 |
| Molecular Weight | N/A |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 212.20 g/mol gives 5-(3-Hydroxy-3-methylbut-1-yn-1-yl)furan-2-carboxylic acid hydrate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies 5-(3-Hydroxy-3-methylbut-1-yn-1-yl)furan-2-carboxylic acid hydrate (CAS 1609400-90-9), a certified reference material (molecular formula C10H10O4H2O, MW 212.20 g/mol) for analytical method development and quality control.
5-(3-Hydroxy-3-methylbut-1-yn-1-yl)furan-2-carboxylic acid hydrate (C10H10O4H2O) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. It is notably hygroscopic, 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 | C10H10O4 H2O |
| Molecular Weight | 212.20 g/mol |
| Appearance | Off-white to pale yellow crystalline powder |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), keep sealed and dry |
| Solubility (reference) | Soluble in methanol, ethanol, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 5.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1993 |