| CAS No. | 10231-46-6 |
| Molecular Formula | C10H6O4 |
| Molecular Weight | 190.15 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 190.15 g/mol gives 3-(1,3-Dioxaindan-5-yl)prop-2-ynoic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
3-(1,3-Dioxaindan-5-yl)prop-2-ynoic acid (CAS 10231-46-6) is a high-purity analytical reference standard with the molecular formula C10H6O4 and a molecular weight of 190.15 g/mol.
3-(1,3-Dioxaindan-5-yl)prop-2-ynoic acid (C10H6O4) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. It is notably hygroscopic, 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
CATO manufactures 3-(1,3-Dioxaindan-5-yl)prop-2-ynoic acid 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 | C10H6O4 |
| Molecular Weight | 190.15 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, ethanol, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 8.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1959 |