| CAS No. | 1881295-33-5 |
| Molecular Formula | C13H18F4O2Si |
| Molecular Weight | 310.36 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
The occurrence of 5-[(tert-Butyldimethylsilyl)oxy]-2-fluoro-3-(trifluoromethyl)phenol is closely related to a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies 5-[(tert-Butyldimethylsilyl)oxy]-2-fluoro-3-(trifluoromethyl)phenol (CAS 1881295-33-5), a certified reference material (molecular formula C13H18F4O2Si, MW 310.36 g/mol) for analytical method development and quality control.
The molecular framework of 5-[(tert-Butyldimethylsilyl)oxy]-2-fluoro-3-(trifluoromethyl)phenol (C13H18F4O2Si) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
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 5-[(tert-Butyldimethylsilyl)oxy]-2-fluoro-3-(trifluoromethyl)phenol 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 | C13H18F4O2Si |
| Molecular Weight | 310.36 g/mol |
| Purity | 97%+ |
| Storage | Store at room temperature |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 3.0 |
| UV Absorption | UV-absorbing |
| CAS Registry Year (est.) | 1995 |
| Halogen Content | F-containing |