2-(4-(tert-Butyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol CAS 22796-15-2

Purity 97%+In StockPharmaceutical Standards
CAS No.22796-15-2
Molecular FormulaC13H14F6O
Molecular Weight300.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-(tert-Butyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol CAS 22796-15-2 chemical structure

Description

2-(4-(tert-Butyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (CAS 22796-15-2), molecular formula C13H14F6O and molecular weight 300.24 g/mol, is a CATO reference standard with documented purity and traceability.

2-(4-(tert-Butyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (C13H14F6O) contains a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

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.

As a certified reference material (CRM), 2-(4-(tert-Butyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC13H14F6O
Molecular Weight300.24 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Halogen ContentF-containing

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Why CATO?