(3-Isopropyl-5-(trifluoromethyl)phenyl)boronic acid CAS 2225178-75-4

Purity 97%+In StockPharmaceutical Standards
CAS No.2225178-75-4
Molecular FormulaC10H12BF3O2
Molecular Weight232.01 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-Isopropyl-5-(trifluoromethyl)phenyl)boronic acid CAS 2225178-75-4 chemical structure

Description

CATO manufactures (3-Isopropyl-5-(trifluoromethyl)phenyl)boronic 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.

(3-Isopropyl-5-(trifluoromethyl)phenyl)boronic acid (CAS 2225178-75-4), molecular formula C10H12BF3O2 and molecular weight 232.01 g/mol, is a CATO reference standard with documented purity and traceability.

(3-Isopropyl-5-(trifluoromethyl)phenyl)boronic acid (C10H12BF3O2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, 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 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.

Physical & Chemical Properties

Molecular FormulaC10H12BF3O2
Molecular Weight232.01 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.5
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1998
Halogen ContentF-containing

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