(4-Isopropoxy-3-(trifluoromethyl)phenyl)methanol CAS 1215118-92-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1215118-92-5
Molecular FormulaC11H13F3O2
Molecular Weight234.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Isopropoxy-3-(trifluoromethyl)phenyl)methanol CAS 1215118-92-5 chemical structure

Description

CATO supplies (4-Isopropoxy-3-(trifluoromethyl)phenyl)methanol (CAS 1215118-92-5), a certified reference material (molecular formula C11H13F3O2, MW 234.21 g/mol) for analytical method development and quality control.

The molecular framework of (4-Isopropoxy-3-(trifluoromethyl)phenyl)methanol (C11H13F3O2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. 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 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.

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.

Physical & Chemical Properties

Molecular FormulaC11H13F3O2
Molecular Weight234.21 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing

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