2-(3-FLUOROPHENOXY)-2-METHYLPROPANOIC ACID CAS 605680-36-2

Purity 97%+In StockPharmaceutical Standards
CAS No.605680-36-2
Molecular FormulaC10H11FO3
Molecular Weight198.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-FLUOROPHENOXY)-2-METHYLPROPANOIC ACID CAS 605680-36-2 chemical structure

Description

CATO supplies 2-(3-FLUOROPHENOXY)-2-METHYLPROPANOIC ACID (CAS 605680-36-2), a certified reference material (molecular formula C10H11FO3, MW 198.19 g/mol) for analytical method development and quality control.

The molecular framework of 2-(3-FLUOROPHENOXY)-2-METHYLPROPANOIC ACID (C10H11FO3) 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.

CATO manufactures 2-(3-FLUOROPHENOXY)-2-METHYLPROPANOIC 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.

Physical & Chemical Properties

Molecular FormulaC10H11FO3
Molecular Weight198.19 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF-containing

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