6,6-Bis(4-fluorophenyl)hexanoic acid CAS 667936-71-2

Purity 97%+In StockPharmaceutical Standards
CAS No.667936-71-2
Molecular FormulaC18H18F2O2
Molecular Weight304.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6,6-Bis(4-fluorophenyl)hexanoic acid CAS 667936-71-2 chemical structure

Description

CATO manufactures 6,6-Bis(4-fluorophenyl)hexanoic 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.

CATO supplies 6,6-Bis(4-fluorophenyl)hexanoic acid (CAS 667936-71-2), a certified reference material (molecular formula C18H18F2O2, MW 304.33 g/mol) for analytical method development and quality control.

Owing to a steroid core, a hydroxyl group, an ether linkage, fluorine substitution, 6,6-Bis(4-fluorophenyl)hexanoic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 304.33 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

Physical & Chemical Properties

Molecular FormulaC18H18F2O2
Molecular Weight304.33 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF-containing

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