4-Fluoro-3-iodo-5-methoxyphenol CAS 2385485-76-5

Purity 97%+In StockPharmaceutical Standards
CAS No.2385485-76-5
Molecular FormulaC7H6FIO2
Molecular Weight268.02 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Fluoro-3-iodo-5-methoxyphenol CAS 2385485-76-5 chemical structure

Description

CATO supplies 4-Fluoro-3-iodo-5-methoxyphenol (CAS 2385485-76-5), a certified reference material (molecular formula C7H6FIO2, MW 268.02 g/mol) for analytical method development and quality control.

The molecular framework of 4-Fluoro-3-iodo-5-methoxyphenol (C7H6FIO2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 4-Fluoro-3-iodo-5-methoxyphenol 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 FormulaC7H6FIO2
Molecular Weight268.02 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 methanol, acetonitrile, DMSO, water (slightly soluble)
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.)1999
Halogen ContentF/I-containing

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