8-Fluoro-4-oxo-4H-chromene-2-carboxylic acid CAS 93340-04-6

Purity 97%+In StockPharmaceutical Standards
CAS No.93340-04-6
Molecular FormulaC10H5FO4
Molecular Weight208.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-Fluoro-4-oxo-4H-chromene-2-carboxylic acid CAS 93340-04-6 chemical structure

Description

CATO supplies 8-Fluoro-4-oxo-4H-chromene-2-carboxylic acid (CAS 93340-04-6), a certified reference material (molecular formula C10H5FO4, MW 208.14 g/mol) for analytical method development and quality control.

The molecular framework of 8-Fluoro-4-oxo-4H-chromene-2-carboxylic acid (C10H5FO4) 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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), 8-Fluoro-4-oxo-4H-chromene-2-carboxylic acid 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 FormulaC10H5FO4
Molecular Weight208.14 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1983
Halogen ContentF-containing

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