1-(Fluoromethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylic acid CAS 2253631-32-0

Purity 97%+In StockPharmaceutical Standards
CAS No.2253631-32-0
Molecular FormulaC7H9FO3
Molecular Weight160.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(Fluoromethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylic acid CAS 2253631-32-0 chemical structure

Description

As a certified reference material (CRM), 1-(Fluoromethyl)-2-oxabicyclo[2.1.1]hexane-4-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.

CATO supplies 1-(Fluoromethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylic acid (CAS 2253631-32-0), a certified reference material (molecular formula C7H9FO3, MW 160.14 g/mol) for analytical method development and quality control.

The molecular framework of 1-(Fluoromethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylic acid (C7H9FO3) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution. 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.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC7H9FO3
Molecular Weight160.14 g/mol
Purity97%+
StorageStore at 2-8°C, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1998
Halogen ContentF-containing

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