Furosemide Impurity 60 CAS 866764-34-3

Purity ≥95%In StockPharmacopoeial Impurity Standards
CAS No.866764-34-3
Molecular FormulaC7H2Cl4O4S
Molecular Weight323.97 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Furosemide Impurity 60 CAS 866764-34-3 chemical structure

Description

CATO supplies Furosemide Impurity 60 (CAS 866764-34-3), a pharmacopoeial impurity reference standard (molecular formula C7H2Cl4O4S, MW 323.97 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C7H2Cl4O4S, Furosemide Impurity 60 contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 323.97 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

As a certified reference material (CRM), Furosemide Impurity 60 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 FormulaC7H2Cl4O4S
Molecular Weight323.97 g/mol
Purity≥95%
StorageStore in a cool place (≤25°C), keep sealed and dry
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Sulfur Atoms1

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