4,5-Dibromothiophene-2-carboxylic Acid CAS 6324-10-3

Purity 97%+In StockPharmaceutical Standards
CAS No.6324-10-3
Molecular FormulaC5H2Br2O2S
Molecular Weight285.94 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,5-Dibromothiophene-2-carboxylic Acid CAS 6324-10-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 4,5-Dibromothiophene-2-carboxylic Acid.

CATO supplies 4,5-Dibromothiophene-2-carboxylic Acid (CAS 6324-10-3), a certified reference material (molecular formula C5H2Br2O2S, MW 285.94 g/mol) for analytical method development and quality control.

4,5-Dibromothiophene-2-carboxylic Acid (C5H2Br2O2S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC5H2Br2O2S
Molecular Weight285.94 g/mol
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
CAS Registry Year (est.)1958
Halogen ContentBr-containing
Sulfur Atoms1

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