2-Hydroxy-3-iodobenzaldehyde CAS 23602-64-4

Purity 97%+In StockPharmaceutical Standards
CAS No.23602-64-4
Molecular FormulaC7H5IO2
Molecular Weight248.02 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Hydroxy-3-iodobenzaldehyde CAS 23602-64-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 248.02 g/mol gives 2-Hydroxy-3-iodobenzaldehyde distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

2-Hydroxy-3-iodobenzaldehyde (CAS 23602-64-4) is a high-purity analytical reference standard with the molecular formula C7H5IO2 and a molecular weight of 248.02 g/mol.

2-Hydroxy-3-iodobenzaldehyde (C7H5IO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. 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.

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

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 FormulaC7H5IO2
Molecular Weight248.02 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Halogen ContentI-containing

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