Triiodoresorcinol CAS 58649-90-4

Purity 97%+In StockPharmaceutical Standards
CAS No.58649-90-4
Molecular FormulaC6H3I3O2
Molecular Weight487.80 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Triiodoresorcinol CAS 58649-90-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 487.80 g/mol gives Triiodoresorcinol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Triiodoresorcinol (CAS 58649-90-4) is a high-purity analytical reference standard with the molecular formula C6H3I3O2 and a molecular weight of 487.80 g/mol.

The molecular framework of Triiodoresorcinol (C6H3I3O2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC6H3I3O2
Molecular Weight487.80 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature
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
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Halogen ContentI-containing

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