2,3,4,6-Tetraiodobenzoic acid CAS 71463-71-3

Purity 97%+In StockPharmaceutical Standards
CAS No.71463-71-3
Molecular FormulaC7H2I4O2
Molecular Weight625.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,3,4,6-Tetraiodobenzoic acid CAS 71463-71-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 625.71 g/mol gives 2,3,4,6-Tetraiodobenzoic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2,3,4,6-Tetraiodobenzoic acid (CAS 71463-71-3), a certified reference material (molecular formula C7H2I4O2, MW 625.71 g/mol) for analytical method development and quality control.

Based on its molecular formula C7H2I4O2, 2,3,4,6-Tetraiodobenzoic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 625.71 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

CATO manufactures 2,3,4,6-Tetraiodobenzoic acid under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC7H2I4O2
Molecular Weight625.71 g/mol
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977
Halogen ContentI-containing

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