5-Bromo-2-iodo-4-methoxybenzoic acid CAS 1269292-64-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1269292-64-9
Molecular FormulaC8H6BrIO3
Molecular Weight356.94 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Bromo-2-iodo-4-methoxybenzoic acid CAS 1269292-64-9 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 5-Bromo-2-iodo-4-methoxybenzoic acid.

CATO supplies 5-Bromo-2-iodo-4-methoxybenzoic acid (CAS 1269292-64-9), a certified reference material (molecular formula C8H6BrIO3, MW 356.94 g/mol) for analytical method development and quality control.

Structurally, 5-Bromo-2-iodo-4-methoxybenzoic acid (C8H6BrIO3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, bromine/iodine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 356.94 g/mol, it falls into the moderately-high-molecular-weight range. 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 FormulaC8H6BrIO3
Molecular Weight356.94 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
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.)1990
Halogen ContentBr/I-containing

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