3-Iodo-5-nitroimidazo[1,2-a]pyridine CAS 885276-56-2

Purity 97%+In StockPharmaceutical Standards
CAS No.885276-56-2
Molecular FormulaC7H4IN3O2
Molecular Weight289.03 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Iodo-5-nitroimidazo[1,2-a]pyridine CAS 885276-56-2 chemical structure

Description

CATO manufactures 3-Iodo-5-nitroimidazo[1,2-a]pyridine 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.

3-Iodo-5-nitroimidazo[1,2-a]pyridine (CAS 885276-56-2) is a high-purity analytical reference standard with the molecular formula C7H4IN3O2 and a molecular weight of 289.03 g/mol.

Based on its molecular formula C7H4IN3O2, 3-Iodo-5-nitroimidazo[1,2-a]pyridine contains an amide group, 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 289.03 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC7H4IN3O2
Molecular Weight289.03 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing
Nitrogen Atoms3

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