Ethyl 3-iodoimidazo[1,2-a]pyridine-8-carboxylate CAS 1262409-63-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1262409-63-1
Molecular FormulaC10H9IN2O2
Molecular Weight316.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 3-iodoimidazo[1,2-a]pyridine-8-carboxylate CAS 1262409-63-1 chemical structure

Description

As a certified reference material (CRM), Ethyl 3-iodoimidazo[1,2-a]pyridine-8-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies Ethyl 3-iodoimidazo[1,2-a]pyridine-8-carboxylate (CAS 1262409-63-1), a certified reference material (molecular formula C10H9IN2O2, MW 316.10 g/mol) for analytical method development and quality control.

The molecular framework of Ethyl 3-iodoimidazo[1,2-a]pyridine-8-carboxylate (C10H9IN2O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC10H9IN2O2
Molecular Weight316.10 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
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.)1990
Halogen ContentI-containing
Nitrogen Atoms2

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