6-(tert-Butoxy)-3-cyclopropoxy-2-iodopyridine CAS 1243311-28-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1243311-28-5
Molecular FormulaC12H16INO2
Molecular Weight333.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(tert-Butoxy)-3-cyclopropoxy-2-iodopyridine CAS 1243311-28-5 chemical structure

Description

CATO manufactures 6-(tert-Butoxy)-3-cyclopropoxy-2-iodopyridine 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.

CATO supplies 6-(tert-Butoxy)-3-cyclopropoxy-2-iodopyridine (CAS 1243311-28-5), a certified reference material (molecular formula C12H16INO2, MW 333.17 g/mol) for analytical method development and quality control.

6-(tert-Butoxy)-3-cyclopropoxy-2-iodopyridine (C12H16INO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC12H16INO2
Molecular Weight333.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; 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 ContentI-containing
Nitrogen Atoms1

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