2-(tert-Butyl)-4-cyclopropoxy-6-iodopyridine CAS 1243464-86-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1243464-86-9
Molecular FormulaC12H16INO
Molecular Weight317.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(tert-Butyl)-4-cyclopropoxy-6-iodopyridine CAS 1243464-86-9 chemical structure

Description

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.

2-(tert-Butyl)-4-cyclopropoxy-6-iodopyridine (CAS 1243464-86-9) is a high-purity analytical reference standard with the molecular formula C12H16INO and a molecular weight of 317.17 g/mol.

The molecular framework of 2-(tert-Butyl)-4-cyclopropoxy-6-iodopyridine (C12H16INO) 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), 2-(tert-Butyl)-4-cyclopropoxy-6-iodopyridine 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.

Physical & Chemical Properties

Molecular FormulaC12H16INO
Molecular Weight317.17 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
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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