2-Bromo-3-methyl-5-((trimethylsilyl)ethynyl)pyridine CAS 1338492-80-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1338492-80-0
Molecular FormulaC11H14BrNSi
Molecular Weight268.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Bromo-3-methyl-5-((trimethylsilyl)ethynyl)pyridine CAS 1338492-80-0 chemical structure

Description

CATO supplies 2-Bromo-3-methyl-5-((trimethylsilyl)ethynyl)pyridine (CAS 1338492-80-0), a certified reference material (molecular formula C11H14BrNSi, MW 268.23 g/mol) for analytical method development and quality control.

The molecular framework of 2-Bromo-3-methyl-5-((trimethylsilyl)ethynyl)pyridine (C11H14BrNSi) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, bromine 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.

As a certified reference material (CRM), 2-Bromo-3-methyl-5-((trimethylsilyl)ethynyl)pyridine 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 FormulaC11H14BrNSi
Molecular Weight268.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
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.)1991
Halogen ContentBr-containing
Nitrogen Atoms1

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