Description

8-(3-Azidophenylmethoxy)-1,2,3-Trimethylimidazol(1,2-A)Pyridinium is a specialized heterocyclic organic compound featuring an azido functional group, making it a valuable intermediate for advanced synthesis. This compound is engineered for applications requiring precise molecular conjugation and click chemistry reactions. It is primarily utilized by research institutions and industrial R&D departments focused on pharmaceutical development, materials science, and bioconjugation.

Application

• Click Chemistry Reagent: A key building block for Huisgen 1,3-dipolar cycloaddition reactions, enabling efficient and selective bioconjugation.
• Pharmaceutical Intermediate: Used in the synthesis of novel drug candidates, particularly for targeted therapies and diagnostic agents.
• Bioconjugation & Labeling: Facilitates the attachment of fluorescent dyes, peptides, or other biomolecules to surfaces or carrier molecules for imaging and diagnostic applications.
• Polymer & Materials Science: Serves as a functional monomer or cross-linker for creating smart polymers, hydrogels, and advanced materials with specific surface properties.
• Chemical Biology Probes: Employed in the development of activity-based probes to study enzyme function and protein interactions within biological systems.
• Agrochemical Research: Acts as an intermediate in the development of new crop protection agents with novel modes of action.

Basic Information

Product Name	8-(3-Azidophenylmethoxy)-1,2,3-Trimethylimidazol(1,2-A)Pyridinium
CAS No.	120722-00-1
Molecular Formula	C18H20N6O
Molecular Weight	336.39 g/mol
Synonyms	8-[(3-Azidobenzyl)oxy]-1,2,3-trimethylimidazo[1,2-a]pyridinium; 1,2,3-Trimethyl-8-[(3-azidobenzyl)oxy]imidazo[1,2-a]pyridinium; 8-(3-Azidobenzyloxy)-1,2,3-trimethylimidazo[1,2-a]pyridinium; Azido-functionalized imidazopyridinium salt; Click chemistry azide reagent; CAS 120722-00-1
EINECS	Contact for details

Quality Control

Our production of 8-(3-Azidophenylmethoxy)-1,2,3-Trimethylimidazol(1,2-A)Pyridinium adheres to stringent quality protocols to ensure batch-to-batch consistency and high purity for research and development applications. All materials are characterized using advanced analytical techniques including NMR, HPLC, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to the presence of the azido group, handle and store away from strong reducing agents and sources of heat or shock. For long-term storage, consider storing under an inert atmosphere.

Specification

Item	Specification
Appearance	Off-white to light yellow solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 95%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.