Description

2-(6-Fluoroimidazo[1,2-A]Pyridin-2-Yl)Ethanamine is a high-purity, advanced pharmaceutical intermediate featuring a unique fused heterocyclic structure. This compound is critical for medicinal chemistry research and development, particularly in the synthesis of novel small-molecule therapeutics. It is primarily utilized by pharmaceutical R&D departments and fine chemical manufacturers specializing in active pharmaceutical ingredient (API) production.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates targeting central nervous system (CNS) disorders, oncology, and inflammatory diseases.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization programs due to its imidazopyridine scaffold.
• Biochemical Tool Compound: Serves as a precursor for developing selective enzyme inhibitors or receptor modulators for biological research.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis to introduce the 2-aminoethyl-imidazopyridine moiety into more complex molecular architectures.
• Contract Research & Development (CRO/CMO): Supplied to organizations engaged in custom synthesis and process development for clinical trial materials.
• Academic Research: Used in university and institutional labs for exploratory research in heterocyclic chemistry and drug discovery.

Basic Information

Product Name	2-(6-Fluoroimidazo[1,2-A]Pyridin-2-Yl)Ethanamine
CAS No.	1216295-83-8
Molecular Formula	C9H9FN4
Molecular Weight	192.20 g/mol
Synonyms	2-(6-Fluoroimidazo[1,2-a]pyridin-2-yl)ethan-1-amine; 2-(6-Fluoroimidazo[1,2-a]pyridin-2-yl)ethylamine; 6-Fluoro-2-(2-aminoethyl)imidazo[1,2-a]pyridine; 2-(2-Aminoethyl)-6-fluoroimidazo[1,2-a]pyridine; Ethanamine, 2-(6-fluoroimidazo[1,2-a]pyridin-2-yl)-; 1216295-83-8; FC-IMP-2A
EINECS	Contact for details

Quality Control

Our 2-(6-Fluoroimidazo[1,2-A]Pyridin-2-Yl)Ethanamine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. Certificates of Analysis (COA) are provided with every shipment, detailing all critical quality attributes. We support compliance with cGMP and ISO standards for pharmaceutical intermediates.

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). This compound is hygroscopic (moisture-sensitive); therefore, containers must be kept tightly sealed and may require desiccant. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

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