Description

Piperazine, 1-(6-Fluoro-2-Pyridinyl)- (9Ci) is a high-purity, specialized heterocyclic compound featuring a piperazine core substituted with a fluoropyridinyl group. This molecular architecture makes it a critical intermediate for the synthesis of advanced active pharmaceutical ingredients (APIs) and other fine chemicals. It is primarily needed by pharmaceutical R&D and manufacturing sectors, as well as agrochemical and advanced material research laboratories seeking to develop novel compounds with targeted biological activity.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly in central nervous system (CNS) and anti-infective therapeutic areas.
• Agrochemical Synthesis: Used in the research and development of new-generation pesticides and herbicides, leveraging its fluorinated heterocyclic structure.
• Ligand and Catalyst Development: Serves as a precursor for creating complex ligands used in catalytic processes and metal-organic frameworks (MOFs).
• Chemical Research: Employed in academic and industrial R&D for exploring new reactions and synthesizing complex molecular libraries for screening.
• Fine Chemical Production: Acts as a specialized intermediate in the multi-step synthesis of high-value, low-volume fine chemicals.

Basic Information

Product Name	Piperazine, 1-(6-Fluoro-2-Pyridinyl)- (9Ci)
CAS No.	223514-16-7
Molecular Formula	C9H12FN3
Molecular Weight	181.21 g/mol
Synonyms	1-(6-Fluoropyridin-2-yl)piperazine; 6-Fluoro-2-(1-piperazinyl)pyridine; 2-(Piperazin-1-yl)-6-fluoropyridine; 6-Fluoro-2-piperazin-1-ylpyridine; 1-(6-Fluoro-2-pyridinyl)piperazine; 6-Fluoro-2-(piperazin-1-yl)pyridine; 2-Fluoro-6-(piperazin-1-yl)pyridine; 1-(6-Fluoropyridin-2-yl)piperazine
EINECS	Contact for details

Quality Control

Our Piperazine, 1-(6-Fluoro-2-Pyridinyl)- (9Ci) is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing including HPLC, GC, NMR, and mass spectrometry to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all specified parameters. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical synthesis workflows.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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