Description

1-[6-Chloro-2-(Trifluoromethyl)Quinol-4-Yl]Homopiperazin is a high-value, advanced pharmaceutical intermediate characterized by its complex heterocyclic structure. This compound matters for its critical role in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring targeted molecular design. It is primarily needed by research institutions and manufacturers in the pharmaceutical and agrochemical industries for developing new drug candidates and specialty chemicals.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the research and synthesis of novel drug candidates, particularly in oncology and central nervous system (CNS) therapeutic areas.
• Agrochemical Research: Used in the development of new-generation pesticides and herbicides, leveraging its trifluoromethyl and quinoline motifs for enhanced biological activity.
• Chemical Synthesis: Acts as a versatile precursor for creating complex heterocyclic compounds in medicinal and organic chemistry research.
• Material Science: Potential application in the synthesis of specialty polymers and advanced organic materials with specific electronic or photonic properties.

Basic Information

Product Name	1-[6-Chloro-2-(Trifluoromethyl)Quinol-4-Yl]Homopiperazin
CAS No.	541539-68-8
Molecular Formula	C15H15ClF3N3
Molecular Weight	329.75 g/mol
Synonyms	1-(6-Chloro-2-(trifluoromethyl)quinolin-4-yl)homopiperazine; 4-(Homopiperazin-1-yl)-6-chloro-2-(trifluoromethyl)quinoline; 1-(6-Chloro-2-trifluoromethyl-4-quinolyl)hexahydro-1,4-diazepine; 541539-68-8; UNII-9V6R6Y3J4I; 9V6R6Y3J4I; AKOS025310647; BDBM50389375; ZINC000006947777; 1-(6-Chloro-2-(trifluoromethyl)-4-quinolinyl)hexahydro-1H-1,4-diazepine
EINECS	Contact for details

Quality Control

Our 1-[6-Chloro-2-(Trifluoromethyl)Quinol-4-Yl]Homopiperazin is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with every shipment, detailing all specifications and test results. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical research and development processes.

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 its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed under an inert atmosphere (e.g., nitrogen or argon) after opening to prevent degradation from moisture absorption. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
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.