Description

5-(Trifluoromethyl)Quinolin-7-Amine is a high-purity, advanced pharmaceutical intermediate characterized by its quinoline core and reactive amine group. This compound matters for its critical role as a key building block in the synthesis of novel, high-value active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring targeted molecular design. It is primarily needed by research institutions and manufacturers in the pharmaceutical, agrochemical, and material science industries for developing new drugs, crop protection agents, and specialty chemicals.

Application

• Pharmaceutical Intermediate: A crucial precursor in the synthesis of potential drug candidates, especially for oncology, antiviral, and central nervous system (CNS) targeted therapies.
• Agrochemical Research: Serves as a building block for developing new generation pesticides and herbicides with improved efficacy and selectivity.
• Material Science: Used in the research and development of advanced organic electronic materials, such as OLED (Organic Light-Emitting Diode) components and conductive polymers.
• Chemical Synthesis: Acts as a versatile reagent for introducing the trifluoromethylquinoline moiety into more complex molecular architectures in organic chemistry.
• Ligand & Catalyst Development: Employed in the creation of novel ligands for catalytic systems and metal-organic frameworks (MOFs).

Basic Information

Product Name	5-(Trifluoromethyl)Quinolin-7-Amine
CAS No.	1447606-61-2
Molecular Formula	C10H7F3N2
Molecular Weight	212.17 g/mol
Synonyms	7-Amino-5-(trifluoromethyl)quinoline; 5-(Trifluoromethyl)-7-quinolinamine; 5-Trifluoromethylquinolin-7-ylamine; 5-Trifluoromethyl-7-aminoquinoline; 7-Quinolinamine, 5-(trifluoromethyl)-; 1447606-61-2; 5-CF3-Quinolin-7-amine
EINECS	Contact for details

Quality Control

Our 5-(Trifluoromethyl)Quinolin-7-Amine 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 each shipment, detailing all specification results. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical R&D and scale-up 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 (typically 15-25°C). Keep away from strong bases and incompatible materials. For long-term storage, consider an inert atmosphere to maximize stability.

Specification

Item	Specification
Appearance	Off-white to light yellow crystalline powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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