Description

2,6-Dimethoxy-4-Methyl-5-[3-(Trifluoromethyl)Phenoxy]Quinolin-8-Amine is a high-purity, advanced pharmaceutical intermediate characterized by its complex quinoline-based molecular structure. This compound is of significant commercial importance for its role in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring targeted molecular scaffolds. It is primarily sought by research institutions and manufacturers in the pharmaceutical, agrochemical, and specialty chemical industries for developing new drug candidates and high-value fine chemicals.

Application

• Pharmaceutical Intermediate: A key building block in the research and synthesis of novel quinoline-based drug candidates.
• Agrochemical Research: Used in developing advanced active ingredients for crop protection products.
• Organic Synthesis: Serves as a versatile precursor for creating complex heterocyclic compounds in laboratory and pilot-scale production.
• Material Science: Potential application in the development of organic electronic materials and functional dyes.
• Biochemical Research: Utilized as a probe or inhibitor in studying enzymatic and biological pathways.

Basic Information

Product Name	2,6-Dimethoxy-4-Methyl-5-[3-(Trifluoromethyl)Phenoxy]Quinolin-8-Amine
CAS No.	106635-86-3
Molecular Formula	C19H17F3N2O3
Molecular Weight	378.35 g/mol
Synonyms	8-Amino-2,6-dimethoxy-4-methyl-5-[3-(trifluoromethyl)phenoxy]quinoline; 5-[3-(Trifluoromethyl)phenoxy]-2,6-dimethoxy-4-methylquinolin-8-amine; 2,6-Dimethoxy-4-methyl-5-(α,α,α-trifluoro-m-tolyloxy)-8-quinolinamine; 106635-86-3; Quinolin-8-amine, 2,6-dimethoxy-4-methyl-5-[3-(trifluoromethyl)phenoxy]-
EINECS	Contact for details

Quality Control

Our production of 2,6-Dimethoxy-4-Methyl-5-[3-(Trifluoromethyl)Phenoxy]Quinolin-8-Amine adheres to stringent quality management protocols. Every batch undergoes comprehensive analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with each shipment, confirming compliance with agreed specifications. Our quality system is designed to support cGMP requirements for advanced pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from strong oxidizing agents. For long-term storage, consider an inert atmosphere to preserve stability.

Specification

Item	Specification
Appearance	Off-white to light yellow crystalline powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Loss on Drying	≤ 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.