Description

4-(2-(6,7-Dimethoxy-3,4-Dihydroisoquinolin-2(1H)-Yl)Ethyl)Aniline is a high-purity, advanced pharmaceutical intermediate characterized by its complex heterocyclic structure. This compound is critical for the synthesis of sophisticated active pharmaceutical ingredients (APIs), particularly those targeting neurological and cardiovascular pathways. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of novel therapeutic agents. The product is supplied with a focus on batch-to-batch consistency and stringent impurity control to meet the rigorous demands of modern drug development.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of complex alkaloid-derived APIs and investigational new drugs.
• Neurological Research: Used in the development of compounds targeting neurotransmitter systems and neurological disorders.
• Cardiovascular Drug Development: Serves as a precursor for molecules with potential vasodilatory or receptor-binding activity.
• Chemical Synthesis Research: Employed in academic and industrial R&D for constructing novel isoquinoline-based molecular libraries.
• Process Chemistry: Used in scale-up and optimization studies for the commercial production of specialty fine chemicals.

Basic Information

Product Name	4-(2-(6,7-Dimethoxy-3,4-Dihydroisoquinolin-2(1H)-Yl)Ethyl)Aniline
CAS No.	82924-84-3
Molecular Formula	C19H24N2O2
Molecular Weight	312.41 g/mol
Synonyms	4-[2-(6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]aniline; 4-(2-(6,7-Dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)ethyl)benzenamine; 2-[2-(4-Aminophenyl)ethyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline; 82924-84-3; 4-(2-(6,7-Dimethoxy-1,2,3,4-tetrahydro-2-isoquinolyl)ethyl)aniline
EINECS	Contact for details

Quality Control

Our production of 4-(2-(6,7-Dimethoxy-3,4-Dihydroisoquinolin-2(1H)-Yl)Ethyl)Aniline adheres to strict quality management protocols. Each batch is analyzed using advanced techniques including HPLC, GC, and NMR to ensure identity, purity, and the absence of critical impurities. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all relevant specifications. Our quality systems are designed to support cGMP compliance for pharmaceutical applications, ensuring traceability and documentation integrity.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated place at a controlled room temperature (15-25°C). Due to its sensitivity to oxidation, it is recommended to store the product under an inert atmosphere (e.g., nitrogen or argon) for long-term stability. Keep away from heat, sparks, and open flame.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Meets ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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