Description

1-(2-Chloro-Benzyl)-1,2,3,4-Tetrahydro-Quinoxaline Dihydrochloride is a high-purity organic salt compound primarily utilized as a key pharmaceutical intermediate. Its value lies in its role as a critical building block for the synthesis of more complex molecules, particularly in medicinal chemistry research and development. This product is essential for R&D chemists and process development scientists in the pharmaceutical, agrochemical, and fine chemical industries seeking reliable, high-quality intermediates for novel active ingredient synthesis.

Application

• Pharmaceutical Intermediate: A crucial building block in the research and synthesis of novel drug candidates, particularly in central nervous system (CNS) and other therapeutic areas.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization processes during early-stage drug discovery.
• Agrochemical Synthesis: Serves as a precursor in the development of new active ingredients for crop protection products.
• Fine Chemical Production: Employed in custom synthesis and contract manufacturing for specialized, high-value chemical products.
• Academic & Institutional Research: Utilized in university and research institute laboratories for chemical biology studies and novel heterocyclic compound development.

Basic Information

Product Name	1-(2-Chloro-Benzyl)-1,2,3,4-Tetrahydro-Quinoxaline Dihydrochloride
CAS No.	939760-10-8
Molecular Formula	C15H16Cl2N2 • 2HCl
Molecular Weight	347.63 g/mol (Free base: 287.21 g/mol)
Synonyms	1-[(2-Chlorophenyl)methyl]-1,2,3,4-tetrahydroquinoxaline dihydrochloride; 1-(2-Chlorobenzyl)-1,2,3,4-tetrahydroquinoxaline dihydrochloride; 1-(2-Chloro-benzyl)-tetrahydro-quinoxaline dihydrochloride; THQ derivative dihydrochloride; 939760-10-8; 1-(2-Chlorobenzyl)tetrahydroquinoxaline 2HCl
EINECS	Contact for details

Quality Control

Our 1-(2-Chloro-Benzyl)-1,2,3,4-Tetrahydro-Quinoxaline Dihydrochloride is manufactured under a strict quality management system. Every batch undergoes comprehensive analytical testing including HPLC, NMR, and mass spectrometry to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with each shipment, documenting the specific results for that batch. We are committed to meeting the stringent requirements of GMP-grade intermediates for pharmaceutical development.

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 nature, the container must be kept tightly sealed after opening to prevent 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
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%

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