Description

n-(2,6-Dichlorophenyl)-4,5-Dihydro-1H-Imidazol-2-Amine Hydrochloride is a high-purity organic compound, primarily recognized as a key intermediate in advanced pharmaceutical synthesis. Its value lies in its role as a critical building block for active pharmaceutical ingredients (APIs), particularly those targeting the central nervous system. This compound is essential for research and manufacturing organizations in the pharmaceutical, agrochemical, and fine chemical industries seeking reliable, high-quality intermediates for complex synthesis pathways.

Application

• Pharmaceutical Intermediate: A crucial precursor in the synthesis of various active pharmaceutical ingredients (APIs), particularly for neurological and cardiovascular applications.
• Agrochemical Synthesis: Used in the research and development of novel pesticides and herbicides, leveraging its imidazoline core structure.
• Biochemical Research: Serves as a valuable reference standard and reagent in pharmacological studies and biochemical assays.
• Fine Chemical Manufacturing: Employed as a specialized intermediate for producing complex organic molecules in custom synthesis projects.
• Material Science Research: Investigated for its potential in creating novel organic compounds with specific electronic or binding properties.

Basic Information

Product Name	n-(2,6-Dichlorophenyl)-4,5-Dihydro-1H-Imidazol-2-Amine Hydrochloride
CAS No.	7555-15-9
Molecular Formula	C9H10Cl3N3
Molecular Weight	274.55 g/mol
Synonyms	2-(2,6-Dichloroanilino)-4,5-dihydro-1H-imidazole Hydrochloride; 2-(2,6-Dichlorophenylamino)-2-imidazoline Hydrochloride; 2-(2,6-Dichloroanilino)-2-imidazoline Hydrochloride; 2-[(2,6-Dichlorophenyl)amino]-4,5-dihydro-1H-imidazole Hydrochloride; 2-(2,6-Dichlorophenylimino)imidazolidine Hydrochloride; Lofexidine Impurity; Lofexidine Related Compound A Hydrochloride; Guanfacine Intermediate
EINECS	Contact for details

Quality Control

Our n-(2,6-Dichlorophenyl)-4,5-Dihydro-1H-Imidazol-2-Amine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the high standards required for pharmaceutical intermediate applications. A comprehensive Certificate of Analysis (COA) detailing purity, residual solvents, and related substances is provided with every shipment.

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 to prevent moisture absorption, which can affect stability and handling properties.

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%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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