Description

Chlormethiazole Hydrochloride is a high-purity pharmaceutical intermediate and active ingredient with significant therapeutic applications. Its value lies in its specific pharmacological activity, making it a critical component in the development and production of specialized medications. This compound is primarily needed by the pharmaceutical industry for research, formulation, and manufacturing of sedative-hypnotic and anticonvulsant drugs.

Application

• Primary active pharmaceutical ingredient (API) in sedative and hypnotic formulations.
• Key intermediate in the synthesis of advanced neuropharmacological agents.
• Research and development of treatments for alcohol withdrawal syndrome and agitation.
• Manufacturing of anticonvulsant medications for controlling seizures.
• Use in preclinical and clinical studies for central nervous system (CNS) disorders.
• Reference standard in analytical laboratories for quality control and method validation.

Basic Information

Product Name	Chlormethiazole Hydrochloride
CAS No.	6001-74-7
Molecular Formula	C5H8ClNS•HCl
Molecular Weight	186.55 g/mol
Synonyms	Chlormethiazole HCl; Clomethiazole Hydrochloride; 5-(2-Chloroethyl)-4-methylthiazole Hydrochloride; Heminevrin; Distraneurin; Chlorethiazol Hydrochloride; Hemineurin
EINECS	227-873-8

Quality Control

Our Chlormethiazole Hydrochloride is manufactured under strict quality management systems, ensuring it meets the rigorous standards required for pharmaceutical applications. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC and other pharmacopeial methods. Certificates of Analysis (COA) detailing purity, related substances, and residual solvents are available upon request to support your regulatory and quality assurance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area 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 purity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.5%
Related Substances (HPLC)	Total impurities ≤1.5%
Loss on Drying	≤0.5%
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.