Description

Xylazine Hydrochloride CAS NO 23076-35-9 is a potent α-2 adrenergic receptor agonist, widely recognized for its sedative, analgesic, and muscle relaxant properties. This compound is of critical importance in veterinary medicine for the safe and effective chemical restraint of large animals. It is primarily utilized by veterinary pharmaceutical manufacturers, research institutions, and compounding pharmacies for the formulation of sedative and anesthetic preparations.

Application

• Veterinary Sedation & Anesthesia: Key component in injectable formulations for the sedation, analgesia, and muscle relaxation of large animals such as horses, cattle, and deer.
• Veterinary Drug Manufacturing: Active Pharmaceutical Ingredient (API) for the production of commercial veterinary anesthetic and tranquilizer products.
• Research & Development: Used in pharmacological and neurobiological research to study α-2 adrenergic receptor mechanisms and effects.
• Wildlife Management: Employed in wildlife capture and immobilization protocols for safe handling and veterinary procedures.
• Compounding Pharmacy: Sourced by specialized pharmacies for the preparation of custom veterinary medication formulations.
• Analytical Reference Standard: High-purity grade serves as a reference material for quality control and analytical method development in laboratories.

Basic Information

Product Name	Xylazine Hydrochloride
CAS No.	23076-35-9
Molecular Formula	C12H16N2S • HCl
Molecular Weight	256.80 g/mol
Synonyms	Xylazine HCl; 2-(2,6-Dimethylphenylamino)-4H-5,6-dihydro-1,3-thiazine Hydrochloride; Rompun (Veterinary Brand Name); Bayer 1470; Sedazine; Anased; Chanazine; N-(2,6-Dimethylphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine Hydrochloride
EINECS	245-409-5

Quality Control

Our Xylazine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. We provide full traceability and Certificates of Analysis (COA) are available for every shipment, detailing key parameters such as assay, related substances, and residual solvents. Our quality commitment aligns with cGMP principles for active pharmaceutical ingredients.

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). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White or almost white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.5% - 101.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any individual impurity ≤ 0.5%
Heavy Metals	≤ 20 ppm

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