Description

Medetomidine is a highly potent and selective α-2 adrenergic receptor agonist. This compound is of significant importance in pharmaceutical research and development due to its sedative and analgesic properties. It is primarily needed by manufacturers and research institutions in the veterinary and human pharmaceutical sectors for the formulation of anesthetic and sedative agents.

Application

• Primary active pharmaceutical ingredient (API) in veterinary sedative and anesthetic formulations.
• Key intermediate in the synthesis of dexmedetomidine, a more selective isomer used in human intensive care.
• Research chemical for neurological and pharmacological studies targeting α-2 adrenergic pathways.
• Component in pre-anesthetic medication protocols for small and large animals.
• Used in the development of long-acting tranquilizers for wildlife management and veterinary procedures.
• Reference standard in analytical laboratories for quality control and method development.

Basic Information

Product Name	Medetomidine
CAS No.	86347-14-0
Molecular Formula	C13H16N2
Molecular Weight	200.28 g/mol
Synonyms	4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole; (RS)-Medetomidine; (±)-Medetomidine; Domitor (Veterinary Brand Name); MPV-785; 86347-14-0; Medetomidine Hydrochloride (Salt Form)
EINECS	Contact for details

Quality Control

Our Medetomidine is produced under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0%
Single Maximum Impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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