Description

Zoletil is a potent injectable anesthetic agent widely used in veterinary medicine. Its primary value lies in providing rapid induction, reliable surgical anesthesia, and smooth recovery for a variety of animal species. This product is essential for veterinary surgeons, research facilities, and wildlife management professionals requiring effective chemical restraint and analgesia. The compound is supplied as a high-purity active pharmaceutical ingredient (API) for formulation.

Application

• Veterinary Anesthesia: Primary use for surgical procedures and invasive examinations in cats, dogs, and non-domestic species.
• Wildlife Immobilization: Critical for the safe capture, translocation, and medical treatment of free-ranging wildlife.
• Veterinary Research: Used as a standard anesthetic in preclinical and pharmacological studies involving laboratory animals.
• Zoological Park Management: Facilitates routine health checks, dental work, and minor surgeries on zoo animals.
• Formulation: Serves as the key active ingredient in the manufacture of finished injectable veterinary medicinal products.

Basic Information

Product Name	Zoletil
CAS No.	39307-54-5
Molecular Formula	C13H16FN3O
Molecular Weight	249.29 g/mol
Synonyms	Tiletamine Hydrochloride; Telazol (combination product with Zolazepam); CL-369; CI-634; Phencyclidine derivative anesthetic; 2-(Ethylamino)-2-(2-thienyl)cyclohexanone hydrochloride
EINECS	Contact for details

Quality Control

Our Zoletil (Tiletamine HCl) is manufactured under strict quality systems to meet the exacting standards of the pharmaceutical industry. Each batch is supported by a comprehensive Certificate of Analysis (COA) confirming identity, purity, and conformance to specifications. We ensure compliance with relevant Good Manufacturing Practice (GMP) guidelines for active pharmaceutical ingredients (APIs).

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive); ensure the container is kept tightly sealed in a low-humidity environment.

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)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Microbial Limits	Meets Ph. Eur. requirements for non-sterile substances

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