Description

Oxantel is a specialized anthelmintic compound belonging to the tetrahydropyrimidine class, recognized for its targeted activity against specific parasitic nematodes. Its primary value lies in its efficacy as a veterinary pharmaceutical active ingredient, offering a critical tool for animal health management. This product is essential for manufacturers in the veterinary pharmaceutical industry, particularly those formulating treatments for livestock and companion animals.

Application

• Active Pharmaceutical Ingredient (API) in veterinary anthelmintic formulations.
• Key component in combination therapies for broad-spectrum parasite control in animals.
• Manufacturing of medicated feed additives for livestock deworming programs.
• Production of oral pastes, drenches, or tablets for equine and ruminant health.
• Research and development of novel antiparasitic agents and drug combinations.
• Reference standard for quality control and analytical testing in pharmaceutical labs.

Basic Information

Item	Detail
Product Name	Oxantel
CAS No.	36531-26-7
Molecular Formula	C13H16N2O
Molecular Weight	216.28 g/mol
Synonyms	Oxantel Pamoate (common salt); Oxantel Embonate; 1-Methyl-2-[3-(2-thienyl)-2-propenylidene]-1,4,5,6-tetrahydro-4-pyrimidinamine; CP-14,445; Meta-oxantel; trans-Oxantel; Oxantel Base
EINECS	Contact for details

Quality Control

Our Oxantel is produced under a strict quality management system to ensure batch-to-batch consistency and reliability. Quality assurance includes comprehensive testing for identity, purity, and specified impurities. A Certificate of Analysis (COA) documenting all test results is provided with each shipment, supporting compliance with cGMP guidelines for active pharmaceutical ingredients.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	NMT 1.0%
Residue on Ignition	NMT 0.1%
Related Substances (HPLC)	Total impurities: NMT 2.0% Any individual impurity: NMT 0.5%

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