Description

Oxantel Pamoate is a salt form of the anthelmintic agent oxantel, combined with pamoic acid to enhance stability and bioavailability. This compound is a critical active pharmaceutical ingredient (API) primarily valued for its targeted efficacy against specific intestinal nematode infections. It is essential for pharmaceutical manufacturers developing veterinary and human anti-parasitic formulations, particularly those focused on combination therapies for broad-spectrum parasite control.

Application

• Veterinary Anthelmintic Formulations: A key API in medications for treating parasitic worm infections (e.g., whipworms) in livestock, companion animals, and poultry.
• Human Pharmaceutical Products: Used in the manufacture of prescription anthelmintic drugs, often in combination with other agents like pyrantel pamoate.
• Broad-Spectrum Parasite Control: Integral to combination therapy products designed to target multiple parasite species simultaneously.
• Pharmaceutical Intermediates: Serves as a starting material or intermediate in the synthesis of more complex anthelmintic compounds.
• Research & Development: Used in biochemical and pharmacological studies to understand anti-parasitic mechanisms of action and drug resistance.
• Public Health Programs: Incorporated into mass drug administration (MDA) initiatives in regions endemic for soil-transmitted helminthiasis.

Basic Information

Item	Details
Product Name	Oxantel Pamoate
CAS No.	68813-55-8
Molecular Formula	C34H30N2O9
Molecular Weight	610.61 g/mol
Synonyms	Oxantel Embonate; 1-Methyl-2-[trans-3-(2-thienyl)acryloyl]tetrahydro-1,4-thiazine Pamoate; CP-14445-16; Oxantel Pamoate Salt; trans-1-Methyl-2-(3-(2-thienyl)acryloyl)tetrahydro-1,4-thiazine Compound with 4,4'-Methylenebis(3-hydroxy-2-naphthoic acid); Oxantel Pamoate (USP); Oxantel Pamoate (Vet.)
EINECS	Contact for details

Quality Control

Our Oxantel Pamoate is manufactured under strict quality management systems. Each batch is tested to ensure it meets high-purity standards suitable for pharmaceutical applications, with specifications aligned with pharmacopeial guidelines. A comprehensive Certificate of Analysis (COA), detailing identity, purity, and impurity profiles, is provided with every shipment to ensure traceability and regulatory compliance.

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 (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	Yellow to pale yellow 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)	≤ 5.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any individual impurity ≤ 0.5%

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