Description

Pyrantel Tartrate is a salt form of the broad-spectrum anthelmintic agent pyrantel, offering enhanced stability and solubility. This compound is a critical active pharmaceutical ingredient (API) in both human and veterinary medicine for the effective treatment of intestinal parasitic infections. It is essential for manufacturers in the pharmaceutical and animal health industries producing anti-parasitic formulations. Our supply of Pyrantel Tartrate CAS NO 7635-10-1 is backed by stringent quality control to ensure efficacy and safety in final products.

Application

• Human Pharmaceutical API: Primary active ingredient in anthelmintic medications for treating pinworm, roundworm, and hookworm infections.
• Veterinary Pharmaceutical API: Key component in deworming pastes, suspensions, and feed additives for livestock, companion animals, and equines.
• Oral Suspension Formulations: Used in the production of palatable liquid medications for easy administration, particularly in pediatric and veterinary applications.
• Tablet and Chewable Tablet Manufacturing: Incorporated into solid dosage forms for precise dosing and convenience.
• Feed Premix and Additives: Utilized in medicated feed for herd-level parasite control in agricultural animal production.
• Research and Development: Serves as a reference standard and building block in pharmacological research for novel anti-parasitic agents.

Basic Information

Product Name	Pyrantel Tartrate
CAS No.	7635-10-1
Molecular Formula	C34H30N2O6S
Molecular Weight	594.68 g/mol
Synonyms	Pyrantel Tartrate Salt; Pyrantel Acid Tartrate; Pyrantel Hydrogen Tartrate; 1-Methyl-2-[(E)-2-(2-thienyl)ethenyl]-5,6-dihydro-4H-pyrimidine Tartrate; Antiminth (as tartrate salt); Combantrin (as tartrate salt); Helmintox (as tartrate salt); Strongid (as tartrate salt)
EINECS	231-559-4

Quality Control

Our Pyrantel Tartrate is manufactured under a quality management system and undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical use. We can supply material compliant with various pharmacopeial monographs. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each batch to support your regulatory and formulation needs.

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). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent absorption of atmospheric moisture, which can affect stability and handling properties.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Conforms to standard
Assay (HPLC)	98.0% - 102.0% (on dried basis)
Loss on Drying	≤ 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./USP criteria

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