Description

Rac-Monepantel is a key intermediate and reference standard in the development and quality control of veterinary anthelmintic pharmaceuticals. This compound is critical for researchers and manufacturers focused on combating parasitic infections in livestock, ensuring the efficacy and safety of end-use treatments. It serves as an essential building block for the synthesis of active pharmaceutical ingredients and is vital for analytical method development and validation within the animal health sector.

Application

• Veterinary Pharmaceutical Intermediate: Primary use as a synthetic precursor in the manufacture of anthelmintic drugs.
• Reference Standard: Serves as a critical analytical standard for HPLC, GC, and LC-MS methods to quantify active ingredients and impurities.
• Research & Development: Used in pharmacological studies to investigate mode of action, metabolism, and structure-activity relationships of anthelmintic compounds.
• Quality Control & Assurance: Essential for validating manufacturing processes and ensuring batch-to-batch consistency in final drug products.
• Veterinary Parasitology: Employed in laboratory research to study parasite resistance and screen for new therapeutic agents.

Basic Information

Product Name	Rac-Monepantel
CAS No.	851976-50-6
Molecular Formula	C18H21F2N3O2S
Molecular Weight	381.44 g/mol
Synonyms	rac-Monepantel; (±)-Monepantel; 4-[(RS)-[4-(Trifluoromethyl)phenyl](pyridin-3-yl)methyl]morpholine; Zolvix Impurity; Zolvix Intermediate; AAD 1566 (racemate); N-(2-Acetamido-2-(4-fluorophenyl)ethyl)-4-(trifluoromethyl)benzamide (racemic form)
EINECS	Contact for details

Quality Control

Our Rac-Monepantel is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity determination and identity confirmation via spectroscopic methods (IR, NMR, MS). We provide a detailed Certificate of Analysis (COA) with every shipment, ensuring traceability and compliance with your research or cGMP-grade requirements. Specifications are designed to meet the high standards of the pharmaceutical and fine chemical industries.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled accordingly to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Any individual impurity ≤ 0.5%
Total Impurities	≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Water Content (KF)	≤ 0.5% w/w

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