Description

Des(Methoxycarbonyl) Febantel is a key pharmaceutical intermediate and metabolite of the anthelmintic drug Febantel. This compound is critical for research and development in veterinary and human medicine, particularly in the study of drug metabolism, efficacy, and the synthesis of novel therapeutic agents. It is primarily utilized by pharmaceutical R&D laboratories, analytical reference standard providers, and manufacturers of active pharmaceutical ingredients (APIs) for quality control and regulatory compliance purposes.

Application

• Pharmaceutical Intermediate: A crucial building block in the synthesis and research of anthelmintic agents.
• Metabolite Reference Standard: Used in analytical laboratories for the identification and quantification of Febantel metabolites in biological and environmental samples.
• Veterinary Drug Research: Essential for studies on the pharmacokinetics, metabolism, and mode of action of benzimidazole-class parasiticides.
• Quality Control & Assurance: Serves as a certified reference material (CRM) for HPLC, LC-MS, and other analytical methods to ensure batch consistency and purity of final drug products.
• Regulatory Compliance Testing: Supports studies required for drug registration dossiers submitted to agencies like the FDA and EMA.

Basic Information

Item	Details
Product Name	Des(Methoxycarbonyl) Febantel
CAS No.	92088-58-9
Molecular Formula	C₁₈H₁₇N₃O₄S
Molecular Weight	371.41 g/mol
Synonyms	Febantel Impurity C; Febantel Metabolite; N-[[(2-Methoxyacetyl)amino]-4-(phenylthio)phenyl]-2-methoxyacetimidate; 2-Methoxy-N-[2-methoxy-1-[[2-(phenylthio)phenyl]imino]ethyl]acetamide; Des(methoxycarbonyl)febantel; Febantel Related Compound C
EINECS	Contact for details

Quality Control

Our Des(Methoxycarbonyl) Febantel is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and MS, and residual solvent analysis, to ensure it meets the high standards required for pharmaceutical research. A detailed Certificate of Analysis (COA) with batch-specific data is provided with every shipment.

Storage

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

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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