Description

Fenoverine CAS NO 37561-27-6 is a synthetic organic compound belonging to the class of spasmolytic agents. It is a high-purity active pharmaceutical ingredient (API) valued for its smooth muscle relaxant properties, primarily targeting the gastrointestinal tract. This compound is essential for pharmaceutical manufacturers and research institutions developing treatments for functional gastrointestinal disorders, such as irritable bowel syndrome (IBS). Consistent quality and reliable supply are critical for ensuring the efficacy and safety of the final medicinal products.

Application

• Pharmaceutical API: Primary use as the active ingredient in antispasmodic and gastroprokinetic medications.
• Gastrointestinal Therapeutics: Formulation into tablets, capsules, or other dosage forms for the treatment of irritable bowel syndrome (IBS) and related functional disorders.
• Clinical Research: Utilization as a reference standard or investigational compound in pharmacological studies and clinical trials.
• Drug Development: Serves as a key intermediate or final API in the R&D pipeline for new spasmolytic drugs.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the production of finished pharmaceutical products.
• Analytical Testing: Used as a certified reference material (CRM) in quality control laboratories for method development and validation.

Basic Information

Item	Details
Product Name	Fenoverine
CAS No.	37561-27-6
Molecular Formula	C24H30N2O3
Molecular Weight	394.51 g/mol
Synonyms	Fenoverine; 1-Piperazineacetic acid, α-phenyl-α-(2-pyridinyl)-, ethyl ester; Ethyl 2-phenyl-2-(2-pyridyl)glycolate piperazinium salt; Spasmopriv; Fenoverinum; Phenyl(2-pyridyl)glycolic acid ethyl ester piperazine salt
EINECS	Contact for details

Quality Control

Our Fenoverine is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent pharmaceutical-grade specifications. We provide full traceability and support regulatory filings. Certificates of Analysis (COA) documenting compliance with agreed specifications are available for every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 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
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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