Description

Prenoverine is a high-purity pharmaceutical intermediate and active ingredient. It is a key compound valued for its specific pharmacological activity, primarily as an antispasmodic agent. This product is essential for manufacturers in the pharmaceutical and fine chemical industries engaged in the development and production of therapeutic formulations.

Application

• Pharmaceutical Active Ingredient (API): Primary use as an antispasmodic agent in prescription medications.
• Research & Development: A critical reference standard and building block in pharmacological and medicinal chemistry research.
• Formulation Development: Used in the development of solid dosage forms (e.g., tablets, capsules) and injectable solutions.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for GMP production.
• Analytical Standard: Serves as a high-purity standard for quality control and method validation in analytical laboratories.

Basic Information

Product Name	Prenoverine
CAS No.	66022-25-1
Molecular Formula	C₂₃H₂₉NO₄
Molecular Weight	383.48 g/mol
Synonyms	Prenoverine; 2-(Diethylamino)ethyl 1-phenylcyclopentanecarboxylate; 1-Phenylcyclopentanecarboxylic acid 2-(diethylamino)ethyl ester; Egazil; Egazyl; Spasmopriv; Spasmopriv
EINECS	Contact for details

Quality Control

Our Prenoverine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent pharmaceutical-grade specifications, including identity, purity, and impurity profile. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

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). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
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.