Description

Spasmofen is a specialized pharmaceutical intermediate and active ingredient known for its antispasmodic properties. It is a high-purity compound critical for ensuring the efficacy and safety of final pharmaceutical formulations. This product is essential for manufacturers in the pharmaceutical industry developing treatments for conditions involving smooth muscle spasms, such as certain gastrointestinal or urinary tract disorders.

Application

• Primary active pharmaceutical ingredient (API) in antispasmodic medications.
• Key intermediate in the synthesis of advanced therapeutic agents targeting smooth muscle hyperactivity.
• Used in research and development for novel spasmolytic drug formulations.
• Component in combination therapies for treating abdominal cramps and irritable bowel syndrome (IBS).
• Reference standard in analytical laboratories for quality control and method development.

Basic Information

Product Name	Spasmofen
CAS No.	82824-08-6
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Fenoverine; Spasmopriv; Fenoverine Hydrochloride; 82824-08-6; 1-Piperazinepropanoic acid, α-phenyl-, ethyl ester; Ethyl 3-phenyl-3-(1-piperazinyl)propionate
EINECS	Contact for details

Quality Control

Our Spasmofen is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) documenting identity, purity, and impurity profiles are available upon request to support your regulatory and quality assurance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which can affect stability and purity.

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 ≤ 1.5%
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.