Description

Spasfon is a pharmaceutical active ingredient with the CAS registry number 79173-14-1. This compound is valued for its antispasmodic properties, making it a critical component in the formulation of medications designed to relieve smooth muscle spasms. It is primarily required by pharmaceutical manufacturers and research institutions developing treatments for gastrointestinal and urological disorders.

Application

• Pharmaceutical Manufacturing: Primary active ingredient in antispasmodic and analgesic drug formulations.
• Gastrointestinal Therapeutics: Used in medications for treating irritable bowel syndrome (IBS), abdominal cramps, and related functional disorders.
• Urological Spasm Relief: Key component in drugs addressing renal colic, bladder spasms, and dysmenorrhea.
• Clinical Research: Serves as a reference standard and active compound in pharmacological studies and new drug development.
• Veterinary Medicine: Employed in veterinary pharmaceutical products for managing spasmodic conditions in animals.
• Analgesic Combination Drugs: Often formulated in combination with other analgesics for enhanced spasmolytic and pain-relief effects.

Basic Information

Product Name	Spasfon
CAS No.	79173-14-1
Molecular Formula	C₁₈H₂₃ClN₂O₃
Molecular Weight	350.84 g/mol
Synonyms	Phloroglucinol Trimethyl Ether; Alverine Citrate (common salt form); Spasfon Lyoc; Spasfon (Alverine Citrate); 1,3,5-Trimethoxybenzene; 1,3,5-Trimethoxybenzene Citrate Salt; Alverine; 3,5-Dimethoxyphenol Methyl Ether
EINECS	Contact for details

Quality Control

Our Spasfon (CAS 79173-14-1) is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity pharmaceutical standards, including identity, assay, and impurity profile verification. Certificates of Analysis (COA) documenting compliance with relevant specifications are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, protect from moisture and store under inert conditions if the container is opened frequently.

Specification

Item	Specification
Appearance	White or almost white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 1.0%; Any single impurity ≤ 0.5%

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