Description

Eperisone Hydrochloride is a centrally acting muscle relaxant pharmaceutical compound. It matters for its ability to relieve muscle stiffness and spasticity by acting on the central nervous system and improving blood flow. This active pharmaceutical ingredient (API) is primarily needed by pharmaceutical manufacturers and research institutions developing treatments for musculoskeletal disorders and related neurological conditions.

Application

• Primary API in the formulation of prescription muscle relaxant medications.
• Used in clinical research for studying spasticity and musculoskeletal pain management.
• Key ingredient in the development of combination therapies for chronic back pain and cervical spondylosis.
• Essential for pharmaceutical companies producing generic versions of eperisone-based drugs.
• Utilized in preclinical and pharmacological studies to understand its mechanism of action.
• Serves as a reference standard in analytical laboratories for quality control and method development.

Basic Information

Item	Details
Product Name	Eperisone Hydrochloride
CAS No.	56839-43-1
Molecular Formula	C17H25NO•HCl
Molecular Weight	295.85 g/mol
Synonyms	4'-Ethyl-2-methyl-3-piperidinopropiophenone Hydrochloride; Myonal (brand name); Eperisone HCl; (2-Methyl-3-piperidinopropyl) 4'-ethylphenyl ketone hydrochloride; 1-(4-Ethylphenyl)-2-methyl-3-(1-piperidinyl)-1-propanone hydrochloride
EINECS	Contact for details

Quality Control

Our Eperisone Hydrochloride is manufactured under strict quality systems. The product undergoes rigorous testing to ensure it meets high-purity pharmaceutical standards, with specifications typically aligned with major pharmacopoeial requirements. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each batch to ensure full traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric 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)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%; Any single impurity ≤ 0.5%

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