Description

Inaperisone Hydrochloride is a high-purity pharmaceutical intermediate and active ingredient. This compound is valued for its role in the research and development of centrally acting muscle relaxants. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the synthesis of therapeutic agents targeting muscle spasticity and related neurological conditions. Our supply ensures consistent quality and reliability for critical production and development processes.

Application

• Pharmaceutical Active Ingredient (API): Primary use in the formulation of muscle relaxant medications.
• Research & Development: Key intermediate in the synthesis and study of novel centrally acting therapeutic agents.
• Reference Standard: Serves as an analytical standard for quality control and method validation in pharmaceutical laboratories.
• Preclinical Studies: Used in pharmacological and toxicological research to evaluate efficacy and safety profiles.
• Chemical Synthesis: Intermediate for further chemical modification and derivative preparation in medicinal chemistry.

Basic Information

Product Name	Inaperisone Hydrochloride
CAS No.	118230-97-0
Molecular Formula	C₁₇H₂₄N₂O•HCl
Molecular Weight	308.85 g/mol
Synonyms	4'-Ethyl-2-methyl-3-piperidinopropiophenone Hydrochloride; Inaperisone HCl; YF-477; YF 477; (±)-Inaperisone Hydrochloride; rac-Inaperisone Hydrochloride; 1-[4-Ethylphenyl]-2-methyl-3-(1-piperidinyl)-1-propanone Hydrochloride
EINECS	Contact for details

Quality Control

Our Inaperisone Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing purity, identity, and impurity profiles 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). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.5%
Related Substances (HPLC)	Total impurities ≤1.5%
Any single unknown impurity	≤0.5%
Water Content (KF)	≤1.0%
Residue on Ignition	≤0.1%

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