Description

Isoxsuprine Hydrochloride is a pharmaceutical active ingredient belonging to the class of vasodilators and β-adrenergic agonists. It is a critical compound for the development and production of medications aimed at improving peripheral circulation. This high-purity substance is primarily utilized by pharmaceutical manufacturers and research institutions in the life sciences sector. Its reliable quality is essential for ensuring the efficacy and safety of the final drug formulations.

Application

• Pharmaceutical API: Primary active ingredient in prescription medications for peripheral vascular disorders.
• Vasodilator Formulations: Used in drugs to treat conditions like Raynaud's phenomenon, arteriosclerosis obliterans, and other circulatory issues.
• Tocolytic Agent: Employed in some obstetric preparations to manage premature labor.
• Research & Development: Serves as a reference standard and building block in pharmacological and biochemical research.
• Veterinary Medicine: Potential application in veterinary pharmaceuticals for circulatory support.
• Generic Drug Manufacturing: Key component for producing generic versions of established vasodilator drugs.

Basic Information

Product Name	Isoxsuprine Hydrochloride
CAS No.	579-56-6
Molecular Formula	C18H23NO3·HCl
Molecular Weight	337.84 g/mol
Synonyms	Isoxsuprine HCl; 4-Hydroxy-α-[1-[(1-methyl-2-phenoxyethyl)amino]ethyl]benzyl alcohol hydrochloride; Vasodilan; Duvadilan; Xuprin; Phenylisopropylamine derivative; 1-(4-Hydroxyphenyl)-2-((1-methyl-2-phenoxyethyl)amino)-1-propanol hydrochloride
EINECS	209-447-4

Quality Control

Our Isoxsuprine Hydrochloride is manufactured under strict quality management systems. It is produced to meet high-purity standards suitable for pharmaceutical applications, with potential alignment to pharmacopeial monographs such as USP or EP. Every batch undergoes comprehensive analytical testing including assay, impurity profiling, and identification. A Certificate of Analysis (COA) documenting purity, related substances, residual solvents, and other critical parameters is provided to ensure full traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White or almost white, crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any individual impurity ≤ 0.5%
Heavy Metals	≤ 20 ppm

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