share

Moxaverine Hydrochloride CAS NO 1163-37-7


Unit Price:

CAS No.:1163-37-7

Grade:Pharmacy Grade

Content:99.0%

Brand:Customizable

Packaging:Customizable

Description

Moxaverine Hydrochloride is a synthetic, spasmolytic pharmaceutical compound. It is primarily valued for its potent smooth muscle relaxant properties, targeting vascular and gastrointestinal systems. This active pharmaceutical ingredient (API) is essential for manufacturers in the pharmaceutical industry developing treatments for circulatory disorders and spasmodic conditions.

Application

  • Pharmaceutical API: Core active ingredient in the formulation of antispasmodic and vasodilator medications.
  • Vasodilator Formulations: Used in drugs aimed at improving peripheral and cerebral blood circulation.
  • Gastrointestinal Spasm Relief: Key component in medications for treating spasms of the digestive tract.
  • Research & Development: Serves as a critical reference standard and building block in pharmacological research for new therapeutic agents.
  • Generic Drug Manufacturing: Sourced by generic pharmaceutical companies for the production of cost-effective alternatives to branded spasmolytic drugs.
  • Veterinary Pharmaceuticals: Applicable in veterinary medicine for managing spasmodic conditions in animals.

Basic Information

Product Name Moxaverine Hydrochloride
CAS No. 1163-37-7
Molecular Formula C₁₉H₂₉N₃O₃·HCl
Molecular Weight 383.91 g/mol
Synonyms Moxaverine HCl; 4-Ethoxy-3-methoxybenzyl 3,4,5-trimethoxybenzoate hydrochloride; 3,4,5-Trimethoxybenzoic Acid 4-Ethoxy-3-methoxybenzyl Ester Hydrochloride; Benzoic acid, 3,4,5-trimethoxy-, 4-ethoxy-3-methoxybenzyl ester, hydrochloride; Moxaverin Hydrochloride; UP 507-04
EINECS Contact for details

Quality Control

Our Moxaverine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent pharmaceutical-grade specifications. Certificates of Analysis (COA) documenting compliance with relevant pharmacopeial standards (such as USP/EP) are provided with every shipment.

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). The product is hygroscopic (moisture-sensitive); ensure containers are sealed after each use to prevent degradation.

Specification

Item Specification
Appearance White to off-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) ≤ 0.5%
Residue on Ignition ≤ 0.1%
Related Substances (HPLC) Total impurities ≤ 1.0% Any single 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.

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.