Description

Moxaverine is a synthetic, spasmolytic pharmaceutical compound with the CAS registry number 10539-19-2. It is valued for its selective action on smooth muscle, making it a critical intermediate in the synthesis of therapeutic agents targeting vascular and gastrointestinal disorders. This high-purity compound is essential for pharmaceutical manufacturers and research institutions engaged in drug development, formulation, and advanced pharmacological studies.

Application

• Pharmaceutical Active Ingredient (API): Primary use as the active component in antispasmodic and vasodilator medications.
• Research & Development: Key intermediate in preclinical and clinical research for studying smooth muscle relaxants.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Formulation Development: Used in the development of various dosage forms, including tablets and injectables.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production.
• Academic Research: Utilized in university and institutional studies on pharmacology and medicinal chemistry.

Basic Information

Product Name	Moxaverine
CAS No.	10539-19-2
Molecular Formula	C24H29N3O4
Molecular Weight	423.51 g/mol
Synonyms	Moxaverine Hydrochloride; 4-Ethoxy-3-methoxybenzaldehyde 1-[3-(diethylamino)propyl]-1,7-dihydro-6H-purine-2,6-dione; 1-[3-(Diethylamino)propyl]-3-ethyl-7-(4-ethoxy-3-methoxybenzyl)xanthine; Eupaverin; Upaverin; Moxaverina; Moxaverinum
EINECS	234-104-8

Quality Control

Our Moxaverine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC and other pharmacopeial methods, to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) documenting full compliance 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). Keep the container tightly sealed to protect from 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 ≤ 1.0%
Any single unknown impurity	≤ 0.10%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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