Description

Denaverine CAS NO 3579-62-2 is a synthetic antispasmodic agent belonging to the class of papaverine derivatives. It is valued for its potent smooth muscle relaxant properties, making it a critical intermediate in the synthesis of specialized pharmaceutical formulations. This compound is primarily required by pharmaceutical manufacturers and research institutions developing treatments for gastrointestinal and genitourinary spasms.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of antispasmodic and vasodilator medications.
• Research & Development: Used in pharmacological studies investigating smooth muscle relaxation and related therapeutic pathways.
• Active Pharmaceutical Ingredient (API) Synthesis: Serves as a precursor in the manufacturing of finished dosage forms like tablets or injectables.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.

Basic Information

Item	Details
Product Name	Denaverine
CAS No.	3579-62-2
Molecular Formula	C₁₈H₂₃NO₃
Molecular Weight	301.38 g/mol
Synonyms	Denaverine Hydrochloride; 1-(3,4-Dimethoxybenzyl)-6,7-dimethoxy-3-methylisoquinoline; Fenoverine (common name); NSC 113986; Papaverine derivative; Isoquinoline antispasmodic
EINECS	Contact for details

Quality Control

Our Denaverine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and spectroscopic identification, to ensure it meets stringent specifications. A Certificate of Analysis (COA) detailing all test results 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 place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%

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