Description

Febuverine is a high-purity pharmaceutical intermediate and active ingredient with significant importance in modern therapeutic development. Its value lies in its role as a key building block for synthesizing advanced drug compounds, ensuring reliable and scalable production. This product is essential for research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in the development and production of specialized medications.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of active pharmaceutical ingredients (APIs) for various therapeutic classes.
• Antispasmodic Drug Research: Used in the research and development of novel antispasmodic and smooth muscle relaxant medications.
• Chemical Synthesis: Serves as a versatile building block in complex organic synthesis for creating new molecular entities.
• Analytical Reference Standard: Employed as a high-purity standard in quality control laboratories for method development and validation.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production.
• Academic & Industrial R&D: Utilized in both academic research and industrial R&D departments for pharmacological studies.

Basic Information

Product Name	Febuverine
CAS No.	7077-33-0
Molecular Formula	C20H24N2O2
Molecular Weight	324.42 g/mol
Synonyms	Febuverine; 1-(3,4-Dimethoxybenzyl)-6,7-dimethoxy-3-methylisoquinoline; 6,7-Dimethoxy-1-veratryl-3-methylisoquinoline; 1-Veratryl-6,7-dimethoxy-3-methylisoquinoline; 3-Methyl-1-veratryl-6,7-dimethoxyisoquinoline; 1-(3,4-Dimethoxyphenyl)methyl-6,7-dimethoxy-3-methylisoquinoline
EINECS	Contact for details

Quality Control

Our Febuverine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We adhere to relevant industry standards, and each lot is supported by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. Certificates of Analysis (COA) are available upon request to support your regulatory and quality assurance requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials and sources of ignition.

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)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
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.