Description

Pyridofylline is a synthetic xanthine derivative with significant pharmacological activity. This compound is valued for its role as a key intermediate in the synthesis of advanced pharmaceutical agents targeting cardiovascular and respiratory systems. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of new therapeutic molecules. Our supply ensures high purity and consistent quality for critical R&D and production processes.

Application

• Pharmaceutical Intermediate: Serves as a crucial building block in the synthesis of novel vasodilator and bronchodilator drugs.
• Biochemical Research: Used in laboratory studies to investigate phosphodiesterase (PDE) inhibition mechanisms and related cellular pathways.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
• Preclinical Development: Utilized in the formulation of drug candidates for pharmacological and toxicological profiling during early-stage development.

Basic Information

Product Name	Pyridofylline
CAS No.	53403-97-7
Molecular Formula	C₁₃H₁₈N₆O₂
Molecular Weight	290.32 g/mol
Synonyms	Pyridofylline; 7-[2-[(3-Pyridinylmethyl)amino]ethyl]-1,3-dimethylpurine-2,6-dione; 1,3-Dimethyl-7-[2-[(3-pyridinylmethyl)amino]ethyl]xanthine; BL 191; 3-Pyridinemethanamine, N-(2-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-7H-purin-7-yl)ethyl)-
EINECS	Contact for details

Quality Control

Our Pyridofylline is manufactured under a strict quality management system. Every batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the high standards required for pharmaceutical research and development. A detailed Certificate of Analysis (COA) is provided with each shipment, documenting all critical quality attributes.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after each use to minimize exposure to atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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