Description

Verofylline CAS NO 66172-75-6 is a high-purity pharmaceutical intermediate and research chemical. This compound is valued for its specific biological activity and role in the synthesis of more complex therapeutic agents. It is primarily required by pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and fine chemical suppliers serving the life sciences sector.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) targeting specific therapeutic pathways.
• Biochemical Research: Used as a reference standard or tool compound in pharmacological and metabolic studies.
• Contract Manufacturing: Supplied to CMOs for the production of clinical trial materials or commercial drug substances.
• Academic Research: Utilized in university and institutional labs for medicinal chemistry and drug discovery programs.
• Process Development: Serves as a starting material for optimizing scalable synthetic routes in process chemistry.

Basic Information

Product Name	Verofylline
CAS No.	66172-75-6
Molecular Formula	C13H18N4O4
Molecular Weight	294.31 g/mol
Synonyms	1,3-Dimethyl-7-(2-oxopropyl)-3,7-dihydro-1H-purine-2,6-dione; 1,3-Dimethyl-7-(2-oxopropyl)xanthine; 7-(2-Oxopropyl)-1,3-dimethylxanthine; 1,3-Dimethyl-7-(2-oxopropyl)-1H-purine-2,6(3H,7H)-dione; Verofyllinum; Vero-fylline
EINECS	Contact for details

Quality Control

Our Verofylline is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation by IR and NMR spectroscopy, to ensure it meets the stringent requirements for pharmaceutical development. Certificates of Analysis (COA) with full traceability 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 a controlled room temperature (typically 15-25°C). Keep away from incompatible materials.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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