Description

Tazifylline is a specialized pharmaceutical intermediate and research chemical with significant potential in therapeutic development. This compound matters for its role as a key building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly those targeting respiratory and inflammatory pathways. It is primarily needed by pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and advanced chemical synthesis facilities focused on creating next-generation drug candidates.

Application

• Pharmaceutical Intermediate: Serves as a critical precursor in the multi-step synthesis of proprietary drug substances.
• Research & Development: Used in medicinal chemistry programs for structure-activity relationship (SAR) studies and lead optimization.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
• Biochemical Research: Investigated for its biological activity and potential mechanism of action in preclinical studies.
• Contract Synthesis: Supplied to CMOs and CDMOs for custom synthesis projects under cGMP or non-GMP conditions.
• Academic Research: Utilized in university and institutional labs for pharmacological and chemical research.

Basic Information

Product Name	Tazifylline
CAS No.	79712-55-3
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	7H-Purine-2,6-dione, 8-(2-hydroxyethyl)-1,3,7-trimethyl-; 8-(2-Hydroxyethyl)-1,3,7-trimethyl-7H-purine-2,6-dione; 1,3,7-Trimethyl-8-(2-hydroxyethyl)xanthine; Tazifyllinum; Tazifylline (USAN)
EINECS	Contact for details

Quality Control

Our Tazifylline is produced and tested under a strict quality management system to ensure batch-to-batch consistency and high purity. We provide comprehensive analytical data supporting identity, purity, and strength. Certificates of Analysis (COA) are available for every batch, detailing results from tests such as HPLC assay, related substances, residual solvents, and identification. Our quality commitment aligns with ICH guidelines, and we can support projects requiring material for cGMP manufacturing.

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 powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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