Description

Nitroso-Prodenafil CAS NO 1266755-08-1 is a high-purity chemical intermediate of significant interest in advanced pharmaceutical research and development. This compound is valued for its role in the synthesis pathway of active pharmaceutical ingredients (APIs) targeting specific therapeutic areas. It is primarily utilized by research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in the development of novel therapeutic agents. Our supply is characterized by stringent quality control, ensuring reliability for critical R&D and scale-up processes.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of advanced active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for the discovery and optimization of new drug candidates.
• Process Chemistry: Serves as a critical reagent in scaling up synthetic routes from laboratory to pilot and commercial production.
• Reference Standard: Employed as an analytical standard for quality control and method validation in pharmaceutical analysis.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Academic Research: Utilized in university and institutional labs for pharmacological and biochemical studies.

Basic Information

Product Name	Nitroso-Prodenafil
CAS No.	1266755-08-1
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Prodenafil Nitroso Derivative; N-Nitroso Prodenafil; 1-[[3-(6,7-Dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-5-yl)-4-ethoxyphenyl]sulfonyl]-4-methylpiperazine N-Oxide; 1266755-08-1; Nitroso Prodenafil; N-Oxide Prodenafil Analog
EINECS	Contact for details

Quality Control

Our Nitroso-Prodenafil is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Quality is verified through a comprehensive suite of analytical techniques including HPLC, NMR, and mass spectrometry. A Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with each shipment to support your quality assurance protocols.

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. For long-term storage, consider under an inert atmosphere.

Specification

Item	Specification
Appearance	Off-white to light yellow powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5%
Total Impurities	≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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