Allylestrenol represents a premium-grade progestogen hormone analog supplied as white to off-white crystalline powder with characteristic odor. Specifically engineered for pharmace...

Allylestrenol represents a premium-grade progestogen hormone analog supplied as white to off-white crystalline powder with characteristic odor. Specifically engineered for pharmaceutical applications, this high-purity compound ensures exceptional stability and compliance with rigorous industry standards. It demonstrates solubility in methanol and chloroform while remaining insoluble in water, undergoing comprehensive testing for identity, potency, and impurities to meet the exacting requirements of pharmaceutical manufacturers and distributors seeking dependable raw materials.

This product finds essential application across pharmaceutical manufacturing, biotechnology development, and veterinary medicine sectors. It serves as a fundamental component in producing hormonal therapies, fertility treatments, and gynecological medications. Companies operating in these specialized fields value Allylestrenol for its unwavering quality consistency, which directly supports the creation of safe and effective medications for both human and animal health applications while maintaining regulatory compliance.

Businesses benefit from Allylestrenol's proven reliability and strict adherence to quality control protocols, significantly reducing production risks while ensuring end-product safety. Its compatibility with diverse pharmaceutical formulations and consistent compliance with international regulatory standards makes it a preferred choice for serious buyers focused on maintaining quality assurance and operational efficiency throughout their supply chain operations.

Key Features:
- High-purity white to off-white crystalline powder with characteristic odor
- Soluble in methanol and chloroform while insoluble in water
- Controlled melting range between 78-81C with moisture content below 1.0%
- Purity assay maintained between 97% to 103% with minimal impurities
- Clear solution formation in methanol at 65C without insoluble particles

Benefits:
- Consistent quality ensures reliable therapeutic performance in final products
- High purity levels support precise dosing in pharmaceutical formulations
- Stable chemical properties enable long shelf life and storage reliability
- Compliance with industry standards reduces regulatory compliance risks
- Versatile solubility characteristics facilitate diverse manufacturing processes