Product Overview

Ospemifene is a selective estrogen receptor modulator widely used in gynecology, primarily for treating urogenital atrophy in postmenopausal women. As an active pharmaceutical ingredient (API), its core function is as a high-purity, highly stable pharmaceutical intermediate, suitable for various stages of research, pilot-scale, and industrial production. This product exhibits excellent chemical stability and biological activity, meeting the pharmaceutical companies' demand for high-quality starting materials and serving as a crucial foundation for related formulation development and process optimization.

Applications

• Gynecological drug development
• Synthesis of drugs for the treatment of urogenital system diseases
• Intermediates for selective estrogen receptor modulators
• Customized production of pharmaceutical intermediates
• Drug impurity research and analysis

Quality & Supply Capability

English Name: Ospemifene Properties: White to off-white crystalline powder with good chemical stability. Its molecular structure contains a benzofuran ring and a piperidine group, meeting pharmaceutical-grade API standards. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the COA/MSDS. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches. Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging. Document Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from laboratory sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust the supply plan according to the customer's specific requirements for purity, impurity control, packaging specifications, delivery cycle, and quality documentation. Simultaneously, we have a professional technical support team to assist customers in process development, route optimization, and project transformation, ensuring stable product supply and technology implementation at different stages.

Why Choose Bioncan

Focused on pharmaceutical intermediates, with extensive experience in API supply. Full-scale supply capabilities, covering all stages from laboratory to commercial production. Provides complete quality control documentation, including COA, MSDS, HPLC, NMR, etc. Supports customized needs, adjusting purity, impurity control, and packaging specifications according to customer requirements. Comprehensive process optimization technical support to help customers achieve a smooth transition from R&D to scale-up.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 128607-22-7, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.