Megestrol Intermediate | GMP-Certified API Synthesis | USP/EP-Compliant
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Product Overview
Megestrol Intermediate is a high-purity chemical precursor essential for synthesizing megestrol acetate, a progesterone analogue widely used in hormonal therapies and oncology treatments13. It ensures precision in API manufacturing for contraceptive drugs, cancer therapies, and hormone replacement formulations25.
Key Advantages
✔ >99% HPLC Purity: Batch-specific chromatographic validation with full traceability34.
✔ GMP/ICH Compliance: Produced under ISO 9001 and ICH Q7 guidelines for pharmaceutical-grade quality25.
✔ Scalable Synthesis: Supports bulk production with 98% yield optimization36.
Applications
◈ Contraceptive API synthesis (e.g., oral contraceptives, hormonal IUDs)25.
◈ Oncology drug development (adjuvant therapy for breast/endometrial cancer)36.
◈ Veterinary hormone formulations (appetite stimulants for companion animals)56.
Quality Certifications
◼ USP/EP/ICH compliant: Full analytical profiles (NMR, IR, MS)34.
◼ Stability tested: 36-month shelf life under controlled storage (2-8°C)25.
Market Trends
The global hormonal therapy market is projected to reach $45.2B by 2030, driven by rising demand for oncology and reproductive health solutions56. Megestrol acetate holds 22% share in progesterone-based cancer therapies, with 15% annual growth in contraceptive API demand35.
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Optimized Keywords:
- Hormonal Therapy Intermediate
- Contraceptive API Synthesis
- Oncology Drug Precursor
- USP/EP-Compliant Megestrol
- GMP-Certified Progesterone Analog
Additional High-Value Keywords:
High-Yield Hormone Synthesis
Veterinary Pharmaceutical Grade
Breast Cancer Adjuvant Intermediate
Oral Contraceptive Manufacturing
Stability-Validated API Precursor
China
