Dehydroepiandrosterone Acetate | GMP-Certified DHEA API | ≥98% HPLC
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Product Overview
Dehydroepiandrosterone Acetate (DHEA Acetate) is a synthetic steroid precursor widely utilized in hormone therapy formulations and anti-aging supplements13. As a key intermediate in steroid biosynthesis, it supports the production of adrenal hormones, enhances metabolic regulation, and serves as a critical raw material for nutraceutical and pharmaceutical industries24. Compliant with USP/EP standards, it ensures high bioactivity and batch consistency for API manufacturing15.
Key Advantages
✔ ≥98% HPLC-Verified Purity: Meets pharmacopeial specifications for steroid intermediates, guaranteeing reliable hormonal activity14.
✔ Stability-Tested: 18-month shelf life under controlled conditions (20-25°C, protected from light and moisture)36.
✔ GMP-Certified Production: Traceable impurities (<0.5% total impurities) with batch-specific COA and ISO 9001:2025 compliance25.
Applications
◈ Hormone Replacement Therapy (HRT): Core ingredient for adrenal insufficiency and menopause management formulations36.
◈ Anti-Aging Supplements: Key raw material for DHEA-based nutraceuticals targeting cellular rejuvenation45.
◈ Sports Nutrition: Enhances metabolic support in performance-enhancing supplements13.
Quality Certifications
■ USP/EP Monograph Compliance: Validated residual solvents (e.g., acetone <3000 ppm)12.
■ ISO 17025 Accredited Testing: ≤1.0% intra-batch variability confirmed by third-party laboratories35.
Market Trends
The global DHEA market is projected to grow at CAGR 7.2% by 2030, driven by rising demand for anti-aging and metabolic health products46. DHEA Acetate accounts for 12% of steroid precursor APIs, with a 15% annual increase in clinical research procurement25.
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