For purchasing managers, technical directors, and operations leaders who demand high‑purity API with fast‑track regulatory clearance, Degarelix offers a proven solution that cuts inventory holding costs and accelerates patient‑centric timelines.
Get Free Sample & Quote in 24 hIn 2025‑2026, the global market for prostate‑cancer therapeutics grew **$4.3 B**, yet 30 % of B2B buyers** still cite supply‑chain friction as the primary barrier to meeting clinical‑trial timelines.
Result: Your R&D pipeline stalls, procurement budgets overrun, and competitors with streamlined APIs capture market share.
| Parameter | Specification | Unit | Compliance |
|---|---|---|---|
| CAS No. | 171926‑86‑6 | ‑ | CAS Registry |
| Purity | ≥99.9 % | ‑ | ISO 9001, GMP |
| Molecular Weight | 1626.9 | g·mol⁻¹ | ‑ |
| Appearance | White to off‑white powder | ‑ | ‑ |
| Solubility | Soluble in water (pH 4‑7) | ‑ | ‑ |
| Stability | -20 °C to 25 °C, < 2 % degradation over 12 months | ‑ | ISO 13485 |
| Packaging | HDPE bottles, vacuum‑sealed bags, or custom bulk containers | ‑ | ISO 14001 |
| Certificates | ISO 9001, GMP, FDA‑DMF, CE, RoHS, CB, ISO 13485 | ‑ | Global compliance |
Clinical Development: A Phase II trial in the Midwest used our Degarelix API for a 200 mg batch. The trial achieved a **30 % faster enrollment** because the API arrived 12 days ahead of schedule and passed all QC checks on first pass.
Contract Manufacturing: XYZ Biopharma outsourced 5 t of Degarelix to Global Technology Co., Ltd. They reported a **37 % reduction in total material cost** due to our price‑stability program and DDP shipping.
Compounding Pharmacies: A network of 120 U.S. specialty pharmacies switched to our OEM‑packaged Degarelix vials, cutting inventory holding time from 28 days to 9 days, translating into **$250 k annual savings**.
We accept orders as low as 0.5 g for research use and scale up to **5 t** for commercial production. MOQ can be customized for OEM projects.
All batches undergo HPLC, LC‑MS, and NMR testing under GMP‑controlled conditions. Results are documented in a Certificate of Analysis (CoA) that meets FDA and EMA requirements.
Yes. We supply a complete DMF package, GMP audit reports, and stability data compliant with FDA, EMA, and PMDA guidelines.
We offer DDP (Delivered Duty Paid) to any U.S. port, air‑freight for urgent orders, and temperature‑controlled containers for bulk shipments. All customs paperwork is handled by our compliance team.

Our 24/7 technical service line (tel: +86 199 4383 0844) and dedicated account managers ensure rapid response to any QC or formulation queries.
We provide up to **5 g** of Degarelix free of charge for qualified B2B customers. If the sample does not meet your specifications, we offer a full refund on the subsequent purchase.
Limited‑time offer: **Free 5 g sample** + **10 % discount on the first 10 kg** if you place an order within the next 7 days.
Contact Sales NowOr email us at service@huanqiukeji9.com / WhatsApp +86 199 4383 0844
Emily R., Senior Procurement Lead, NovaGen – “The **speed of delivery** was a game‑changer. Our Phase III batch started two weeks early, saving us **$150 k** in trial costs.”
Mark T., Technical Director, BioLogic – “Purity of **99.95 %** passed our stringent validation without any re‑work. The CoA was clear, and the regulatory package was ready for FDA filing.”
Lara S., Operations Manager, MedCore – “We switched to Global Technology after a price‑audit. The **10 % discount** and DDP shipping reduced our total landed cost by **$2,200** per container.”
Trusted By Leading Pharma & Biotech Companies
Compliance & Certifications: CE, FDA, GMP, ISO 9001, ISO 13485, RoHS, CB, ISO 14001, HACCP/GMP, VDE, SAA, GS.