Accelerate your clinical pipeline with a GMP‑certified Degarelix API that guarantees consistent potency, low impurity profile, and fast‑track delivery to the USA. Ideal for purchasing managers, technical directors, and operations leaders seeking a reliable partner for large‑scale or custom‑batch production.
Get Free Quote in 24 hIn 2025‑2026, over 60 % of U.S. pharmaceutical firms reported supply‑chain bottlenecks when sourcing critical APIs such as Degarelix. The most common pain points you likely experience are:
Imagine a scenario where a Phase II trial stalls because the Degarelix batch fails purity testing. The resulting delay can cost your company **$1.2 million** in lost market opportunity and **12 months** of development time. That risk is avoidable.
| Parameter | Specification |
|---|---|
| CAS No. | 221227-05-0 |
| Purity (HPLC) | ≥ 99.5 % (single‑peak) |
| Appearance | White to off‑white crystalline powder |
| Moisture Content | ≤ 0.5 % (Karl Fischer) |
| Molecular Weight | 1628.37 g mol⁻¹ |
| Solubility | Soluble in 0.9 % NaCl, pH 4‑6 buffer |
| Stability | Shelf‑life ≥ 24 months (25 °C, 60 % RH) |
Case Study – Mid‑Size Oncology Firm (2024): Switched from a 2‑year lead‑time supplier to Global Technology’s Degarelix. Resulted in:
Case Study – Academic Research Consortium (2025): Required 500 g of GMP‑grade Degarelix for a multi‑center trial. Our OEM service delivered a custom lyophilized formulation within 3 weeks, enabling simultaneous enrollment across 12 sites.
Our standard MOQ is **1 kg** for GMP‑grade Degarelix. For research‑grade material, we can supply as low as **100 mg** with a fast‑track quote.
Yes. Our OEM/ODM team offers **salt‑form conversion, micronization, and spray‑drying** to meet your formulation needs. Lead‑time for custom batches is typically **10‑14 days** after specification approval.
Every consignment includes a **Certificate of Analysis (CoA)**, **Batch Manufacturing Record (BMR)**, **FDA 510(k) correspondence**, **CE Declaration of Conformity**, and **ISO‑9001 compliance certificate**.
We operate a **dedicated U.S. logistics hub in Los Angeles**. All shipments are pre‑cleared with US Customs and Border Protection (CBP) and are eligible for **DAP (Delivered at Place)** or **DDP (Delivered Duty Paid)** terms.

Yes. New customers can request a **100 mg free sample** with a **30‑day money‑back guarantee** if the CoA does not meet the agreed specifications.
Act now—stock of GMP‑certified Degarelix is limited to **5 tons** for Q3 2026. Secure your allocation and enjoy:
Emily R., Senior Procurement Officer, NovaPharm – “The **purity** of the Degarelix batch was exactly 99.6 % as promised. We saved **$45 k** on our quarterly purchase and received the shipment in **10 days**. The process was seamless, and the compliance package was audit‑ready.”
Michael T., Technical Director, OncoSolutions – “Custom particle‑size engineering helped us formulate a stable injectable. Global Technology delivered the OEM batch **two weeks early**, enabling us to meet the IND filing deadline.”
Sarah L., Operations Manager, BioCore Labs – “Their **fast‑track logistics** from Zhengzhou to LA cut shipping costs by **$1.8 k** per ton. The real‑time tracking portal gave us full visibility, which is crucial for tight trial schedules.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Contact Page | service@huanqiukeji9.com
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