Accelerate your prostate‑cancer formulation pipeline with a GMP‑certified Degarelix Intermediate that guarantees ≥98% purity, on‑time delivery, and flexible OEM/ODM support.
In 2025‑2026, the global market for androgen‑blocking agents grew by 12%, yet many pharmaceutical manufacturers still grapple with **three critical bottlenecks** that erode ROI and delay patient access.
Scenario: A mid‑size biotech firm in the United States postponed its Phase III trial because the Degarelix batch failed purity testing, costing them an estimated US$ 2.3 million in lost time and extra testing.
Global Technology Co., Ltd leverages a **powerful factory network** certified by GMP, FDA, ISO 9001, and HACCP. Our **CAS 920014-72-8 Degarelix Intermediate** is engineered for **high‑yield synthesis**, **cost‑effective scaling**, and **regulatory compliance**.
| Parameter | Value | Unit | Method |
|---|---|---|---|
| CAS Number | 920014-72-8 | — | N/A |
| Purity (HPLC) | ≥98.5 | % | Validated method 2024 |
| Appearance | White to off‑white powder | — | Visual inspection |
| Moisture Content | ≤0.5 | % | Karl Fischer |
| Residual Solvents | ≤10 ppm | ppm | GC‑MS |
| Stability | 24 months | — | ICH‑Q1A(R2) |
Case A – Mid‑Size Oncology Startup (USA)
Needed 2 kg of Degarelix Intermediate for a Phase II trial. Our fast‑track production cut lead time from 45 days to 14 days, saving US$ 150,000 in storage and expediting patient enrollment.
Case B – Contract Manufacturing Organization (CMO) in Europe
Required custom‑sized particles (<200 µm) for a novel depot formulation. Our OEM service delivered a **tailored batch** within 21 days, meeting both **EMA** and **FDA** specifications.
The standard MOQ is **10 g** for research‑grade material. For commercial‑grade API, the MOQ starts at **5 kg**, with volume discounts available beyond 20 kg.
Yes. We ship a **5 g trial kit** within 48 h, fully documented with CoA and MSDS. If the sample does not meet your specifications, the cost is reimbursed.
We support **T/T**, **L/C at sight**, and **PayPal for smaller quantities**. For trusted partners, we can arrange **30‑day net** after the first successful shipment.
All batches are produced in GMP‑certified facilities, accompanied by a **Full FDA‑compliant Dossier**, Certificate of Analysis, and a **US‑Customs Bond**. We also assist with IND/DMF submissions if required.

Standard air freight (DAP) arrives in **12‑18 days**. Express courier (DHL, UPS) can deliver within **4‑6 days** for orders under 5 kg. Sea freight is available for >10 kg, with a 30‑day transit window.
Absolutely. Our OEM/ODM team can produce **Degarelix acetate, phosphate, or custom salts**, adjust particle size distribution, and provide **sterile‑filled vials** upon request.
Place your order within the next 7 days and receive a **5% price reduction** plus **free expedited shipping** on orders ≥10 kg.
Risk‑Free Guarantee: If the product does not meet the agreed specifications, we will provide a **full refund** or a **replacement shipment** at no extra cost.
Laura M., Procurement Lead – MedTech USA
“The **speed** of delivery was outstanding. We received 8 kg of Degarelix Intermediate within 10 days, allowing us to meet our FDA filing deadline. The **CoA** was crystal‑clear, and the product performed exactly as expected.”
James T., CEO – BioPharma Solutions
“Switching to Global Technology saved us **~30%** on raw material costs while improving purity from 96% to 99.1%. Their **OEM flexibility** helped us launch a new depot formulation in record time.”
Dr. Ahmed K., Head of Clinical Ops – European Oncology Center
“Regulatory documentation was **complete and audit‑ready**. The product’s stability (24 months) gave us confidence for long‑term clinical supply.”
Tel: +86 199 4383 0844 Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
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