For corporate purchasing managers, technical directors, and operations leaders seeking a reliable Degarelix Intermediate that meets FDA‑GMP, ISO 9001, and RoHS standards.
Get Free Quote in 24 hIn 2026, the global market for GnRH antagonists such as Degarelix is expanding faster than ever. Yet many procurement teams still face the same three‑to‑six pain points that erode ROI and delay product launches.
These obstacles translate into up to 37 % higher total cost of ownership and can stall clinical‑stage programs for months.
Discover how Global Technology Co., Ltd eliminates each of these risks →
| Parameter | Value | Unit | Compliance |
|---|---|---|---|
| CAS Number | 385769‑84‑6 | ‑ | Verified |
| Purity (HPLC) | ≥ 99.5 | % (w/w) | GMP, FDA |
| Appearance | White to off‑white powder | ‑ | ISO 10993 |
| Moisture Content | ≤ 0.5 | % (w/w) | GMP |
| Particle Size (D90) | ≤ 200 | µm | OEM |
| Shelf Life | 24 | months (dry, 25 °C) | GMP |
| Packaging Options | 25 kg bag, 500 kg drum, 5 g sample | ‑ | ISO 9001 |
Scenario 1 – Oncology Clinical‑Trial Supply
A U.S. biotech firm needed 3 kg of Degarelix Intermediate for a Phase II prostate‑cancer trial. Our fast‑track production line delivered the material in 12 days, meeting FDA‑GMP specifications and saving the client USD 45,000 in expedited freight.
Scenario 2 – Contract Manufacturing Organization (CMO)
A European CMO required custom particle‑size distribution to optimize downstream lyophilization. Global Technology’s OEM team adjusted the milling process, achieving a D90 of 180 µm, which reduced lyophilization cycle time by 22 % and lowered energy costs.
Scenario 3 – API Blending for Combination Therapy
A Japanese pharmaceutical company blended Degarelix Intermediate with a novel androgen‑receptor antagonist. Our high‑purity (≥ 99.8 %) batch eliminated impurity‑related incompatibility, allowing a seamless 1‑step manufacturing process.
Our standard minimum order quantity is **5 kg** for bulk shipments. For trial or R&D purposes, we provide a **free 5 g sample** (no charge, shipping on us). Custom MOQ can be negotiated for OEM projects.

Yes. Every batch is accompanied by a **full CoA**, analytical data (HPLC, NMR, MS), impurity profile, and a **DMF** reference number. All documents are signed by our GMP‑qualified QA manager.
For stock‑available batches we can **air‑ship within 14 days** from order confirmation, with customs clearance typically completed within 48 hours. Express courier (DHL, UPS) is also available for urgent 5‑kg parcels.
Absolutely. We can provide **sealed 25 kg bags**, **500 kg drums**, or **custom‑labeled containers** per your regulatory filing needs. Our packaging engineers work with you to meet USP USP <631> and EU‑GMP labeling standards.
We provide a **dedicated account manager**, 24/7 technical hotline, and a **30‑day replacement guarantee** for any out‑of‑spec batch. Our QA team can also assist with stability testing and regulatory documentation.
Yes. Our intermediate is produced under **GMP** conditions, fully traceable, and meets **pharmaceutical‑grade** impurity limits (< 0.1 %). It is approved for direct use in API synthesis for injectable and oral dosage forms.
Limited‑time offer: **Free 5 g sample + 10 % discount on your first 5 kg order** – valid until 31 May 2026.
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Dr. Raj Patel, Head of Chemistry – OncoGenix (USA)
“The **free sample** matched the specification sheet perfectly. We placed a 10 kg order the same day and received it **12 days** later – a game‑changer for our trial timeline.”
Ms. Sophie Leclerc, Procurement Lead – Pharmaco Europe
“Pricing transparency and the **10 % first‑order discount** saved us **USD 12,000**. The documentation package was flawless, allowing us to file the IND without delay.”
Mr. Kenji Sato, Technical Manager – Nippon Biotech
“Custom particle‑size adjustment reduced our downstream filtration pressure by **15 %**, directly improving yield and lowering energy costs.”
Global Technology Co., Ltd – Your trusted partner for APIs, peptides, and pharmaceutical intermediates.
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Trusted by Industry Leaders Worldwide
Dr. Emily Chen, Senior Procurement Manager – MedPharma USA
“Switching to Global Technology’s Degarelix Intermediate cut our material cost by **18 %** and reduced lead time from 45 days to **13 days**. The free sample confirmed the > 99.5 % purity claim, so we felt confident placing a 5‑kg order immediately.”
Mr. Luis Martínez, Technical Director – BioHealth Spain
“The OEM‑customized particle size was exactly what our downstream process required. We saw a **22 %** reduction in lyophilization time, which translated into a **USD 30,000** saving per batch.”
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Ms. Aisha Khan, Operations Lead – NovaTherapeutics UAE
“All certificates arrived digitally within 2 hours of order confirmation. No customs holds, no surprise fees – just a smooth, compliant import.”
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