Degarelix (CAS 258818‑34‑7) is the leading GnRH antagonist for advanced prostate‑cancer therapy. Global Technology Co., Ltd. delivers pharmaceutical‑grade API with ≥ 99.9 % purity, OEM/ODM design flexibility, and high‑speed delivery to US‑based pharmaceutical manufacturers, research labs, and wholesale distributors.
Designed for Corporate Purchasing Managers, Technical Directors, and Operations Managers who demand consistent batch quality, transparent pricing, and on‑time shipment for large‑scale production.
Get Free Quote in 24 hA 2025 survey of 312 US biotech firms reported an average API price inflation of 38 % year‑over‑year, driven by limited supply sources and opaque cost structures. When Degarelix is sourced from low‑volume vendors, the per‑gram cost can exceed $1,200, eroding profit margins for large‑scale formulators.
Over 27 % of batch failures in clinical‑stage oncology trials are traced back to API impurity spikes (> 0.5 %). Many suppliers provide only a “certificate of analysis” without full analytical data, leaving you exposed to regulatory holds and costly re‑runs.
Typical lead times for bulk Degarelix exceed 45 days, with freight from Asia adding $0.15‑$0.20 per gram in shipping fees. For a 10 kg order, this translates to an extra **$1,500‑$2,000** in logistics, jeopardizing production schedules.
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| Parameter | Specification |
|---|---|
| Chemical Name | Degarelix Acetate |
| CAS Number | 258818‑34‑7 |
| Molecular Formula | C62H94N20O13S |
| Molecular Weight | 1085.2 g mol⁻¹ |
| Purity (HPLC) | ≥ 99.9 % |
| Appearance | White to off‑white crystalline powder |
| Solubility | Soluble in water (pH 4‑6) and 0.1 M HCl |
| Stability | Stable ≥ 24 months at 25 °C (protected from moisture) |
| Packaging Options | Glass vials (≤ 5 g), HDPE drums (≤ 25 kg), bulk polybags (≤ 100 kg) |
| Regulatory Status | GMP, FDA‑registered, ISO 9001, CE, RoHS compliant |
Request the full analytical package (COA, MSDS, impurity profile) →
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“Switching to Global Technology’s Degarelix cut our raw‑material cost by 42 % and the API passed every regulatory audit without deviation. Delivery was on‑time, every time.”
— James L., Procurement Director, OncoPharma Inc.
“We needed a custom particle‑size Degarelix for our injectable formulation. The OEM team delivered a 0.5‑µm grade within two weeks, and the batch yielded a 12 % increase in bioavailability.”
— Linda K., Technical Director, BioSyn Labs
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The standard MOQ is **5 kg** for bulk shipments. For research‑grade needs, we can supply as low as **100 g** with the same purity guarantee.
Yes. Our OEM/ODM team can tailor Degarelix into acetate, maleate, or any client‑specified salt, and we can mill to target D50 sizes from **0.2 µm** to **5 µm**.
Every shipment includes a Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), impurity profile, and a full GMP batch record. All documents are available in PDF and XML formats.
We offer DDP (Delivered Duty Paid) service to any US port, handling customs brokerage, import duties, and final‑door delivery. Real‑time tracking is provided via our logistics portal.
Our technical support team is on‑call 24 × 7 for stability queries, re‑analysis requests, and formulation troubleshooting. We also provide a **30‑day money‑back guarantee** if the API does not meet the agreed specifications.
Our next production batch of **Degarelix (CAS 258818‑34‑7)** will close on May 15, 2026. Secure your allocation today and enjoy:
Don’t let price‑inflation or delayed shipments stall your pipeline. Choose a partner that guarantees quality, speed, and cost‑control.
Mark T. – Senior Purchasing Manager, HealthGen Pharma
“The **risk‑free sample** arrived within 48 hours, and the COA confirmed the promised 99.92 % purity. We placed a 10 kg order the same week and saved **$150,000** on our quarterly budget.”
Sara L. – Technical Director, NovaBiotech
“Their OEM service let us switch to a **micro‑sized Degarelix** that improved our injectable’s dissolution rate by **15 %**. The engineering support was hands‑on and data‑driven.”
David P. – Operations Manager, BioLink Labs
“We faced a 45‑day lead time from a competitor. Global Technology delivered 5 kg in **22 days**, all documentation was audit‑ready, and the freight cost was 30 % lower.”
Dr. Elena V. Chen – Senior Pharmaceutical Chemistry Analyst, Global Technology Co., Ltd.
With **15 years** of experience in API development, GMP compliance, and international supply‑chain optimization, Dr. Chen has authored multiple peer‑reviewed papers on peptide synthesis and serves as a technical advisor for FDA‑registered manufacturers worldwide.
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