Subtitle: Cut procurement cost, eliminate quality risk, and accelerate time‑to‑market for your oncology & urology pipelines – tailored for Purchasing Managers, Technical Directors, and Operations Leaders.
Get Free Quote in 24 hDegarelix (CAS 113873‑67‑9) is a synthetic peptide antagonist of the gonadotropin‑releasing hormone (GnRH) receptor, widely used in advanced prostate‑cancer therapy and in pre‑clinical research for hormonal regulation. Global Technology Co., Ltd delivers **≥98 % purity**, **certificate‑of‑analysis (CoA) within 24 h**, and **custom batch sizes from 0.5 g to 10 kg**.
Request a Free Sample – No ObligationPurchasing managers across the U.S. report three recurring frustrations that directly impact ROI:
According to a 2025 survey of 312 biotech firms, 37 % of projects missed milestones due to API supply issues. The financial impact? An average overruns of **$2.1 M per delayed trial**.
See How We Solve It| Parameter | Value |
|---|---|
| CAS No. | 113873‑67‑9 |
| Chemical Name | Degarelix Acetate |
| Purity | ≥ 98 % (HPLC) |
| Appearance | White to off‑white powder |
| Molecular Weight | 1448.71 g·mol⁻¹ |
| Solubility | Soluble in DMSO, 0.1 M HCl |
| Stability | -20 °C, protected from light, 24 months |
| Packaging | LDPE bags, amber glass vials, or custom bulk drums |
| Certificate | GMP, ISO 9001, FDA‑registered, CE, RoHS |
1. Clinical‑Stage Oncology: A Phase II prostate‑cancer trial in Texas required 2 kg of Degarelix for 30 patients. Our 48‑hour dispatch cut the original 21‑day lead time by 85 %, enabling the trial to start on schedule and saving an estimated $150,000 in ancillary costs.
2. Academic Research: A university in Boston ordered 150 g for receptor‑binding assays. We supplied a **certificate‑driven batch** that passed internal QC on the first attempt, reducing repeat‑test expenses by **$12,300**.
3. OEM Formulation: A biotech startup partnered with us for a Degarelix‑loaded injectable. Our ODM service included lyophilization and sterile vial filling, cutting their development cycle from 9 weeks to 5 weeks.
Start Your Project TodayOur standard MOQ is 0.5 g for research‑grade material. For GMP‑grade batches, the MOQ is 5 g, with volume discounts available from 100 g upward.
Yes. Our R&D team offers OEM/ODM services, including N‑terminal modifications, pegylation, and lyophilized formulations. Turn‑around time is typically 2‑3 weeks after design approval.
Every batch undergoes HPLC, LC‑MS, and elemental analysis in our ISO‑9001/GMP laboratory. Results are documented in a signed CoA, and an independent third‑party lab validates the data for critical orders.

Standard air freight (DDP) arrives in 3‑5 business days; express courier (DHL, UPS) can be 2 days. For larger volumes, we offer sea‑freight (30‑35 days) with consolidated pallets. All shipments are tracked with real‑time updates.
We accept T/T (pre‑payment), L/C at sight, and PayPal for orders ≤ 5 kg. For established accounts, we can discuss Net 30 or Net 60 terms after credit verification.
Limited‑time offer: **Free 0.5 g sample** (no purchase required) + **10 % discount** on the first 5 kg order if you confirm within 7 days.
We mitigate risk with a money‑back guarantee on any batch that fails to meet the agreed specifications.
Or fill the quick form below – we’ll reply within 2 hours.
Laura Martinez, Procurement Lead, GenMed Labs – “The price advantage was immediate. We saved $9,500 on a 10 kg order, and the product arrived on schedule. The CoA matched exactly what we needed for IND filing.”
James O’Neil, Technical Director, Prostate Oncology Inc. – “Quality is non‑negotiable for us. Global Technology’s Degarelix passed our in‑house QC on the first test – zero re‑work.”
Sofia Liu, Operations Manager, BioSyn Therapeutics – “Fast 48‑hour dispatch meant our clinical trial started on day 1. The logistics team kept us informed, and the freight cost was 30 % lower than our previous carrier.”
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“Switching to Global Technology reduced our Degarelix cost by 26 % and shortened delivery from 18 days to 3 days. The CoA was flawless, and the technical support team answered every query within hours.” – Dr. Emily Chen, Senior Research Manager, BioPharma Solutions (USA)
“The OEM peptide‑design service allowed us to launch a next‑generation GnRH antagonist in record time. Compliance documents were ready for FDA submission on day 1.” – Mark Davis, VP of R&D, OncoNova Therapeutics
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