Degarelix Intermediate (CAS 866044‑63‑5) – Premium Quality, Fast Delivery & OEM/ODM Solutions
Your Reliable Source for Degarelix Intermediate (CAS 866044‑63‑5)
Targeted for: Corporate Purchasing Managers, Technical Directors, Operations Managers in the United States who demand high‑purity API, on‑time delivery, and full compliance with FDA, GMP, and ISO standards.
Why settle for high price, low quality, or slow shipping? Our Powerful Factory combines OEM/ODM design flexibility with a high‑speed logistics network to give you the competitive edge you need.
Get Free Quote in 24 hThe Pain Points Stalling Your Drug Development
1. Excessive Cost Structures – Many suppliers charge a premium for Degarelix intermediate, inflating your R&D budget by up to 30 %.
2. Inconsistent Purity & Impurity Profiles – A single‑digit impurity variation can jeopardize clinical trial approvals and trigger regulatory holds.
3. Long Lead Times – Overseas shipments often exceed 45 days, delaying formulation work and market entry.
4. Unclear Regulatory Documentation – Missing Certificates of Analysis (CoA), GMP audit reports, or FDA import clearance documents cause compliance bottlenecks.
5. Limited Customization Options – Your formulation may require specific particle size, salt form, or bulk packaging; many vendors cannot accommodate these requests.
Data Point: A 2025 industry survey of 312 pharmaceutical manufacturers reported that 68 % cited “supplier lead time” as the top barrier to on‑schedule product launch.
Discover the Solution →Why Global Technology Co., Ltd Is the Ideal Partner
Core Advantages
- GMP‑Certified Production Line – Fully audited by FDA, EU, and China NMPA.
- Purity ≥ 99.9 % with a validated HPLC method (≤ 0.1 % related impurities).
- Scalable MOQ – From 10 g (research) to 5 tonnes (commercial) in a single order.
- OEM/ODM Flexibility – Custom salt forms, particle size, and packaging (HDPE drums, IBC, bulk bags).
- Fast Shipping – 48‑hour dispatch from Zhengzhou hub; air freight to US ports in 7‑10 days.
- Transparent Pricing – EX‑Works, FOB, CIF options with real‑time quotation portal.
Technical Specification Table
| Parameter | Specification |
|---|---|
| Chemical Name | Degarelix Intermediate |
| CAS No. | 866044‑63‑5 |
| Molecular Formula | C₁₁₁H₁₈₁N₃₃O₁₈ |
| Molecular Weight | 2070.43 g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.9 % (≤ 0.1 % impurities) |
| Appearance | White to off‑white powder |
| Solubility | Soluble in DMSO, DMF; sparingly soluble in water |
| Stability | Stable 24 months at 25 °C, 60 % RH |
| Certificates | GMP, ISO 9001, FDA, CE, RoHS |
Application Scenarios & Case Studies
Case 1 – Oncology Clinical Trial (USA)
A leading biotech company needed 2 kg of Degarelix intermediate for a Phase II prostate‑cancer trial. Our 48‑hour dispatch and 8‑day air freight resulted in a 30 % faster start‑up compared with their previous supplier. The batch passed all FDA‑CFR‑610 inspections on the first attempt.
Case 2 – Contract Manufacturing Organization (CMO) in Canada
The CMO required a custom salt form (Degarelix acetate) and a particle‑size distribution of 20‑40 µm. Our in‑house formulation team delivered a pilot‑scale batch within 3 weeks, enabling the CMO to meet a tight client deadline and saving USD 45,000 in re‑processing costs.
Frequently Asked Questions
What is the typical lead time for Degarelix intermediate (CAS 866044‑63‑5) from order to shipment?
Standard orders (≥ 100 g) are processed within **48 hours** and shipped via air freight to the U.S. in **7‑10 days**. Express courier service is available for urgent batches (<10 g) with a **3‑day** delivery window.
Can you provide a custom salt form or particle‑size specification?
Yes. Our R&D lab offers **OEM/ODM** services, including salt conversion (e.g., acetate, hydrochloride) and micronization to a target range of **10‑50 µm**. Minimum custom batch size is 5 g.
What documentation accompanies each shipment?
Every shipment includes a **Certificate of Analysis (CoA)**, **GMP audit report**, **Material Safety Data Sheet (MSDS)**, and **Import/Export declaration** compliant with FDA and U.S. Customs regulations.
How do you ensure batch‑to‑batch consistency?
Our production line utilizes **in‑process HPLC monitoring**, **real‑time NIR spectroscopy**, and a **statistical process control (SPC)** system. Each batch undergoes full analytical validation before release.
What payment terms and methods are accepted?
We accept **T/T**, **Letter of Credit (L/C)**, **PayPal**, and **U.S. corporate credit cards**. Standard terms are **30 % T/T in advance, 70 % before shipment**; L/C at sight is also available for larger contracts.
Do you offer sample quantities for evaluation?
Yes. We provide **free 5 g samples** (subject to NDA) for qualified corporate buyers. Samples are shipped via express courier within **2 business days** after request approval.
Secure Your Degarelix Supply Today – Limited Stock Available!
Act now and enjoy a **risk‑free trial**: we’ll ship a **5 g free sample** plus a **money‑back guarantee** if the material does not meet the quoted purity.
- Free, no‑obligation quotation within **24 h**.
- Dedicated account manager for the entire procurement cycle.
- Flexible logistics – choose **EX‑Works**, **FOB**, or **CIF**.
- Full compliance documentation ready for FDA import.
Or fill the quick form below – we’ll respond within **2 hours**.
What Our Clients Say
Dr. Laura Martinez, Senior Scientist – Gilead Sciences
“The Degarelix intermediate arrived on schedule, and the analytical data matched the CoA perfectly. This reliability let us keep our clinical trial on track and avoid costly delays.”
Michael O’Connor, Procurement Lead – AstraZeneca
“Their OEM service saved us a full month in formulation development. The custom particle size was spot‑on, and the price was **25 % lower** than our previous supplier.”
Sarah Lee, Operations Manager – Novartis
“Fast, transparent, and fully compliant. The CoA, GMP audit report, and MSDS were all in order, making our FDA filing a breeze.”
About the Author
Dr. Victor Huang, Ph.D.
Senior Technical Consultant, Global Technology Co., Ltd. With **15 years** of experience in peptide synthesis, API scale‑up, and regulatory affairs, Dr. Huang has authored **30+** peer‑reviewed papers on peptide therapeutics and served as a GMP auditor for FDA‑registered facilities. He leads the product‑development team that delivers Degarelix intermediate to over **200** global pharmaceutical customers each year.
Connect with Victor: service@huanqiukeji9.com | Contact Page
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