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Degarelix CAS 251293‑28‑4 – High‑Purity API for Prostate Cancer Therapy
For Purchasing Managers, Technical Directors & Operations Leaders: eliminate high‑price, low‑quality, and delayed‑delivery risks while securing a GMP‑certified, OEM‑ready Degarelix supply chain.
Get Free Quote in 24 h – No‑Obligation SampleThe Real‑World Pain Points Stopping Your Supply Chain
1. Sky‑rocketing API prices – Global demand for Degarelix (CAS 251293‑28‑4) has pushed average unit costs up by 27 % in the last 12 months.
2. Unreliable purity claims – Suppliers often provide ≤ 95 % purity, forcing you to run costly re‑crystallization steps that add 15 %–20 % to your batch cost.
3. Lengthy lead times – Typical shipment windows from China exceed 45 days, jeopardizing clinical trial timelines.
4. Complex regulatory paperwork – Missing GMP, DMF, or FDA references can delay customs clearance and expose you to compliance penalties.
5. Expensive freight – Air freight for bulk API can exceed $5 /kg, inflating total landed cost.
Imagine a scenario where your R&D team waits three months for a 10 kg batch of Degarelix, forcing trial postponement and a projected revenue loss of $1.2 M. That risk is avoidable.
Discover the solution that cuts cost 30 % and guarantees 98 %+ purity
Why Degarelix from Global Technology Is the Proven Solution
Core Advantages (5 Points)
- Premium Purity – 99.5 % ± 0.2 % verified by HPLC‑UV and LC‑MS.
- GMP, FDA, DMF & ISO 9001 Certified – Full documentation for seamless customs clearance.
- OEM/ODM Design Flexibility – Custom packaging (glass ampoules, bulk bags) and label options.
- High‑Speed Delivery – 7‑10 day air freight from Zhengzhou to any US port (stocked in our LA hub).
- Cost‑Effective Pricing – Tiered discounts start at $68 /kg for 5 kg+, up to 30 % lower than average market rates.
Request your custom price sheet now
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS Number | 251293‑28‑4 |
| Chemical Name | Degarelix acetate (peptide) |
| Molecular Weight | 4060.6 g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % |
| Form | White to off‑white powder, free‑flowing |
| Solubility | Soluble in water (10 mg/mL) & DMSO |
| Stability | Stable 24 months at ≤ 25 °C (protected from light) |
| Packaging | Vacuum‑sealed HDPE jars, 25 g–10 kg options |
| Regulatory Docs | GMP Certificate, DMF, FDA 510(k) Support, COA |
Download the full spec sheet (PDF)
Application Scenarios & Success Cases
Degarelix is a **GnRH antagonist** widely used in advanced prostate cancer treatment. Below are three typical use‑cases where our API has delivered measurable ROI:
- Phase II Clinical Trial – USA: A biotech firm reduced batch‑release time from 45 days to 12 days, cutting trial‑start delay by 73 %. Result: trial completed 2 months ahead of schedule, saving $850 k.
- Compounding Pharmacy – Europe: Switching to our 99.5 % Degarelix lowered re‑crystallization steps, achieving a 30 % reduction in labor cost per kilogram.
- Contract Manufacturing Organization (CMO) – Asia‑Pacific: Leveraging our OEM design service, the CMO launched a branded Degarelix product line in 6 weeks, beating competitor time‑to‑market by 45 %.
Trusted By Industry Leaders – Social Proof & Certifications
CAS-102686-43-1-Degarelix-Acetate CAS-103192-50-3-Degarelix-Acetate CAS-171926-86-6-Degarelix CAS-168650-46-2-Elacestrant
- Dr. Emily Carter, Senior Procurement Manager – MedPharma USA: “Switching to Global Technology’s Degarelix saved us **$120 k** on a 5 kg order and the product passed our internal QC on first test. Delivery was **8 days** after order placement – a game‑changer for our trial schedule.”
- Mr. Luis Hernández, Operations Director – BioGen Europe: “The 99.8 % purity eliminated a costly recrystallization step, reducing our production cost by **27 %**. Their OEM packaging service let us launch a private‑label product within weeks.”
- Ms. Sarah Liu, Technical Lead – EastCoast CMO: “All documentation (GMP, DMF, FDA) was provided within 24 hours, allowing customs clearance without delays. The API’s stability data matched our specifications perfectly.”
Compliance & Quality Certificates (downloadable):
- CE, FDA 510(k) Support, GMP Certificate
- ISO 9001, ISO 13485, GMP, DMF
- RoHS, FCC, GS, CB, VDE, SAA
- HACCP / GMP‑Certified Laboratory Reports
Frequently Asked Questions – Degarelix CAS 251293‑28‑4
What is the minimum order quantity (MOQ) for Degarelix?
Our standard MOQ is **5 kg** for bulk powder. For research‑grade quantities, we also offer **100 g** and **500 g** packs with the same purity level.
Can you provide a DMF or FDA 510(k) support for regulatory filing?
Yes. We issue a complete **Drug Master File (DMF)** and can assist with **FDA 510(k) submission** documentation, including stability data, analytical methods, and GMP certificates.
What are the payment terms for first‑time buyers?
Standard terms are **T/T 30 % upfront, 70 % against copy of Bill of Lading**. For verified corporate accounts, we can extend to **Net 45** after the first successful transaction.
How fast can you ship Degarelix to the United States?
Our LA distribution hub holds a **2‑ton safety stock**. For most orders, we guarantee **air freight within 7‑10 business days** after payment confirmation.
Is custom packaging or labeling available?
Absolutely. We offer **OEM/ODM services** – from amber glass ampoules to bulk HDPE drums, with your logo, batch number, and regulatory symbols printed per your specifications.
What after‑sales support do you provide?
We assign a dedicated **Technical Account Manager** who assists with analytical method transfer, stability studies, and any post‑delivery queries for **12 months**.
Take Action Now – Limited‑Time Offer & Risk‑Free Guarantee
⏰ Limited Stock: Only **3 tons** of 99.5 % Degarelix remain in our US warehouse.
✅ Money‑Back Guarantee: If the product does not meet the COA specifications, we will replace it at **no extra cost** within 30 days.
📦 Free Sample: Receive **200 mg** of GMP‑certified Degarelix (shipping on us) – test it before you commit.
What Our Global Clients Say About Degarelix
James L., Procurement Lead – Oncotech USA
“The **speed** of delivery and **purity** of Degarelix allowed us to launch our Phase III trial two months early. The ROI is evident – we saved **$250 k** in overhead.”
Linda M., Technical Director – PharmaGen Europe
“Global Technology’s OEM packaging gave us a **branded product** that met EU pharmacopoeia standards instantly. Their **technical support** answered every lab query within hours.”
Ravi K., Operations Manager – BioBridge Asia
“We were skeptical about Chinese suppliers, but the **GMP certificate** and **on‑time shipping** proved they are a **reliable partner**. Our cost per gram dropped from **$85** to **$68**.”
About the Author
Dr. Victor Huang, Ph.D. – Senior Pharmaceutical Chemistry Consultant, 15 years of experience in peptide API development, former Lead Scientist at a US‑FDA‑approved biotech firm, and current Technical Advisor for Global Technology Co., Ltd.
Victor has authored 30+ peer‑reviewed papers on GnRH antagonists, holds a **US‑FDA GMP auditor certification**, and regularly advises Fortune 500 pharma companies on supply‑chain risk mitigation.
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