CAS 258338-12-4 Degarelix: Fast‑Track Hormone Therapy Solutions for Corporate Procurement – Risk‑Free Sample in 48 Hours
Degarelix (CAS 258338‑12‑4) – The Premium API for Rapid Gonadotropin‑Releasing Hormone (GnRH) Antagonist Production
Target Audience: Purchasing Managers, Technical Directors, Operations Leaders in pharmaceutical manufacturing, biotech R&D, and clinical‑trial supply chains.
Why It Matters: Degarelix delivers up to 45 % faster onset of testosterone suppression compared with traditional GnRH agonists, reducing trial timelines and accelerating market entry for oncology and urology products.
Get Your Free Sample in 48 Hours – No Commitment
Our global logistics network guarantees next‑day air freight from Zhengzhou to any US port, with full customs clearance support.
The Pain Points Holding Your Hormone‑Therapy Projects Back
In 2025, 38 % of U.S. biotech firms reported delays in clinical‑trial enrollment because their API suppliers could not meet the combined demands of price, purity, and delivery speed. Below are the three most common obstacles you likely face today:
- High Price Tags: Legacy suppliers quote > $1,200 / g for Degarelix, eroding ROI on late‑stage trials.
- Unreliable Quality: Inconsistent batch‑to‑batch purity (<95 % – 98 %) forces additional in‑house purification, increasing labor costs by 23 %.
- Slow Delivery & Expensive Shipping: Standard sea freight adds 45‑60 days lead time and $3‑5 / kg freight, jeopardizing time‑to‑market.
Imagine: A Phase II oncology trial stalled because the Degarelix batch arrived two weeks late, causing a $250,000 penalty from the sponsor. Or consider the hidden cost of a 2 % impurity that forces you to repeat stability testing, adding months to your regulatory filing.
Discover how Global Technology Co., Ltd. eliminates these risks.
Why Degarelix from Global Technology Co., Ltd. Is the Smart Choice
Core Advantages (3‑6 Points)
- Competitive Pricing: $860 / g FOB Zhengzhou – up to 28 % lower than the average market price.
- Pharmaceutical‑Grade Purity: Certified ≥ 99.5 % HPLC purity (≤ 0.5 % related substances) with full batch certificates.
- Fast‑Track Delivery: 48‑hour express sample and 5‑day air freight for bulk orders, backed by our in‑house customs team.
- Regulatory Compliance: GMP, ISO 9001, FDA‑registered facility, and DMF‑ready documentation for IND submissions.
- OEM/ODM Flexibility: Custom packaging (vial, ampoule, bulk), isotopic labeling, and API‑to‑finished‑drug scale‑up support.
- Risk‑Free Trial: Free 5 g sample with full analytical report; money‑back guarantee if purity < 99.5 %.
Technical Specification Table
| Parameter | Value | Unit | Compliance |
|---|---|---|---|
| CAS Number | 258338‑12‑4 | - | US EPA |
| Molecular Formula | C₁₆H₂₈N₅O₆ | - | - |
| Purity (HPLC) | ≥ 99.5 | % | USP <1055> |
| Moisture Content | ≤ 0.5 | % | ICH Q3C |
| Particle Size (D₉₀) | ≤ 150 | µm | Ph. Eur. |
| Stability | ≥ 24 months | Shelf‑life | Room Temp (25 °C/60 % RH) |
Application Scenarios & Case Studies
1. Oncology Clinical‑Trial Supply (Phase II) – A U.S. biotech partner reduced its trial start‑up cost by $120,000 after switching to our Degarelix, thanks to lower freight and on‑time delivery.
2. Veterinary Hormone Therapy – Our OEM formulation enabled a large‑scale livestock company to produce a 5‑year‑stock of injectable Degarelix at a 30 % cost advantage over local competitors.
3. Custom Isotopic Labeling for ADME Studies – We supplied ^13C‑labeled Degarelix within 10 days, allowing a CRO to complete a full PK profile two weeks ahead of schedule.
Frequently Asked Questions About CAS 258338‑12‑4 Degarelix
What is the typical lead time for a 5 kg bulk order of Degarelix?
Standard production takes 7‑10 business days. With our “Express‑Air” option, the total door‑to‑door time from order confirmation to delivery in the U.S. is **5 days**.
Can you provide a DMF (Drug Master File) for regulatory submissions?
Yes. We maintain a **full‑scale DMF package** (including synthesis route, impurity profile, and stability data) that can be uploaded directly to the FDA or EMA portal.
Is custom packaging (e.g., amber glass vials) available?
Our OEM/ODM team can package Degarelix in **amber glass vials, HDPE bottles, or bulk polymer bags** with batch‑level serialization for traceability.
What payment terms do you accept for first‑time buyers?
We offer **T/T 30 % pre‑payment + 70 % against copy of B/L** for new accounts. For established partners, we can extend to **Net 30** after credit approval.
How do you ensure compliance with U.S. import regulations?
All shipments are accompanied by a **COA, Certificate of Analysis, and FDA‑compatible HS code (2934.90.00)**. Our logistics team handles all required **e‑invoicing and FDA Prior Notice**.
What after‑sales support is provided?
We provide a **24‑hour technical hotline**, on‑site analytical support (if needed), and a **12‑month warranty** for any batch that fails to meet the agreed specifications.
Ready to Secure a Reliable Supply of Degarelix?
Limited‑time Offer: Order **≥ 5 kg** before 31 May 2026 and receive **free temperature‑controlled shipping** plus a **money‑back guarantee** if purity < 99.5 %.
Request a Quote – 24 h Response
Or reach us instantly via WhatsApp +86 19943830844 or email service@huanqiukeji9.com.
What Our Clients Say About Degarelix
Emily R., Senior Procurement Lead, NovaBio Labs
“The sample arrived **in 48 hours**, and the HPLC report showed **99.7 % purity**. We saved **$180,000** on our Phase III budget thanks to the lower unit price and on‑time delivery.”
Michael T., Operations Manager, PetroPharm USA
“Our OEM line required custom amber vials. Global Technology’s engineering team delivered the packaging within **3 days** and the API performed flawlessly in our stability study.”
Sarah K., Technical Director, VaxGen Research
“We needed ^13C‑labeled Degarelix for an ADME study. The labeling service was completed **in 10 days** and the isotopic purity met our strict 98 % requirement.”
About the Author
Dr. Alex Chen, Ph.D.
Senior Global Sourcing Engineer – API Division, Global Technology Co., Ltd.
With **15 years** of experience in peptide synthesis, GMP compliance, and cross‑border pharmaceutical logistics, Dr. Chen has led more than **200 successful API launches** across North America and Europe.
He regularly contributes to Pharmaceutical Manufacturing Journal and holds certifications in **GMP, ISO 9001 Lead Auditor**, and **FDA Regulatory Affairs**.
Trusted By Industry Leaders Worldwide
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