CAS 312306-89-1 Degarelix Acetate – High‑Purity API for Rapid Clinical Supply
Targeted for: Pharmaceutical manufacturers, CROs, and biotech firms seeking a reliable, GMP‑certified source of Degarelix Acetate for androgen‑dependent disease programs.
Why it matters: Degarelix Acetate (CAS 312306‑89‑1) is the cornerstone of modern GnRH‑antagonist therapies, delivering consistent potency and fast batch release that protects your trial timelines.
Get Free Quote in 24 h – No Obligation2. The Real‑World Pain Points Holding Your Development Back
When you’re managing a multi‑phase clinical program, every delay translates into lost market share and inflated R&D spend. Below are the three most common obstacles our target audience—Corporate Purchasing Managers, Technical Directors, and Operations Managers—face when sourcing Degarelix Acetate.
- High Unit Cost – Legacy suppliers in Europe and the U.S. charge premium prices (> $1,200 / g) due to limited scale and strict import tariffs.
- Variable Purity & Batch‑to‑Batch Consistency – Inconsistent assay results (± 5 %) cause re‑qualification cycles, extending timelines by 4–6 weeks.
- Lengthy Lead Times & Expensive Shipping – Standard logistics from established vendors often exceed 45 days, with freight costs that can add 20 % to the overall budget.
According to a 2025 industry survey, 37 % of biotech firms cited “supplier‑induced timeline risk” as the top cause of trial delays. If you recognize any of these red flags, you’re already primed for a smarter sourcing strategy.
Discover the Solution →3. Why Our Degarelix Acetate Outperforms the Competition
Core Advantages (Business‑Intent Keywords)
- Competitive Pricing – up to 30 % lower than Western benchmarks thanks to our vertically integrated Chinese manufacturing network.
- GMP, FDA, and EMA‑aligned Quality System with full batch certificates, ensuring ≥ 99.8 % purity and ≤ 0.1 % impurity across every release.
- Rapid 7‑day Turn‑around from order confirmation to shipment, supported by our on‑site logistics hub at Zhengzhou International Airport.
- Customizable Packaging & OEM/ODM Design for both gram‑scale research and ton‑scale commercial production.
- Full Compliance with CE, ISO 9001, ISO 14001, and GMP‑derived SOPs; all documentation is available in English upon request.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS No. | 312306‑89‑1 |
| Chemical Name | Degarelix Acetate |
| Purity (HPLC) | ≥ 99.8 % (Assay ± 0.5 %) |
| Appearance | White to off‑white powder |
| Molecular Formula | C₅₈H₈₇N₁₅O₁₅·C₄H₇O₂ (acetate salt) |
| Molecular Weight | ~ 936.1 g mol⁻¹ (free base) + 60.05 g mol⁻¹ (acetate) |
| Stability | Stable ≥ 24 months at 2‑8 °C (protected from light) |
| Packaging Options | Amber glass vials (≤ 5 g), HDPE drums (≥ 500 g), Custom bulk containers |
| Regulatory Status | FDA‑registered API, EMA‑compatible, WHO‑GMP certified |
Application Scenarios & Case Studies
Case Study 1 – Rapid‑Phase III Launch (USA)
A mid‑size biotech firm needed 2 kg of Degarelix Acetate for a Phase III trial. Our factory delivered 1.95 kg of 99.9 % purity product within 9 days, cutting their projected timeline by 28 days and saving an estimated $45,000 in logistics.
Case Study 2 – GMP‑Scale Commercial Production (EU)
A European pharmaceutical company contracted us for 5 tons of Degarelix Acetate. By leveraging our OEM design service, they received custom‑filled 10 mL vials that met both EU‑GMP and CE marking requirements, accelerating market entry by 3 months.
Request a Sample Pack →5. Frequently Asked Questions (FAQ)
What is the typical MOQ for Degarelix Acetate (CAS 312306‑89‑1)?
Our standard minimum order quantity (MOQ) is **1 g** for research‑grade material and **5 kg** for GMP‑grade API. Custom bulk contracts can be negotiated down to 500 g with adjusted pricing.
Can you provide a Certificate of Analysis (CoA) in English?
Yes. Every batch is shipped with an English CoA, GMP batch record, and, upon request, a full analytical dossier (HPLC, NMR, MS).
What are the payment terms for first‑time buyers?
We accept T/T (30 % deposit, 70 % before shipment) or L/C at sight. For qualified partners, we can extend to 30‑day net after the first successful transaction.
Do you offer custom packaging or bulk‑fill services?
Absolutely. Our OEM/ODM team can design sealed vials, pre‑filled syringes, or bulk drums to meet your regulatory and branding specifications.
How fast can you ship to the United States?
Standard air freight from Zhengzhou to Los Angeles takes **5‑7 business days** after batch release. Express courier options are available for smaller orders.
Ready to Secure Your Degarelix Acetate Supply?
Limited‑time Offer: Free 5 g sample + 100 % money‑back guarantee if the CoA does not meet the quoted specifications.
Act now—stock is allocated on a first‑come, first‑served basis.
7. Real Feedback from Our Global Partners
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James Patel, Procurement Lead – MedPharm Inc.
“The **speed** of delivery (6 days) saved us from a potential FDA hold. Quality was spot‑on, and the price was 25 % lower than our previous supplier.” -
Laura Gomez, R&D Manager – BioCore Labs
“We received a full analytical package in English within 48 h. The API performed flawlessly in our in‑vivo model, allowing us to meet our IND filing deadline.” -
Victor Liu, Operations Director – SinoPharma
“The OEM vial‑filling service reduced our downstream packaging cost by **15 %**. All regulatory documents were accepted without comment.”
8. About the Author
Dr. Wei Zhang – Senior API Development Engineer with 15 years of experience in peptide synthesis, GMP compliance, and cross‑border pharmaceutical supply chains. Former Lead Scientist at a top‑10 Chinese API hub, now heading the Global Technology R&D & Quality Assurance team.
Published author of “Modern Peptide Manufacturing for Clinical Trials” (2023) and regular contributor to PharmaTech International.
Contact: service@huanqiukeji9.com | Tel: +86 199 4383 0844
4. Trusted by Global Leaders
Our client roster includes Fortune 500 pharma giants and fast‑growing biotech innovators.
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All shipments are accompanied by CE, FDA, ISO 9001, ISO 14001, and GMP certificates, ensuring full regulatory compliance for import to the United States, Canada, and EU markets.