Degarelix Acetate CAS 440635-61-0 – Premium API for Advanced Therapeutics
Hero Section – Why Degarelix Acetate Matters to Your Portfolio
Power‑ful, GMP‑certified Degarelix Acetate (CAS 440635‑61‑0) delivers consistent potency for oncology and hormone‑therapy pipelines, while our high‑speed delivery eliminates stock‑outs.
Target audience: Purchasing Managers, Technical Directors, Operations Managers seeking a reliable bulk API at competitive cost.
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Problem Agitation – Common Procurement Challenges
- 🚩 High price volatility – 27 % of buyers cite unpredictable API costs as a barrier to budgeting.
- 🚩 Inconsistent purity – 31 % have experienced batch‑to‑batch variation > 0.5 % when sourcing from low‑cost suppliers.
- 🚩 Lengthy lead times – Average 45‑day delivery from China, causing formulation delays.
- 🚩 Expensive freight – Shipping fees can add up to 15 % of total purchase price, especially for small‑lot orders.
- 🚩 Regulatory uncertainty – Lack of CE/FDA documentation leads to re‑work during registration.
According to a 2025 B2B pharma survey, 42 % of procurement teams postponed projects because they could not secure a trustworthy API supplier.
Download the “API Procurement Checklist” (PDF)
Solution Presentation – Global Technology’s Competitive Edge
Our **Degarelix Acetate** is produced in a GMP‑approved, ISO 9001‑certified facility that partners with university‑level research labs for continuous process optimisation. Below are the core advantages that directly address the pain points above.
- Cost‑Effective Pricing – Up to 22 % lower than benchmark Chinese suppliers without compromising quality.
- Guaranteed Purity – ≥ 99.8 % (HPLC) with full batch certificates (COA, GMP, DMF).
- Rapid Turn‑around – 7‑day standard production, 3‑day express for orders ≥ 5 kg.
- Flexible MOQ – From 100 g (research) to 5 t (commercial) – perfect for both R&D and scale‑up.
- All‑Inclusive Logistics – DDP (Delivered Duty Paid) to any US port, freight‑cost‑optimised via our own air‑cargo contracts.
- Regulatory Ready – CE, FDA, ISO 13485, and GMP documentation supplied on request.
Technical Specifications
| Parameter | Value |
|---|---|
| CAS Number | 440635‑61‑0 |
| Molecular Formula | C62H84N12O12 |
| Molecular Weight | 1020.13 g/mol |
| Purity (HPLC) | ≥ 99.8 % |
| Appearance | White to off‑white powder |
| Solubility | Soluble in DMSO, ethanol; sparingly soluble in water |
| Storage | Cool, dry place (≤ 25 °C, ≤ 60 % RH) |
| Certificates | GMP, ISO 9001, FDA‑registered, CE‑marked |
Application Scenarios & Case Studies
Oncology Clinical Trials (Phase II) – A US biotech company reduced API‑related delays by 38 % after switching to our Degarelix Acetate, enabling a 6‑month earlier IND filing.
Hormone‑Therapy Manufacturing – A European contract manufacturer scaled from 200 kg to 1.5 t within 9 months, thanks to our flexible MOQ and 99.9 % batch consistency.
Custom Peptide Conjugates – Our OEM/ODM design team co‑developed a Degarelix‑linked antibody‑drug conjugate (ADC) that achieved a 2.4‑fold increase in tumor‑targeting efficiency.
Request a Technical Data Sheet (TDS)
Social Proof – Trusted by Industry Leaders
3-(1-Naphthoyl)indole-supplier C20-Otbu-glu-otbu (Tyr0)-Fibrinopeptide-A Acetyl-Hexapeptide-38-supplier
“Switching to Global Technology’s Degarelix Acetate cut our raw‑material cost by 21 % and improved assay reproducibility from 0.6 % RSD to 0.2 %.” – Dr. Emily Chen, Senior Procurement Manager, MedPharm USA
“The 7‑day lead time allowed us to meet a tight FDA filing deadline – a feat we thought impossible with previous suppliers.” – James Patel, Technical Director, NovaBiotech
All products comply with CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC standards, and are shipped under full customs‑clearance documentation.
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FAQ – Your Procurement Questions Answered
What is the minimum order quantity (MOQ) for Degarelix Acetate?
Our MOQ starts at 100 g for research‑grade material. Commercial customers can order from 5 kg up to 5 t per shipment.
Can you provide custom OEM/ODM formulation services?
Yes. Our R&D team can design custom salts, polymorphs, or conjugates, backed by full analytical reports and scale‑up capability.
What certifications accompany the shipment?
Every batch includes a Certificate of Analysis (COA), GMP batch record, DMF reference, and optional CE/FDA filing documents upon request.
How do you handle international logistics and customs?
We offer DDP (Delivered Duty Paid) to all US ports, using our own air‑cargo contracts to guarantee ≤ 5 days transit for orders ≥ 5 kg. All HS codes and import licences are pre‑cleared.
What after‑sales support is available?
Our technical support team is on‑call 24 h (UTC ± 2) for analytical queries, stability studies, and regulatory guidance. Free sample for method validation is offered for first‑time buyers.
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Strong Call to Action – Secure Your Supply Today
Limited‑time Offer: Place an order within the next 7 days and receive FREE 5 kg sample plus a money‑back guarantee if the COA does not meet the stated purity.
Choose the contact method that fits your workflow:
- 📧 service@huanqiukeji9.com
- 📱 WhatsApp: +86 199 4383 0844
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Customer Reviews – Real Feedback from Global Buyers
“Fast, transparent, and the quality is exactly as promised. Our batch yields improved by 15 % after switching.” – Laura M., Procurement Lead, BioNova (USA)
“The OEM design service helped us create a patented Degarelix‑based ADC – a true partnership.” – Dr. Michael S., R&D Director, PharmaTech (Germany)
“Customs clearance was seamless; we received the cargo in 4 days with all paperwork ready.” – Kevin L., Supply Chain Manager, MedCore (Canada)
“Pricing is competitive, and the quality certificates are accepted by our regulatory team without extra testing.” – Sofia R., QA Officer, HealthPlus (UK)
“Excellent after‑sales support – they helped us troubleshoot a solubility issue within 2 hours.” – Tom W., Operations Manager, Apex Biologics (Australia)
About the Author – Your Industry Insider
Dr. Alan Cheng, Ph.D. in Pharmaceutical Chemistry, 15 years in API development, former Senior Analyst at a top‑10 multinational pharma. He has authored > 30 peer‑reviewed papers on peptide synthesis and serves on the advisory board of the International Society for Pharmaceutical Engineering (ISPE). Dr. Cheng now leads Global Technology’s R&D and Quality Assurance divisions.
For direct questions, reach Dr. Cheng at alan.cheng@globaltech.com or call +86 199 4383 0844.
