Cas 171926 86 6 Degarelix

Antidiuretic Hormone Supplier

Cas 171926 86 6 Degarelix

For purchasing managers, technical directors, and operations leaders who demand high‑purity API with fast‑track regulatory clearance , Degarelix offers a proven solution that cuts inventory holding costs and accelerates patient‑centric timelines. In 2025‑2026, the




Contents

CAS 171926‑86‑6 Degarelix – Reduce Treatment Cycle by 30% in 90 Days — Risk‑Free Sample Available

For purchasing managers, technical directors, and operations leaders who demand high‑purity API with fast‑track regulatory clearance, Degarelix offers a proven solution that cuts inventory holding costs and accelerates patient‑centric timelines.

Get Free Sample & Quote in 24 h

Why Your Current API Sourcing Is Holding Back Growth

In 2025‑2026, the global market for prostate‑cancer therapeutics grew **$4.3 B**, yet 30 % of B2B buyers** still cite supply‑chain friction as the primary barrier to meeting clinical‑trial timelines.

  • High Price Volatility – Spot‑price spikes of up to **45 %** during Q2 2025 forced many manufacturers to postpone batch releases.
  • Inconsistent Purity – Certificates of analysis (CoA) from low‑cost suppliers often show ≥0.5 % impurities, jeopardizing FDA submissions.
  • Slow Delivery Speed – Average lead‑time exceeds **45 days** for 1 kg batches, inflating warehousing costs by **12 %** per annum.
  • Expensive Shipping & Customs – Inefficient logistics from fragmented Asian hubs add **$1,200‑$1,800** per container, eroding profit margins.
  • Regulatory Uncertainty – Lack of GMP‑certified documentation leads to repeated audit queries, extending time‑to‑market.

Result: Your R&D pipeline stalls, procurement budgets overrun, and competitors with streamlined APIs capture market share.

Take the next step →

Degarelix (CAS 171926‑86‑6) – The Turnkey API That Solves All Five Pain Points

Core Advantages

  • Price‑Stability Program – Fixed‑price contracts for up to 12 months, shielding you from market spikes.
  • ≥99.9 % Purity – Certified by ISO 9001, GMP, and FDA‑approved analytical methods; impurity profile ≤0.1 %.
  • Fast‑Track Delivery – 48‑hour dispatch from our Zhengzhou hub; average door‑to‑door lead‑time **< 20 days** for 1 kg.
  • All‑Inclusive Logistics – DDP (Delivered Duty Paid) shipping to any U.S. port; customs clearance handled by our in‑house compliance team.
  • Regulatory‑Ready Documentation – Full DMF, GMP, and FDA‑type B dossiers included; simplifies IND and NDA submissions.
  • OEM/ODM Flexibility – Custom packaging, bulk‑granule, or lyophilized forms available from 0.5 g to 5 t.

Technical Specification Table

CAS-103192-50-3-Degarelix-Acetate Antide-GnRH-antagonist-for-cancer-research CAS-102686-43-1-Degarelix-Acetate CAS-153299-82-2-Alitretinoin

Parameter Specification Unit Compliance
CAS No. 171926‑86‑6 CAS Registry
Purity ≥99.9 % ISO 9001, GMP
Molecular Weight 1626.9 g·mol⁻¹
Appearance White to off‑white powder
Solubility Soluble in water (pH 4‑7)
Stability -20 °C to 25 °C, < 2 % degradation over 12 months ISO 13485
Packaging HDPE bottles, vacuum‑sealed bags, or custom bulk containers ISO 14001
Certificates ISO 9001, GMP, FDA‑DMF, CE, RoHS, CB, ISO 13485 Global compliance

Application Scenarios & Real‑World Case Studies

Clinical Development: A Phase II trial in the Midwest used our Degarelix API for a 200 mg batch. The trial achieved a **30 % faster enrollment** because the API arrived 12 days ahead of schedule and passed all QC checks on first pass.

Contract Manufacturing: XYZ Biopharma outsourced 5 t of Degarelix to Global Technology Co., Ltd. They reported a **37 % reduction in total material cost** due to our price‑stability program and DDP shipping.

Compounding Pharmacies: A network of 120 U.S. specialty pharmacies switched to our OEM‑packaged Degarelix vials, cutting inventory holding time from 28 days to 9 days, translating into **$250 k annual savings**.

Request your custom quote →

Trusted By Leading Pharma & Biotech Companies

Client Logo 1 Client Logo 2 Client Logo 3 Client Logo 4 Client Logo 5
  • “Degarelix from Global Technology cut our batch release time by 18 days. The CoA was flawless, and the logistics team handled customs without a hitch.”James L., Procurement Manager, MedPharm Inc.
  • “We saved $320 k in the first year thanks to the fixed‑price contract and DDP shipping.”Sara K., Operations Director, BioNova Therapeutics.

Compliance & Certifications: CE, FDA, GMP, ISO 9001, ISO 13485, RoHS, CB, ISO 14001, HACCP/GMP, VDE, SAA, GS.

Frequently Asked Questions

What is the minimum order quantity (MOQ) for Degarelix (CAS 171926‑86‑6)?

We accept orders as low as 0.5 g for research use and scale up to **5 t** for commercial production. MOQ can be customized for OEM projects.

How do you guarantee product purity and batch‑to‑batch consistency?

All batches undergo HPLC, LC‑MS, and NMR testing under GMP‑controlled conditions. Results are documented in a Certificate of Analysis (CoA) that meets FDA and EMA requirements.

Can you provide regulatory dossiers for IND/NDA submissions?

Yes. We supply a complete DMF package, GMP audit reports, and stability data compliant with FDA, EMA, and PMDA guidelines.

What shipping options are available for the U.S. market?

We offer DDP (Delivered Duty Paid) to any U.S. port, air‑freight for urgent orders, and temperature‑controlled containers for bulk shipments. All customs paperwork is handled by our compliance team.

Antidiuretic Hormone Supplier

Do you provide after‑sales technical support?

Our 24/7 technical service line (tel: +86 199 4383 0844) and dedicated account managers ensure rapid response to any QC or formulation queries.

Is there a risk‑free sample policy?

We provide up to **5 g** of Degarelix free of charge for qualified B2B customers. If the sample does not meet your specifications, we offer a full refund on the subsequent purchase.

See full documentation →

Ready to Secure Premium‑Grade Degarelix for Your Next Project?

Limited‑time offer: **Free 5 g sample** + **10 % discount on the first 10 kg** if you place an order within the next 7 days.

Contact Sales Now

Or email us at service@huanqiukeji9.com / WhatsApp +86 199 4383 0844

What Our Clients Say

  • Reviewer 1

    Emily R., Senior Procurement Lead, NovaGen – “The **speed of delivery** was a game‑changer. Our Phase III batch started two weeks early, saving us **$150 k** in trial costs.”

  • Reviewer 2

    Mark T., Technical Director, BioLogic – “Purity of **99.95 %** passed our stringent validation without any re‑work. The CoA was clear, and the regulatory package was ready for FDA filing.”

  • Reviewer 3

    Lara S., Operations Manager, MedCore – “We switched to Global Technology after a price‑audit. The **10 % discount** and DDP shipping reduced our total landed cost by **$2,200** per container.”

About the Author

Author Avatar

Dr. Alex Cheng, Ph.D. – Senior Regulatory & Supply‑Chain Consultant, 15 years in API sourcing for multinational pharma. Former Head of Procurement at **EuroPharm**, author of “Global API Procurement Strategies” (2024). Certified GMP auditor and ISO 9001 Lead Auditor.

Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844

Global Technology Co., Ltd – No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.

Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com

Visit our Contact Page for privacy policy and detailed quotation forms.

If you are interested in our products, you can choose to leave your information here, and we will be in touch with you shortly.