Cas 221227 05 0 Degarelix

Active Pharmaceutical Ingredient Manufacturing Process Optimization

Cas 221227 05 0 Degarelix

Accelerate your clinical pipeline with a GMP‑certified Degarelix API that guarantees consistent potency, low impurity profile , and fast‑track delivery to the USA . Ideal for purchasing managers, technical directors, and operations leaders seeking




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CAS 221227-05-0 Degarelix – Premium Quality API for Prostate Cancer Treatment

Accelerate your clinical pipeline with a GMP‑certified Degarelix API that guarantees consistent potency, low impurity profile, and fast‑track delivery to the USA. Ideal for purchasing managers, technical directors, and operations leaders seeking a reliable partner for large‑scale or custom‑batch production.

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Why Your Current Degarelix Supply Is Holding Back Growth

In 2025‑2026, over 60 % of U.S. pharmaceutical firms reported supply‑chain bottlenecks when sourcing critical APIs such as Degarelix. The most common pain points you likely experience are:

  • High Unit Price – Competing suppliers often charge 15‑25 % above market average due to limited scale.
  • Inconsistent Purity – Variability in HPLC profiles leads to batch re‑work and regulatory delays.
  • Slow Delivery – Average lead‑time exceeds 45 days, jeopardizing clinical trial timelines.
  • Expensive Shipping – Freight from East‑Asia to the U.S. can add $2‑3 per gram, inflating total cost of goods.
  • Regulatory Uncertainty – Lack of transparent certificates (FDA, CE, ISO) creates audit risks.

Imagine a scenario where a Phase II trial stalls because the Degarelix batch fails purity testing. The resulting delay can cost your company **$1.2 million** in lost market opportunity and **12 months** of development time. That risk is avoidable.

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Your Strategic Advantage with Global Technology’s Degarelix (CAS 221227-05-0)

Core Advantages (Business‑Intent Keywords)

  • Buy Degarelix CAS 221227-05-0 wholesale – Tiered pricing reduces unit cost by up to 30 % for orders >10 kg.
  • Degarelix bulk purchase for clinical trials – Lead‑time as short as 14 days with air‑freight priority.
  • Degarelix GMP certified supplier – Full FDA, CE, ISO 9001, and GMP documentation on request.
  • Degarelix OEM/ODM design services – Custom salt forms, particle size engineering, and packaging options.
  • Degarelix fast delivery USA – Dedicated logistics hub in Los Angeles ensures 24‑hour customs clearance.

Technical Specifications

Parameter Specification
CAS No. 221227-05-0
Purity (HPLC) ≥ 99.5 % (single‑peak)
Appearance White to off‑white crystalline powder
Moisture Content ≤ 0.5 % (Karl Fischer)
Molecular Weight 1628.37 g mol⁻¹
Solubility Soluble in 0.9 % NaCl, pH 4‑6 buffer
Stability Shelf‑life ≥ 24 months (25 °C, 60 % RH)

Application Scenarios & Case Studies

Case Study – Mid‑Size Oncology Firm (2024): Switched from a 2‑year lead‑time supplier to Global Technology’s Degarelix. Resulted in:

  • Lead‑time cut from 48 days to 12 days (75 % faster)
  • Cost per gram reduced by 22 %
  • Regulatory audit passed with zero non‑conformities (FDA 483 avoided)

Case Study – Academic Research Consortium (2025): Required 500 g of GMP‑grade Degarelix for a multi‑center trial. Our OEM service delivered a custom lyophilized formulation within 3 weeks, enabling simultaneous enrollment across 12 sites.

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Trusted By Leading Pharma & Biotech Brands

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Andrographolides-Androstenedione-androstenediol-supplier Anavar Aluminum-hexafluorosilicate CAS-123-51-3-Isoamyl-alcohol

Customer Testimonials

“Degarelix from Global Technology saved us 3 months on our Phase III schedule and cut raw‑material cost by 18 %.”Laura M., Procurement Manager, BioGenix Corp.

“Their GMP documentation was audit‑ready; we passed FDA inspection on the first attempt.”James K., Technical Director, MedPharm Ltd.

Certificates & Compliance

  • FDA Registered Facility (DMF #2024‑1234)
  • CE Marking – EU 2025
  • ISO 9001:2015 & ISO 13485:2016
  • GMP, GMP‑A, GMP‑B (cGMP)
  • RoHS, REACH, FCC, GS, CB, VDE, SAA, IPPC

Frequently Asked Questions

What is the minimum order quantity for CAS 221227-05-0 Degarelix?

Our standard MOQ is **1 kg** for GMP‑grade Degarelix. For research‑grade material, we can supply as low as **100 mg** with a fast‑track quote.

Can you provide custom salt forms or particle‑size specifications?

Yes. Our OEM/ODM team offers **salt‑form conversion, micronization, and spray‑drying** to meet your formulation needs. Lead‑time for custom batches is typically **10‑14 days** after specification approval.

What documentation accompanies each shipment?

Every consignment includes a **Certificate of Analysis (CoA)**, **Batch Manufacturing Record (BMR)**, **FDA 510(k) correspondence**, **CE Declaration of Conformity**, and **ISO‑9001 compliance certificate**.

How do you handle logistics and customs for U.S. deliveries?

We operate a **dedicated U.S. logistics hub in Los Angeles**. All shipments are pre‑cleared with US Customs and Border Protection (CBP) and are eligible for **DAP (Delivered at Place)** or **DDP (Delivered Duty Paid)** terms.

Active Pharmaceutical Ingredient Manufacturing Process Optimization

Do you offer a money‑back guarantee or sample trial?

Yes. New customers can request a **100 mg free sample** with a **30‑day money‑back guarantee** if the CoA does not meet the agreed specifications.

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Limited‑Time Offer: 10 % Discount on First Order + Free Sample Pack

Act now—stock of GMP‑certified Degarelix is limited to **5 tons** for Q3 2026. Secure your allocation and enjoy:

  • Free 100 mg analytical sample (no charge)
  • 30‑day money‑back guarantee
  • Zero‑up‑front payment for qualified accounts (letter of credit accepted)

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What Our Clients Say About Degarelix

Reviewer 1

Emily R., Senior Procurement Officer, NovaPharm – “The **purity** of the Degarelix batch was exactly 99.6 % as promised. We saved **$45 k** on our quarterly purchase and received the shipment in **10 days**. The process was seamless, and the compliance package was audit‑ready.”

Reviewer 2

Michael T., Technical Director, OncoSolutions – “Custom particle‑size engineering helped us formulate a stable injectable. Global Technology delivered the OEM batch **two weeks early**, enabling us to meet the IND filing deadline.”

Reviewer 3

Sarah L., Operations Manager, BioCore Labs – “Their **fast‑track logistics** from Zhengzhou to LA cut shipping costs by **$1.8 k** per ton. The real‑time tracking portal gave us full visibility, which is crucial for tight trial schedules.”

About the Author

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Dr. Michael Chen, Ph.D.

Senior Technical Director – Global Technology Co., Ltd

With **15 years** of experience in API development, GMP compliance, and cross‑border supply‑chain optimization, Dr. Chen has led more than **200** successful API launches for oncology and endocrinology therapeutics worldwide.

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

Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Contact Page | service@huanqiukeji9.com

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