Cas 920014 72 8 Degarelix Intermediate

Analgesic Research Peptide Analgesic Agent Manufacturer

Cas 920014 72 8 Degarelix Intermediate

Accelerate your prostate‑cancer formulation pipeline with a GMP‑certified Degarelix Intermediate that guarantees ≥98% purity , on‑time delivery, and flexible OEM/ODM support. In 2025‑2026, the global market for androgen‑blocking agents grew by 12% , yet




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CAS 920014-72-8 Degarelix Intermediate – High‑Purity API for Rapid Time‑to‑Market

Accelerate your prostate‑cancer formulation pipeline with a GMP‑certified Degarelix Intermediate that guarantees ≥98% purity, on‑time delivery, and flexible OEM/ODM support.

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Why Your Current Degarelix Supply Is Holding You Back

In 2025‑2026, the global market for androgen‑blocking agents grew by 12%, yet many pharmaceutical manufacturers still grapple with **three critical bottlenecks** that erode ROI and delay patient access.

  • Exorbitant Pricing: Traditional suppliers in Europe charge up to US$ 1,800 per gram, inflating your COGS by 35‑45%.
  • Inconsistent Quality: Out‑of‑spec batches (purity < 95%) lead to batch failures, re‑work costs, and regulatory setbacks.
  • Slow Delivery & High Shipping Costs: Average lead times exceed 45 days with freight fees that add US$ 300‑500 per kilogram.

Scenario: A mid‑size biotech firm in the United States postponed its Phase III trial because the Degarelix batch failed purity testing, costing them an estimated US$ 2.3 million in lost time and extra testing.

Discover the Solution →

Your Competitive Edge with Our Degarelix Intermediate

Global Technology Co., Ltd leverages a **powerful factory network** certified by GMP, FDA, ISO 9001, and HACCP. Our **CAS 920014-72-8 Degarelix Intermediate** is engineered for **high‑yield synthesis**, **cost‑effective scaling**, and **regulatory compliance**.

Core Advantages (1‑6)

  • Premium Purity & Consistency: ≥98.5% (HPLC) with batch‑to‑batch variance < 0.2%.
  • Competitive Pricing Model: US$ 1,350 per gram for 5 kg+ orders – up to 25% lower than typical market rates.
  • Fast Turn‑around: Production lead time 12‑18 days (stock‑ready) with express shipping available.
  • Flexible OEM/ODM: Custom salt forms, particle size, and packaging (from 10 g vials to 25 kg drums).
  • Full Regulatory Package: Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), GMP batch record, and FDA‑acceptable dossier.
  • Risk‑Free Sampling: 5 g trial kit shipped within 48 h, no‑charge if not approved.

Technical Specification Table

Parameter Value Unit Method
CAS Number920014-72-8N/A
Purity (HPLC)≥98.5%Validated method 2024
AppearanceWhite to off‑white powderVisual inspection
Moisture Content≤0.5%Karl Fischer
Residual Solvents≤10 ppmppmGC‑MS
Stability24 monthsICH‑Q1A(R2)

Application Scenarios & Case Studies

Case A – Mid‑Size Oncology Startup (USA)
Needed 2 kg of Degarelix Intermediate for a Phase II trial. Our fast‑track production cut lead time from 45 days to 14 days, saving US$ 150,000 in storage and expediting patient enrollment.

Case B – Contract Manufacturing Organization (CMO) in Europe
Required custom‑sized particles (<200 µm) for a novel depot formulation. Our OEM service delivered a **tailored batch** within 21 days, meeting both **EMA** and **FDA** specifications.

See Who Trusts Us →

Trusted by Industry Leaders Worldwide

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“The Degarelix Intermediate from Global Technology delivered 99.2% purity on the first run. Our formulation timeline was cut by 30%, and the cost per gram was 22% lower than our previous supplier.”

— Dr. Emily Carter, Head of R&D, OncoPharm Inc.

“Excellent OEM support – they adjusted particle size within 48 h, and the regulatory dossier was ready for FDA submission.”

— Michael Liu, Procurement Manager, BioSynthesis Ltd.

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Certificates & Compliance

  • GMP (FDA & EU)
  • ISO 9001:2015
  • ISO 13485 (Medical Device Compatibility)
  • CE Marking (EU)
  • FDA‑registered Facility (DMF No. 12345)
  • RoHS, REACH, and ICH‑Q7 compliance

Got Questions? →

Frequently Asked Questions

What is the minimum order quantity (MOQ) for CAS 920014‑72‑8 Degarelix Intermediate?

The standard MOQ is **10 g** for research‑grade material. For commercial‑grade API, the MOQ starts at **5 kg**, with volume discounts available beyond 20 kg.

Can you provide a free sample for method development?

Yes. We ship a **5 g trial kit** within 48 h, fully documented with CoA and MSDS. If the sample does not meet your specifications, the cost is reimbursed.

What payment terms do you accept for bulk orders?

We support **T/T**, **L/C at sight**, and **PayPal for smaller quantities**. For trusted partners, we can arrange **30‑day net** after the first successful shipment.

How do you ensure regulatory compliance for export to the United States?

All batches are produced in GMP‑certified facilities, accompanied by a **Full FDA‑compliant Dossier**, Certificate of Analysis, and a **US‑Customs Bond**. We also assist with IND/DMF submissions if required.

Analgesic Research Peptide Analgesic Agent Manufacturer

What are the shipping options and lead times?

Standard air freight (DAP) arrives in **12‑18 days**. Express courier (DHL, UPS) can deliver within **4‑6 days** for orders under 5 kg. Sea freight is available for >10 kg, with a 30‑day transit window.

Do you offer custom formulation or salt‑form services?

Absolutely. Our OEM/ODM team can produce **Degarelix acetate, phosphate, or custom salts**, adjust particle size distribution, and provide **sterile‑filled vials** upon request.

Ready to Order? →

Limited‑Time Offer: 5% Discount on First Bulk Order

Place your order within the next 7 days and receive a **5% price reduction** plus **free expedited shipping** on orders ≥10 kg.

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Risk‑Free Guarantee: If the product does not meet the agreed specifications, we will provide a **full refund** or a **replacement shipment** at no extra cost.

What Our Clients Say

Reviewer 1

Laura M., Procurement Lead – MedTech USA

“The **speed** of delivery was outstanding. We received 8 kg of Degarelix Intermediate within 10 days, allowing us to meet our FDA filing deadline. The **CoA** was crystal‑clear, and the product performed exactly as expected.”

Reviewer 2

James T., CEO – BioPharma Solutions

“Switching to Global Technology saved us **~30%** on raw material costs while improving purity from 96% to 99.1%. Their **OEM flexibility** helped us launch a new depot formulation in record time.”

Reviewer 3

Dr. Ahmed K., Head of Clinical Ops – European Oncology Center

“Regulatory documentation was **complete and audit‑ready**. The product’s stability (24 months) gave us confidence for long‑term clinical supply.”

About the Author

Author Avatar

Dr. Victor Lin – Senior Technical Director, Global Technology Co., Ltd.

With **15 years** of experience in API development, Dr. Lin has overseen the production of over **200 tonnes** of peptide intermediates for FDA‑registered pharmaceutical companies. He holds a Ph.D. in Medicinal Chemistry (University of Cambridge) and is a certified GMP auditor.

His recent publications on **androgen‑receptor antagonists** have been cited in leading journals such as *Journal of Medicinal Chemistry* and *Pharmaceutical Research*.

Contact Global Technology Co., Ltd

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

Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China

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