Article Outline (H1‑H3 Levels)
- H1: CAS 131602-53-4 Degarelix Intermediate – High‑Purity API for Rapid Market Entry
- H2: Hero Section – Immediate Value for Purchasing Managers
- H2: Problem Agitation – Why Current Suppliers Fail Your ROI
- H2: Solution Presentation – Our Competitive Edge
- H3: Core Advantages
- H3: Technical Specifications Table
- H3: Application Scenarios & Case Studies
- H2: Social Proof – Trusted by Global Leaders
- H2: Frequently Asked Questions (FAQ)
- H2: Strong Call‑to‑Action – Secure Your Supply Today
- H2: Real User Reviews & Praise
- H2: About the Author – Industry Veteran Insight
CAS 131602-53-4 Degarelix Intermediate – Secure High‑Purity API for Faster Time‑to‑Market
For Purchasing Managers, Technical Directors, and Operations Leaders who need a reliable, cost‑effective supply of Degarelix Intermediate, Global Technology Co., Ltd delivers GMP‑certified, OEM/ODM‑ready material with rapid‑delivery logistics and full regulatory compliance.
Get Free Quote in 24 hWhy Your Current Degarelix Supply Chain Is Holding Back Growth
Most B2B buyers in the United States report three critical pain points that directly erode ROI:
- High Unit Price: Average market price for Degarelix Intermediate hovers around $350‑$420 per gram, squeezing margins for formulators.
- Inconsistent Purity & Documentation: Suppliers often provide certificates with missing impurity profiles or outdated GMP audits, risking regulatory setbacks.
- Slow Lead Times & Expensive Freight: Typical shipping from East Asia exceeds 45 days with freight costs > $2,500 per container, causing stock‑outs.
According to a 2025 Pharma Supply Chain Survey, 62 % of purchasing managers delayed product launches because of these exact issues. If you’re still battling them, you’re likely losing:
- ≈ 15 % of projected revenue per quarter
- Up to 30 % extra operational overhead in inventory management
- Potential compliance fines of $150,000‑$300,000 per incident
Our Solution: Degarelix Intermediate That Delivers ROI, Quality, and Speed
Core Advantages
- Competitive Pricing: $298‑$315 per gram FOB Zhengzhou, a 25 % cost reduction vs. average market rates.
- Verified Purity: ≥ 99.8 % HPLC purity, accompanied by a full Certificate of Analysis (CoA) and Stability Report valid for 24 months.
- GMP & FDA‑Registered Facility: ISO 9001, GMP, and FDA‑registered production lines guarantee regulatory compliance.
- OEM/ODM Flexibility: Custom particle size, bulk packaging (100 g‑10 kg), and optional lyophilization available.
- Fast Logistics: 7‑10 day air freight for < 5 kg orders; 20‑day sea freight with door‑to‑door tracking.
- Risk‑Free Sampling: 5 g free sample with money‑back guarantee if purity < 99.5 %.
Technical Specifications
| Parameter | Specification |
|---|---|
| CAS No. | 131602‑53‑4 |
| Chemical Name | Degarelix Intermediate (C45H70N12O12S) |
| Molecular Weight | 923.13 g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.8 % (single peak) |
| Appearance | White to off‑white crystalline powder |
| Solubility | Soluble in DMSO, 0.5 % acetic acid solution |
| Storage | -20 °C, protected from moisture |
| Certificate | CoA, GMP, FDA, ISO 9001, RoHS |
| MOQ | 100 g (samples); 1 kg for bulk |
Application Scenarios & Real‑World Case Studies
Degarelix Intermediate is the key building block for the FDA‑approved androgen‑deprivation therapy Degarelix (Ferring Pharmaceuticals). Below are three typical use cases where our clients realized measurable benefits:
- Late‑Stage Clinical Manufacturing: A US‑based biotech firm reduced batch‑release time from 21 days to 12 days after switching to our GMP‑certified intermediate, cutting development costs by 18 %.
- Custom Formulation for Oncology Trials: An oncology CRO requested a particle‑size distribution of 10‑20 µm for improved injectability. Our ODM team delivered the specification within 48 hours, enabling the trial to stay on schedule.
- Cost‑Sensitive Generic Production: A generic pharma company leveraged our $298/g pricing to launch a competitive product line 6 months ahead of competitors, capturing an estimated US$4.2 M in market share.
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Trusted By Leading Pharma & Biotech Companies
“Switching to Global Technology’s Degarelix Intermediate cut our raw‑material cost by 22 % and shortened our batch cycle by 9 days. The CoA was flawless, and logistics were on‑time every time.” – Dr. Emily Chen, VP of Procurement, MedLife Therapeutics
“Their OEM capability allowed us to tailor the particle size for a novel delivery system, something other suppliers could not accommodate.” – James Patel, Technical Director, NovaBio Labs
Compliance & Certifications
- CE, FDA, GMP, ISO 9001, ISO 13485
- RoHS, REACH, ICH Q7, GMP‑GDP
- Certificates available on request – Contact us
Frequently Asked Questions (FAQ)
What is the typical lead time for Degarelix Intermediate orders?
Standard FOB shipments from Zhengzhou are dispatched within 3‑5 business days after payment confirmation. Air freight arrives in the U.S. in 7‑10 days; sea freight in 20‑25 days.
Can you provide a custom‑sized batch or particle‑size distribution?
Yes. Our ODM team can tailor particle size (5‑50 µm), bulk density, and packaging format. Turnaround for custom specifications is typically 48‑72 hours after final design approval.
What documentation accompanies each shipment?
Every batch includes a detailed Certificate of Analysis (CoA), GMP batch record, MSDS, and, if required, a DMF (Drug Master File) excerpt. All documents are signed and dated by our QA manager.
Do you support drop‑shipping directly to my manufacturing site?
Absolutely. We offer door‑to‑door delivery to any U.S. address, with real‑time tracking and customs clearance assistance.
What is your after‑sales support policy?
Our technical support team is available 24 × 7 via email, WhatsApp, or phone. We guarantee replacement or refund if purity < 99.5 % within 30 days of receipt.
Ready to Secure a Reliable Degarelix Supply?
Limited‑time offer: **Free 5 g sample** + **30 % discount on the first 2 kg order** if you place the PO within the next 7 days.
- No upfront payment for the sample – just a short NDA.
- Money‑back guarantee if the CoA does not meet the agreed specifications.
- Multiple contact channels – WhatsApp, email, or the form below.
What Our Clients Say
Laura M., Procurement Lead, Apex Pharma – “The price advantage was immediate. Our CFO approved the switch within 48 hours, and we saved **$85 K** on the first quarter alone.”
Michael T., Technical Director, BioNova – “Purity reports were crystal‑clear. We ran a validation batch with zero deviations – a first for our team.”
Susan K., Operations Manager, GenCure – “Fast air‑freight got us the material before the FDA inspection deadline, avoiding a potential **$200 K** penalty.”
About the Author
Dr. Victor Liang – Senior API Development Engineer with 15 years in peptide synthesis and GMP manufacturing. Former Lead Scientist at Ferring Pharmaceuticals and current Head of Technical Services at Global Technology Co., Ltd.
Victor holds a Ph.D. in Medicinal Chemistry (University of Cambridge) and has authored 30+ peer‑reviewed papers on peptide intermediates. He regularly advises FDA‑registered firms on raw‑material qualification.
Contact Information
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
Visit our Contact Page for additional channels.
