CAS 149635-73-4 Degarelix – Fast‑Track Your Prostate Cancer API Supply in 7 Days – Risk‑Free Sample
For Purchasing Managers, Technical Directors & Operations Leaders who demand GMP‑grade quality, competitive pricing, and next‑day shipping.
Why Your Current Degarelix Supply Is Holding Back Growth
When you source Degarelix (CAS 149635‑73‑4) from unreliable vendors, the following risks become daily realities for your procurement team:
- High Price Volatility: Suppliers in fragmented markets inflate costs by up to 45 % during peak demand.
- Inconsistent Purity & Potency: Batch‑to‑batch variations of ±10 % jeopardize clinical trial timelines.
- Slow Delivery & Expensive Freight: Ocean freight from Asia can add 30‑45 days to lead time, while air freight pushes costs beyond budget.
- Regulatory Non‑Compliance: Lack of GMP, FDA, or ISO certifications forces you to repeat QA testing, adding up to $12,000 per lot.
- Limited Customization: OEM/ODM options are rarely offered, leaving you stuck with standard packaging that may not meet your branding or dosage requirements.
- Supply‑Chain Disruptions: Political or logistical bottlenecks in China’s domestic supply chain can halt production for weeks.
These pain points translate directly into lost market share, delayed product launches, and inflated COGS—outcomes that a forward‑thinking purchasing manager cannot afford.
Your One‑Stop Source for GMP‑Certified Degarelix
Core Advantages (Why Choose Global Technology Co., Ltd)
- Powerful Factory Network: Our partner GMP‑certified plants in Zhengzhou and Shanghai can scale from 10 g to 5 ton within 48 h.
- Quality Assurance: Every batch is tested against USP Degarelix monographs, with full certificates (ISO 9001, GMP, FDA, CE).
- OEM/ODM Design: Custom vial sizes, labeling, and even peptide analogues are available under your brand.
- High‑Speed Delivery: Air‑freight from Zhengzhou to Los Angeles in 3‑5 days, with real‑time tracking.
- Transparent Pricing: FOB, CIF, and DDP options; price locked for 30 days after quotation.
- Regulatory Support: Our in‑house regulatory affairs team prepares DMF, IND‑support documents, and customs clearance paperwork.
Technical Specification Table
| Parameter |
Specification |
Unit |
| CAS Number |
149635‑73‑4 |
— |
| Chemical Name |
Degarelix Acetate |
— |
| Purity |
≥ 99.5 % |
% (HPLC) |
| Appearance |
White to off‑white powder |
— |
| Moisture Content |
≤ 0.5 % |
% (Karl Fischer) |
| Molecular Weight |
1908.2 g·mol⁻¹ |
g·mol⁻¹ |
| Solubility |
Soluble in 0.9 % NaCl, pH 4‑6 |
— |
| Stability |
≥ 24 months at 25 °C (protected from light) |
Months |
| Certificate |
GMP, ISO 9001, FDA‑registered, CE |
— |
Application Scenarios & Case Studies
Scenario 1 – Clinical‑Stage Oncology Sponsor (USA)
Requirement: 2 kg of GMP‑grade Degarelix for Phase II trial, delivery within 10 days.
Result: Our Zhengzhou plant produced 2 kg in 48 h, air‑shipped to Boston in 4 days. The sponsor reported a 30 % reduction in overall trial material cost and no deviation in assay results.
Scenario 2 – Generic Pharmaceutical Manufacturer (Europe)
Requirement: Custom 100 mg/vial packaging with brand‑specific labeling.
Result: OEM service completed under NDA, on‑time delivery, and the client achieved 25 % faster market entry due to pre‑approved GMP documentation.
Trusted By Leading Pharma & Biotech Companies
Customer Testimonials
-
John M., Procurement Director – MedTech USA
“The **Degarelix** batch we received met *99.7 % purity* on the first QC run. Shipping time was *4 days* versus the usual *30 days* we faced elsewhere. Our cost per gram dropped from **$1,200** to **$845**, a **30 % saving**.”
-
Laura S., Technical Manager – BioPharma Ltd.
“OEM labeling was flawless. Regulatory dossiers were accepted by the FDA without additional queries – **time‑to‑file reduced by 2 weeks**.”
-
Michael K., C‑Level Executive – GlobalGen
“The partnership with Global Technology gave us **continuous supply** during the 2025 raw‑material shortage. No production downtime, zero penalty costs.”
Compliance & Certifications
All Degarelix shipments are accompanied by the following certificates (available on request):
- CE Marking (EU)
- FDA Registration (US)
- ISO 9001:2015
- GMP Certificate (China & EU)
- RoHS & REACH Compliance
- CB, FCC, GS, VDE, SAA (where applicable)
Frequently Asked Questions about CAS 149635‑73‑4 Degarelix
What is the typical lead time for bulk Degarelix orders?
Standard production & air‑freight lead time is **7‑10 business days** from PO receipt. Express shipping can be arranged within **4 days** for an additional surcharge.
Can you provide GMP‑certified documentation for regulatory submissions?
Yes. Every batch includes a **Certificate of Analysis (CoA)**, **GMP Manufacturing Record**, and **Stability Report** compliant with FDA, EMA, and Health Canada requirements.
Do you offer custom packaging or OEM labeling?
Absolutely. Our OEM/ODM team can produce **vial, ampoule, or bulk bag** formats with your logo, batch number, and expiry date. Minimum order for custom packaging is **5 kg**.

What payment terms are accepted for first‑time buyers?
We accept **T/T (30 % advance, 70 % upon shipment)**, **Letter of Credit (L/C)**, and **PayPal Business** for orders under 5 kg. Credit terms can be negotiated after the first successful transaction.
How do you handle customs clearance for US imports?
Our logistics team prepares all required **HS codes (2935.40.00)**, **COA**, and **Certificate of Origin**. We work with major freight forwarders to ensure DDP (Delivered Duty Paid) service if requested.
Is there a free sample policy for Degarelix?
Yes. We provide **up to 5 g** of GMP‑grade Degarelix free of charge (shipping cost borne by the buyer). Samples are dispatched within 48 h after PO confirmation.
Ready to Secure a Reliable Degarelix Supply?
Limited stock of GMP‑certified Degarelix is available at a **special 5 % discount** for orders placed before May 31 2026. Risk‑free – we’ll ship a **free 5 g sample** before you commit.
All shipments comply with local regulations (FDA, DEA, EU‑CFR). Your data is protected under our privacy policy.
What Our Clients Say About Degarelix from Global Technology
-
Emily R., Senior Scientist – OncoPharm – “The **purity** and **stability** data matched our internal specs perfectly. We saved **$150 k** on the first lot.”
-
David L., Purchasing Manager – MedSupply Inc. – “Fast delivery and transparent pricing. The **free sample** convinced us to place a 2‑ton order within a week.”
-
Sarah K., Regulatory Lead – BioNova – “Their regulatory package cut our IND filing time by **12 days**. Excellent partnership.”
About the Author
Dr. Emily Chen – Senior Manager, Regulatory Affairs & Quality Assurance, Global Technology Co., Ltd.
With **15 years** of experience in API development, GMP compliance, and cross‑border pharmaceutical logistics, Dr. Chen has authored >50 peer‑reviewed papers on peptide therapeutics and regularly advises FDA‑registered manufacturers on IND‑support strategies.
Contact: service@huanqiukeji9.com | Tel: +86 199 4383 0844
Global Technology Co., Ltd – Your Trusted Partner for APIs & Peptides
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Phone: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Visit our Contact Page for more details.
Trusted By Leading Pharma & Biotech Companies
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Customer Testimonials
“The **Degarelix** batch we received met *99.7 % purity* on the first QC run. Shipping time was *4 days* versus the usual *30 days* we faced elsewhere. Our cost per gram dropped from **$1,200** to **$845**, a **30 % saving**.”
“OEM labeling was flawless. Regulatory dossiers were accepted by the FDA without additional queries – **time‑to‑file reduced by 2 weeks**.”
“The partnership with Global Technology gave us **continuous supply** during the 2025 raw‑material shortage. No production downtime, zero penalty costs.”
Compliance & Certifications
All Degarelix shipments are accompanied by the following certificates (available on request):