Targeted for: Corporate Purchasing Managers, Technical Directors, and Operations Managers who demand pharmaceutical‑grade Cetrorelix Acetate for fertility‑treatment pipelines, research‑grade studies, or OEM production.
1. Sky‑rocketing Prices – Global market surveys (2025) show average unit cost > $450 / g for non‑GMP sources, eroding R&D budgets.
2. Unreliable Purity Claims – Over 30 % of suppliers fail to provide certified > 98 % purity, leading to batch failures and regulatory setbacks.
3. Lengthy Lead Times – Traditional Asian factories quote 4‑6 weeks, jeopardizing time‑to‑market for new fertility drugs.
4. Hidden Shipping Costs – Freight from remote ports adds 15‑25 % to landed cost, especially for bulk (>10 kg) orders.
5. Compliance Uncertainty – Lack of GMP, DMF, or FDA certificates forces extra audits, consuming legal resources.
6. Limited Customization – Many vendors cannot adjust particle size, salt form, or provide bespoke packaging, forcing you to compromise on formulation stability.
Result: Delayed clinical trials, inflated budgets, and missed market windows. Take action now to eliminate these bottlenecks.
| Parameter | Value |
|---|---|
| CAS Number | 81840-57-5 |
| Chemical Name | Cetrorelix Acetate |
| Molecular Formula | C45H68N12O12 |
| Molecular Weight | 860.99 g/mol |
| Purity (HPLC) | ≥ 99.5 % (Single‑peak) |
| Appearance | White to off‑white crystalline powder |
| Solubility | Soluble in water (1 mg/mL) and 0.1 M HCl |
| Storage | -20 °C, protected from moisture |
| Package Options | 5 g, 25 g, 100 g, 1 kg, 10 kg (customizable) |
| Certificates | ISO 9001, GMP, FDA DMF, CE, RoHS |
Clinical Development – As a GnRH antagonist, Cetrorelix Acetate is essential for controlled ovarian hyperstimulation protocols, reducing premature luteinizing hormone surges.
API Manufacturing – Integrated into injectable formulations, the high‑purity salt ensures consistent dosing and longer shelf‑life.
Research & Discovery – Ideal for in‑vitro receptor‑binding assays, cell‑culture studies, and pharmacokinetic profiling.
Contract Manufacturing Organizations (CMOs) – Our OEM service lets CMOs blend Cetrorelix Acetate into multi‑peptide cocktails without cross‑contamination.
The MOQ is **5 g** for research‑grade samples. For bulk production, we accept **1 kg** increments, with discounts beginning at **10 kg**.
Yes. Every shipment includes a full CoA, GMP batch record, and, upon request, the FDA DMF dossier and ISO 9001 audit report.
Absolutely. Our R&D team can tailor salt form, particle size, or add protecting groups. Lead time for custom batches is **14‑21 days** after final specification approval.
We partner with DHL, FedEx, and UPS for **express air freight** (3‑7 days) and offer **sea‑freight consolidation** for orders ≥ 10 kg at a 12 % cost reduction. All shipments are temperature‑controlled and fully insured.
Our technical support team is available 24/7 via email, WhatsApp, or phone. We assist with formulation troubleshooting, stability studies, and regulatory filing guidance.
Limited‑time Offer: Place an order within the next 48 hours and receive **free 5 g sample** + **30 % off** the first bulk shipment. Stock is limited to **10 tons** per quarter.
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
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“Switching to Global Technology’s Cetrorelix Acetate cut our batch‑failure rate by **37 %** and saved **$120 k** in raw‑material costs per year. The 7‑day delivery window kept our Phase II trial on schedule.”
“The free 5 g sample matched the analytical certificate exactly. After verification we placed a 5 kg order and received it **3 days** ahead of the quoted ETA.”
“OEM customization (particle size 30 µm) was completed within 2 weeks, enabling us to launch a novel sub‑cutaneous formulation without additional engineering work.”
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