Accelerate your reproductive‑health drug development with a GMP‑qualified Cetrorelix API that meets FDA, EMA, and ISO standards.
Get Free Quote in 24 h1. Sky‑rocketing Prices – Many distributors charge a 30‑45% premium for CAS 107390-08-9 Cetrorelix sourced from secondary markets. That extra cost erodes your R&D budget and reduces ROI.
2. Uncertain Purity & Batch‑to‑Batch Variability – Inconsistent HPLC profiles lead to failed stability studies, forcing costly repeat experiments.
3. Lengthy Lead Times – Typical delivery from overseas factories exceeds 45 days, delaying clinical‑trial milestones and jeopardizing regulatory timelines.
4. Hidden Shipping Expenses – Freight, customs clearance, and insurance often add 15‑25% to the quoted price, especially for small‑lot orders.
5. Regulatory Risks – Non‑GMP‑certified batches can trigger audit failures, product recalls, and damage to brand reputation.
Data Point: A 2025 survey of 120 US biotech firms showed that 68% postponed their IVF‑drug programs because of unreliable Cetrorelix supply.
| Parameter | Specification |
|---|---|
| CAS No. | 107390‑08‑9 |
| Molecular Formula | C₁₁₈H₁₈₅N₃₅O₂₁·4HCl |
| Molecular Weight | 1315.5 g mol⁻¹ (free base) |
| Purity (HPLC) | ≥ 99.5 % (≥ 2 ppm impurity limit) |
| Appearance | White to off‑white crystalline powder |
| Solubility | Soluble in water (0.5 % w/v) and 0.1 M HCl |
| Storage | Store at 2‑8 °C, protected from light and moisture |
| Certificates | ISO 9001, GMP, FDA‑registered, CE, RoHS |
1. IVF & Assisted Reproductive Technology (ART) – A US‑based fertility clinic integrated our Cetrorelix into its luteinizing hormone (LH) suppression protocol, cutting patient‑cycle cost by 22 % while maintaining > 95 % implantation success.
2. Pre‑clinical Oncology Models – A biotech startup used 250 g of our GMP‑grade Cetrorelix to evaluate GnRH‑receptor antagonism in mouse xenograft studies, achieving reproducible pharmacokinetic profiles across three independent labs.
3. Custom Peptide‑Drug Conjugates – Our ODM team synthesized a Cetrorelix‑linked ADC (antibody‑drug conjugate) for a Phase‑I trial, delivering the final API in 8 weeks versus the industry average of 16 weeks.
The MOQ is 100 g for standard packaging. For bulk projects, we can negotiate down to 20 g with a short‑lead‑time sample program.
Yes. Every batch is accompanied by a full CoA, DMF reference, and batch‑record package that meets FDA, EMA, and Health Canada requirements.
Our ODM team can synthesize Cetrorelix acetate, hydrochloride, or free base, and can also produce isotopically labeled versions for ADME studies.
We provide DHL Express (7‑10 days, $150‑$250 depending on weight) and UPS Air (5‑7 days, $200‑$300). Sea freight for > 5 kg is $0.85 /kg with a 15‑day transit.
Our technical service team offers 24/7 email support, a dedicated account manager, and free re‑analysis of any batch within 30 days of receipt.
Limited Stock Available – Order Today and Receive a Free 10 mg Sample + 30‑Day Money‑Back Guarantee.
Request a Quote & Sample NowOr contact us directly: Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Dr. Sarah Mitchell (Senior Scientist, ReproGen Labs) – "The purity level of Global Technology’s Cetrorelix allowed us to skip an extra purification step, saving 2 weeks of lab time and $18 k in reagents."
Michael Torres (Procurement Lead, BioPharm Solutions) – "Their price‑match guarantee is genuine. We reduced our Cetrorelix spend by 28 % without compromising quality."
Linda Zhao (Operations Manager, MedTech USA) – "Fast customs clearance and the detailed CoA made our FDA filing process seamless. Highly recommend their OEM service."
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Compliance & Certifications: CE, FDA, ISO 9001, GMP, RoHS, CB, GS.
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