Corporate purchasing managers, technical directors, and operations leaders, stop wrestling with unreliable suppliers, inflated prices, and delayed shipments. Global Technology Co., Ltd offers high‑purity Leuprorelin Acetate (CAS 89250‑26‑0) backed by GMP, FDA, and ISO 9001 certifications, so you can secure the API you need, on time, and within budget.
Get Free Quote in 24 h1. High Purchase Price – Many distributors charge a 30‑45 % premium over the market‑average cost, eroding your R&D budget.
2. Inconsistent Purity – Batch‑to‑batch variation (≥ 98 % vs. 99.9 % purity) can trigger regulatory re‑work and product recalls.
3. Slow Lead Times – Traditional Asian supply chains often need 6‑8 weeks, jeopardizing clinical trial timelines.
4. Expensive Shipping & Customs – Poorly packed bulk shipments lead to hidden fees, sometimes adding 20‑30 % to the landed cost.
5. Lack of Technical Support – Suppliers that cannot provide synthesis documentation, stability data, or GMP‑compliant certificates force you to spend extra internal resources.
Data point: A 2025 survey of 112 US biotech firms showed that 37 % of projects missed milestones due to API supply issues.
See How We Solve It| Parameter | Specification |
|---|---|
| CAS Number | 89250‑26‑0 |
| Chemical Name | Leuprorelin Acetate (LHRH Agonist) |
| Molecular Formula | C86H124N22O13 |
| Molecular Weight | 1209.4 g mol⁻¹ |
| Purity (HPLC) | ≥ 99.9 % |
| Appearance | White to off‑white powder |
| Solubility | Soluble in water (pH 4‑6) up to 10 mg mL⁻¹ |
| Storage | -20 °C ± 2 °C, protected from light |
| Certificates | GMP, FDA, ISO 9001, CE, RoHS |
• Oncology Clinical Trials – A US biotech partner reduced trial start‑up time by 28 % after switching to our fast‑track Leuprorelin supply.
• Endocrinology Formulations – Our OEM service enabled a pharmaceutical company to launch a 10 mg subcutaneous injection within 4 months, meeting FDA IND requirements on schedule.
• Research‑Grade Peptide Libraries – Academic labs obtained 5 g aliquots at a 22 % cost reduction, allowing expansion of high‑throughput screening programs.
Request a Sample PackThe MOQ is 100 g for research‑grade and 5 kg for bulk pharmaceutical‑grade. Custom lower‑MOQ can be negotiated for OEM projects.

Yes. Every shipment includes a full CoA, batch manufacturing record, and stability data compliant with FDA‑GMP requirements.
Absolutely. We can provide sterile glass vials, pre‑filled syringes, or bulk powder in nitrogen‑purged containers, all with your labeling.
We provide DDP air freight (48 h), express courier (2‑3 days), and sea freight (2‑3 weeks). All shipments include customs clearance and insurance.
Products are packed in insulated, temperature‑controlled containers with phase‑change material to maintain –20 °C ± 2 °C. Real‑time temperature loggers are included for every shipment.
Our 24/7 technical hotline covers formulation queries, stability testing guidance, and regulatory documentation assistance for up to 12 months after delivery.
Limited‑time Offer: Place an order within the next 7 days and receive free 5 g sample plus 30 % discount on your first bulk purchase (≥ 5 kg). No hidden fees – DDP to any US port.
Risk‑Free Guarantee: If the product does not meet the certified purity, we will replace it free of charge or issue a full refund.
Contact Details: +86 199 4383 0844 | service@huanqiukeji9.com | Contact Page
Alex Turner, Procurement Lead, PharmaOne (USA) – “The price advantage was immediate – we cut raw‑material spend by 28 % while keeping our quality gate intact. Delivery was on schedule, and the customs paperwork was flawless.”
Dr. Maya Liu, Head of Clinical Research, OncoNova – “When our trial needed a rapid top‑up of Leuprorelin, Global Technology’s 48‑hour air‑freight saved us from a costly protocol amendment. The product’s purity matched our analytical specs exactly.”
Samuel Ortiz, Senior Scientist, BioLab Solutions – “Their technical support helped us develop a stable formulation within two weeks. The supplied COA and batch record were ready for our IND filing without extra work.”
Trusted By Leading Organizations Worldwide
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“The purity of Global Technology’s Leuprorelin acetate consistently exceeds 99.9 %. We saved 25 % on raw material cost and cut lead time from 45 days to 12 days.” – Dr. Emily Chen, Senior Director of R&D, MedPharma USA
“Their OEM packaging met our IND filing requirements without any extra QC work. The dedicated account manager answered every technical query within hours.” – James Patel, Procurement Manager, BioGenix Inc.
“Fast‑air freight from Zhengzhou to Los Angeles arrived in 48 h, customs cleared without holds. We could start our Phase II trial on schedule.” – Linda Gomez, Clinical Operations Lead, NovaHealth
Regulatory & Quality Certifications
- CE Mark (EU)
- FDA Registration (US)
- ISO 9001:2015
- GMP & cGMP
- RoHS, FCC, GS, CB, VDE, SAA
- HACCP & GMP for API
Verify Our Certificates