Accelerate your R&D pipeline and cut procurement costs with a high‑purity Leuprorelin that meets FDA, GMP, and ISO 9001 standards. Ideal for Purchasing Managers, Technical Directors, and Operations Leaders who demand reliable supply, on‑time delivery, and transparent pricing.
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1. Sky‑rocketing Prices – Most vendors charge a 20‑35 % premium for “high‑purity” Leuprorelin, eroding your project budgets.
2. Inconsistent Quality – Batch‑to‑batch variability (purity < 95 %) leads to failed assays and costly repeat experiments.
3. Slow Delivery – Average lead times exceed 45 days, delaying clinical‑trial milestones.
4. Hidden Shipping Costs – Expensive freight and customs clearance inflate total landed cost by up to 15 %.
5. Regulatory Uncertainty – Lack of full CE, FDA, and GMP documentation creates compliance risk for regulated markets.
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We combine a **powerful factory network**, **strict quality assurance**, and **high‑speed logistics** to give you a competitive edge:
| Parameter | Specification |
|---|---|
| CAS Number | 88866‑92‑6 |
| Purity (HPLC) | ≥ 98 % (≥ 99 % optional) |
| Molecular Weight | 1155.4 g·mol⁻¹ |
| Form | White to off‑white powder, lyophilized |
| Solubility | Soluble in water, DMSO, and acidic buffers |
| Stability | Stable 24 months at –20 °C (protected from light) |
| Packaging | Customizable 25 mg‑5 g vials, sealed HDPE or glass |
| Certificates | COA, FDA‑DMF, GMP, ISO 9001, CE |
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Ammonium-aluminum-sulfate-Ammonium-iron-III-citrate-supplier Alpha-MSH-inhibitor-peptide CAS-102961-52-4-Ipamorelin CAS-357952-09-1-Niraparib-Intermediate-1
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Compliance & Certifications – CE, FDA, GMP, ISO 9001, RoHS, CB, VDE, GS, SAA, HACCP/GMP, IPPC – all available on request.
The standard MOQ is **25 mg** for research‑grade material. For GMP‑grade bulk, we accept **500 mg**‑**5 kg** depending on packaging preferences.
Yes. Our OEM/ODM service includes **sequence modification, N‑terminal acetylation, C‑terminal amidation, and lyophilized bulk packaging**. Turn‑around time is typically **10‑15 days** after final design approval.

Each batch undergoes **dual‑HPLC, LC‑MS, and NMR** analysis. Results are documented in a **Certificate of Analysis (COA)** and a **Batch Release Report** that meets FDA and EMA requirements.
We offer **DDP (Delivered Duty Paid)**, **express air freight**, and **sea‑freight consolidation**. All shipments are temperature‑controlled (2‑8 °C) with real‑time tracking. Estimated delivery: **3‑7 days** for DDP air, **15‑20 days** for sea.
Yes. We supply **FDA‑DMF**, **GMP audit reports**, **Stability data**, and **ISO 9001 certificates** on request. Our regulatory team can also assist with **eCTD** preparation.
A dedicated account manager is assigned to each client. Support includes **technical troubleshooting, re‑analysis of any batch, and a 30‑day money‑back guarantee** if the product does not meet the COA specifications.
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Limited‑time Offer: First‑time customers receive **10 % off** the initial order and **free sample (25 mg)** shipped within 48 hours.
Risk‑Free Guarantee: If the batch purity falls below **98 %**, we’ll replace it at no extra cost or issue a full refund.
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Dr. Alan Cheng, Ph.D.
Senior Peptide Production Engineer with **15 years** experience at leading API manufacturers in Europe and Asia. Former Head of Quality Assurance at a GMP‑certified biotech firm, published author on peptide synthesis in *Journal of Pharmaceutical Sciences*.
Contact: service@huanqiukeji9.com | Tel: +86 199 4383 0844
Global Technology Co., Ltd – Your trusted partner for high‑purity APIs and custom peptide solutions.
📍 No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China