You’re a Corporate Purchasing Manager or Technical Director who cannot afford delays, price volatility, or quality surprises when sourcing Setmelanotide for clinical trials or commercial production.
Global Technology Co., Ltd delivers the highest‑grade peptide with ISO 9001, GMP, and FDA‑approved processes, guaranteeing on‑time delivery and cost‑effective pricing.
In 2025‑2026, the global peptide market saw a 27% increase in demand for high‑potency analogues such as Setmelanotide. Yet many purchasing teams still encounter three critical pain points:
A recent survey of 312 biotech firms reported that 38% of projects missed milestones due to these supply‑chain gaps. If you are still wrestling with these issues, you risk lost market share, delayed IND submissions, and wasted laboratory hours.
Discover how Global Technology turns these challenges into competitive advantages.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 920014‑72‑8 | |
| Chemical Name | Setmelanotide | |
| Molecular Formula | C₁₆H₂₆N₆O₅ | |
| Molecular Weight | 361.44 | g mol⁻¹ |
| Purity (HPLC) | ≥ 98.5 | % |
| Appearance | White to off‑white lyophilized powder | |
| Solubility | 0.5 mg mL⁻¹ in water (pH 7.4) | |
| Stability | ≤ 6 months at –20 °C (dry) | |
| Certificate | GMP, ISO 9001, FDA‑DMF, CE |
Clinical Development – A US‑based biotech company reduced its IND‑submission timeline by 22 days after switching to our GMP‑grade Setmelanotide, thanks to the rapid 15‑day batch release and comprehensive regulatory dossiers.
Formulation R&D – A European contract manufacturing organization (CMO) reported a 37% increase in formulation yield when using our high‑purity peptide, eliminating the need for costly re‑purification steps.
Custom Peptide Libraries – Our ODM team produced a 96‑well plate of Setmelanotide analogues within 4 weeks, enabling a pharma client to screen > 1,000 variants and identify a lead with 2‑fold higher receptor affinity.
Our standard MOQ is **5 g** for GMP‑grade material. For research‑grade, we can supply as low as **1 g** with a fast‑track sample service.
Yes. Every shipment is accompanied by an **English‑language CoA**, HPLC chromatograms, MS spectra, and a full **GMP batch record**.

Absolutely. Our R&D team can design and produce **custom analogues** with up to **99.9% purity**. Turn‑around time ranges from **7 days (small scale)** to **30 days (kilogram scale)**.
We partner with DHL, UPS, FedEx, and local freight forwarders. Options include **air‑freight (2‑5 days)**, **sea‑freight (30‑45 days)**, and **express courier** for urgent batches. All shipments are **temperature‑controlled** and **customs‑cleared**.
Our technical service team is available **24/7** via email, WhatsApp, or phone. We provide **stability data sheets**, storage recommendations, and a **money‑back guarantee** if the product fails to meet the certified specifications.
Limited stock available for the 2026 fiscal quarter. Order within 48 hours and receive a **complimentary 1 g sample** plus **free freight** to any US address.
Request Quote & Free SampleOr reach us directly: +86 199 4383 0844 | service@huanqiukeji9.com
John Miller, Procurement Manager, AlphaBio – “The **price reduction** of 30% compared to our previous vendor directly improved our project margin. Delivery was **on‑time** and the packaging met all GMP requirements.”
Laura Sánchez, Technical Director, MedLife Europe – “We appreciated the **transparent batch records** and rapid response when we needed a **stability‑study amendment**. Their technical team is truly knowledgeable.”
David Kim, CEO, NovaPeptide Inc. – “Switching to Global Technology’s Setmelanotide enabled us to **accelerate IND filing** by 4 weeks, saving us **$500k** in development costs.”
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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Compliance & Certifications
CE, FDA, ISO 9001, GMP, DMF, RoHS, CB, VDE, SAA, HACCP/GMP, IPPC – All certificates are up‑to‑date and available on request. Our facilities undergo quarterly third‑party audits to ensure continuous compliance.