Accelerate your research and product development with globally‑certified Neurotensin peptide series, engineered for consistency, scalability, and regulatory compliance. Ideal for pharmaceutical R&D, biotech startups, and CROs in the USA and other English‑speaking markets.
Get Free Quote in 24 hIn 2025, 37 % of biotech firms reported project delays due to unreliable peptide supplies. If you’re a purchasing manager or technical director, you probably recognise at least one of the following challenges:
These obstacles translate directly into up to 25 % higher operational costs and delayed market entry. You need a partner that eliminates the guesswork.
See How We Solve It →Global Technology Co., Ltd leverages a state‑of‑the‑art manufacturing hub in Zhengzhou, China, backed by GMP, ISO 9001, and FDA‑registered facilities. Our peptide line offers:
| Parameter | Neurotensin 1‑11 | Neurotensin 1‑8 | Neurotensin 8‑13 | Neurotensin 9‑13 |
|---|---|---|---|---|
| Sequence (AA) | pELYENKPRRPY | pELYENKP | PRRPY | RPY |
| Molecular Weight (Da) | 1384.8 | 1061.5 | 699.8 | 447.6 |
| Purity (HPLC) | ≥98 % | ≥98 % | ≥98 % | ≥98 % |
| Form | Lyophilized powder / 10 mg‑ml solution | Lyophilized powder | Lyophilized powder | Lyophilized powder |
| Storage | -20 °C, desiccated | -20 °C, desiccated | -20 °C, desiccated | -20 °C, desiccated |
Case Study – Academic Lab (USA): A neuroscience department needed 500 mg of Neurotensin 1‑11 for a high‑throughput receptor binding assay. Our 7‑day delivery reduced their lead time by 45 % compared with their previous supplier, and the batch’s 99.2 % purity eliminated the need for a repeat assay, saving an estimated $12,800 in reagents.
Case Study – CRO (Canada): Requested a custom‑blended Neurotensin 1‑8/8‑13 mixture (1:1) for a GLP toxicology study. We delivered a GMP‑certified bulk within 10 days, providing full batch records and stability data, enabling the client to meet FDA IND filing deadlines.
Request a Sample →The standard MOQ is 10 mg for research‑grade powder. For bulk GMP orders, we accept 100 g increments, and custom volumes can be negotiated.
Yes. Every batch ships with a detailed CoA, including HPLC chromatograms, mass‑spectrometry data, and impurity profiling, all signed by our GMP‑qualified QA team.
Absolutely. Our OEM/ODM service covers N‑terminal acetylation, C‑terminal amidation, cyclization, and isotopic labeling. Turn‑around is typically 14‑21 days depending on complexity.
Standard air freight is 3‑5 business days after production. For express orders (≥10 g), we can dispatch within 48 hours, with DHL tracking and customs clearance assistance.
Our technical support team is available 24 h/7 d via email, WhatsApp, and phone. We offer assay troubleshooting, stability guidance, and free re‑analysis if purity falls outside the guaranteed range.

Limited‑time Offer: Order before June 30 2026 and receive a free 100 mg sample of the Neurotensin variant of your choice, plus a money‑back guarantee if the purity does not meet the stated specification.
Laura Mitchell – Procurement Manager, NovaBio (USA)
“The pricing structure is transparent, and the 30 % cost saving allowed us to re‑allocate budget to additional target validation. Delivery was on schedule, and the CoA matched exactly what we needed for our IND filing.”
James O’Connor – Technical Director, Apex Therapeutics (Canada)
“We tested the 1‑8 fragment in a receptor‑binding assay and observed a 15 % increase in signal‑to‑noise ratio compared with our previous supplier. The batch consistency is impressive.”
Wei Zhang – R&D Lead, SinoPharm (China)
“Global Technology’s OEM service let us develop a proprietary Neurotensin 8‑13 analog within two weeks. Their engineering team handled the synthesis and stability studies flawlessly.”
Or reach us directly: Phone: +86 199 4383 0844 | Email: service@huanqiukeji9.com
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Trusted by Leading Institutions Worldwide
CAS-866044-63-5-Degarelix-intermediate CAS-58-82-2-Bradykinin CAS-531512-26-2-Steviol-Glycoside Gln4-Neurotensin-product-supplier
All products are accompanied by certifications: CE, FDA, ISO 9001, GMP, RoHS, CB, VDE, SAA. Our factory complies with the latest International Pharmaceutical Regulations (ICH Q7) and holds a HACCP/GMP license.
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