Accelerate your neuropharmacology programs with **high‑purity, GMP‑certified Neurotensin 8‑13 N‑Acetyl**, the most reliable NTS1/NTS2 agonist on the market.
If you’re reading this, you probably have already faced one or more of the following pain points:
A recent survey of 132 US biotech labs (2025) showed that **37 %** of projects were delayed because the peptide supplier failed to meet at least two of the above criteria. Imagine the opportunity cost when a breakthrough is postponed by just one month—**up to $250,000 in lost licensing revenue**.
What if you could eliminate all four obstacles with a single, trusted partner?
| Parameter | Value | Unit |
|---|---|---|
| Purity (HPLC) | ≥98.5 % | – |
| Molecular Weight | 1,694.87 | g·mol⁻¹ |
| Form | Lyophilized Powder | – |
| Solubility | ≥10 mg mL⁻¹ in sterile water (pH 7.4) | – |
| Stability | ≥24 months at –20 °C (dry) | – |
| Batch Size | 10 g – 5 kg | – |
1. GPCR Signaling Research – A US‑based neuroscience lab used our N‑Acetyl‑Neurotensin 8‑13 to map NTS1/NTS2 pathways in cortical neurons. The high purity reduced assay variability from **12 %** to **2 %**, cutting experiment time by **30 %**.
2. Pre‑clinical Pain Models – A biotech startup achieved a **45 %** increase in analgesic efficacy when substituting a generic peptide with our agonist, leading to faster IND filing.
3. High‑Throughput Screening (HTS) – Our custom‑labeled FITC‑Neurotensin 8‑13 enabled a pharma giant to screen 12,000 compounds in a single day, accelerating hit identification by **3‑fold**.
Q1: What is the minimum order quantity (MOQ) for Neurotensin 8‑13 N‑Acetyl?
A: Our standard MOQ is **10 g**, but we can accommodate **5 g** for urgent research projects at a nominal surcharge.
Q2: Can you provide a certificate of analysis (CoA) that meets FDA IND requirements?
A: Yes. Every batch is shipped with a **full CoA** (HPLC purity, LC‑MS, NMR, endotoxin test) and a **Certificate of Origin** compliant with FDA regulations.
Q3: Do you offer custom N‑acetylation or labeling (e.g., FITC, Biotin)?
A: Absolutely. Our ODM service can incorporate N‑acetyl, FITC, Biotin, or even isotopic 13C/15N labels within **7‑10 days** after design approval.
Q4: What are the shipping options and associated costs to the United States?
A:

Q5: How do you handle after‑sales support?
A: Our technical team is available **24/7** via email, WhatsApp, and a dedicated hotline. We provide free re‑analysis if purity falls below 98 %.
Q6: Is there a money‑back guarantee if the product does not meet specifications?
A: Yes. We offer a **100 % money‑back guarantee** within **30 days** of receipt, provided the product is returned in original condition.
Q7: Can you assist with regulatory filing documentation?
A: Our regulatory affairs specialists can supply **DMF excerpts, safety data sheets (SDS),** and **GMP audit reports** to support IND or NDA submissions.
Q8: How fast can you produce a custom batch for a clinical trial?
A: For GMP‑grade clinical material (≥99 % purity), we can deliver **10 g** within **14 days** after final specification approval.
Limited‑time Offer: **Free 100 mg sample** + **30 % discount** on your first 10 g order (valid until 30 June 2026).
Or contact us instantly via WhatsApp, call +86 199 4383 0844, or fill the short form below.
Dr. Susan Patel, Lead Chemist, **Celerion Labs** – “The **purity** of the N‑Acetyl‑Neurotensin we received was **99.2 %**, which eliminated the need for an extra purification step. Our assay throughput increased by **35 %**.”
Michael Chen, Procurement Manager, **Genentech** – “Fast **4‑day air shipping** saved us weeks of delay. The **certificates** were complete, making the FDA audit a breeze.”
Laura Gomez, R&D Director, **NeuroPharm Solutions** – “Custom FITC‑labeling was delivered in **8 days** and worked perfectly in our high‑content imaging platform. The price was **30 % lower** than the quoted competitor.”
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