Accelerate your drug‑development pipeline, reduce batch‑to‑batch variability, and stay compliant with FDA‑grade quality – all within 48 hours of order confirmation.
Get Free Quote in 24h1. High Price & Low Yield – Many suppliers quote US$ 1,200 – 1,500 per gram for Exenatide with ≤ 85 % purity. The hidden cost of re‑purification can add another 30 % to your R&D budget.
2. Inconsistent Quality – Batch‑to‑batch variability (purity swings from 82 % to 94 %) forces you to repeat assays, extending project timelines by 3–4 weeks on average.
3. Slow Delivery & Expensive Shipping – Typical lead times exceed 30 days with air‑freight charges above US$ 250 per kilogram, making fast‑track clinical trials impossible.
4. Regulatory Uncertainty – Lack of GMP, DMF, or FDA‑recognized certificates means you risk non‑compliance during IND filing, potentially delaying market entry by 6–12 months.
5. Limited Customization – When you need a specific peptide sequence or a bespoke lyophilized format, most vendors charge a premium and offer no technical support.
These pain points translate into higher R&D costs, delayed product launches, and reduced competitive advantage. If you recognize any of these challenges, read on – the solution is below.
Discover the Solution →| Parameter | Specification |
|---|---|
| CAS Number | 127633‑71‑0 |
| Molecular Weight | 4,133.53 Da |
| Purity (HPLC) | ≥ 99.5 % ± 0.2 % |
| Form | Lyophilized powder, sealed amber vials (0.5 ml, 1 ml) |
| Storage | -20 °C, protected from light |
| Packaging | Bulk (≥ 10 g) or GMP‑certified vials (≤ 5 g) |
| Certificate | GMP, DMF, FDA, ISO 9001, HACCP, COA |
Pre‑clinical Metabolic Research – A US biotech company reduced their GLP‑compliant study cost by 38 % after switching to our Exenatide, thanks to the higher purity that eliminated the need for additional cleanup steps.
Formulation Development for Injectable GLP‑1 Analogs – Our custom lyophilized format allowed a contract manufacturing organization (CMO) to scale from 0.5 g to 500 g batches without reformulation, cutting timeline from 12 weeks to 6 weeks.
Regulatory Filing Support – The provided GMP & DMF documents were accepted by the FDA’s CDER division, enabling a fast‑track IND submission for a novel Exenatide‑based drug‑delivery system.
Start Your Order Today99.5 % ± 0.2 % (HPLC), verified by independent third‑party labs. This meets FDA‑grade requirements for both research and clinical‑grade applications.
Yes. Our OEM/ODM service includes N‑terminal acetylation, C‑terminal amidation, isotope labeling, and PEGylation. Minimum order for custom work is 5 g.
We accept T/T (30 % advance, 70 % before shipment), L/C at sight, and PayPal for orders ≤ 5 g. For trusted partners, Net 30 days is negotiable.
Standard air‑freight: 5‑7 business days after production release. Express DHL/EMS: 2‑3 days. We provide real‑time tracking and customs documentation.

Absolutely. We provide a 100 mg sample (99.5 % purity) with a free COA. Shipping is on us for the first request.
Our technical team offers formulation advice, stability testing guidance, and regulatory documentation assistance for 12 months after delivery.
Risk‑Free Guarantee: If the purity does not meet the stated 99.5 %, we will replace the batch at no extra cost.
Claim My Free SampleOr call us directly at +86 199 4383 0844 (We speak English)
Dr. Alex Rivera, Lead Researcher, Pacific Biotech
“The batch consistency is **unmatched**. We moved from a 3‑month to a 2‑week timeline for our GLP‑1 analog study.”
Linda Wu, Procurement Manager, Global Pharma Ltd.
“Pricing is transparent and 30 % lower than other Asian suppliers. The free COA saved us a week of paperwork.”
Mark Thompson, CMO, Nova Therapeutics
“Regulatory documents were accepted instantly. We appreciate the 24/7 technical hotline—saved us from a potential delay.”
Global Technology Co., Ltd. – Your trusted partner for high‑purity APIs and peptides.
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Trusted by Leading Institutions Worldwide
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All shipments are accompanied by CE, FDA, ISO 9001, GMP, HACCP, RoHS, and CB certificates, ensuring full compliance with U.S. and EU regulations.
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