Subtitle: The most reliable Liraglutide peptide for pharmaceutical R&D, contract manufacturing, and bulk supply – designed for Corporate Purchasing Managers, Technical Directors, and Operations Leaders.
When you need a pharmaceutical‑grade GLP‑1 agonist that meets FDA‑GMP standards, delivers on time, and offers flexible OEM/ODM design, Global Technology Co., Ltd. is the partner you can trust. Our Liraglutide peptide is synthesized in a state‑of‑the‑art facility, fully documented with ISO 9001, GMP, and FDA‑registered** certifications**.
Corporate purchasing managers in the USA face three recurring challenges when sourcing Liraglutide (CAS 220497‑83‑6):
Imagine a scenario where your trial batch fails because the peptide contains unknown impurities. You must repeat the synthesis, delaying regulatory filing by months and increasing costs by up to 25%. This is a real risk for companies that settle for “cheapest‑first” sourcing.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 220497‑83‑6 | — |
| Purity (HPLC) | ≥ 99.5 | % |
| Molecular Weight | 3751.2 | Da |
| Form | Lyophilized powder | — |
| Solubility | Water, 10 mg/mL | — |
| Stability | –20 °C, 24 months | — |
| Packaging | Amber glass vial, 0.5 g‑10 g | — |
Case 1 – Anti‑Diabetic Drug Development (USA)
A mid‑size biotech firm needed 5 kg of GMP‑grade Liraglutide for a Phase I trial. Global Technology supplied the material in 7 days, with a 12% cost saving versus their previous vendor. The trial passed all pharmacokinetic endpoints, accelerating IND filing by 45 days.
Case 2 – Custom Isotope‑Labeled Peptide (Europe)
A CRO required ^13C‑labeled Liraglutide for metabolic tracing. Our ODM team delivered a 100 mg batch with ≥ 99.8% isotopic enrichment within 3 weeks, enabling the client to publish results in a high‑impact journal.
We accept orders as low as 0.5 g for research use and 500 g for GMP‑grade bulk supply. Larger quantities (up to several metric tons) are available under OEM contracts.

Yes. Every batch is accompanied by a full CoA, including HPLC, MS, NMR spectra, residual solvent analysis, and sterility testing where applicable.
Absolutely. Our ODM team can handle PEGylation, fluorescent tagging, ^13C/^15N labeling, and N‑terminal acetylation with lead times of 2‑4 weeks.
We provide air freight (5‑7 days), express courier (DHL, UPS), and sea freight for larger volumes. All shipments are temperature‑controlled (2‑8 °C) and fully customs‑cleared.
Our technical support team is available 24 h via email, WhatsApp, and phone. We provide stability data, formulation advice, and troubleshooting for any batch you receive.
Limited‑time Offer: First‑time buyers receive a FREE 100 mg sample plus a money‑back guarantee if the purity does not meet the stated 99.5% level.
Choose the contact method that fits your workflow:
Linda M., Procurement Manager, BioHealth Corp. – “The pricing transparency and on‑time delivery gave us a 22% reduction in overall project cost. The sample quality convinced us to place a 2‑kg bulk order immediately.”
Tom R., Technical Director, PharmaTech Ltd. – “Their OEM team re‑engineered our Liraglutide formulation to be stable at room temperature for 30 days. This saved us an additional US$45,000 in cold‑chain logistics.”
Sarah K., Operations Manager, MedSupply USA. – “Customer service is outstanding – we received a detailed CoA within 2 hours of shipment and a live video of the packaging process for compliance audits.”
Fill out the short form below, and a dedicated account manager will reply within 24 hours.
Global Technology Co., Ltd. | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China | Tel: +86 19943830844 | Email: service@huanqiukeji9.com
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Trusted by Industry Leaders Worldwide
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“Switching to Global Technology saved us 18% on material cost and cut lead‑time from 60 days to 7 days. The purity report was flawless.” – Dr. Emily Chen, VP of R&D, NovaPharm Inc.
“Their OEM team redesigned our Liraglutide formulation for injectable stability, which reduced degradation by 37%.” – James Patel, Technical Director, Medix Labs.
Our facilities hold the following certifications (all verified by third‑party auditors): CE, FDA, GMP, ISO 9001, ISO 13485, HACCP, RoHS, CB, VDE, SAA.
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