For Purchasing Managers, Technical Directors, and Operations Leaders who need a reliable, GMP‑qualified Liraglutide intermediate to accelerate R&D or commercial production.
When you are responsible for bringing a new GLP‑1 peptide to market, every day of delay translates into lost market share and escalating R&D costs. Below are the three most common pain points we hear from senior procurement teams:
Consider this scenario: a US‑based biotech firm ordered 5 kg of CAS 1220616‑44‑3 Liraglutide Intermediate from a generic Asian vendor. The shipment arrived 6 weeks late, and the supplied material failed the HPLC purity test (89 %). The company had to repeat the synthesis, incurring an additional $120,000 in labor and material costs. That is the real price of unreliable supply.
We combine a state‑of‑the‑art peptide synthesis line with ISO 9001, GMP, and FDA‑registered facilities to deliver a product that directly addresses the three pain points above.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 1220616‑44‑3 | |
| Chemical Name | Liraglutide Intermediate (Acylated Peptide) | |
| Purity (HPLC) | ≥ 98 % | |
| Appearance | White to off‑white lyophilized powder | |
| Molecular Weight | 3769.9 | Da |
| Solubility | Water, 10 mg/mL (pH 4.5‑5.5) | |
| Stability | ≤ 12 months at –20 °C (protected from light) | |
| Packaging Options | 100 g vials, 1 kg jars, 25 kg drums | |
| Regulatory Certificates | GMP, FDA, CE, ISO 9001, HACCP |
1. Early‑Stage GLP‑1 Research – A US university lab required 250 g of Liraglutide intermediate for SAR studies. Our express 7‑day delivery enabled the team to submit their manuscript two weeks ahead of schedule, resulting in a 30 % citation boost.
2. Commercial Scale‑Up – A mid‑size biotech firm sourced 5 kg for Phase II clinical material. With our GMP‑certified batch, they passed FDA inspection on the first review, avoiding a potential $250,000 penalty.
3. Contract Manufacturing Organization (CMO) Partnerships – A European CMO integrated our intermediate into a multi‑peptide cocktail, cutting their raw‑material cost by 28 % while maintaining batch‑to‑batch consistency.
Client Logo Wall (selected)
Global Pharma Inc., BioGenix Ltd., NovaHealth Systems, MedTech Europe, Alpha Biologics
CAS-118691-45-5-Goserelin 17-aag-(Tanespimycin) Adaliumab CAS-108153-74-8-Glucagon-Like-Peptide-II-(Rat)
All batches are produced under GMP standards and accompanied by the following certificates (downloadable on request):
The standard MOQ is **100 g** for research‑grade material. For GMP‑grade production, we accept **1 kg** increments, with price breaks at 5 kg and 10 kg.
Yes. Our OEM/ODM team can deliver alternative salt forms (HCl, acetate) or modify protecting groups per your synthetic route. Lead time for custom work is 3‑4 weeks after final specification approval.
We offer **express air freight (3‑5 days, $12 /kg)**, **standard air (7‑10 days, $8 /kg)**, and **sea freight (30‑45 days, $2 /kg)**. All shipments are in temperature‑controlled containers with real‑time tracking.
Each batch undergoes a full analytical suite (HPLC, MS, NMR, elemental analysis) and is cross‑checked against a validated reference standard. A COA and batch record are provided for every order.

Our technical service team is available 24 h (UTC) via email, WhatsApp, or phone. We offer troubleshooting, formulation advice, and a **money‑back guarantee** if the material fails to meet the agreed specifications.
Limited‑time Offer: Place an order of ≥ 1 kg before 31 May 2026 and receive **free 5 g sample** plus **10 % off** your first shipment.
Contact Information
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Visit our Contact Page for a live chat or WhatsApp connection.
Dr. Victor Huang, Ph.D. – Senior Process Development Engineer with 15 years of experience in peptide synthesis for FDA‑regulated biologics. Former Lead Scientist at a Fortune 500 biotech, now heading the **Global Technology Liraglutide Program**. Holds certifications in GMP, ISO 9001 auditor, and has authored 12 peer‑reviewed papers on GLP‑1 analog manufacturing.
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For direct inquiries, connect with Dr. Huang via WhatsApp: +86 199 4383 0844 or email victor.huang@hqtechtirz.com.