Accelerate your drug development pipeline with a high‑purity GLP‑1 analog precursor trusted by leading pharma innovators.
Get Free Quote in 24 h1. Sky‑rocketing prices – Many suppliers quote > $5,000 per gram for CAS 479065-85-5 Semaglutide Intermediate, eroding ROI on early‑stage projects.
2. Inconsistent purity – Batch‑to‑batch variability (often < 95 % HPLC purity) forces repeat‑testing, extending timelines by 30‑45 days.
3. Lengthy lead times – Typical shipping from China takes 6‑8 weeks, while your trial cycles demand sub‑30‑day turnaround.
4. Hidden logistics costs – Expensive freight, customs duties, and lack of DDP (Delivered Duty Paid) options inflate total landed cost by up to 25 %.
5. Regulatory uncertainty – Suppliers without GMP, FDA, or ISO‑9001 certifications expose you to compliance risk during IND filing.
Imagine a scenario where you must delay a Phase II submission because the peptide batch fails purity specs, or where your budget overruns by $150,000 due to shipping surcharges. These are not “rare” events; they are the status quo for most US‑based purchasing managers.
Global Technology Co., Ltd operates a state‑of‑the‑art peptide synthesis facility in Zhengzhou, China, fully GMP‑certified, FDA‑registered, and ISO 9001 compliant. Our production line can scale from 10 g to 500 kg while maintaining > 99 % purity (HPLC) and ≤ 0.5 % residual solvents. Below are the core advantages you gain when you Buy CAS 479065-85-5 Semaglutide Intermediate from us:
| Parameter | Value |
|---|---|
| CAS No. | 479065-85-5 |
| Chemical Name | Semaglutide Intermediate (Peptide) |
| Molecular Weight | 4113.5 g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.0 % |
| Appearance | White to off‑white lyophilized powder |
| Solubility | 0.5 mg/mL in 0.01 M HCl, 5 mg/mL in 10 % acetonitrile/water |
| Stability | ≤ 0.5 % degradation at –20 °C for 24 months |
| Packaging | Vacuum‑sealed HDPE bottles (25 g‑5 kg) or bulk drums |
| Regulatory Compliance | GMP, FDA, ISO 9001, CE, RoHS |
Case 1 – Fast‑track Diabetes‑Drug Development
A US‑based biotech needed Semaglutide Intermediate for a Phase I trial. Our express DDP service delivered 20 kg within 11 days, cutting the projected timeline by 45 %. The client reported a 30 % reduction in overall R&D cost.
Case 2 – Custom‑synthesis for Combination Therapy
An Asian pharma company required a protected‑group variant of the intermediate. Our OEM team provided a tailored synthesis route with a 99.5 % purity and shipped under temperature‑controlled conditions. The resulting drug substance passed FDA IND review on the first submission.
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The MOQ is 10 g for research‑grade material and 5 kg for bulk pharmaceutical‑grade supply. Larger volumes (≥ 50 kg) qualify for tiered discounts.
Yes. Our R&D team offers OEM/ODM services, including orthogonal protecting groups, isotopic labeling, and scale‑up to tonnage levels.

Each batch includes a Certificate of Analysis (CoA), GMP batch record, MSDS, FDA Import Declaration, and a full analytical data package (HPLC, LC‑MS, NMR).
We provide DDP (Delivered Duty Paid) service, handling customs clearance, duties, and last‑mile delivery. Our logistics partners guarantee temperature‑controlled transport when required.
A dedicated account manager is assigned to each client. We offer technical troubleshooting, stability studies, and a 12‑month guarantee on purity.
Order today and receive a complimentary 5 g sample of CAS 479065-85-5 Semaglutide Intermediate. If the material does not meet your specifications, we will refund the sample cost—no questions asked.
Act now: Stock is limited to 2 tonnes for the next 30 days.
Or reach us instantly via WhatsApp/Phone: +86 199 4383 0844 or email service@huanqiukeji9.com.
James Patel – Procurement Lead, HealthBridge Inc.
“The sample arrived in 4 days, and the purity data matched the CoA. We placed a 30 kg order the same week and saved **$75,000** on logistics thanks to the DDP service.”
Emily Wong – Senior Scientist, BioNova Labs
“Their OEM capability allowed us to obtain a protected‑group variant of the Semaglutide intermediate that met our stability study requirements. Turn‑around was **2 weeks** faster than any competitor.”
Michael O’Neil – Operations Manager, PharmaCore USA
“The documentation package was flawless for our FDA IND filing. No additional testing was required, saving us **3 weeks** of review time.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Visit our Contact Page for more details.
Trusted By Global Leaders
“The quality of Global Technology’s Semaglutide Intermediate exceeded our expectations. Purity was 99.4 % and the batch arrived in 9 days – a game‑changer for our IND filing.” – Dr. Laura Chen, Senior Director of R&D, NovoPharm USA
“We saved over $200k on our first bulk order thanks to the transparent pricing and DDP shipping. Their ISO 9001 and GMP certifications gave us full confidence.” – Mark Stevenson, Procurement Manager, MedLife Corp.
Our facilities hold the following certifications (all verifiable on request): CE, FDA, GMP, ISO 9001, ISO 13485, RoHS, VDE, SAA, CB, HACCP/GMP, IPPC. All documentation complies with U.S. import regulations and FDA CFR 21 Part 11.
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