Accelerate your R&D pipeline, reduce batch‑to‑batch variability, and secure on‑time delivery – designed for Corporate Purchasing Managers, Technical Directors, and Operations Leaders.
In 2025‑2026, more than 42% of biotech firms reported delays in clinical‑trial material due to unreliable peptide suppliers. The following pain points are repeatedly cited by decision‑makers like you:
Imagine a scenario where your next‑generation HIV‑1 fusion inhibitor trial is postponed because the peptide you ordered arrived late, under‑purified, and without a proper Certificate of Analysis. The resulting delay can cost $1.2 M in lost opportunity and regulatory fees.
Our state‑of‑the‑art manufacturing platform combines GMP‑certified facilities, university‑level R&D labs, and a dedicated quality‑assurance team. Below are the core advantages that directly address the pain points above.
| Parameter | Specification | Compliance |
|---|---|---|
| CAS No. | 156012-92-9 | – |
| Chemical Name | Enfuvirtide (T‑20) | – |
| Molecular Weight | 3,468 Da | – |
| Purity (HPLC) | ≥ 99.9 % | ISO 9001, GMP |
| Form | Lyophilized powder, 5 mg‑5 kg | FDA, CE, ISO |
| Storage | ‑20 °C, desiccated | – |
| Lead Time | 7‑10 business days | – |
| Certificates | CoA, MSDS, GMP, ISO 9001, FDA DMF | All |
Case Study 1 – US‑Based Biotech Startup: Needed 250 mg of Enfuvirtide for pre‑clinical mouse models. Our rapid 7‑day production saved the client 30% in overall project cost and allowed IND filing two weeks ahead of schedule.
Case Study 2 – European Contract Research Organization (CRO): Required a GMP‑grade batch with isotopic labeling for PK studies. Delivered 1 kg of 99.9% pure, ^13C‑labeled Enfuvirtide within 12 days, meeting EMA documentation standards without additional testing.
CAS-1143-70-0-4-Hydroxybenzophenone Aminotadalafil-tadalafil-analog-standard-supplier Biotin-NKA-and-Biotin-NMS-conjugate-supplier Amylin-(8-37)-human-antagonist
Case Study 3 – Asian Pharmaceutical Manufacturer: Switched from a legacy supplier to our OEM service, cutting raw‑material cost by 22% while maintaining batch consistency across a 5‑year production run.Our standard MOQ is 100 mg. For OEM/ODM projects we can accommodate as low as 50 mg with a short lead‑time surcharge.
Yes. Every batch is accompanied by a full CoA, including HPLC purity, LC‑MS mass confirmation, residual solvent analysis, and a signed GMP statement.
We ship DDP (Delivered Duty Paid). Our logistics team prepares all HS codes, commercial invoices, and FDA import documentation to ensure a smooth clearance.
Absolutely. We offer ^13C, ^15N, and deuterium labeling with the same 99.9 % purity standard. Lead time is an additional 3‑5 days.
We assign a dedicated Technical Account Manager, 24/7 email support, and a 30‑day guarantee for any purity‑related issues.
Limited‑time Offer: Place an order before 30 June 2026 and receive free sample (50 mg) + 5 % discount on the first full‑scale purchase.

Laura Mitchell, Procurement Manager, NovaPharma (USA)
“The 99.9% purity of Enfuvirtide allowed us to skip a costly re‑analysis step. Delivery in 8 days saved us a critical month in our IND timeline.”
James O’Neil, Technical Director, MedGen Labs (UK)
“Their OEM service gave us a custom‑labeled batch within two weeks – a feat no other supplier could match.”
Rita Singh, Operations Manager, BioCore (Canada)
“Transparent pricing and a fixed‑rate contract eliminated the 20% price spikes we experienced with previous vendors.”
Global Technology Co., Ltd | Tel: +86 19943830844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Website: www.hqtechtirz.com | Contact Page
All product information complies with local regulations, pricing methods, and approved usage. For detailed terms, please request our latest compliance package.
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Compliance & Certifications: CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC – all verified by third‑party auditors.