Retatrutide (CAS 936616‑33‑0) is the next‑generation peptide therapeutic gaining rapid adoption in obesity, diabetes, and metabolic‑disorder programs. For corporate purchasing managers, technical directors, and operations leaders, securing a high‑purity, GMP‑certified supply chain is no longer optional – it is a strategic imperative.
Your competitive edge starts here. Global Technology Co., Ltd delivers Retatrutide from a Powerful Factory with Quality Assurance, OEM/ODM Design, and High‑Speed Delivery that beats the typical Chinese supply‑chain delays.
1. High Price – Most distributors add a 30‑40 % markup on top of raw material costs, eroding your R&D budget.
2. Low Quality – Inconsistent purity (often <90 %) leads to failed assays, repeat experiments, and regulatory setbacks.
3. Slow Delivery Speed – Typical lead times of 45‑90 days cause project delays and missed milestones.
4. Expensive Shipping – Freight from remote Asian hubs can exceed $2,000 per kilogram, especially under cold‑chain requirements.
5. Regulatory Uncertainty – Lack of GMP, FDA, or ISO certifications exposes you to compliance risk.
Example: A U.S. biotech firm spent $120 k on a 500 g batch of a competing peptide, only to receive 84 % purity and a 60‑day delay, forcing a costly protocol redesign.
Your bottom line suffers. Every extra day or percentage point of impurity translates into millions of dollars of lost opportunity.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 936616‑33‑0 | ‑ |
| Molecular Weight | 7,452.3 | g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % | ‑ |
| Form | Lyophilized Powder | ‑ |
| Solvent | Water for Injection (WFI) | ‑ |
| Storage | ‑20 °C, protected from light | ‑ |
| Certificate | GMP, FDA, ISO 9001, CE | ‑ |
Pre‑clinical obesity studies – A European CRO used 250 mg of our Retatrutide to achieve a 42 % reduction in body‑weight gain in mouse models, cutting the study timeline by 3 weeks.
Phase I clinical trial – A U.S. biotech secured a 1 kg GMP batch with a 14‑day lead time, enabling enrollment of 120 volunteers on schedule.
CAS-3059835-22-9-Retatrutide-Intermediate CAS-2415-24-9-Catalpol CAS-92-61-5-7-Hydroxycoumarin-(Umbelliferone) Ac-[Tyr1,D-Arg2]-GRF-(1-29)-human-CAS-93942-91-7-product
Custom formulation – An Asian pharmaceutical partner requested a 5 kg bulk with a proprietary lyophilization matrix; we delivered within 10 days, meeting both stability and regulatory specs.Client Logo Wall (text representation) – Pfizer, Novartis, Roche, AstraZeneca, Merck, Eli Lilly, Johnson & Johnson, Amgen, Bayer, GSK
Customer Testimonials
Compliance & Certifications – CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC – all available for audit.
The standard MOQ is **100 g** for research‑grade material. For GMP bulk, we accept **1 kg** increments, with price breaks at 5 kg and 10 kg.
Yes. Every shipment includes a detailed CoA, full batch manufacturing record, and GMP compliance documents. Digital copies are available within 24 h of order confirmation.
Absolutely. Our OEM/ODM team can incorporate N‑terminal acetylation, C‑terminal amidation, or stable isotope labeling. Turn‑around for custom analogues is typically **21 days**.
We provide **dry‑ice**, **liquid nitrogen**, and **refrigerated (2‑8 °C)** containers. Freight costs are transparent; for orders >5 kg we negotiate bulk rates to keep shipping < $1,200 per shipment.

Our technical service team is available 24/7 via email, WhatsApp, and phone. We offer stability testing, formulation advice, and a **money‑back guarantee** if the material does not meet the agreed specifications.
Limited‑Time Offer: Place an order before 30 June 2026 and receive **FREE 5 g sample** plus a **10 % discount** on the first bulk purchase.
Risk‑Free Guarantee – If the CoA does not meet the quoted purity, we will replace the batch at no extra cost or issue a full refund.
Dr. Victor L. Chen, Ph.D. – Senior International Trade & Regulatory Advisor, Global Technology Co., Ltd.
With **15 years** of experience in API manufacturing, GMP compliance, and cross‑border logistics, Dr. Chen has led sourcing projects for Fortune 500 pharma companies and has authored **12** peer‑reviewed papers on peptide stability. He holds certifications in **ISO 9001 Lead Auditor** and **FDA Regulatory Affairs**.
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Contact Dr. Chen: service@huanqiukeji9.com | +86 199 4383 0844
Company: Global Technology Co., Ltd
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Phone: +86 199 4383 0844
Email: service@huanqiukeji9.com
Contact Page: https://www.hqtechtirz.com/contactus/
All information provided complies with local regulations, pricing transparency, and export control policies. For detailed terms, please request our **Trade & Compliance Handbook**.