HPLC purity
Reverse-phase HPLC with UV detection; ≥99% area-purity target on each production lot.
GLP-1 family · research-use
Lyophilized retatrutide (triple GLP-1 / GIP / glucagon receptor research compound) for research labs and private-label brand evaluation worldwide. ≥99% HPLC purity target, batch-linked COA, HPLC chromatogram and MS identity record.
On 2026-04-30 the FDA proposed removing GLP-1 medications from the regulatory bulk-substance framework, with public comment open through 2026-06-29. Pending finalization, this compound is positioned for research and private-label brand evaluation worldwide. Read the GLP-1 2026 update →
Vial illustrations reflect supplied lyophilized format. Lot codes are sample identifiers; production lots carry their own batch references.
| Compound | Retatrutide |
|---|---|
| CAS number | 2381089-83-2 |
| Class | Triple GLP-1 / GIP / glucagon receptor agonist (research) |
| Molecular weight | Confirmed on batch-linked COA for each production lot |
| Form | Lyophilized powder, glass vial |
| Purity target | ≥ 99% by HPLC |
| Vial formats | 5 mg, 10 mg, 15 mg, 20 mg |
| Documentation | Batch-linked COA + HPLC chromatogram + MS identity record for every production lot |
| Distribution scope | Research use, worldwide |
| Storage | 2–8 °C protected from light; long-term −20 °C |
| Tier | Quantity | Lead time |
|---|---|---|
| Sample lot | From 100 vials | 5–10 days |
| Production lot | 500–2,000 vials | 14–21 days |
| OEM repeat | 2,000+ vials | 21–28 days, scheduled |
All retatrutide quotes require a destination country and buyer track. Inquiries from US regulated facilities are answered with the regulatory bulk-substance framework proposal and routed to non-GLP-1 alternatives.
Documentation
COA, HPLC chromatogram, MS identity confirmation, water content and storage notes. Buyer track and destination confirmed before invoicing.
Reverse-phase HPLC with UV detection; ≥99% area-purity target on each production lot.
Mass spectrometry identity confirmation against the Retatrutide reference profile.
Lot code printed on vial label and reflected in the document pack. Reorders cite the prior lot for continuity.
FAQ
On 2026-04-30 the FDA proposed removing GLP-1 medications from the regulatory bulk-substance framework. While retatrutide itself is the target of separate clinical-stage development, Pepti supplies it as a research peptide worldwide for research and private-label brand evaluation; buyers confirm local compliance.
Latin America, Southeast Asia, parts of the Middle East, and select EMEA distributors with appropriate local registration.
Yes — lyophilized retatrutide is supplied for laboratory research with COA, HPLC, and MS. Research inquiries are reviewed before quoting.
Sample lots from 100 vials; production lots from 500 vials with tier pricing.
HPLC purity (target ≥99%), MS identity, water content, related-substance profile on request, and lot traceability tied to the document pack.
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