HPLC purity
Target specification: ≥99% area purity by reverse-phase HPLC with UV detection; actual acceptance criteria and result are confirmed for the applicable product and 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 containing chromatographic purity and molecular-weight identity results.
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 against available documentation for the applicable product, specification and lot |
| Form | Lyophilized powder, glass vial |
| Purity target | ≥ 99% by HPLC |
| Vial formats | 5 mg, 10 mg, 15 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 100 mg |
| Documentation | Batch-linked COA containing chromatographic purity and molecular-weight identity results for the confirmed lot |
| Distribution scope | Research use, worldwide |
| Storage | 2–8 °C protected from light; long-term −20 °C |
| Tier | Quantity | Lead time |
|---|---|---|
| Sample lot | 1 kit (10 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
Batch-linked COA with chromatographic purity, molecular-weight identity, water-content and storage results. Buyer track and destination confirmed before invoicing.
Target specification: ≥99% area purity by reverse-phase HPLC with UV detection; actual acceptance criteria and result are confirmed for the applicable product and 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 development programs, 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 a COA containing chromatographic purity and molecular-weight identity results. Research inquiries are reviewed before quoting.
Sample lots from 1 kit (10 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.
Related compounds
Current Batch COA
Batch-linked COA PDF for each Retatrutide specification below, with the reported chromatographic purity and molecular-weight identity results. Independent local verification is welcome. Confirmed quality issues are eligible for replacement or refund under the quality policy.