HPLC purity
Reverse-phase HPLC with UV detection; ≥99% area-purity target on each production lot.
PeptiOEM · Catalog · Retatrutide
GLP-1 family · Engine 2 (OUS only)
Lyophilized retatrutide (triple GLP-1 / GIP / glucagon receptor research compound) for OUS (non-US) distribution, research labs, and private-label brand evaluation outside the United States. 99%+ HPLC purity, per-batch COA + MS.
On 2026-04-30 the FDA proposed removing GLP-1 medications from the 503B bulks list, with public comment open through 2026-06-29. Pending finalization, this compound is positioned for OUS (non-US) distribution markets, research, and private-label brand evaluation only. 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 |
|---|---|
| Class | Triple GLP-1 / GIP / glucagon receptor agonist (research) |
| Molecular weight | ≈ 4731 g/mol |
| Form | Lyophilized powder, sterile glass vial |
| Purity target | ≥ 99% by HPLC |
| Vial formats | 5 mg, 10 mg, 15 mg, 20 mg |
| Documentation | COA + HPLC + MS, per-batch lot file |
| Distribution scope | OUS markets & research only |
| 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 (OUS) | 2,000+ vials | 21–28 days, scheduled |
All retatrutide quotes require a destination country and buyer track. Inquiries from US compounding facilities are answered with the 503B bulks list 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 503B bulks list. While retatrutide itself is the target of separate clinical-stage development, PeptiOEM positions it for OUS distribution markets, research, and private-label brand evaluation rather than US compounding.
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. US-bound research inquiries are reviewed against current FDA guidance and the 2026 503B bulks proposal.
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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