Pepti · Catalog · Retatrutide 20mg + Tirzepatide 40mg

Dual-incretin research blend · research-use

Retatrutide + Tirzepatide blend supply.

Co-formulated 60 mg research vials (retatrutide 20 mg / tirzepatide 40 mg) with per-lot HPLC purity and mass-spec identity documentation, for laboratory and private-label programs.

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Research use — supplied as research peptides; buyers confirm local compliance

On 2026-04-30 the FDA proposed removing GLP-1 medications from the 503B bulks list. Pending finalization, US 503B facilities cannot compound these from bulk substances. Pepti positions GLP-1 compounds for research and private-label brand evaluation worldwide. Read the GLP-1 2026 update →

Retatrutide 20mg + Tirzepatide 40mg lyophilized vial
Retatrutide 20mg +HPLC ≥ 98%MS confirmed60mg

Vial illustrations reflect supplied lyophilized format. Distribution scope and destination market confirmed before invoicing.

CompoundRetatrutide 20mg + Tirzepatide 40mg
ClassBlends
FormLyophilized powder, sterile glass vial
Purity target≥ 98% by HPLC
Vial formats60mg
DocumentationCOA + HPLC + MS, batch lot file where available
Distribution scopeResearch use, worldwide
StorageStore the lyophilized blend at -20 °C, protected from light and moisture in a desiccated, sealed container. After reconstitution keep at 2-8 °C and use within the validated stability window. Ships under cold chain / with ice packs.

MOQ & lead time

TierQuantityLead time
Sample lotFrom 100 vials5–10 days
Production lot500–2,000 vials14–21 days
OEM repeat2,000+ vials21–28 days, scheduled

Retatrutide 20mg + Tirzepatide 40mg is a co-formulated 60 mg research blend pairing retatrutide (a GLP-1/GIP/glucagon triple agonist) with tirzepatide (a GIP/GLP-1 dual agonist), supplied as a lyophilized powder for research use only.

Documentation

Batch documentation support for Retatrutide 20mg + Tirzepatide 40mg lots.

COA / HPLC / MS document support where available. Distribution scope confirmed before invoicing.

HPLC purity

Reverse-phase HPLC with UV detection; purity target reported per lot with related-substance reporting on request.

MS identity

Mass spectrometry identity confirmation against the Retatrutide 20mg + Tirzepatide 40mg reference profile.

Lot traceability

Compound prefix and lot serial printed on the vial label and repeated in the document pack and carton.

FAQ

Retatrutide 20mg + Tirzepatide 40mg — frequently asked by B2B buyers.

What exactly is in the Retatrutide 20 mg + Tirzepatide 40 mg vial?

Each 60 mg vial is a physical co-formulation of 20 mg retatrutide and 40 mg tirzepatide presented as a single lyophilized cake. It is not a novel single molecule, so it carries no combined CAS or molecular weight; both peptides are documented individually on the certificate of analysis.

What documentation ships with each lot?

A per-lot certificate of analysis reporting HPLC purity for each peptide and identity confirmation by mass spectrometry (MS), together with appearance, water/residual-solvent and endotoxin data available on request. Third-party lab verification can be arranged for qualified buyers.

What are the minimum order quantity and available formats?

The catalog format is the 60 mg co-formulated vial (retatrutide 20 mg / tirzepatide 40 mg) at a 50-vial MOQ. Alternative ratios, single-component vials, different fill volumes and bulk lyophilized powder are quoted via RFQ for OEM and private-label programs.

Can the ratio and labeling be customized for private-label?

Yes. As an OEM/private-label supplier we can adjust the retatrutide-to-tirzepatide ratio, vial fill and unbranded labeling and packaging to buyer specification, subject to documentation and destination-market compliance review.

Is this product intended for human or clinical use?

No. All material is supplied strictly for laboratory research and as a manufacturing input. Retatrutide and tirzepatide are incretin-class compounds subject to regulatory restrictions; the buyer is responsible for compliance in their jurisdiction and must not represent the product for human consumption.

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