HomeCatalogueRoyal Pharma Retatrutide Triple-Agonist (40mg)
Royal PharmaGLP-1/GIP/GCGR40mg / 50mg EU

Independent HPLC & CoA Verified

COA Verified

Batch tested for chemical identity, assay purity, sterility, endotoxins and particulate clearance.

Verified Partner • Royal Pharma•Independent HPLC & Sequence Verified

Royal Pharma Retatrutide Triple-Agonist (40mg)

Next-generation 40mg triple hormone receptor agonist (GLP-1, GIP, and GCGR) by Royal Pharma engineered for advanced metabolic energy expenditure investigations, glucagon receptor modulation, and hepatic lipid oxidation research (50mg regional formulation available for Portugal protocols).

Technical Specifications

RUO Certified

Assay Purity

99.4% Purity (HPLC Verified)

Storage Protocol

-20°C (lyophilized), 4°C (reconstituted)

Format / Concentration

40mg / 2mL multiple-dose triple-agonist lyophilized vial

Synthesis Origin

Royal Pharma European Biotech Labs

Access Status

Authorized Researchers Only

Available for Dispatch

Strictly Research Use Only (RUO). Not for diagnostic, veterinary, or human medical procedures. Handled exclusively by authorized laboratory investigators.

Triple Hormone Receptor Agonist (GLP-1 / GIP / GCGR)

Retatrutide is an investigational multi-receptor synthetic peptide sequence exhibiting balanced agonist activity across GLP-1, GIP, and glucagon (GCGR) receptors in metabolic energy expenditure and hepatic lipid oxidation assays.

Provided by Royal Pharma in sealed 40mg lyophilized multi-dose vials (with 50mg EU regional specification support), each lot is released with full chromatogram identity and peptide assay verification.

Receptor Class

GLP-1 / GIP / GCGR

Triple receptor engagement

Vial Capacity

40mg / 50mg EU

Lyophilized reference cake

Purity Standard

99.4% HPLC

Sequence & mass verified

Manufacturing & Analytical Standards

Synthesized and verified under strict aseptic analytical controls with full batch-level chain-of-custody documentation and independent chromatographic identity release testing.

Compounding StandardRoyal Pharma EU Synthesis
Analytical VerificationRP-HPLC & Mass Spectrometry
AccreditationBatch Traceable CoA