
Triple Receptor Agonist (GLP-1, GIP & Glucagon) | Fat Loss, Appetite Suppression & Metabolic Enhancement | For Research Use Only
Retatrutide is a cutting-edge investigational peptide that acts as a triple agonist of the GLP-1, GIP, and glucagon receptors. This triple mechanism has demonstrated unprecedented weight loss, improved glycaemic control, and enhanced energy expenditure in early-phase research studies. It is currently one of the most promising agents under investigation for obesity, type 2 diabetes, and metabolic dysfunction.
With a long half-life and superior fat-burning properties, Retatrutide is paving the way for next-generation peptide therapeutics.
Triple Receptor Activation: GLP-1, GIP & Glucagon
Potent Appetite Suppression & Satiety Induction
Accelerates Fat Burning & Promotes Lean Mass Retention
Improves Insulin Sensitivity & Glucose Regulation
Superior to Semaglutide & Tirzepatide in Preclinical Trials
Ideal for Advanced Weight Management & Diabetic Research Models
Compound Name: Retatrutide
CAS Number: 2381089-83-2
Molecular Formula: C₂₀₉H₃₂₉N₅₅O₆₆
Molecular Weight: ~4717.35 g/mol
Purity: ≥ 98% (HPLC Verified)
Form: Lyophilised powder
Unit Size: 50mg per vial
Storage (lyophilised): Store at –20°C, protected from light and moisture
Reconstitution: Reconstitute with sterile bacteriostatic water (1–2ml recommended)
Post-Reconstitution: Store at 2–8°C and use within 10–14 days
Avoid: Heat exposure, light, and repeated freeze-thaw cycles
Retatrutide – 50mg is intended strictly for scientific, non-human research purposes. It is not approved for human use, medical treatment, or diagnostic procedures.
Explore our high-purity compounds — including Retatide (Retatrutide 30 mg), Semaglutide, and more.
Fast UK shipping. Lab-tested quality. Strictly for research use only.