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Preloaded Autoinjector | Retatrutide | 3ml Pen | 15mg

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Safety data sheet PL-SDS-141 GHS: Warning · H361 · Read the SDS · PDF

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Retatrutide preloaded pen: 3 mL of LY3437943, a lipidated GIP, GLP-1 and glucagon receptor agonist, in bacteriostatic water at 5 mg/mL, 15 mg per pen. Filled from a peptide lot tested in PrymaLab’s own laboratory, with a certificate. Research use only.

Description

PrymaLab · Research use only

Preloaded Autoinjector | Retatrutide | 3ml Pen | 15mg

Retatrutide in solution at 5 mg/mL: 15 mg in a 3 mL preloaded pen cartridge

Retatrutide (LY3437943) is an investigational peptide agonist of the GIP, GLP-1 and glucagon receptors, with a 20-carbon diacid side chain on lysine 17. This listing is a preloaded pen holding a 3 mL glass cartridge of ready-made solution at 5 mg/mL, 15 mg of peptide in all, so there is no powder to reconstitute. Research on retatrutide runs from receptor pharmacology and mouse work to phase 2 and phase 3 clinical trials.

Specifications

Preloaded Autoinjector | Retatrutide | 3ml Pen | 15mg at a glance
Property Value
Compound Retatrutide LY3437943; GIP/GLP-1/glucagon receptor triple agonist
CAS number 2381089-83-2
Molecular formula C221H342N46O68
Theoretical mass 4731.4 Da
Sequence / structure H-Y-Aib-QGTFTSDYSI-[αMeLeu]-LDKK(AEEA-γGlu-C20 diacid)AQ-Aib-AFIEYLLEGGPSSGAPPPS-NH₂ (39 residues; Aib2, α-methyl-Leu13, Aib20; Lys17 acylated with eicosanedioic acid via γ-Glu and AEEA; C-terminal amide)
Contents Retatrutide: 15 mg per 3 mL pen (0.5% w/v)
Form Sterile aqueous solution in bacteriostatic water (0.9% benzyl alcohol), supplied in a 3 mL glass cartridge inside a preloaded autoinjector pen fitted with a needle
Storage, sealed Store at 2–8 °C in the original carton, protected from light
Safety data sheet PL-SDS-141

What is in the pen

The cartridge holds 3 mL of sterile aqueous solution. Retatrutide is present at 0.5% w/v, which is 5 mg/mL and 15 mg per pen; at the certificate’s theoretical mass of 4731.4 Da that works out to about 1.06 mM, or roughly 3.2 µmol in the whole pen. The solvent is bacteriostatic water with 0.9% benzyl alcohol as an antimicrobial preservative. On the safety data sheet, benzyl alcohol carries hazard statements for harm if swallowed or inhaled, serious eye irritation and allergic skin reactions, and retatrutide itself is classified Repr. 2 (H361), suspected of damaging fertility or the unborn child.

Keep the pen at 2 to 8 °C in its original carton, away from light, capped once in use and stored locked up. It must not be frozen, and a pen whose solution has frozen, discoloured or turned cloudy should be discarded. The same peptide is sold freeze-dried in the retatrutide 10 mg vial and the other fills, and peptide pen vs vial sets out the general differences between the two formats.

What the research covers

Coskun and colleagues introduced LY3437943 in 2022 as a triple agonist whose in vitro activity at the glucagon and GLP-1 receptors was balanced, with stronger activity at the GIP receptor1. In obese mice they found that energy expenditure driven through the glucagon receptor added to the reduced calorie intake attributed to the two incretin receptors1.

Human evidence comes from trials of an investigational drug run under medical supervision. The phase 2 obesity trial randomised 338 adults to retatrutide or placebo, with percentage change in body weight at 24 weeks as the primary end point and follow-up to 48 weeks2. How much each receptor contributes in people has not been worked out; the receptor-level evidence comes from cell and mouse experiments1. Phase 3 trials in type 2 diabetes, non-alcoholic fatty liver disease and obesity were started in August 2023, according to a 2024 review3.

None of these papers examined retatrutide held in solution, and none tested a preloaded pen or research-grade material, so the storage limits on the safety data sheet are the ones that apply to this format. The full literature, including the liver fat substudy, the diabetes trials and the 2026 phase 3 announcements, is in the retatrutide vs tirzepatide guide.

How each lot is tested

Every lot is tested in PrymaLab’s own laboratory in Ashland, Kentucky before release: RP-HPLC for purity, LC-MS for identity, Karl Fischer titration for water, LAL for endotoxin and USP <71> for sterility. Published certificates are listed on the results page and can be checked by number and key on the verify page. The certificate covers the peptide lot used to fill the pen, not the finished solution. These are in-house results from PrymaLab Analytical, not an independent test, and the lab is not accredited to ISO 17025. The third-party testing guarantee on this page still applies: if any independent laboratory finds the wrong compound, or less than the stated purity or amount, the order is refunded and the cost of the test is reimbursed.

Frequently asked questions

How does the pen differ from the retatrutide vials?

The vials hold freeze-dried powder, stored at −20 °C and dissolved in the lab at whatever volume the work calls for. The pen holds 15 mg already dissolved at a fixed 5 mg/mL in bacteriostatic water, and it is refrigerated at 2 to 8 °C, never frozen.

What does the certificate cover for a pen?

The peptide lot used to fill it, not the finished solution in the cartridge. The testing section on this page explains where published certificates are listed and how to check one by its number and key.

Is there published stability data for retatrutide in solution?

Not in the references on this page. The discovery and trial papers describe the molecule and its effects rather than how long it lasts in bacteriostatic water, so follow the storage conditions and discard criteria on the safety data sheet.

Is the pen meant for use in people?

No. It is sold for laboratory research only and has no approval from the FDA or any other regulator for human or veterinary use. Nothing here should be read as instructions for using it in people or animals.

References

  1. Coskun T, Urva S, Roell WC, et al. LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept. Cell Metab. 2022;34(9):1234-1247.e9. DOI · PubMed
  2. Jastreboff AM, Kaplan LM, Frías JP, et al. Triple-Hormone-Receptor Agonist Retatrutide for Obesity – A Phase 2 Trial. N Engl J Med. 2023;389(6):514-526. DOI · PubMed
  3. Kaur M, Misra S. A review of an investigational drug retatrutide, a novel triple agonist agent for the treatment of obesity. Eur J Clin Pharmacol. 2024;80(5):669-676. DOI · PubMed

Research use only

For laboratory research use only. This product is not a drug, food, cosmetic or dietary supplement, is not approved by the FDA or any comparable authority for human or veterinary use, and must not be given to people or animals. It is sold to qualified researchers and institutions, and the buyer is responsible for lawful handling and disposal.

Other formats of Retatrutide

Retatrutide is also stocked as Retatrutide 5mg, Retatrutide 20mg, Retatrutide 30mg, Retatrutide 40mg, Retatrutide 50mg and Retatrutide 60mg. Each listing states its own quantity and concentration, and the pen and vial comparison explains what changes between formats. The retatrutide buying guide covers what to check on a certificate before ordering.

Additional information

Weight N/A
Dimensions N/A

Safety data sheet PL-SDS-141 · Retatrutide

GHS safety data sheet for this product (solution, preloaded autoinjector pen), revision 1.0 of October 3, 2026. Read all 16 sections or download the PDF to keep with the material.

Warning
  • H361 Suspected of damaging fertility or the unborn child.
CompositionRetatrutide (CAS 2381089-83-2) · 0.5% w/v, 15 mg per 3 mL pen
Benzyl alcohol (preservative) (CAS 100-51-6) · 0.9% w/v
Water for injection (CAS 7732-18-5) · balance to 100%
ClassificationReproductive toxicity (Category 2)
Physical stateLiquid. Clear, colourless to faintly yellow aqueous solution.
Storage2–8 °C, protected from light; do not freeze
HandlingHandle the device as a sharp: never recap or reuse needles, keep fingers away from the needle, and discard used devices into a rigid sharps container. Avoid splashes to eyes and skin. Wash hands after handling.
First aidEyes: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do; continue rinsing. If eye irritation persists, get medical advice. Skin: Take off contaminated clothing. Wash the skin with plenty of soap and water. If irritation or a rash develops, get medical advice. Ingestion: Rinse mouth. Do not induce vomiting. Call a POISON CENTER or doctor if you feel unwell.
DisposalChemical waste through a licensed contractor; do not pour down the drain. Used pens and needles go into a sharps container.
TransportNot regulated as a dangerous good (DOT / IATA / IMDG).

For laboratory research use only. Not for human or veterinary use.

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