Retatrutide 30 mg kit — analytical-grade research peptideLY-3437943 · 30 mg / vial
Fig. 01 · Specimen
Lyophilised kit
In the box
  • ·3 mL bacteriostatic water
  • ·10 × 1 mL insulin syringes
  • ·Alcohol swabs
MetabolicClass IIILY-3437943

Retatrutide 30 mg kit

Triple-receptor agonist — 30 mg vial, full research kit.

Retatrutide 30 mg lyophilised vial kit — the mid-dose research presentation. Includes bacteriostatic water, syringes, and swabs.

Designation
LY-3437943
CAS no.
2381089-83-2
Molecular formula
C221H343N51O66
MW (Da)
4729.4
Residues
39
Purity
≥ 99.2%
Form
Lyophilised kit
Dose
30 mg / vial
Class
Class III
Dispatch · per unit
£195GBP
≈ €230 · 0.00361 BTC
1
In stock·Same-day dispatch (order by 09:30 UK)·Tracked24 Royal Mail £6.50·Not shipped to USA
Clinical status: Investigational. Phase 3 trials under the TRIUMPH programme. Not approved anywhere.
§ A Overview

What the peptide is.

Retatrutide (LY-3437943) is an investigational triple-agonist peptide being studied in Phase 3 trials. The 30 mg vial is the mid-dose presentation, widely used in extended research protocols and analytical-chemistry reference work.

Every lot is tested by Janoshik Analytical in Slovakia: HPLC for purity, ESI-MS for identity. COA is published on the product page before the lot lists for sale.

Proposed mechanism

Simultaneous agonism at GLP-1, GIP, and glucagon receptors. The added glucagon-receptor agonism is proposed to drive energy-expenditure effects in addition to incretin-mediated insulin secretion.

§ B Laboratory handling

Reconstitution, storage, and handling.

Lab-technical guidance for the researcher handling the material. Not therapeutic dosing, not administration guidance — those are not within the scope of this supply.

Reconstitution
Recommended solvent
Bacteriostatic water for injection (0.9% benzyl alcohol) — included with kit
Typical volume
1 – 2 mL
Notes
  • Inject diluent slowly down the side of the vial onto the cake.
  • Swirl gently — do not shake.
  • Solution should be clear and colourless. Discard if not.
Storage
Lyophilised
−20 °C, desiccated, protected from light. Stable at 15–25 °C for up to 30 days in transit.
Reconstituted
2–8 °C, original vial, consumed within 4 weeks.
Shelf life · sealed
24 months from date of manufacture when stored lyophilised at −20 °C.
Shelf life · reconstituted
Up to 4 weeks refrigerated.
Handling notes
  • Amber glass vial, argon-purged headspace, butyl stopper.
  • Do not refreeze reconstituted solution.
§ C Certificate of Analysis

This lot, documented.

Every shipment is accompanied by a signed four-page analytical report including the HPLC chromatogram, ESI-MS spectrum, purity calculation, and sample handling chain-of-custody.

The report you will receive is specific to the lot dispatched to you. The display below is a current representative example.

retatrutide 30mg kit · batch.log
LIVE
04:22:11lot 26-04-A received ┈ 5.00 g
04:22:40weight check ┈ PASS ±0.4 mg
04:23:12sample → janoshik ┈ 50 mg
04:23:12tracking #jnk-9218334
05:18:03HPLC result ┈ 99.24 %
05:18:04MS obs 4729.42 Da ┈ PASS
05:18:05coa.pdf signed ┈ attached
05:18:06lot approved ┈ LIVE
janoshik.report.txt
SIGNED
REPORT ID     JA-26-04-012
SUBJECT       Retatrutide 30 mg kit
DESIGNATION   LY-3437943
LOT           26-04-A
METHOD        RP-HPLC, ESI-MS
COLUMN        C18, 250 x 4.6 mm, 5 um
MOBILE PHASE  A: 0.1% TFA in H2O
              B: 0.1% TFA in ACN
GRADIENT      5 -> 65% B over 20 min
FLOW RATE     1.0 mL/min
DETECTION     UV 214 nm
INJECTION     20 uL @ 0.5 mg/mL
---
PURITY (A%)   99.20
MASS EXP.     4729.40 Da
MASS OBS.     4729.42 Da
---
CONCLUSION    Identity CONFIRMED · Purity PASS
SIGNED BY     J. Novak, MSc · Janoshik Analytical SVK
DATE          2026-04-11
representative chromatogram · A214 nmRT 8.42 min
Representative trace · Lot-specific COA included with every dispatch
purity≥ 99.2%
§ D Clinical trials

Registered clinical investigation.

Links below resolve to the ClinicalTrials.gov registry. Trial status reflects publicly disclosed information at the time of publication.

NCTPhaseTitleStatus
NCT05929066Phase 3TRIUMPH-1: Retatrutide in obesityOngoingRegistry ↗
§ E Peer-reviewed studies

Research references for Retatrutide 30 mg kit.

2 peer-reviewed publications. Links resolve to PubMed. DOIs are provided where available.

  1. [01]
    Jastreboff AM, et al.

    Triple-Hormone-Receptor Agonist Retatrutide for Obesity — Phase 2 Trial

    NEJM · 2023
  2. [02]
    Rosenstock J, et al.

    Retatrutide in people with type 2 diabetes — Phase 2

    The Lancet · 2023
§ F Questions

About this peptide.

For general site, shipping, and payment questions see the full FAQ.

Q.How does this differ from the 40 mg pen?
A.Same active peptide. The vial kit is lyophilised and requires reconstitution (bac water and syringes included); the pen is pre-filled and shipped cold-chain. Vial kits have a longer shelf life and do not require cold-chain shipping.
Research use only

This peptide is supplied by Omega Grade for in vitro laboratory research use. It is not a drug, food, cosmetic, or dietary supplement. It is not approved by the FDA, EMA, MHRA, PMDA, or any other regulatory authority for any therapeutic indication.

No claim of therapeutic benefit is made or implied. The material is not intended for human or veterinary consumption, administration, or any form of self-experimentation. By purchasing, you acknowledge the researcher terms and accept full responsibility for local import compliance and all handling.