Ask sales for the lot-numbered COA. Net peptide content, RP-HPLC, ESI-MS, or other results appear only when they are part of that batch's agreed analytical scope.
Lot-numbered COA available; the certificate states the tests actually completed.
Batch COA records net peptide content when included in the agreed specification.
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GIP / GLP-1 / glucagon tri-agonist · 39-mer metabolic research peptide
Overview
Lyochem supplies Retatrutide (investigational development code LY3437943) as a sequence-verified analytical reference standard for tri-agonist incretin research. It is a 39-residue synthetic peptide that engages three receptors — GIP, GLP-1, and glucagon — and it is the glucagon arm that separates it from the dual-agonist entities, layering a direct hepatic-energy-expenditure mechanism on top of the incretin signalling; that third axis is the mechanistic rationale offered for the larger body-composition readouts in its published Phase 2 metabolic-research literature. As an investigational molecule it is not an approved finished drug anywhere, and the material here is characterized and labelled strictly as a research reagent. Production volume for this peptide is far smaller than for Semaglutide or Tirzepatide, so the closely-eluting deletion-sequence profile of a low-throughput 39-mer SPPS run is the dominant analytical concern. Where included in the agreed analytical scope, the applicable batch record can contain RP-HPLC purity (gradient method, UV 214 nm), ESI-MS identity, sequence confirmation by LC-MS/MS, counter-ion content, and water content by Karl Fischer — with the tandem-MS sequence read available when required by an agreed qualification protocol, since intact mass alone cannot resolve a correct 39-mer from its deletion by-products. Bacterial endotoxin (LAL) and microbial limits are available on request for in vivo metabolic-model work. Fills run mg-scale for reproducible aliquoting; this is reference-grade research material, distinct from compounding-scale API supply.
Applications & buyer fit
GLP-1 and metabolic-peptide buyers run incretin-pathway and related research. Ask sales for the COA matched to the offered or supplied lot. If the buyer's written procedure requires tandem-MS sequence evidence or other expanded methods, agree the analytical scope, timing, and cost before quotation.
Academic Laboratories
Universities, medical schools, and government research institutes qualifying a reference standard for a method-development or in vivo workflow.
Biotech R&D Groups
Preclinical biotech and pharmaceutical discovery teams sourcing characterized peptides for receptor-pharmacology, screening, and method-development campaigns.
Every release ships with its own batch-specific CoA — identity, purity, and the analytical scope agreed at quote stage, tied to the exact lot you receive.
Review a representative batch CoA before you order, so you can confirm the packet matches what your method or sponsor audit needs.
Supplied strictly as a research reagent to research institutions — not a finished dosage form and not for human administration. Buyer qualification runs at the inquiry stage.
Specifications
Documentation available on request
Product- and strength-matched first-page previews are shown separately from the Batch COA. Contact sales with the report number for the complete high-resolution file.
Third-party testing in Tianjin
Independent HPLC and mass-spectrometry reports from Qorix , the professional, authoritative third-party analytical laboratory at tjqxgd.com, affiliated with the Tianjin International Joint Academy of Biomedicine.
Regulatory note
Investigational compound in clinical development; not approved as a finished drug in any jurisdiction. Sold for Research Use Only under the receiving laboratory's institutional and jurisdictional regulations — not a finished dosage form and not labelled for human administration. Buyers are responsible for institutional biosafety review and verifying import eligibility in the destination market.
Selected literature
Frequently asked questions
At this length, the impurities that matter most are near-isobaric to the target. Single-residue deletions and aspartimide rearrangements co-elute closely on RP-HPLC and can fall within the resolution of intact-mass measurement, so a clean ESI-MS peak does not by itself prove the labelled sequence. We therefore run LC-MS/MS on the lot: the b/y-ion ladder confirms residue order across the full 39-mer and demonstrates the supplied sequence matches the label. The certificate carries the RP-HPLC purity, the ESI-MS intact mass against the theoretical value for the supplied form, and the tandem-MS sequence result together.
The isolated material is a salt, and the counter-ion and residual water vary with the purification route and source. Those components change the average mass and the effective molecular formula of what is actually in the vial, so a single fixed catalog figure would misrepresent net peptide content for weighing. For an investigational lipidated 39-mer this matters directly to concentration accuracy in metabolic-model work. We confirm identity by ESI-MS against the theoretical mass for the specific supplied form and reproduce that lot-specific value on the certificate, so a lab cites the measured number for its actual material rather than a nominal one.
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