We report net peptide content, not just purity — so the milligrams you dose aren't padded with water and counter-ion. RP-HPLC purity and ESI-MS identity, on a lot-numbered COA.
Net peptide content, not just purity — RP-HPLC + ESI-MS, lot-numbered COA.
Net peptide content on every lot's COA.
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GIP / GLP-1 dual receptor agonist · 39-mer metabolic research peptide
Overview
Lyochem supplies Tirzepatide as a sequence-verified analytical reference standard for incretin-pharmacology research. The molecule is a 39-residue synthetic peptide carrying a C20 fatty-diacid substituent on a lysine side chain; that lipidation governs the reversible albumin binding and the long circulating half-life that set it apart from the GLP-1 mono-agonist series. Functionally it behaves as a balanced co-agonist at both the GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 receptors, which is why the metabolic-research literature treats it as the reference dual-incretin entity. It is the active ingredient of approved finished drugs marketed under separate names, but the material here is characterized and labelled strictly as a research reagent — not a dosage form. Each lot is released against its own analytical packet rather than as an undifferentiated bulk fill: RP-HPLC purity (gradient method, UV 214 nm), ESI-MS identity within 0.5 Da of the theoretical 4813.45 g/mol, sequence confirmation by LC-MS/MS, counter-ion content, peptide content (% net peptide), and water content by Karl Fischer. Because the deletion sequences from a 39-mer SPPS run co-elute closely and are not separable by intact mass alone, the tandem-MS b/y-ion ladder is the test that demonstrates sequence identity, and Lyochem recommends requesting it on the first lot from any new source. Bacterial endotoxin (LAL) is an on-request add-on for in vivo metabolic-model work. Fills run mg-scale for reproducible aliquoting across a study series; this is reference-grade research material, distinct from compounding-scale API supply.
Applications & buyer fit
GLP-1 and metabolic-peptide buyers run incretin-pathway, body-composition, glucose-regulation, and energy-expenditure studies. Because the receptor pharmacology is sequence-sensitive, qualifying a new source means confirming identity within 0.5 Da of theoretical by ESI-MS, sequence verification by tandem MS on the first lot, and lot-to-lot consistency for reproducible metabolic research. Lyochem supplies this class reference-grade and mg-scale — distinct from compounding-grade (g/kg) API supply.
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
Regulatory note
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. Tirzepatide is the active ingredient of approved finished drugs under separate brand names, but the bulk active supplied here is a research reagent; buyers are responsible for institutional biosafety review and verifying import eligibility in the destination market.
Selected literature
Frequently asked questions
Tirzepatide CAS is 2023788-19-2; molecular formula C225H348N48O68; average molecular weight 4813.45 g/mol. It is a 39-amino-acid synthetic peptide carrying a C20 fatty-diacid albumin-binding moiety on a lysine side chain. Every Lyochem lot confirms identity by ESI-MS within 0.5 Da of the theoretical mass, with the full reference set (CAS, formula, MW, sequence-verification result) reproduced on the batch COA so the value can be cited directly in a methods section.
Mass spec alone confirms the intact mass but cannot separate a correctly-synthesized 39-mer from closely-related deletion or aspartimide by-products that co-elute on RP-HPLC. Lyochem confirms identity with a combination of RP-HPLC purity (gradient method, 214 nm), ESI-MS within 0.5 Da of 4813.45 g/mol, and sequence verification by LC-MS/MS (b/y-ion ladder). For a lab qualifying a new source, request the tandem-MS sequence data on the first lot; that is the test that demonstrates the supplied sequence matches the labelled sequence rather than only matching the labelled mass.
Both are once-weekly fatty-acid-conjugated incretin-pathway peptides, but the receptor profile differs: Semaglutide is a selective GLP-1 mono-agonist (31 amino acids, C18 fatty-diacid), while Tirzepatide is a balanced GIP / GLP-1 dual agonist (39 amino acids, C20 fatty-diacid). In published metabolic-research readouts the dual-incretin mechanism produces larger effects on glucose handling and body composition than the GLP-1 mono-agonist class at comparable exposures, which is the reason it is a frequent comparator in incretin-pharmacology studies.
Lyochem supplies Tirzepatide as a reference-grade research reagent, mg-scale, characterized lot-by-lot for reproducible bench and in vivo metabolic research and labelled strictly Research Use Only. That is a different scope from compounding-grade or kg-scale API supply intended for finished-dose preparation. Buyers whose workflow is pharmacy-compounding rather than research should source through a supplier scoped to that use; Lyochem's lots are scoped to the research-documentation chain (HPLC trace, mass spec, sequence verification, stability) that a lab needs to cite in a paper.
Related peptides
GLP-1 receptor agonist · 31-mer metabolic research peptide
GIP / GLP-1 / glucagon tri-agonist · 39-mer metabolic research peptide
Modified HGH fragment 176–191 (anti-obesity drug candidate)