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GLP-2 (T)

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Rigorous third-party testing

Every batch of our research chemicals and peptides undergoes independent third-party laboratory testing for purity and identity.

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For laboratory research use only by qualified professionals. Not for human or veterinary use. Not for ingestion, injection, topical application, diagnostic, therapeutic, prophylactic or cosmetic use.

GLP-2 (T) / Tirzepatide is supplied as a catalogued research material in 10mg, 20mg and 30mg. It is intended only for controlled analytical, biochemical and non-clinical laboratory workflows. The catalogue amount identifies the nominal vial presentation; it is not a dose or a use instruction.

“GLP-2 (T)” is a catalogue alias, not a chemical identity. Tirzepatide is a modified GIP-derived peptide and dual GIP/GLP-1 receptor agonist; GLP-2 is a different endogenous 33-residue hormone. Registry assignment requires confirmation of the complete modified structure and batch form [1–3].

Product identity

Identity must be assigned to the exact batch rather than to a marketed name alone. Sequence, terminal modifications, conjugation, salt or counter-ion, hydration state and excipients may change the applicable mass and registry identifiers. The batch CoA and SDS take precedence over literature identifiers shown below.

Chemical properties and registry information

PropertyValue
Name and synonymsTirzepatide; catalogue alias “GLP-2 (T)” only; not GLP-2
Material categoryModified GIP-derived dual GIP/GLP-1 receptor agonist; prescription-medicine active substance; high-risk research material
Sequence or structural definitionY–Aib–EGTFTSDYSI–Aib–LDKIAQK[acyl]–AFVQWLIAGGPSSGAPPPS–NH₂ (39-residue modified backbone)
Molecular formulaC225H348N48O68 for the defined tirzepatide parent structure; salts, counter-ions and solvates differ
Average molecular mass4813.53 g/mol average mass for the defined parent structure
CAS Registry Number2023788-19-2 for the defined tirzepatide structure, conditional on exact-form confirmation
PubChem CIDCID 156588324 for tirzepatide; use only after modified sequence, conjugate and exact-form confirmation
Structural featuresAib residues at positions 2 and 13, a linker/C20 fatty-diacid substituent on Lys20, and a C-terminal amide; exact conjugation and salt require batch confirmation
Physical formCatalogue vial; the exact physical state, salt or counter-ion and excipients are batch-specific and must be verified in the CoA and SDS.
Catalogue presentations10mg, 20mg and 30mg
Batch identity and quality documentationLot-specific identity and available analytical reports must be verified against the CoA entry associated with the exact product size and batch.
Intended useAnalytical, biochemical and non-clinical laboratory research only; all human and veterinary uses are excluded.

Where an identifier is qualified or omitted, no unambiguous exact-form public assignment has been confirmed. Do not transfer an identifier from a related analogue, salt, conjugate or formulation.

Research context and evidence status

What the literature supports

Defined tirzepatide reference material can support structural confirmation, impurity profiling, receptor-pharmacology research and analytical-method development. That research context requires exact modified-peptide identity and does not make a catalogue vial equivalent to a separately manufactured medicinal product [1,3].

Evidence limitations

Clinical evidence and authorization for branded tirzepatide medicines are formulation-, strength-, indication- and manufacturer-specific. They do not establish identity, purity, bioequivalence, safety, efficacy, dosage, administration or authorization for this catalogue material [3,4].

Tirzepatide is the active substance in the prescription medicine Mounjaro. A research-use label does not confer medicine authorization or permit unapproved human supply; FDA specifically warns about unapproved tirzepatide products and products falsely labelled “for research purposes.” Do not imply equivalence to Mounjaro or any authorised product [3,4].

ImportantResearch-use labeling does not itself determine the substance-specific legal status. The purchaser is responsible for confirming institutional authorization, local restrictions and lawful procurement, possession, import, export, storage and disposal.

Technical comparison

The comparison below is limited to structural and analytical distinctions. It does not compare clinical performance or recommend a use.

AspectThis catalogue materialComparator
IdentityTirzepatide, subject to confirmation of its complete modified structure and batch formNative human GLP-2 peptide
Structural distinctionModified 39-residue GIP-derived peptide with Aib residues and a lipid conjugateDistinct endogenous 33-residue GLP-2 hormone without tirzepatide's structure
Analytical implicationRequires intact-mass, modified-sequence, conjugation-site, amidation, purity and assay controlsGLP-2 sequence, mass and registry data cannot identify tirzepatide
What is not impliedNo conclusion about human or veterinary safety, efficacy, dosage, route, duration or interchangeability.No conclusion about human or veterinary safety, efficacy, dosage, route, duration or interchangeability.

Quality and batch documentation

Quality information is batch- and presentation-specific. Use only the report linked to the exact size and lot. A report listed for another size, lot or similarly named material must not be treated as evidence for this product.

Chromatographic area purity, identity, net peptide or analyte content, water or counter-ion content, sterility, endotoxin and elemental impurities are different measurements. One result does not establish the others. Only tests supported by a visible, matching report should be regarded as available.

Laboratory handling and storage

Store and handle only under the conditions stated on the product label, batch CoA and SDS. Keep the container secured, correctly identified and protected from contamination. Do not infer storage, solvent compatibility or stability from a related compound.

This page intentionally provides no reconstitution, administration or dosing instructions. Laboratory preparation, analytical method selection, risk assessment, personal protective equipment and waste disposal must be defined by the qualified institution and the applicable SDS.

Regulatory and legal status

This catalogue material is not offered as a medicine, medical device, in-vitro diagnostic, food, dietary supplement, cosmetic or veterinary product. It is not intended to diagnose, treat, cure, mitigate or prevent any disease or condition.

A research designation does not override medicinal-product, controlled-substance, chemical, customs or other substance-specific rules. Availability may be restricted by jurisdiction and by the purchaser's verified professional or institutional status.

Sources and references

References document identity and research context only. They do not constitute instructions for use or evidence that this catalogue batch is suitable for any human or veterinary purpose.

  1. [1] PubChem. Tirzepatide structure and registry record, CID 156588324.
  2. [2] IUPHAR/BPS Guide to Pharmacology. GLP-2 structure: distinct endogenous 33-residue peptide.
  3. [3] European Medicines Agency. Mounjaro: authorised prescription tirzepatide medicinal product.
  4. [4] U.S. FDA. Concerns with unapproved GLP-1 drugs, including false research-use labelling.

Frequently Asked Questions

What is this material intended for?

Controlled laboratory research by qualified professionals, including substantiated analytical, biochemical or non-clinical workflows. It is not intended for personal use.

Is the amount shown on the vial a dosage?

No. It is a nominal catalogue presentation used to identify the product variant. It is not a dose, concentration, administration schedule or preparation instruction.

Do the CAS number and PubChem CID apply to every batch form?

Only when the exact sequence or structure, termini, conjugation, salt or counter-ion and hydration state match. The batch CoA and SDS govern; a related-compound identifier must not be substituted.

What does an analytical purity result mean?

It is method- and report-specific. For example, an HPLC area percentage is not automatically the same as identity, net content, sterility, endotoxin status or absence of elemental impurities.

How should the material be stored and handled?

Follow the exact label, batch CoA and SDS, together with the institution's risk assessment. This page does not provide reconstitution or administration guidance.

May this material be used in humans or animals?

No. Human and veterinary use, including ingestion, injection, topical application, diagnosis, treatment, prevention and cosmetic use, is expressly excluded.

RESEARCH USE ONLY. NOT FOR HUMAN OR VETERINARY USE. THE PRODUCT NAME, VIAL AMOUNT AND LITERATURE REFERENCES MUST NOT BE INTERPRETED AS A DOSAGE, ADMINISTRATION INSTRUCTION OR MEDICAL CLAIM.

LABORATORY REAGENT – FOR RESEARCH PURPOSES ONLY

This product is not a drug or food and should be handled by qualified professionals in laboratory conditions. All product information is provided for educational purposes only.

Description

Information:

  • The product (substance) isn't a food or diet supplement and is not suitable for human consumption.
  • Keep out of children's reach
  • Keep container tightly closed.
  • Store in a dry, cool and shaded place; protect from moisture.
  • Store only in the original container.
  • Avoid contact during pregnancy and breast feeding.
  • Consult a doctor in the event of feeling unwell or having adverse effects related to the contact with the substance.