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TIRZEPATIDE

(19)
Tirzepatide · 10MG · GLP-1 / GIP dual agonist
€90
Größe
Menge
  • ≥99 % Reinheit per HPLC
  • Janoshik-COA zu jeder Charge
  • Chargenrückverfolgung ab Synthese
  • In der EU synthetisiert
Auf Lager · Charge NZM-W-0019 · Versand in 3–5 Werktagen (EU)
Für Forschungszwecke verfügbar. Geliefert als lyophilisierte Forschungsverbindung mit chargenspezifischem COA.
Spezifikationen
Lot NumberNZM-W-0019
Purity99.6% (HPLC)
Verified byJanoshik Analytical
Synthesis Date2026-04-08
FormLyophilized powder
StorageBelow 16°C · sealed
Unabhängig im Labor geprüft

Jede Charge wird von Janoshik Analytical unabhängig per HPLC geprüft. Das COA ist chargenspezifisch und stammt vom prüfenden Labor.

ProduktPrüfdatumReinheitLabor
TIRZEPATIDE2026-04-0899.6% (HPLC)JanoshikBericht ansehen ↗
Lagerung & Handhabung

Lyophilisierte Peptide sollten bis zu 24 Monate unter 16 °C sowie licht- und feuchtigkeitsgeschützt gelagert werden. Nach der Rekonstitution gekühlt lagern und innerhalb von 30 Tagen verwenden.

FormLyophilisiertes Pulver
LagerungLyophilized: store below 16°C for up to 24 months. Reconstituted: refrigerate and use within 30 days.
HaltbarkeitVersiegelt bis zu 24 Monate
Rekonstitution

2mL bacteriostatic water for injection (BWI). Yields 5mg per 1.0mL.

Empfohlen2mL bacteriostatic water for injection (BWI). Yields 5mg per 1.0mL.
Produktdetails

The dual agonist
benchmark.

Tirzepatide is the most-studied GLP-1 / GIP dual agonist in metabolic research. Activating both receptors simultaneously produces a steeper glycemic response curve and stronger satiety signaling than GLP-1 alone - the basis for nearly every modern incretin-mimetic protocol design.

Lot-to-lot reproducibility is the primary reason researchers source TIRZEPATIDE from us. Each lot is HPLC-MS verified at ≥99% purity by Janoshik Analytical, with full sequence and mass-match documentation in the Certificate of Analysis.

Produktspezifikationen
VerbindungTirzepatide
Sequenzlänge39 amino acids
Molekulare Masse4813.5 Da
Modellierte Halbwertszeit~5 days (modeled)
Mechanismus / ForschungsklasseDual GLP-1R / GIPR agonist.
Lösungsmittel für die Laborhandhabung2mL bacteriostatic water for injection (BWI)
Berechnete KonzentrationYields 5mg per 1.0mL
LieferformatTirzepatide · 10MG · GLP-1/GIP lyophilisiertes Forschungsvial
Qualitätsstandards

Synthetisiert.
Verifiziert.
Dokumentiert.

Forschungspeptid-Vial mit Molekülstruktur
01
Geprüfte Reinheit
Jede Charge wird von Janoshik Analytical per HPLC geprüft. Unabhängige Verifizierung, nicht ausschließlich intern. Aktuelle Charge: 99.6% (HPLC).
02
Massenspektrometrisch bestätigt
Die Identität wird massenspektrometrisch bestätigt. Theoretische und gemessene Masse stimmen innerhalb einer Toleranz von 0,5 Da überein.
03
Lyophilisiert & versiegelt
Unter Inertgas vakuumgetrocknet und mit Crimpkappe versiegelt. Maximale Stabilität bis zur Rekonstitution. Kein Hitzeeintrag während des Versands.
04
Chargenrückverfolgbar
Von der Synthesecharge bis zur Auslieferung wird jeder Schritt dokumentiert. Charge NZM-W-0019 für die vollständige Rückverfolgbarkeit prüfen.
Studienlage

Durch Forschung gestützt.
In Ergebnissen messbar.

Jedes Themenfeld führt zur zitierten Literatur. Die Referenzen sind mit PubMed verlinkt.

up to 22.5%
Weight Reduction

Tirzepatide is a 39-amino-acid GLP-1 / GIP dual agonist. The dual receptor profile produces a steeper satiety-pathway response than single-pathway GLP-1, with downstream effects on body weight and adiposity in both research models and published clinical literature.

The reference SURMOUNT-1 trial reported a mean body-weight reduction of −22.5% from baseline at 72 weeks in the highest published study arm, with monotonic responses across published study arms. Results referenced for in-vitro / animal-model protocol design only.

Referenzen
  1. Jastreboff AM et al. Tirzepatide once weekly for the treatment of obesity. NEJM. 2022;387(3):205-216.PubMed ↗
  2. Frías JP et al. Tirzepatide vs Semaglutide once weekly in patients with type 2 diabetes. NEJM. 2021;385(6):503-515.PubMed ↗
A1C ↓ 1.9–2.6%
Glycemic Control

GLP-1 / GIP dual agonism amplifies insulin secretion and steepens the glycemic-response curve compared with single-pathway GLP-1 agonism. The reference literature reports HbA1c reductions of 1.87% to 2.59% across published weekly study arms in T2D research populations.

Referenzen
  1. Rosenstock J et al. Efficacy and safety of a novel dual GIP and GLP-1 receptor agonist tirzepatide in patients with type 2 diabetes. The Lancet. 2021;398(10295):143-155.PubMed ↗
up to 73%
Liver Fat Reduction

GLP-1 / GIP co-agonism engages hepatic lipid handling beyond what GLP-1 alone produces. The Tirzepatide MASLD substudy reported relative liver-fat reduction of up to 73% at 52 weeks measured by MRI-PDFF in the highest published study arm.

Referenzen
  1. Hartman ML et al. Effects of tirzepatide on biomarkers of NAFLD/NASH in patients with T2D. Diabetes Care. 2020;43(6):1352-1355.PubMed ↗
Improved
Metabolic Flexibility

Beyond direct glycemic effects, dual incretin agonism improves measured markers of insulin sensitivity (HOMA-IR) and metabolic flexibility in research populations - a profile that distinguishes Tirzepatide from single-pathway references in published comparison studies.

Referenzen
  1. Frías JP et al. SURPASS-2 trial. NEJM. 2021;385(6):503-515.PubMed ↗
Zu TIRZEPATIDE

Fragen?
Hier sind die Antworten.

(01)
Why dual agonism and not single GLP-1?
Adding GIP-receptor activation amplifies the satiety and glycemic effect of GLP-1 without proportionally amplifying GI side effects. Most published metabolic-research protocols using dual-pathway compounds reference Tirzepatide as the canonical example.
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(02)
How is the Certificate of Analysis verified?
Every lot is sent to Janoshik Analytical for independent HPLC and mass spectrometry testing. The COA you receive is theirs, not ours - searchable by lot number at coa.nzmlab.com with no account required.
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(03)
How is the product shipped?
Lyophilized vials are shipped temperature-controlled across the EU and UK. Store sealed vials below 16°C after delivery; normal 3–5 working day transit has no measurable impact on potency.
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(04)
Is this a research product?
Yes. NZM peptides are sold strictly for in vitro and animal research use only. They are not for human consumption, off-label use, or clinical application. Please consult applicable local regulations before ordering.
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(05)
Wie hoch ist der Preis für TIRZEPATIDE in Forschungsqualität?
Der aktuelle Preis für TIRZEPATIDE ist auf dieser Seite angegeben. Die Preisgestaltung gilt ausschließlich für die Forschungsbeschaffung und kann je nach Charge, Format und Verfügbarkeit variieren.
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(06)
Ist TIRZEPATIDE bei NZM Labs für Forschungszwecke erhältlich?
TIRZEPATIDE ist bei NZM Labs ausschließlich für In-vitro- und Tierforschung erhältlich. Nicht zur Anwendung am Menschen, zur klinischen Verwendung oder zur Selbstanwendung bestimmt.
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Rückmeldungen aus der Forschung

Aus dem Labor.

19 reviews for TIRZEPATIDE

  1. M. Virtanen –

    Third order from NZM. HPLC purity on the COA matched the lot number on the vial exactly — our QC ran independent verification and the numbers lined up within margin.

  2. A. Keller –

    Cold-chain packaging done properly, vials arrived sealed with intact stoppers. Reconstitution in bacteriostatic water was clean, no visible particulates.

  3. S. Lindqvist –

    Fast dispatch to Sweden. Documentation for institutional purchasing was handled without friction — invoice, COA and lot traceability all in order.

  4. J. Novak –

    Vial labelling is clear and the lot lookup works as advertised. One spec field on the datasheet was still marked pending, which we would like to see filled in.

  5. L. De Vries –

    Ordered for a receptor-binding assay panel. Lyophilized cake was uniform and dissolved rapidly. Mass spec on our end confirmed identity.

  6. R. Holm –

    Ordered TIRZEPATIDE for a research-protocol pilot. Arrived in 4 days temperature-controlled, vials sealed and properly lyophilized. Reconstituted cleanly in BWI with no haze. Will reorder.

  7. E. Kowalski –

    Procurement was straightforward as a lab customer. VAT invoice issued correctly, delivery to Poland in five working days.

  8. T. Bergström –

    Consistent between lots so far — three separate lots ordered and the COAs have stayed within tight purity bands.

  9. C. Meyer –

    Solid supplier. Packaging generous for the vial count. Minor gripe: tracking updates lagged a day behind actual transit.

  10. P. Jansen –

    The independent third-party COA is the reason we switched suppliers. Lot number searchable, report legible, no account needed.

  11. K. Tamm –

    Shipped to Estonia without customs friction. Vials arrived well within the stated transit window, contents in spec on arrival.

  12. N. Fischer –

    Reordered after an initial trial batch. Reconstituted solution stayed clear under refrigeration across the study window.

  13. O. Nielsen –

    Support answered a technical question about storage temperature the same day, with a reference instead of marketing language.

  14. H. Wagner –

    Product itself checks out — purity as stated. Delivery took nine days to Austria after a customs hold, longer than the estimate. Would order again but plan margins accordingly.

  15. D. Laine –

    Clean COA, accurate fill volumes, sensible packaging. Exactly what a research supplier should be: boring in the best way.

  16. G. Rossi –

    First order as an independent researcher. The verification portal and lot traceability gave enough confidence to proceed; the material matched documentation.

  17. F. Dubois –

    We compared three EU suppliers this quarter. NZM documentation and lot consistency were the differentiator.

  18. I. Petrov –

    Good material and fast handling. The spec table still has a few fields pending, which matters for our SOPs — support filled the gap by email.

  19. V. Andersen –

    Repeat institutional order. Temperature indicators in the shipment showed no excursion; QC accepted the lot without deviation.

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