Tirzepatide 15mg research vial
SwissNova Labs
Tirzepatide 15mg · 15mg
≥99% Purity · COA Included
GLP-1

Tirzepatide 15mg

Purity: 99.5%
Size: 15mg
Grade: Research
Form: Lyophilized
SwissNova Labs · Research Grade
GLP-1NEW!

Tirzepatide 15mg

Dual GIP/GLP-1 receptor agonist — mid-range vial covering full titration through early maintenance.

Dual GIP/GLP-1 agonism — activates two complementary incretin pathways for superior metabolic response vs GLP-1 monotherapyWeight reduction — SURMOUNT-1 demonstrated 22.5% mean body weight reduction at 72 weeks, the highest of any approved weight-loss drugGlucose control — reduces HbA1c by up to 2.46% in T2D research models, outperforming semaglutide in head-to-head trialsAppetite suppression — dual receptor activation produces stronger satiety signaling than single-receptor GLP-1 agonists
Strength15mg
$75.00
15mg · Research use only
Compound Specifications
Purity99.5%
Molecular Weight4813.5 Da
Vial Size15mg
SequenceDual GIP/GLP-1 agonist (C20 fatty diacid chain)
Vial Supply
Duration~10 weeks supply
Week 1Week 10
Why Researchers Choose This Compound

Key Benefits

01
Dual GIP/GLP-1 agonism

activates two complementary incretin pathways for superior metabolic response vs GLP-1 monotherapy

02
Weight reduction

SURMOUNT-1 demonstrated 22.5% mean body weight reduction at 72 weeks, the highest of any approved weight-loss drug

03
Glucose control

reduces HbA1c by up to 2.46% in T2D research models, outperforming semaglutide in head-to-head trials

04
Appetite suppression

dual receptor activation produces stronger satiety signaling than single-receptor GLP-1 agonists

Mechanism of Action

Active Signaling Pathway

BioHuman Research Dossier
Clinical DataResearch use only — not for human consumption

Investigated Pathways

GLP-1 ReceptorGIP ReceptorGlucagon ReceptorAdipose Metabolism

Proposed Mechanism

Tirzepatide is a 39-amino acid peptide with a C20 fatty diacid chain enabling albumin binding and a ~5-day half-life. It acts as a dual agonist at both GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 receptors. GIP receptor activation adds complementary metabolic effects — enhanced insulin secretion, reduced glucagon, and direct adipocyte signaling — producing greater weight reduction than GLP-1 agonism alone.

Research Highlights

  • SURMOUNT-1 trial: 22.5% mean body weight reduction at 15 mg/week over 72 weeks — the highest of any approved weight-loss drug at time of publication
  • SURPASS-2 trial: tirzepatide 15 mg reduced HbA1c by 2.46% vs 1.86% for semaglutide 1 mg
  • FDA approved as Mounjaro (T2D) in 2022 and Zepbound (obesity) in 2023
  • Dual receptor mechanism produces additive metabolic effects beyond GLP-1 monotherapy
Clinical DataEvidence Strength

Randomised controlled trial data available. Results are compound-specific and do not constitute treatment guidance.

Research FocusMetabolic & AMPK
Metabolic & AMPK body system research map
Adipose & MetabolismMitochondrial Health

For laboratory research only

All Research Systems →

For research use only — not for human consumption. No treatment claims.

Full Research Hub →
Supply Calculator

How long will one vial last?

Based on standard research protocols, here's exactly what to expect from a single 15mg vial — and when to plan your next order.

One vial lasts
10
weeks
Approximately 2 months of supply at standard protocol volumes.
Reorder around week 9 to avoid running out
Your supply timeline15mg vial
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Vial supply estimate is based on standard research protocol volumes. Actual duration will vary based on your specific protocol design.

Research Literature

Scientific Background

Mechanism of Action

Tirzepatide is a 39-amino acid peptide with a C20 fatty diacid chain enabling albumin binding and a ~5-day half-life. It acts as a dual agonist at both GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 receptors. GIP receptor activation adds complementary metabolic effects — enhanced insulin secretion, reduced glucagon, and direct adipocyte signaling — producing greater weight reduction than GLP-1 agonism alone.

Clinical Context

Tirzepatide represents the second generation of incretin-based therapy. Its dual mechanism — acting on both GIP and GLP-1 receptors — produces metabolic effects that exceed GLP-1 monotherapy in head-to-head trials. The 15mg vial bridges the full titration phase and the initial maintenance step, reducing the number of vials needed in the first 12 weeks of a protocol.

Research Highlights

  • SURMOUNT-1 trial: 22.5% mean body weight reduction at 15 mg/week over 72 weeks — the highest of any approved weight-loss drug at time of publication
  • SURPASS-2 trial: tirzepatide 15 mg reduced HbA1c by 2.46% vs 1.86% for semaglutide 1 mg
  • FDA approved as Mounjaro (T2D) in 2022 and Zepbound (obesity) in 2023
  • Dual receptor mechanism produces additive metabolic effects beyond GLP-1 monotherapy

Storage & Reconstitution

Store lyophilized at -20°C. Reconstitute with bacteriostatic water (BAC water). Recommended: add 3 mL BAC water to the 15 mg vial → yields 5 mg/mL. On a 100-unit insulin syringe, 1 unit = 50 mcg; 50 units = 2.5 mg (starter dose); 100 units = 5 mg (escalation dose). Inject BAC water slowly down the vial wall — do not shake, gently swirl. Stable 28 days at 2–8°C after reconstitution. Do not freeze reconstituted solution.

Peer-Reviewed Research

Key Studies

2022New England Journal of Medicine

Tirzepatide Once Weekly for the Treatment of Obesity (SURMOUNT-1)

Jastreboff AM et al.

Tirzepatide 15 mg/week produced 20.9% mean body weight reduction at 72 weeks — highest of any approved weight-loss drug at time of publication.

PubMed →
2021New England Journal of Medicine

Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes (SURPASS-2)

Frías JP et al.

Tirzepatide 15 mg reduced HbA1c by 2.46% vs 1.86% for semaglutide 1 mg — superior glycemic control in head-to-head trial.

PubMed →
2022Lancet

Tirzepatide cardiovascular outcomes trial (SURPASS-CVOT)

Dahl D et al.

Tirzepatide demonstrated favorable cardiometabolic profile with significant reductions in cardiovascular risk markers.

PubMed →
Absorption & Distribution

Pharmacokinetics

PK Parameters
Bioavailability~80% SubQ
Peak Plasma8–72 hours post-injection
Half-life~5 days; C20 fatty diacid chain enables albumin binding for once-weekly dosing
ClearanceProteolytic degradation; hepatic/renal clearance; albumin binding
Volume of Distribution~10 L (limited by albumin binding)
What this means

Bioavailability indicates how much of the compound reaches systemic circulation. Peak plasma is when blood levels are highest. Half-life determines dosing frequency — compounds with short half-lives require more frequent dosing to maintain therapeutic levels.

The volume of distribution reflects how widely the compound distributes into tissues. A higher Vd means the compound concentrates in tissues rather than staying in plasma.

Molecular Targets

Receptor Binding Profile

GLP-1 receptorAgonist

Appetite suppression, insulin secretion, gastric emptying delay

GIP receptorAgonist

Enhanced insulin secretion, adipocyte lipolysis — dual mechanism superior to GLP-1 alone

Hypothalamic satiety centersIndirect modulation

Stronger satiety signaling than single-receptor GLP-1 agonists

Pancreatic β-cellsStimulation

Glucose-dependent insulin secretion via dual incretin pathway activation

Safety Profile

Side Effects & Adverse Events

Common
  • Nausea (33%)
  • Diarrhea (23%)
  • Vomiting (18%)
  • Constipation (17%)
Uncommon
  • Injection site reactions
  • Decreased appetite
  • Fatigue
Serious
  • Pancreatitis (rare)
  • Gallbladder disease
  • Thyroid C-cell tumors (rodent data)
NOTE:Superior weight loss vs semaglutide in head-to-head trials. GI profile similar to semaglutide. Titrate over 20 weeks to minimize GI effects.
Research Safety

Contraindications & Interactions

Absolute Contraindications
Personal or family history of MTC or MEN2History of pancreatitis
Relative Contraindications
GastroparesisSevere GI diseaseDiabetic retinopathy
Drug Interactions
Insulin (hypoglycemia risk)Sulfonylureas (hypoglycemia risk)Oral contraceptives (reduced absorption — use backup contraception)
NOTE:Titrate over 20 weeks to minimize GI effects. FDA-approved as Mounjaro (T2D) and Zepbound (obesity).
Stack Protocols

Synergistic Compounds

Lipo-C

Lipo-C provides B12 repletion and lipotropic support during tirzepatide caloric restriction.

Lipo-C 1 mL IM 2–3× per week alongside weekly tirzepatide injection.

View Compound →
Cagrilintide

Adding amylin receptor agonism to dual GIP/GLP-1 agonism for triple-mechanism weight loss.

Tirzepatide 5 mg + Cagrilintide 1.2 mg, both once weekly SubQ — titrate each independently.

View Compound →
Sourcing & Testing

Transparent Global Sourcing

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Manufactured

Sourced through our manufacturing partner in China

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Independent Testing

Analytical reports available from Janoshik Analytical

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Batch Verification

Batch-specific COAs with online verification via janoshik.com

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US Fulfillment

Orders fulfilled from the United States

Testing documentation varies by product and batch. Customers may review available reports and verification information before ordering. COA task numbers and verification keys can be confirmed directly at janoshik.com/verification. For research use only — not for human consumption.
RESEARCH USE ONLY:All products are sold strictly for in vitro research and laboratory use. Not intended for human consumption, clinical use, diagnosis, treatment, or prevention of any disease or condition. By purchasing, you confirm you are a qualified researcher and will use these compounds in accordance with all applicable laws and regulations.