Recorded market$79.45Recorded exact-size market estimate: 79.45 USD for one 10 mg container (7.945308 USD/mg). Arithmetic mean of 10 recorded supplier prices for this same vial or container size and formulation, with no extrapolation from other sizes. Supplier observation dates: Oct 10, 2026 UTC to Oct 11, 2026 UTC. Non-USD prices use ECB exchange rates dated October 9, 2026. Shipping excluded; supplier tax treatment is retained as recorded. This is a dated price comparison, not a former Peptide Serum price or an assurance of potency, purity, dosing or medical equivalence.Public price$79.00Member price$41.6047.6% lessMembers save $37.85 on this item vs. recorded market
Dual GIP/GLP-1 receptor agonist for metabolic research.
Supplier observation dates: Oct 10, 2026 UTC to Oct 11, 2026 UTC. This reference uses recorded prices for the same 10 mg vial or container and formulation. No prices are extrapolated from smaller or larger vials. Peptide Serum member unit prices refresh from the current catalog. Paid PRO membership is required for member pricing.
Member price
$4.16/mg47.6% less
Recorded market average$7.95/mg$79.45 USD / one 10 mg container
Recorded supplier prices10
View source observations and methodology
Peptide Serum reference:Member unit price (USD), available with verified paid PRO membership; excludes shipping and applicable taxes.Read from catalog: Oct 23, 2026 04:31 UTC.1 x 10 mg = 10 mg total.
Source: PeptideSerum-exact-size-market-comparison.xlsx. One selected single-container price per supplier domain, for the same labeled vial size and formulation. Blends match recorded component amounts. The arithmetic mean uses the first ten selected supplier prices in recorded Google discovery order, or the true smaller sample when ten could not be found. No size scaling, mg-to-IU conversion, pack discount or minimum price range is substituted.
The green percentage, when shown, compares the member price for every visitor: (recorded exact-size market average minus Peptide Serum member price) divided by the recorded market average. Unrounded values are used and the percentage is rounded down to one decimal. It is omitted when the member price is equal to or above the reference or the refreshed snapshot cannot be confirmed. Member pricing requires verified paid PRO membership.
These are dated price observations, not live available supplier offers. Shipping is excluded. Supplier tax treatment is retained as recorded and can differ. Memberships, clinical qualifications, ancillary supplies and availability can affect comparability; source notes retain these limitations. Some observations were sold out. Seller domains may be correlated through one manufacturer. This is not a revenue-ranked or complete-market survey.
Non-USD native prices are converted using ECB reference rates dated October 9, 2026. Recorded exchange-rate source. Original prices and currencies are shown below. Currency conversion does not make tax treatment or purchasing conditions identical.
Price observation; no COA authentication is implied by inclusion.
Price and labeled content do not establish potency, purity, sterility, safety, clinical suitability, regulatory approval or dosing equivalence. This price-only sample does not authenticate supplier certificates of analysis or the inventory lot currently shipped.
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A dual GIP and GLP-1 receptor agonist peptide studied in preclinical models of glucose regulation and energy metabolism.
Supplied sealed for laboratory handling. Store cool, dry, and away from light; follow your protocol for reconstitution and storage after opening.
For in-vitro laboratory research only. Not for human or veterinary use.
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Peptide Serum research library
Complete research for Tirzepatide
The updated research profile and study-exposure context appear below, with source links and evidence limitations.
Research-use contextThis source material is not medical advice, a treatment recommendation, or instructions for human or veterinary use.
Tirzepatide research, identity and evidence limits
Tirzepatide has strong clinical evidence for specific diabetes and weight-related indications. Approval belongs to defined prescription products, not generic research vials.
Identity and formulation
Tirzepatide activates GIP and GLP-1 receptors. It is a distinct molecule from semaglutide and from investigational multi-receptor agonists.
Mounjaro and Zepbound contain tirzepatide but have product-specific labeled indications and presentations. Matching the ingredient name is only one part of matching the approved product.
What the studies show
Large randomized trials establish clinically important effects in defined populations. The trials below answer different questions: weight reduction without diabetes, and glucose control in type-2 diabetes against a particular semaglutide comparator. Neither supports a universal claim that tirzepatide is best for every patient or outcome.
Selected directly relevant studies and their limits
SURMOUNT-1: 72-week double-blind randomized trial in 2,539 adults with obesity or qualifying overweight, excluding diabetes
Reading scope: PubMed bibliographic record and abstract
Mean weight reduction was substantially greater with tirzepatide than placebo across the studied groups; gastrointestinal adverse events were common, particularly during escalation.
The findings apply to a monitored trial with lifestyle intervention and specified eligibility; they are not a guarantee for an individual or an unverified product.
SURPASS-2: 40-week open-label randomized trial in 1,879 adults with type-2 diabetes
Reading scope: PubMed abstract
Tirzepatide produced greater HbA1c and weight reductions than the tested semaglutide comparator; gastrointestinal effects occurred with both treatments.
The comparator was semaglutide 1 mg, so this result cannot establish superiority over every semaglutide formulation, exposure or clinical outcome.
For the differences between a mechanism, a biomarker and a clinical outcome, see the evidence-reading guide.
How to interpret the findings
The August 2026 Mounjaro label covers glucose control in adults and children aged 10 years or older with type-2 diabetes, plus reduction of major cardiovascular events in high-risk adults with type-2 diabetes. Older summaries may omit these updates.
The current Zepbound label covers long-term weight reduction in qualifying adults and moderate-to-severe obstructive sleep apnea in adults with obesity, alongside diet and physical activity. These are specific indications rather than a general wellness approval.
Compare absolute changes, eligibility, duration and adverse-event discontinuations. Percent weight loss in a non-diabetic obesity trial cannot be assumed to match a different diabetic population or a brief course.
Safety context
Current labeling includes a boxed warning based on thyroid C-cell tumors in rats; human relevance is unknown. Personal or family medullary thyroid carcinoma history and MEN2 are contraindications.
Gastrointestinal effects are common, and current labels also address pancreatitis, dehydration-related kidney injury and interactions with glucose-lowering therapy. This is not an exhaustive clinical screening list.
Study exposure and units
Dose escalation, maintenance and follow-up are part of the trial design. A headline maintenance amount is not a complete treatment plan and should not be extracted for unsupervised use.
Different presentations contain different total quantities and concentrations. Current product-specific instructions and professional prescribing context take precedence over an old chart or a vendor’s vial-size label.
Match any reported amount or concentration to the exact material, route, population and duration in the original experiment. Read the guide to mass, volume and concentration for the meaning of common units. A calculation cannot establish an appropriate treatment or validate an untested formulation.
Product identity and report checks
Separate identity, concentration, total container content and delivered amount. These are different quantities, especially when comparing single-dose and multidose presentations.
A laboratory result on one research sample does not authenticate Mounjaro or Zepbound. Check the finished product and supply documentation rather than treating an ingredient certificate as proof of pharmaceutical equivalence.
Keep the clinical evidence and the supplier evidence separate. Use the report-verification steps to check the issuer and the batch questions to connect a tested sample with the product offered. Compare prices using the delivered-cost method rather than an isolated discount or purity percentage.
Peptide Serum operates a store as well as this research library. The supplier directory contains imported seller information; a listing is not laboratory certification. Read how this library is prepared and evaluate the documentation for the exact lot offered. A seller rating does not establish clinical safety or effectiveness.
Common questions
Did SURPASS-2 compare every available semaglutide option?
No. It compared a specified semaglutide 1 mg regimen in adults with type-2 diabetes. Broader superiority claims need directly relevant evidence.
Does FDA approval authenticate a research vial?
No. Approval concerns named pharmaceutical products and their specifications; it does not transfer through the ingredient name.
Are all trial weight-loss averages personal forecasts?
No. They are group estimates under defined study conditions, with variable responses and discontinuations.
This companion to the Tirzepatide research profile explains how to interpret experimental quantities. It provides no personal-use regimen.
Read exposure in its original context
Dose escalation, maintenance and follow-up are part of the trial design. A headline maintenance amount is not a complete treatment plan and should not be extracted for unsupervised use.
Different presentations contain different total quantities and concentrations. Current product-specific instructions and professional prescribing context take precedence over an old chart or a vendor’s vial-size label.
Find the tested material, formulation, route, study population, comparison group and observation period in the original paper. Exposure in a cell system or animal model does not supply a human starting amount, schedule or route.
Mass, volume and concentration describe different things
Mass describes an amount of material; concentration describes that amount per final solution volume. One milligram equals 1,000 micrograms. Neither a vial label nor arithmetic establishes identity, stability, sterility or an appropriate use.
The main profile links the selected primary sources, distinguishes the study designs and explains what the findings cannot show. A trial registration is a research plan, not a published result.
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