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GLP-2 T 30mg

Research Specifications

IUPAC Name:
Tirzepatide (LY3298176)
CAS Number:
2023788-19-2
Molecular Weight:
4813.5 Da
Side Chain:
C20 fatty diacid (enables albumin binding, once-weekly dosing)
Form:
Lyophilized powder
Purity:
≥98% (HPLC verified)
Storage:
−20°C long-term / 4°C up to 4 weeks reconstituted
Price per mg:
$9.33

GLP-2 T 30mg

Dual GLP-1/GIP receptor agonist. SURMOUNT-1 trial: 22.5% mean body weight reduction at 15mg — the first approved dual incretin.

−22.5%

Mean Weight Reduction

SURMOUNT-1, 15mg (NEJM 2022)

2 receptors

Simultaneous Targets

GLP-1 + GIP

4813 Da

Molecular Weight

NCBI PubChem

Receptor Targets

GLP-1R↓ appetite, ↓ gastric emptying, ↑ insulin sensitivity
GIPR↑ insulin secretion, ↑ adipocyte lipolysis, ↑ satiety
$279.99In Stock
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≥98% Purity Verified Free Shipping $200+ HPLC Tested

Dual Incretin Agonism: GLP-1 & GIP Receptors

Tirzepatide (LY3298176) is a 39-amino-acid synthetic peptide with a C20 fatty diacid side-chain that enables once-weekly dosing via albumin binding. It simultaneously activates GLP-1 receptors (reducing appetite, slowing gastric emptying, improving insulin sensitivity) and GIP receptors (enhancing glucose-stimulated insulin secretion and promoting adipocyte lipolysis). This dual mechanism outperforms GLP-1 monotherapy in head-to-head trials. It lacks the glucagon receptor component of Retatrutide, making it a 'step 2' rather than 'step 3' in the receptor-targeting progression.

Research Highlights

SURMOUNT-1 Trial (NEJM 2022)

2,539 participants across 72 weeks. The 15mg dose group achieved 22.5% mean body weight reduction vs 2.4% placebo. 37% of participants achieved ≥25% weight loss. The trial also demonstrated significant improvements in waist circumference, blood pressure, lipids, and fasting glucose — a comprehensive cardiometabolic profile.

GIP Receptor Advantage Over Semaglutide

Direct comparison trial (SURPASS-2) showed Tirzepatide 15mg produced 5.5% greater weight loss than Semaglutide 1mg at 40 weeks. The additional GIP agonism drives adipocyte-level lipolysis and may improve insulin secretion more effectively in high-fat dietary contexts.

Body Composition

SURMOUNT body composition sub-analysis showed the majority of weight loss was from fat mass, with lean mass preserved at a higher percentage than caloric restriction alone — consistent with GIP's hypothesized role in adipose-specific energy mobilization.

Research FAQ

What is the difference between Tirzepatide and Semaglutide?
Semaglutide is a GLP-1 only agonist (14.9% mean weight loss in STEP-1). Tirzepatide adds GIP receptor agonism, producing 22.5% mean weight loss in SURMOUNT-1. The additional GIP mechanism enhances adipocyte lipolysis and glucose-stimulated insulin secretion beyond what GLP-1 alone achieves.
How does Tirzepatide compare to Retatrutide?
Tirzepatide is a dual agonist (GLP-1 + GIP). Retatrutide adds a third receptor — glucagon — which drives thermogenesis and hepatic fat oxidation. Phase 2 data shows Retatrutide achieving 24.2% vs Tirzepatide's 22.5% — roughly 2 percentage points higher, attributed primarily to the glucagon component.
What is the 30mg vial pricing per mg?
At $9.33/mg, this 30mg vial offers bulk research value for Tirzepatide research protocols.
What is the C20 fatty diacid modification on Tirzepatide?
Tirzepatide's C20 fatty diacid side chain enables non-covalent binding to serum albumin, dramatically extending its half-life to ~5 days and enabling once-weekly subcutaneous dosing. This lipidation strategy was adopted from Semaglutide's design and refined for Tirzepatide.

Research Use Only. This product is intended for in-vitro laboratory research only. Not for human consumption, injection, or therapeutic use. Not medical advice. Always consult applicable regulations in your jurisdiction.

Price Comparison

SupplierPurityPriceShipping
Apollo (via ClavTides)>98% HPLC$279.99Free over $200
Generic Research SuppliersVaries (often <95%)Similar–HigherVaries
Pharmaceutical (Rx only)Pharmaceutical gradeNot available for researchRx required

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