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Mazdutide
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Standardized safety protocols and material specifications for professional use.

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Certificate of Analysis

Purity verified via High-Performance Liquid Chromatography (HPLC) for #myo-mazdutide-10mg

Official Product Data Sheet

Mazdutide (10mg)

Research Grade >99.2% Purity

Vial Contents
10 mg Mazdutide (lyophilized powder)
Includes
3 ml bacteriostatic water for reconstitution
Form
Lyophilized white powder for optimal stability
Purity
≥99%, third-party tested (COA available)
Sequence
Long-acting GLP-1/Glucagon dual receptor agonist
Molecular Formula
Proprietary peptide structure
Molecular Mass
~4800 g/mol
CAS No.
2413147-09-6
Solubility
Reconstitute with sterile/bacteriostatic water (3 ml for ~3.33 mg/mL)
Storage
Lyophilized frozen at −20°C; reconstituted refrigerated at 2–8°C for up to 28 days

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Scientific Background

Mazdutide (IBI362) is a once-weekly injectable dual agonist targeting both GLP-1 (glucagon-like peptide-1) and glucagon (GCGR) receptors, developed by Innovent Biologics. This dual-receptor mechanism distinguishes it from pure GLP-1 agonists by adding glucagon receptor activation, which increases energy expenditure and enhances hepatic fat mobilization beyond appetite suppression alone.

The GLP-1 component reduces appetite, slows gastric emptying, and improves insulin sensitivity — mechanisms shared with semaglutide. The GCGR component provides a distinct metabolic advantage by increasing basal metabolic rate, promoting hepatic gluconeogenesis suppression, and mobilizing visceral fat through cAMP-mediated lipolysis. This dual action creates synergistic weight loss and metabolic benefits that address both energy intake (GLP-1) and energy expenditure (GCGR).

This 10 mg vial is designed for maintenance dosing in established research protocols where weekly doses of 3–4.5 mg have been titrated and tolerability confirmed. It provides a larger supply per vial, making it cost-effective for longer-duration research programs. Phase 2 and 3 clinical trials have demonstrated significant weight loss (up to ~19%) and cardiometabolic improvements in participants with overweight and obesity.

Intended Research Use

  • GLP-1 and glucagon dual receptor agonism and metabolic pathway research
  • Body weight reduction via appetite suppression and increased energy expenditure
  • Insulin sensitivity and glycemic control research in type 2 diabetes models
  • Hepatic fat mobilization and NAFLD/MASH pathophysiology studies
  • Long-duration metabolic research protocols requiring larger vial quantities
  • Cardiometabolic risk factor modulation (blood pressure, lipids, HbA1c)

Clinical Evidence: Mazdutide Phase 2 trials showed ~11% weight loss at 3 mg/week and up to 19% at 4.5 mg/week over 24 weeks. The 10 mg vial at 3.33 mg/mL concentration provides approximately 2–3 maintenance doses (3–4.5 mg each), making it well-suited for established protocols. Superior hepatic fat reduction versus GLP-1 monotherapy is a key differentiator supported by GCGR-mediated lipolysis.

warning

FOR RESEARCH USE ONLY. This product is intended for laboratory research purposes only and is not for human consumption, medical, or diagnostic use.

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