Reproductive Research

MT-2 (MELANOTAN II)

CAS 121062-08-61024.2 g/molSynthetic cyclic heptapeptide

MT-2 (Melanotan II) is a synthetic cyclic melanocortin analog studied in research models involving melanocortin receptor activity, pigmentation-related pathways, appetite signaling, energy-balance research, and neuroendocrine regulation.

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FOR RESEARCH USE ONLY (RUO). NOT FOR DIAGNOSTIC, MEDICAL, HUMAN, OR ANIMAL USE.

Technical Specifications

Compound Information

Molecular Profile

What is MT-2 (MELANOTAN II)?

CAS Number121062-08-6
Molecular FormulaC50H69N15O9
Molecular Weight1024.2g/mol
Compound ClassSynthetic cyclic heptapeptide
↗ View on PubChem

Storage Requirements

Stability Information

Store sealedProtect from lightKeep dry
2–8°C
Long-term storageLyophilized powder, as shipped. Keep sealed and refrigerated for maximum stability. Protect from light.
Cool & dry
Short-term storageStore sealed in a cool, dry place, protected from light.

For laboratory research use only. Not for human or veterinary use. Chemical data sourced from PubChem.

Peer-Reviewed Literature

The research behind this compound, cited in full.

Every reference below is a published, peer-reviewed record, linked to its PubMed entry. Provided for educational reference only, not product claims. For laboratory research use only.

  1. 01 Chemistry (Weinheim an der Bergstrasse, Germany) · 2024 5-Hydroxypyrroloindoline Affords Tryptathionine and 2,2'-bis-Indole Peptide Staples: Application to Melanotan-II Todorovic M, et al.
  2. 02 Neuroscience · 2006 Melanotan-II: Investigation of the inducer and facilitator effects on penile erection in anaesthetized rat Giuliano F, et al.
  3. 03 CEN case reports · 2020 Melanotan II: a possible cause of renal infarction: review of the literature and case report Peters B, et al.
  4. 04 BMJ case reports · 2019 Melanotan-induced priapism: a hard-earned tan Dreyer BA, et al.
  5. 05 Clinical toxicology (Philadelphia, Pa.) · 2012 Melanotan II injection resulting in systemic toxicity and rhabdomyolysis Nelson ME, et al.