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MT-II (Melanotan II)

Melanocortin receptor research peptide for controlled laboratory studies.

Dose
10 mg
Batch
268010

MT-II (Melanotan II)

Acetyl-[Nle4, Asp5, D-Phe7, Lys10]-cyclo-α-MSH(4–10) amide (melanotan-II, MT-II)

4.7 · 143 researcher reviews

For research purposes only — This compound is not FDA approved. All data presented is from clinical trials for educational reference.

Melanocortin receptor research peptide for controlled laboratory studies.

€4510 mg / vial

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Batch tested
HPLC + LC-MS
Same-day
Dispatch · 1–3 business days
COA included
Batch-traceable
Order quantity

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Certificate of Analysis · 268010On fileEU lab
Lab
Janoshik Analytical
Methods
HPLC · LC-MS
1 test on fileBatch record →

For laboratory research use only. Not for human consumption.

Compound information

Technical specifications

Molecular profile · MT-II (Melanotan II)
Type
Peptide
Scientific name
Acetyl-[Nle4, Asp5, D-Phe7, Lys10]-cyclo-α-MSH(4–10) amide (melanotan-II, MT-II)
Amino acids
7
Sequence
Ac-Nle-c[Asp-His-D-Phe-Arg-Trp-Lys]-NH2
Molecular weight
1024.2 g/mol
Formula
C50H69N15O9
CAS
121062-08-6
Origin
Synthetic cyclic lactam heptapeptide analogue of α-MSH residues 4–10, designed at the University of Arizona (Al-Obeidi/Hruby, 1989); the Asp5–Lys10 lactam bridge forms a 23-membered ring.
Storage requirements
Lyophilized (powder)
-20°C · stable long-term; keep sealed, desiccated and protected from light
Reconstituted
2-8°C · use within 30 days; avoid repeated freeze-thaw cycles
Room temperature
Lyophilized powder tolerates short shipping excursions of a few days, but peptide in solution degrades within days at room temperature — reconstituted vials should not be held above 8°C.
Sources & references

Peer-reviewed research

Published research and registered trials involving this compound. Provided for educational reference only — none of it is a claim about this product.

  • Journal of the American Chemical Society
    Design of a new class of superpotent cyclic α-melanotropins based on quenched dynamic simulations
    Al-Obeidi F, Hadley M, Pettitt B, Hruby V
    1989DOI: 10.1021/ja00191a044
  • Journal of Medicinal Chemistry
    Potent and prolonged acting cyclic lactam analogues of alpha-melanotropin: design based on molecular dynamics
    Al-Obeidi F, Castrucci AM, Hadley ME, Hruby VJ
    1989DOI: 10.1021/jm00132a010PMID: 2555512
  • Life Sciences
    Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study
    Dorr RT, Lines R, Levine N, Brooks C, Xiang L, Hruby VJ, Hadley ME
    1996DOI: 10.1016/0024-3205(96)00160-9PMID: 8637402
  • Nature
    Role of melanocortinergic neurons in feeding and the agouti obesity syndrome
    Fan W, Boston BA, Kesterson RA, Hruby VJ, Cone RD
    1997DOI: 10.1038/385165a0PMID: 8990120
  • The Journal of Urology
    Synthetic melanotropic peptide initiates erections in men with psychogenic erectile dysfunction: double-blind, placebo controlled crossover study
    Wessells H, Fuciarelli K, Hansen J, Hadley ME, Hruby VJ, Dorr R, Levine N
    1998PMID: 9679884
  • Urology
    Effect of an alpha-melanocyte stimulating hormone analog on penile erection and sexual desire in men with organic erectile dysfunction
    Wessells H, Gralnek D, Dorr R, Hruby VJ, Hadley ME, Levine N
    2000DOI: 10.1016/s0090-4295(00)00680-4PMID: 11018622
  • Peptides
    Melanocortin peptide therapeutics: historical milestones, clinical studies and commercialization
    Hadley ME, Dorr RT
    2006DOI: 10.1016/j.peptides.2005.01.029PMID: 16412534
  • International Journal of Dermatology
    Risks of unregulated use of alpha-melanocyte-stimulating hormone analogues: a review
    Habbema L, Halk AB, Neumann M, Bergman W
    2017DOI: 10.1111/ijd.13585PMID: 28266027

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