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Melanotan II

Aliases: MT-2 · MT-II · MT-2 Acetate · Melanotan 2

Last verified: 2026-09-23

DiscontinuedLimited evidencePeptidesHigh interest

The short version

Melanotan-2 is a 'tanning peptide' with a complicated profile: gray use for skin darkening is global, and the official regulatory picture is negative — regulators have warned about its sale multiple times. Side effects are well documented in case reports: nausea, flushing, increased pigmentation (including unwanted), and the melanocortin pathway has theoretical links to melanoma. No controlled data on benefit exist.

Identity & type

Molecular type
analog
Sequence / structure
Ciklični heptapeptid (Ac-Nle-c[Asp-His-D-Phe-Arg-Trp-Lys]-NH2)
Molecular weight
~1024 Da
Origin
Synthetic analog of alpha-MSH that stimulates melanocortin receptors.

Mechanism of action

Melanocortin receptor agonist: MC1R (pigmentation), MC3R/MC4R (appetite, sexual function, energy balance).

not confirmed in humans

Dosing & routes

Official / clinical context

Development was abandoned; no active regulatory document exists. There are no official indications.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

Gray market: 250–500 mcg SC daily until desired tone, then 1–2× weekly maintenance. The community reports fast tanning, strong libido/erection increase, reduced appetite — but also nausea, flushing and darkened moles. The most popular "cosmetic" peptide.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

The community reports fast tanning, strong libido/erection increase, reduced appetite — but also nausea, flushing and darkened moles. The most popular "cosmetic" peptide.

Protocol — official vs community

Official / label

No approved product anywhere. FDA warning letters target injectable tanning products containing MT-II.

Duration: —

The regulatory record is a list of enforcement actions, not a dosing literature.

Community (anecdotal)

0.5–1 mg SC 2–3× weekly until desired pigmentation, then 0.5–1 mg weekly maintenance. Often micro-dosed (250–500 mcg) for 'glow' without nausea.

Cycle:
2–4 weeks loading, indefinite maintenance.
Break:
None — which is precisely the problem: chronic non-selective melanocortin agonism with no safety data.

Documented: nevus darkening, nausea, flushing, BP effects. Unresolved: long-term melanoma signal. Chronic use is an unmonitored experiment.

Human evidence

No controlled trials for tanning; only case reports of adverse effects and gray-market analyses.

Preclinical evidence

Phase I/II in early 2000s (University of Arizona); halted over side effects, focus moved to Bremelanotide (PT-141).

Known risks

  • Nausea, flushing, somnolence (very common on first use)characterized
  • Uneven/unexpected pigmentation (melanosis, darkening of eyes)characterized
  • Theoretical melanocortin-pathway link to melanomatheoretical
  • Regulatory warnings (FDA, TGA et al.) on sale and usecharacterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Cancer risk of chronic melanogenesis stimulation
  • Pharmacokinetics and purity of gray products

Frequently asked questions

References