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Skin & Anti-AgingIntermediateRestricted

Melanotan II

Non-selective melanocortin receptor agonist (MT-II)

Low Dose
0.25 mg/day (loading)
Medium Dose
1 mg 2–3x/wk (maintenance)
Route
SubQ
Cycle Length
10–20 day loading phase, then ongoing maintenance

Mechanism of Action

Cyclic heptapeptide analog of alpha-MSH. Non-selectively activates MC1R (pigmentation), MC3R/MC4R (appetite, energy homeostasis) and MC4R-mediated central pathways implicated in sexual arousal — explaining its broader effect profile relative to the MC1R-selective Melanotan I.

Key Benefits

  • Potent UV-independent tanning, including in poor-tanning skin phototypes
  • Increased sexual desire/erectile response reported in controlled human trials (MC4R-mediated)
  • Appetite suppression via MC3R/MC4R activation
  • Historical basis for development of bremelanotide (PT-141), now FDA-approved as Vyleesi

Dosing Protocol

Low / Starting Dose
0.25 mg/day (loading)
Medium / Maintenance Dose
1 mg 2–3x/wk (maintenance)
Administration Route
SubQ
Half-Life
~30–60 minutes
Frequency
Daily during loading, then 2–3x weekly maintenance
Cycle Length
10–20 day loading phase, then ongoing maintenance
Protocol Notes

Human data exists (Wessells/Hadley/Dorr group, University of Arizona) but from a small controlled ED trial — not a safety-established consumer product. Never approved by FDA; its selective descendant PT-141/bremelanotide is.

Ideal Candidates

Research contexts studying non-selective melanocortin pharmacology, MC4R-linked appetite/sexual arousal pathways, or as historical/comparative reference for PT-141 development.

Side Effects & Safety

Nausea and yawning are the most frequently reported effects in human trials (severe nausea in 12.9% of subjects at 0.025 mg/kg); flushing, spontaneous erections, darkening of nevi, and appetite suppression. Nausea is more prominent and frequent than with Melanotan I.

Regulatory Status

Restricted

Not FDA-approved in any form; FDA has issued warning letters against MT-II marketing. Its truncated/modified analog bremelanotide (PT-141) is FDA-approved as Vyleesi (2019) for HSDD — MT-II itself remains an unapproved research compound.

Evidence & Citations

Frequently asked

What is Melanotan II?+

Melanotan II (Non-selective melanocortin receptor agonist (MT-II)) is a peptide studied for non-selective mc receptor agonism and tanning + libido effects. Cyclic heptapeptide analog of alpha-MSH. Non-selectively activates MC1R (pigmentation), MC3R/MC4R (appetite, energy homeostasis) and MC4R-mediated central pathways implicated in sexual arousal — explaining its broader effect profile relative to the MC1R-selective Melanotan I.

What is the dosing protocol for Melanotan II?+

Literature commonly references 0.25 mg/day (loading) (low) to 1 mg 2–3x/wk (maintenance) (maintenance) via SubQ, on a 10–20 day loading phase, then ongoing maintenance cycle. Educational reference only — a licensed Stackhaus Health provider sets any personalized protocol.

What is the regulatory status of Melanotan II?+

Not FDA-approved in any form; FDA has issued warning letters against MT-II marketing. Its truncated/modified analog bremelanotide (PT-141) is FDA-approved as Vyleesi (2019) for HSDD — MT-II itself remains an unapproved research compound.

Where can I access Melanotan II?+

Research-grade Melanotan II is available through Stackhaus Research. For a personalized, provider-reviewed protocol, consult a licensed clinician through Stackhaus Health.

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Written and reviewed by Stackhaus Academy Editorial Team · Last reviewed July 2026

Educational Only. This page is educational reference material, not medical advice. It does not establish a doctor-patient relationship and is not a substitute for individualized clinical guidance. Personalized protocols and clinical decisions are made through a licensed provider via Stackhaus Health.