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Melanotan II: Complete Guide

Melanotan II is a synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH) that activates melanocortin receptors, primarily MC1R and MC4R. Originally developed at the University of Arizona for photoprotection (preventing skin cancer by stimulating melanin production without UV exposure), melanotan II gained attention for its tanning, libido-enhancing, and appetite-suppressing effects. It is not approved for medical use in any country and remains a research compound.

Last updated: 2026-01-28

Quick Facts

Category
cosmetic
Also Known As
Melanotan 2, MT-2
Related Goals
skin

Who Researches Melanotan II?

Melanotan II is researched by people interested in skin tanning without extensive UV exposure. It's popular among fair-skinned individuals who burn easily and want protective melanin before sun exposure. However, it is not approved for use in any country, and health authorities have issued specific warnings about it. The side effects — nausea, mole changes, blood pressure effects — are more significant than most peptides. If sexual health is your primary interest rather than tanning, PT-141 (which was derived from melanotan II) is FDA-approved for that specific purpose with a better safety profile.

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What Is Melanotan II?

Melanotan II was developed in the 1990s by researchers at the University of Arizona who were investigating ways to stimulate the body's natural tanning response without UV radiation exposure. The goal was photoprotection — creating a "biological sunscreen" that would reduce skin cancer risk by darkening skin through melanin production.

The peptide activates multiple melanocortin receptor subtypes, which explains its diverse effects: MC1R activation causes melanin production (tanning), MC4R activation affects sexual function and appetite, and MC3R activation influences energy balance.

Melanotan II has never received regulatory approval anywhere in the world. Health authorities in the US, EU, UK, and Australia have issued warnings about its use due to safety concerns including potential effects on existing moles and the risk of masking melanoma development.

Mechanism of Action

Melanotan II is a non-selective melanocortin agonist:

  • MC1R (skin): Stimulates melanocytes to produce eumelanin (dark pigment), resulting in skin darkening independent of UV exposure
  • MC4R (brain): Activates hypothalamic pathways involved in sexual desire, appetite regulation, and energy balance
  • MC3R (metabolic): Influences energy homeostasis and fat metabolism

The tanning effect is cumulative — repeated doses produce progressive darkening over days to weeks. The effect persists for weeks after discontinuation before gradually fading.

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Dosage Overview

Melanotan II is typically used at 0.25–0.5 mg per day via subcutaneous injection during an initial "loading" phase, then reduced to 0.25–0.5 mg once or twice weekly for maintenance. Some protocols include brief UV exposure (10-20 minutes) within hours of dosing to enhance melanin activation.

Use the peptide calculator for reconstitution volumes.

Side Effects & Safety Warnings

Melanotan II carries significant safety concerns:

  • Nausea (very common): Often severe with initial doses
  • Facial flushing
  • Mole changes: Can darken existing moles and make melanoma detection more difficult — a serious dermatological concern
  • Blood pressure changes: Transient increases
  • Spontaneous erections (in males)
  • Appetite suppression
  • Injection site reactions
  • Unknown long-term cancer risk: While designed to be photoprotective, the effect on existing melanocytic lesions raises concern about melanoma risk

Health authorities in the US, UK, EU, and Australia have issued public warnings about melanotan II use. The peptide is not approved for human use and its long-term safety profile is unknown.

Frequently Asked Questions

References

  1. Dorr RT, et al.. Effects of a superpotent melanotropic peptide in combination with solar UV radiation on tanning of the skin in human volunteers. Archives of Dermatology, 2004.
  2. Habbema L, et al.. Risks of unregulated use of alpha-melanocyte-stimulating hormone analogues: a review. British Journal of Dermatology, 2017.

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Peptides Insider Editorial Team

Our content is reviewed for accuracy and grounded in peer-reviewed research where available. We do not provide medical advice. Always consult a qualified healthcare professional.