DATABASE
SYS.ONLINE
🔒 SECURE
Other ● Verified

Melanotan 2

Alpha-MSH analogue used for extreme tanning and libido stimulation.
Half-Life
~1 Hour
Onset
30min - 2h
Duration
Days (Tan)
Route
Injectable
Mechanism of Action

Non-selective agonist of melanocortin receptors (MC1R, MC3R, MC4R, MC5R). Stimulates melanogenesis (tanning) and central sexual arousal.

Key Benefits
  • Skin tanning without excessive sun exposure
  • Appetite suppression
  • Dramatic increase in libido
  • Spontaneous erectionsTanning of the skin without excessive sun exposure
  • Spontaneous erections
Evidence Notes
RESEARCH RANGE (Non-prescriptive): Very low doses (50mcg-100mcg) to start. Level of Evidence: B.
Risk Profile
  • Severe nausea, flushing, priapism (attention), darkening of moles.
Overview

Melanotan 2 (MT-2) is a synthetic analogue of alpha melanocyte-stimulating hormone (α-MSH) that acts non-selectively on melanocortin receptors (MC1R to MC5R).

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What it is (in plain language)
- MT-2 does two main things: it stimulates melanin production (tanning) without the need for intense sun exposure and it acts on the central nervous system to significantly increase libido. It mimics the body's natural signal to 'darken' the skin and 'activate' sexual desire.

Why do you appear online so much
- It is extremely popular for its ability to provide a deep tan and for its effectiveness in treating erectile dysfunction and low libido. However, it is also one of the peptides that requires the most caution due to its systemic effects.

How it is framed today (pragmatic view)
- 1) Evidence: Widespread historical use, although not approved by the FDA for tanning. 2) Purpose: Aesthetics (pigmentation) and sexual health. 3) Risk: Can cause intense nausea, darkening of moles (nevi) and prolonged erections.

How to use this form
- Carefully read the warnings about monitoring moles and freckles in the risks section.

- Quick profile (curated by Subject 157)
- Class: Other
- Status: Verified
- Use case: Other
- Route: Injectable
- Tags: Injectable|Tanning|Libido
- Half-life: ~1 Hour
- Start: 30min - 2h
- Duration: Days (Tan)

- Mechanism (high level)
Non-selective agonist of melanocortin receptors (MC1R, MC3R, MC4R, MC5R). Stimulates melanogenesis (tanning) and central sexual arousal.

- Evidence (what the literature covers)
RESEARCH RANGE (Non-prescriptive):
Very low doses (50mcg-100mcg) to start with.
Level of Evidence: B.

- Safety and harm-reduction (non-prescriptive)
Risks: Severe nausea, flushing, priapism (attention), darkening of moles.
Interactions: Naltrexone.

- References (anchors)
- Dorr, R. T. (1996) - Melanotan-II synthetic analogue of alpha-MSH - https://doi.org/10.1016/0024-3205(96)00160-9 | PubMed:8667634
- Hadley, M. E. (2005) - Melanotan-II clinical results summary - https://doi.org/10.1016/j.peptides.2005.01.023 | PubMed:15862168

Note: Educational/research content. Does not constitute medical advice, diagnosis or prescription.

Scientific References
Dorr, R. T. (1996) - Melanotan-II synthetic analogue of alpha-MSH -
Hadley, M. E. (2005) - Melanotan-II clinical results summary - R. T. (1996) - Melanotan-II synthetic analogue of alpha-MSH -
Hadley, M. E. (2005) - Melanotan-II clinical results summary -
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Snapshot
Use CaseOther
AliasesMT-2|Barbie Drug
StorageRefrigerator (2-8°C).
HandlingProtect from light.
Interactions
Naltrexone.
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