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Melanotan I vial

Melanotan I

Melanotan-1 (afamelanotide) is a synthetic linear analog of alpha-melanocyte-stimulating hormone (alpha-MSH) that selectively activates the melanocortin-1 receptor (MC1R) on melanocytes. It is studied for its ability to stimulate eumelanin production, producing skin darkening and increased UV photoprotection. It differs from Melanotan-2 in being highly MC1R-selective, so it lacks MT-2's pronounced appetite and libido effects.

Best for

Research contexts focused on melanogenesis, UV photoprotection, and fair (Fitzpatrick I-II) skin phototype pigmentation studies.

What to expect

Visible pigment changes generally develop gradually over 1-2 weeks of daily dosing, deepening with continued exposure to UV or the peptide.

Pairs with

Typically run standalone; a photoprotective/pigment agent rather than a stack component.

Research protocol

In human research the free peptide is given subcutaneously, most commonly 0.25-1 mg once daily, with a conservative starting point of 0.25 mg/day. Doses are individualized to skin type, and a loading period of daily injections is typically followed by reduced maintenance dosing.

Typical research dosing
Typical start0.25 mgstarting0.63 mgtitration1 mghigher
How often
Daily
When
Morning
Route
Subcutaneous
Vial & water
10 mg vial in 3 mL = 3.33 mg/mL · 0.25 mg = 7.5 units on a U-100 syringe
Cycle
Loading phase of daily doses to build pigment, then a reduced maintenance frequency; typically run in defined multi-week cycles rather than indefinitely.
CautionIMPORTANT: increasing pigment does NOT prevent UV damage or skin cancer — keep using normal sun protection. Can darken/enlarge existing moles; get a baseline mole check and watch for changes (melanoma risk). Not FDA-approved. Avoid with a personal/family history of melanoma or atypical moles; consult a dermatologist before use.

The same numbers the goodtides app and the Dose Calc use — a research reference, not a prescription. Responses are individual; research protocols start at the low end.

How it works

Melanotan-1 is the research designation for afamelanotide, a synthetic 13-amino-acid analog of the natural hormone alpha-MSH, modified at positions 4 and 7 ([Nle4, D-Phe7]-alpha-MSH) to resist enzymatic breakdown and prolong receptor activity relative to native alpha-MSH.

It is important to be clear that the injectable research peptide sold as 'Melanotan-1' is NOT the same as an approved medicine, is not FDA-approved for tanning or cosmetic use, and is offered for research use only.

It acts as a potent agonist at the melanocortin-1 receptor (MC1R) expressed on epidermal melanocytes; MC1R activation raises intracellular cyclic AMP, upregulating tyrosinase and shifting melanin synthesis toward eumelanin, the darker, more photoprotective pigment. Clinical pharmacology studies of the free peptide report short plasma exposure after subcutaneous dosing, whereas the approved clinical product uses a slow-release subcutaneous implant to sustain levels.

Controlled research has shown meaningful increases in skin eumelanin content in fair-skinned subjects, and afamelanotide as a sustained-release implant (Scenesse) is approved in some jurisdictions specifically for erythropoietic protoporphyria to reduce phototoxic reactions. Long-term safety of unregulated injectable use has not been established, and because melanocortin agonists can affect pre-existing pigmented lesions, dermatologic monitoring of moles and skin is prudent.

Anyone considering it should do so only under qualified physician guidance; nothing here is medical advice.

References4
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This page is educational reference material about compounds studied in research settings. It is not medical advice, and nothing here is a recommendation to buy, possess, or use any compound. Research findings described are from published literature; individual compounds may not be approved for human use. Talk to a licensed clinician about anything that affects your health.