Cosmetic & Skin

Melanotan I

Also known as: Afamelanotide, MT-I

Molecular Identifiers

Molecular Formula

C78H111N21O19

PubChem CID

16197727

Molecular Weight

1646.85 Da

Overview

Synthetic α-MSH analog with high affinity for the MC1R receptor. Promotes tanning and photoprotection by stimulating eumelanin production in melanocytes. Developed as a treatment for erythropoietic protoporphyria (EPP) and photoprotection in sensitive skin.

Extended notation: Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH₂

Contains non-natural amino acids (Nle, D-Phe)

Half-life

~30 minutes

Administration Route

Subcutaneous

Category

Cosmetic & Skin

Mechanism of Action

  • Selective MC1R receptor agonism in melanocytes
  • Stimulation of melanogenesis and eumelanin production
  • Photoprotection through increased skin pigmentation
  • Activation of the cAMP/PKA pathway in melanocytes
  • Protective effect against UV radiation damage

Dosage Protocol

Data compiled from the literature. This does not constitute medical advice.

Parameter Value
Dose 0.5-1 mg per injection
Frequency Every other day (loading phase), weekly (maintenance)
Timing Any time of day
Duration Loading 10-14 days, continuous weekly maintenance

Reported Side Effects

Adverse effects described in the literature. Severity and frequency vary between individuals.

  • Nausea
  • Facial flushing
  • Fatigue
  • Darkening of nevi
  • Pain at injection site

Presentations & Preparation

Vials of Melanotan I found in the research market:

5 mg10 mg

Reconstitution

  • Diluent: Bacteriostatic water
  • Volume: 2 ml per vial
  • Inject the diluent slowly against the vial wall
  • Gently swirl until fully dissolved
  • Never shake

Storage

  • Lyophilized: Refrigerated 2-8°C
  • Reconstituted: Refrigerated 2-8°C (up to 30 days)
  • Protect from direct light
  • Do not freeze after reconstitution
Reconstitution Calculator

Scientific Studies

Published studies on Melanotan I.

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