Skip to content
Recovery & Performance PeptidesRecovery research and practical context
Source comparison

Melanotan-1 Dosage Protocol Guide: Comparison Table

Starting Dose 0.25mg 0.05mL (5 units) Tolerance assessment, first 5 days Minimal visible change; receptor priming phase 10–15% mild nausea, typically resolves within 48 hours Essential baseline. Skipping this phase increases side effect risk 3× Low Maintenance

This comparison does not assign a generated winner or score.

  • Starting Dose
  • 0.25mg
  • 0.05mL (5 units)
  • Tolerance assessment, first 5 days
  • Minimal visible change; receptor priming phase
  • 10–15% mild nausea, typically resolves within 48 hours
  • Essential baseline. Skipping this phase increases side effect risk 3×
  • Low Maintenance
  • 0.5mg
  • 0.1mL (10 units)
  • Maintenance for fair-skinned subjects (Fitzpatrick I–II)
  • Noticeable darkening by day 10–12 with UV co-exposure
  • 5–10% transient nausea or facial flushing
  • Minimum effective dose for most subjects; higher doses rarely needed
  • Standard Maintenance
  • 0.75mg
  • 0.15mL (15 units)
  • Maintenance for moderate skin types (Fitzpatrick III–IV)
  • Visible pigmentation by day 7–10 with UV co-exposure
  • 15–20% mild nausea; <5% spontaneous erections (males)
  • Standard research dose; exceeding this provides diminishing returns
  • Maximum Maintenance
  • 1.0mg
  • 0.2mL (20 units)
  • Maximum dose; reserved for subjects unresponsive at 0.75mg
  • Accelerated melanogenesis by day 5–7 with UV co-exposure
  • 25–30% nausea; 10% spontaneous erections; 5–8% darkening of existing moles
  • Ceiling dose. Further escalation increases off-target binding without additional benefit
More references

Related material