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Melanotan-2 Clearance: Full Comparison Table

Blood Plasma 33 minutes (t½) Renal filtration and enzymatic degradation Undetectable after 2–3 hours Standard pharmacokinetic half-life. Does NOT predict biological effect duration Urine (intact peptide) Detectable 12–18 hours Glomerular filtration of unmetabo

This comparison does not assign a generated winner or score.

  • Blood Plasma
  • 33 minutes (t½)
  • Renal filtration and enzymatic degradation
  • Undetectable after 2–3 hours
  • Standard pharmacokinetic half-life. Does NOT predict biological effect duration
  • Urine (intact peptide)
  • Detectable 12–18 hours
  • Glomerular filtration of unmetabolised MT2
  • Up to 24 hours post-injection
  • Mass spectrometry required for detection; standard urinalysis will not identify MT2
  • Tissue (melanocytes)
  • 48–72 hours (receptor occupancy)
  • MC1R binding and tyrosinase upregulation
  • Pigmentation visible 24–96 hours
  • Tanning effect peaks at 72 hours, persists 5–7 days as melanin granules shed
  • Adipose Tissue
  • 24–48 hours (depot release)
  • Lipophilic partitioning and slow diffusion
  • Not directly measurable
  • Acts as secondary reservoir; higher body fat = slightly prolonged tanning duration
  • Hypothalamus (MC4R sites)
  • 2–4 days (functional suppression)
  • MC4R-mediated appetite signalling reduction
  • Appetite changes resolve 3–5 days post-dose
  • Receptor downregulation occurs with chronic daily dosing; washout requires 7–10 days
  • Complete System Clearance
  • 5–7 days (all biological effects)
  • Combination of renal excretion, receptor dissociation, melanin turnover
  • No measurable tanning or appetite effect after 7 days
  • Standard washout period for research protocols transitioning between peptides
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