Melanotan-2 (MT-2)Melanocortin PeptideSafety Rating 3/10

TypeCyclic lactam heptapeptide
CAS121062-08-6
MW1,024.18 g/mol
AAs7
Primary research areaMelanocortin research

Research-literature reference data, NOT patient instructions. Not for human use. Consult a licensed clinician for any human application.

Research dose range0.025 mg/kg/day (~1.5–2 mg) in Phase 1; research loading 0.25–0.5 mg/daysource ↗
AdministrationSubcutaneous injection
Half-life~30–60 minutes (plasma); pigmentation effects last weeks
Safety3/10 · Not FDA-approved
NCAA D1Not listed

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Overview

About Melanotan-2

Mechanism of action

Non-selective melanocortin agonist (MC1R, MC3R, MC4R); stimulates melanin production; activates MC4R for potent sexual arousal; significantly more sexual effect than MT-1.

Safety profile

Nausea, facial flushing, fatigue, spontaneous erections, increased libido, yawning, hyperpigmentation, mole changes (monitor), potential cancer promotion concerns. · Documented serious harms: peer-reviewed melanoma/eruptive-nevi case reports with formal MHRA and TGA safety warnings, plus priapism (a urological emergency). Directly stimulates melanocytes. Nausea and flushing are common.

Storage

Stability & handling

❄️Lyophilized (powder)2–8°Cstable
💉Reconstituted2–8°C30 days
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Safety & Interactions

Contraindications & Drug Interactions

Research use only — not medical advice. Consult a licensed physician before using any peptide. Sources are cited where available.

! CautionContraindication

Personal or family history of melanoma or atypical nevi — melanocortin agonists darken moles; theoretical melanoma risk debated but unproven.

! CautionCaution

Priapism (prolonged painful erection) — reported in literature. Emergency medical evaluation required if erection lasts >4 hours.

! CautionCaution

Rhabdomyolysis — case reports of muscle breakdown with high doses.

Sources: Br J Dermatol

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Research

Studies & key findings

  • Synthetic cyclic α-MSH analog that binds MC1R, MC3R, MC4R and MC5R — the broad receptor profile is what drives both the tanning response (MC1R → tyrosinase → eumelanin) and the central pro-erectile/anorexic effects (MC4R in the hypothalamus), and is also why side effects cluster across so many systems.
  • Originally developed at the University of Arizona in the 1980s for UV-sparing skin photoprotection in patients at high melanoma risk; Dorr et al. 1996 (Life Sciences) showed dose-dependent tanning in a Phase I trial, and Wessells 1998 (J Urology) demonstrated improved erections in men with psychogenic erectile dysfunction.

7 peer-reviewed sources cited — clinical, preclinical, and regulatory.

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