Earn points on every order New products in stock Free 51-page beginner’s guide
← Back to Compound Library

Melanotan II (MT-2)

Gives you a deep tan. Side effects include nausea, a libido boost, and unprompted erections. Keep an eye on your moles, they darken too.

Research referenceCommunity compiled

Molecular profile

The molecule itself: sequence, composition, mass, target, and registry identifiers.

Molecular formula
C₅₀H₆₉N₁₅O₉
Average mass
1024.2 Da
CAS number
121062-08-6
Registry
PubChem CID 92432
Receptor / pathway
MC1RMC4R
Formula, mass and identifiers from PubChem CID 92432.
Research & reference information

This profile compiles research and community-sourced reference information for educational purposes. Information may evolve as research and community knowledge develop. It is not individualized medical advice.

Overview

Melanotan II (MT-2) is a potent, non-selective cyclic analogue of alpha-melanocyte-stimulating hormone that stimulates skin tanning while strongly boosting libido.

What problem it targets: It targets fair skin prone to severe sunburning, inability to tan, and central psychogenic and physical erectile dysfunction or low sexual desire.

What It Does

• Stimulates rapid melanin production (MC1R): Signals skin melanocytes to produce rich, dark eumelanin, producing a deep tan with very little sun exposure.

• Ignites central libido and erections (MC4R): Crosses into the central nervous system to activate MC4R in the hypothalamus, triggering spontaneous sexual arousal and robust erections in men and women.

• Suppresses appetite: Activation of central melanocortin pathways produces moderate appetite suppression during active administration.

• Realistic expectations: MT-2 is fast-acting and potent. Common initial side effects include mild nausea, facial flushing, and darkening of existing moles and freckles; starting with conservative micro-doses is crucial.

Reconstitution

Vial sizeBAC water / SolventConcentration
10 mg+ 3 mL3.33 mg/mL

Protocol

PhaseFrequencyDoseNotes
Load Week 1Nightly167 mcgStart low.
Load Week 2Nightly333 mcgStep up.
Maintenance1–2×/week500 mcgSustain pigmentation. Cycle: 2-week loading phase then ongoing maintenance. Timing: Daily SubQ during loading; anytime; libido use 1–2 hr before activity. Evidence: not approved; afamelanotide is the only approved α-MSH analog. Reviews flag melanoma/mole risk. By sex: Melanocortin effects hit both sexes: skin/mole darkening (melanoma monitoring), nausea, appetite drop. MT-2 also raises libido/arousal (same MC4R pathway as PT-141).

Handling & Stacking

Injection site
SubQ abdomen. Rotate.
Storage
Freeze-dried: -4°F. Reconstituted: 36–46°F. Best used within 28 days, otherwise potency gradually fades over ~6–8 weeks (inferred from a marketed analog). Protect from light.
Side effects
Flushing/nausea (dose-dependent, resolves). Darkening of all pigmented lesions. Libido increase.
What to expect
Skin darkens within days; flushing/nausea at loading (ease with titration); spontaneous erections in men. Monitor all moles. Supply math 10mg → 1 vial (2-wk @ 500 mcg × 2/wk)
Pairs well with
PT-141 (libido/erectile complement); GH secretagogues (skin regeneration); B12 (energy + nausea support)
Avoid
Personal or family history of melanoma. Atypical mole syndrome. Recent prolonged unprotected sun exposure

Safety & Patient Education

Contraindications
Personal or family history of melanoma Atypical mole syndrome / dysplastic nevus syndrome Active skin cancer or pre-malignant skin lesions Uncontrolled hypertension Cardiovascular disease (significant) Pregnancy and lactation
Warnings
  • Hyperpigmentation of all melanocytes including existing moles, mole monitoring required New mole formation Transient BP elevation (PT-141: mean ~6 mmHg systolic per FDA Vyleesi label) Nausea, especially MT-2 during loading Priapism risk in men (MT-2 specifically) Spontaneous erections (MT-2) Reduced response and tachyphylaxis with frequent use Priapism risk in men.
  • Spontaneous erections expected.
  • Greater pigmentation magnitude than MT-1.
Drug interactions
PDE5 inhibitors (sildenafil, tadalafil, vardenafil): additive BP effects with PT-141; separate timing per label Antihypertensives: additive or paradoxical BP effects Vasoactive drugs in general
Labs
Dermatology mole mapping (photo-documented) at baseline + ABCDE recheck every 12 weeks on-cycle, then every 6–12 months Blood pressure log at baseline and before each dose
Stop criteria
New atypical mole or rapid change in existing mole (ABCDE criteria) Sustained BP elevation above 140/90 in previously normotensive patient Priapism (sustained erection more than 4 hours): seek emergency care Severe nausea not resolving with dose reduction
Patient education
Use sunscreen during MT-1/MT-2, extra melanin doesn’t replace UV protection Photograph moles at baseline; recheck monthly ABCDE warning signs: Asymmetry, Border irregularity, Color variation, Diameter >6mm, Evolution MT-2: erections are pharmacologic, >4 hours is a medical emergency PT-141: do not exceed 1 dose per 24 hours
References
researchdosing · peptidedosages · PubMed · thepeptidereport · peptides.id · Wessells 2000 · Dorr 1996