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Skin & hair

Melanotan II

MT-2 · MT-II · Melanotan 2

PreclinicalReviewed 12 Aug 2026

Melanotan II is a synthetic analogue of alpha-MSH, the hormone that signals pigment cells to produce melanin. Injecting it darkens skin over weeks, with far less sun exposure than would otherwise be needed. That is the effect people want and it does work.

It is not approved anywhere, and it is the compound on this site where regulators have been most vocal. Several national medicines agencies have issued public warnings about it by name. That is unusual.

The concern that matters is dermatological. Melanotan II stimulates melanocytes, the same cells melanoma arises from. Case reports describe existing moles darkening, changing shape, and in some instances melanoma being diagnosed in users. Causation in individual case reports is never settled, but the mechanism makes the association biologically plausible rather than coincidental, and that combination is why this page is written the way it is.

How it works

Melanotan II activates melanocortin receptors broadly. MC1R activity on melanocytes is what drives melanin production and the resulting tanning; MC4R activity in the brain accounts for the appetite suppression and sexual effects users also report.

Because it is non-selective, all of those effects arrive together. There is no dose at which it tans without also acting on the other receptors, which is the design difference between it and PT-141.

Regulatory status — United States

Not approved for human use in any jurisdiction. Multiple national medicines regulators have issued public safety warnings specifically about melanotan products, citing unregulated manufacture and dermatological risk. Sold only as a research chemical.

Last reviewed 12 Aug 2026. Regulatory positions in this category change frequently; we date this line so you can see how current it is.

What it is studied for

Each entry states the evidence behind it. We do not rank indications by effectiveness — for most compounds here, that would be a claim nobody can support.

Skin pigmentation

Published review

The effect it is used for.

EvidenceWell documented that it produces tanning. No controlled trial establishes safety for this use.

Appetite suppression and sexual effects

Community practice

Reported alongside the tanning.

EvidenceFollow from MC4R activity. Not studied as endpoints for this compound.

Identity and clearance

Molecule

Class
Cyclic heptapeptide, non-selective melanocortin agonist
Molecular weight
1024.2 Da
Length
7 amino acids

Sequence

Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-NH2

Structurally almost identical to PT-141. The difference in terminal group changes receptor selectivity substantially.

Pharmacokinetics

Published review
Half-life1 h
Substantially cleared6 h
100%50%25%0%half-life 1hdose2h3h5h6h
Modelled from the half-life above, assuming first-order elimination. Illustrative rather than measured — it shows the shape of clearance, not a prediction for any individual.

Short-acting, but the pigmentation effect accumulates over weeks and persists for months after stopping.

Dose protocols reported in sources

Displayed for reference only. Every row says where it came from, and a trial protocol and a community convention are not the same kind of information. None of this is fed into the calculator, and none of it is a recommendation.

Dose protocols reported in sources, with the source of each.
GoalDoseFrequencyRouteUnits, 10 mg vialSourceStart this protocol
Loading, commonly described250 mcg – 500 mcgDaily until the desired pigmentation is reachedSubcutaneousCommunity sources describe starting low specifically because nausea is dose-related and pronounced.12.5–25 uCommunity practiceStart this
Maintenance, commonly described500 mcg – 1 mgOne to two times weeklySubcutaneous25–50 uCommunity practiceStart this

Start this copies a row into a protocol of your own, which you can then edit. Where a source gave a dose range or an ambiguous frequency, those fields arrive empty — we will not pick a number on your behalf.

CheckRows marked community practice describe what people commonly do, drawn from public discussion. They are not derived from any trial and are not evidence that a dose is safe or effective.

Calculator

Work out what to draw

Pre-filled with a 10 mg vial as a worked example. These are not recommended values — change them to match the vial in front of you.

Dose unit
Your syringe
01020304050607080901005 units0.05 mL

Draw to 5 units on a 1 mL U-100 syringe. That is 0.05 mL, containing 250 mcg of Melanotan II.

Concentration5mg / mL
Volume drawn0.05mL
Doses per vial40doses
Per unit50mcg / unit

Check5 units falls between the printed lines on a 1 mL U-100 syringe. Mixing with 1.6 mL of water instead would put this dose at 4 units.

Bioalmanac performs arithmetic on values you enter. It does not recommend doses, schedules or compounds, and nothing here is medical advice. Confirm every calculation against your vial and syringe before drawing, and speak with a licensed healthcare provider.

Open this calculation in the full calculator

Units, concentration, bacteriostatic water — the glossary defines the vocabulary, and a unit is not a fixed volume.

Safety

Reported effects

  • Nausea, sometimes severeCommunity practice

    Very commonly reported

    Dose-related and often pronounced in the first week.

  • Facial flushingCommunity practice

    Very commonly reported

  • Darkening of existing moles and frecklesPublished review

    Commonly reported

    Expected from the mechanism, and the reason skin monitoring matters here more than anywhere else on this site.

  • Spontaneous erectionsCommunity practice

    Commonly reported in men

    MC4R activity, the same mechanism PT-141 was developed around.

  • New or changing pigmented lesions, including reported melanomaPublished review

    Reported in case literature

    Case reports describe melanoma diagnosed in users. Individual case reports cannot establish causation, but the mechanism makes the association plausible rather than coincidental.

When to stop

  • Any mole that changes in size, shape, colour or border, or that bleeds or itches. Stop and see a dermatologist promptly. This is the specific risk this compound carries.
  • Any new pigmented lesion.
  • Severe or persistent nausea and vomiting.
  • Any allergic response: rash, hives, facial swelling or difficulty breathing. Seek urgent care.
  • An erection lasting more than four hours is a medical emergency — seek immediate care.

Interactions and situations that need care

  • Melanoma history, atypical mole syndrome, or many molesAvoid

    This compound stimulates the exact cell type melanoma arises from. Case reports describe melanoma diagnosed in users, and while individual reports cannot prove causation, deliberately stimulating melanocytes in someone already at elevated risk is the clearest avoidable hazard described anywhere on this site.

  • Fair skin with heavy frecklingUse caution

    The skin types most drawn to a tanning compound are the same ones at highest baseline melanoma risk, which makes dermatological monitoring more important rather than less.

  • Pregnancy and breastfeedingAvoid

    No reproductive or developmental safety data.

  • Uncontrolled hypertension or cardiovascular diseaseUse caution

    Melanocortin agonists raise blood pressure transiently, which is documented for the approved compound in this family.

What to expect

HonestlyThere is no human efficacy data for this compound, so there is no evidence-based timeline to give. Any site publishing a week-by-week schedule of expected effects has invented it.

  • The tanning effect is real and develops over weeks, not days. It fades over months after stopping.
  • Nausea in the first week is close to universal in community reports and is dose-related.
  • It does not prevent sunburn. Darker skin is not protection from UV damage, and treating it as such is how people get burned while believing they are covered.
  • Baseline photographs of your moles before starting, and a dermatologist who knows you are using it, are the two things that most reduce the risk this compound actually carries.

Storage and handling

Freeze-dried powder
Refrigerated at 2–8 °C, protected from light.
After mixing
Refrigerated at 2–8 °C. Do not freeze once mixed.
Long-term, frozen
Unopened powder is stable at −20 °C or colder.

Printable one-pagerHow to reconstitute a vial, step by step

With other peptides

  • PT-141caution

    Both act on melanocortin receptors. Combining them stacks the same receptor family, compounding nausea, blood pressure effects and pigmentation changes.

  • Both drive pigmentation through the same receptor. Combining them stacks melanocyte stimulation for no additional effect, while adding melanotan II's nausea and blood pressure effects to a compound that avoids them.

Check this against a whole stack

Checking your vial

Research chemicals carry no manufacturing standard, so what the vial looks like is often the only quality signal available before you use it. More on assessing quality and COAs.

  • White cake, clear solution

    Standard for a short cyclic peptide.

  • Collapsed cake, or any colour in the solution

    Indicates degradation. A tanning peptide does not produce a coloured solution.

Questions

Does Melanotan II protect against sunburn?
No. It increases melanin, which is not the same as being protected from UV damage, and people using it routinely overestimate how much sun they can tolerate. It does not replace sunscreen.
What is the melanoma concern exactly?
The compound stimulates melanocytes, which are the cells melanoma arises from. Case reports describe moles darkening and changing in users, and melanoma being diagnosed. Case reports cannot establish causation, but the biological mechanism makes the association plausible. Which is why skin monitoring is the single most important thing on this page.
How is it different from PT-141?
They are structurally almost identical, differing in one terminal group. That one difference changes receptor selectivity substantially. PT-141 has weak pigmentation activity and holds an FDA approval; melanotan II is non-selective, tans strongly, and is approved nowhere.

References

  1. Melanotan-associated melanoma and pigmented lesion change: a review of reported cases

    Dermatology review literature, 2019 · Review of case reports

    Humans

    Collects reports of pigmented lesion change and melanoma diagnosis in melanotan users, and notes that causation cannot be established from case reports while the melanocyte-stimulating mechanism provides biological plausibility.

  2. Commonly reported community protocols

    Bioalmanac editorial summary of public community sources, 2026 · Not a study

    Summarises loading and maintenance dose patterns described in public discussion. Carries no evidential weight about safety or effect.

Keep this page honest

If something here is wrong, out of date, or missing a source, tell us and we will fix it and say that we did.

Suggest a correction

This page is educational. It describes what published research reports, not what you should do. Peptides discussed here are largely not approved for human use, and nothing on Bioalmanac is medical advice. No clinician reviews these pages.

Page last updated 12 Aug 2026