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Melanotan I

Tanning; approved for rare sun sensitivity

Afamelanotide (Scenesse)

Match every finding to its exact substance, formulation, route and study population. A related molecule or approved medicine does not validate a catalog vial.

Human / product-specific records
AcSYSNleEHfRWGKPVNH₂AcSYSNleEHfRWGKPVNH₂
Schematic illustration · View structure evidenceAc-S-Y-S-Nle-E-H-f-R-W-G-K-P-V-NH₂
Color key
NonpolarAromaticPositive chargeNegative chargePolar Copper ion D-form or non-natural

At a glance

Why people take it. And what backs it up.

  1. Get a deeper tan

    Early human studies

    Tanners inject gray-market vials alongside sun or sunbeds, often choosing it over Melanotan II hoping for milder side effects; health agencies warn against unlicensed melanotan.

    Sources (5)
  2. Tolerate sunlight without pain

    Implant approved for rare sun sensitivity

    Approved as the Scenesse implant for adults with a rare inherited disease that makes light painful; it lets them spend longer in light without pain.

    Sources (3)
  3. Restore color in vitiligo

    Small trial; not approved for this

    Some people with vitiligo use it with light therapy, hoping white patches regain color faster; the trial used the implant, not vials.

    Sources (3)

Evidence briefing

Sources checked

What the sources support.

Afamelanotide is a long-acting alpha-MSH analog commonly called Melanotan I. FDA approval is for the specified 16 mg Scenesse subcutaneous implant, administered by a trained clinician to increase pain-free light exposure in adults with erythropoietic protoporphyria (EPP). It does not approve online Melanotan-I vials or cosmetic tanning use.

Keep in mind

Approval attaches to the tested implant, indication, adults with EPP and trained-clinician administration; the shared nickname does not establish that vendor products contain afamelanotide or match Scenesse.

Identity and research status reviewRead the original sources

The research. What’s been studied.

  • Human evidence

    EPP light tolerance

    The FDA-approved Scenesse implant increases pain-free light exposure in adults with EPP; it is given by a trained clinician.

  • Human evidence

    Skin pigmentation

    Afamelanotide stimulates pigmentation, but the approved use is EPP and does not make it a cosmetic tanning treatment.

  • Early human studies

    Vitiligo research

    Afamelanotide has been studied with light therapy for vitiligo; this is not an approved indication.

What do these labels mean?
  • Human evidence: approved-drug data or larger human studies, within the populations and uses studied.
  • Early human studies: small, preliminary or limited human studies.
  • Animal & lab studies: animal or laboratory findings that do not establish effects in people.
  • Unverified: a proposed use or claim without verified supporting clinical evidence.
How each claim was reviewed (4)

Reported effects and evidence.

A citation may support, qualify or correct a claim. Read the study scope; a laboratory result is not an established benefit in people. Each review covers a claim as it was first collected; the tiles above show the collection’s current wording.

  1. Approved-product pigment pharmacology; misleading protection headline

    Review of “Protective tan”

    Afamelanotide increases eumelanin. This does not establish safe recreational tanning or substitute for sun protection.

    Limitations and applicability. Pigmentation is not a guarantee of safe tanning or skin-cancer prevention; approved implant population and precautions matter.

    Original collected claim and review history

    Original title: Protective tan

    Increases eumelanin, the dark pigment that protects skin from UV.

    Original label: proven. Preserved for traceability; the reviewed wording above qualifies this record.

    Record melanotan-i:benefit:1 · Annotated 2026-10-01 · Review method

  2. FDA-approved implant indication

    Review of “Sun tolerance in EPP”

    Scenesse implants increase pain-free light exposure in adults with EPP and a history of phototoxic reactions.

    Limitations and applicability. Indication is adult EPP with phototoxic reactions; approval does not cover vendor research injections.

    Original collected claim and review history

    Original title: Sun tolerance in EPP

    Approved to let people with a painful sunlight disorder spend more time in light.

    Original label: proven. Preserved for traceability; the reviewed wording above qualifies this record.

    Record melanotan-i:benefit:2 · Annotated 2026-10-01 · Review method

  3. Human randomized combination study

    Review of “Vitiligo repigmentation”

    A randomized study investigated afamelanotide implants plus narrowband UV-B for vitiligo repigmentation.

    Limitations and applicability. Combination with NB-UVB and selected skin types; not approval for vitiligo or isolated peptide efficacy.

    Original collected claim and review history

    Original title: Vitiligo repigmentation

    Studied with light therapy to restore color in vitiligo patches.

    Original label: early. Preserved for traceability; the reviewed wording above qualifies this record.

    Record melanotan-i:benefit:3 · Annotated 2026-10-01 · Review method

  4. Receptor pharmacology; comparative clinical safety unresolved

    Review of “More targeted than Melanotan II”

    Afamelanotide acts at MC1R. A comparative claim about fewer appetite or sexual effects requires a specific study.

    Limitations and applicability. MC1R agonism is supported; fewer libido/appetite effects versus MT-II needs a direct comparative source.

    Original collected claim and review history

    Original title: More targeted than Melanotan II

    Mainly acts on skin pigment cells, with fewer effects on appetite and libido.

    Original label: proven. Preserved for traceability; the reviewed wording above qualifies this record.

    Record melanotan-i:benefit:4 · Annotated 2026-10-01 · Review method

The research in detail

Evidence category

FDA-approved (US)

The approved afamelanotide implant increases pain-free light exposure in adults with EPP. That clinical evidence and approval concern the regulated implant and its EPP indication; they do not establish quality or safety of unverified seller products or cosmetic tanning.

Evidence is assessed claim by claim above. Regulatory approval, study design, findings and relevance are separate questions; there is no single evidence score.

Risks and unknowns. What to know first.

Collected cautions follow. These are not an exhaustive or independently validated safety assessment; claim references do not automatically support every caution.

  • Nausea, headache, darkening of moles and skin.
  • Regular skin checks are required on the approved drug.
  • Injected research versions lack the implant’s controlled release.

What people report

Show all 4 cautionsShow fewer cautions

Read this first: what “research use only” means

Published dosing records. What the approved label says.

Historical label and trial records for the named product, route, population and indication. These records are not a personal schedule or a validated regimen for a catalog vial. Source attribution does not establish applicability.

Scenesse

Adults with erythropoietic protoporphyria (EPP), a rare condition that makes light exposure painful, to increase pain-free time in light

Given by a clinicianApproved label

Source: Scenesse prescribing information (FDA, revised 08/2024) (opens in a new tab)

Every 2 months
16 mg
How
Implant placed under the skin, just above the front of the hip bone
How often
One implant every 2 months
How long
No set length
  • The approved product is a slow-release 16 mg implant (a rod about 1.7 cm long) placed under the skin through a special cannula, not an injectable liquid. A health care professional who has completed the maker’s (Clinuvel’s) training inserts it.
  • The patient is watched for 30 minutes after insertion, and the dressing stays on for 24 hours.
  • Sun and light protection continues during treatment.
  • The EU label (updated 10/2025) gives one implant every 2 months before and during times of stronger sunlight. It sets no yearly cap: a specialist at a porphyria centre decides how many implants and for how long, and it notes limited data on 4–6 implants a year.

These are the label’s doses for the approved medicine, started and adjusted by a prescriber. A research vial is not that medicine: no regulator has checked what’s in it, or how much.

Community protocols. Reported online. Not clinically validated.

Community reports Collection date: 30 Sep 2026

Grey-market melanotan I (research vials, not the approved implant) is used like melanotan II: about 250–500 mcg injected daily for roughly 1–2 weeks with sun or sunbed exposure, then 250–500 mcg once or twice a week to maintain.

More about this

Many only dose on sun days, and some push to 0.75–1 mg while others start as low as 50–100 mcg.

Not testedFrequently encountered in reviewed sources

Loading, then maintenance

Collected report · exact form and route are only as reported below. Source date and reporter identity are not separately verified. Collection checked 30 Sep 2026; presentation annotated 2026-10-01.

Frequency labels describe this collection, not a measured population. Contradictory records remain available.

Details and sourcesHide details
Dose
Loading: 250–500 mcg. Maintenance: 250–500 mcg.
How often
Loading: every day. Maintenance: once or twice a week.
Route
Injection under the skin
Timing
Before sun or sunbed exposure (often 30–60 minutes of sun)
How long
Loading about 1–2 weeks, or until the wanted colour
Ramp
250 mcg on day 1 to test tolerance, then 500 mcg
Mixing
10 mg vial + 2 mL bacteriostatic water is typical
  • Some choose it over melanotan II hoping for fewer side effects and fewer new freckles.
  • Often started in spring (April or May) for the summer season.
Sources (4)

Not testedCommon

Only on sun or sunbed days

Collected report · exact form and route are only as reported below. Source date and reporter identity are not separately verified. Collection checked 30 Sep 2026; presentation annotated 2026-10-01.

Frequency labels describe this collection, not a measured population. Contradictory records remain available.

Details and sourcesHide details
Dose
250–500 mcg
How often
Only on days with UV exposure (about 3–4 times a week)
Route
Injection under the skin
Timing
Before 30–60 minutes of sun or a sunbed
How long
Through the summer
Sources (2)
Show all 4 protocolsShow fewer protocols

Not testedSometimes seen

Higher dose (0.75–1 mg or more)

Collected report · exact form and route are only as reported below. Source date and reporter identity are not separately verified. Collection checked 30 Sep 2026; presentation annotated 2026-10-01.

Frequency labels describe this collection, not a measured population. Contradictory records remain available.

Details and sourcesHide details
Dose
750 mcg–1 mg or more
How often
Most days
Route
Injection under the skin
Timing
Before sun
Ramp
Stepped up after a plateau at 500 mcg
  • Other users argue high doses waste product because the skin’s receptors are already saturated.
Sources (2)

Not testedSometimes seen

Very slow start

Collected report · exact form and route are only as reported below. Source date and reporter identity are not separately verified. Collection checked 30 Sep 2026; presentation annotated 2026-10-01.

Frequency labels describe this collection, not a measured population. Contradictory records remain available.

Details and sourcesHide details
Dose
50–100 mcg, rising to about 300 mcg
How often
Daily for about 1–2 weeks, then twice a week
Route
Injection under the skin
Timing
Some take an antihistamine about 40 minutes before
How long
About 2 weeks
Ramp
Gradual increase over about 2 weeks
  • Used by people worried about nausea or allergic-type reactions.
Sources (2)

Where the numbers come from

Forum practice copies the melanotan II “loading and maintenance” pattern at similar microgram doses. The approved form of the drug, afamelanotide, is a slow-release implant used for a rare light-sensitivity disease; grey-market users do not copy that dosing.

Home-made sprays and serums

Home-made nasal spray. Community recipes. Not tested.

Original source recordsHide

A few users take melanotan I (or tanning peptides generally) as vendor or home-made nasal sprays; one household mixes a 10 mg vial with 1 mL bacteriostatic water and uses one puff a day. Community only, and the key recipe may refer to melanotan II.

Best evidence: Community only (Reddit r/Peptides, 2025). No trial or approved nasal product; the approved form (Scenesse) is an implant.

Collected strength records

Not testedNasal sprayFringe

10 mg vial + 1 mL bacteriostatic water, one puff a day

Original source-specific report. Collection checked 30 Sep 2026; presentation annotated 2026-10-01. Source date and reporter identity are not separately verified. Exact form and route are limited to the source’s description.

Batch: 1 mL

Ingredients and methodHide the recipe

Ingredients

IngredientAmountRole
Melanotan (vial)10 mgActive
Bacteriostatic water1 mLLiquid / preservative
How it’s used
One puff a day; after about a month, every other day. Taking it just after breakfast helped with nausea.
Per dose
Not worked out by the poster.
Preservative
Bacteriostatic water.
  • Posted in a melanotan I thread, but the poster does not say whether their spray is melanotan I or II.
Sources (3)
Editorial synthesis and reported strength comparison

This synthesized method combines source records. It has not been validated for preparation, sterility, compatibility, absorption or storage. Select a reported strength to inspect the arithmetic; no strength is selected for you.

Strength per spray
What people report
Research notes

Grey-market melanotan I is a research-vial product, unrelated in dosing to the approved afamelanotide implant. Many users also take melanotan II, retatrutide or other peptides, so side effects are hard to attribute. Doses in forum posts are sometimes written in “units”, which depend on how the vial was mixed.

Nasal spray

Melanotan I vs II is unclear in the main source.

What it is. In plain English.

Afamelanotide is an alpha-MSH analog approved as a specific implant for adults with erythropoietic protoporphyria, not for cosmetic tanning.

A long-acting alpha-MSH analog also commonly called Melanotan I. FDA approval applies to the specified 16 mg Scenesse subcutaneous implant administered by a trained clinician for adults with erythropoietic protoporphyria (EPP), not to online Melanotan-I vials or tanning use.

Afamelanotide stimulates pigmentation. The approved Scenesse implant is used to increase pain-free light exposure in adults with EPP; this does not establish a cosmetic tanning use or approve seller vials.

Reviewed 2026-10-01.

Structure. What it really looks like.

Experimental

Cryo-EM structure of melanotan I (coral) bound to the human melanocortin-1 receptor (gray).

Melanotan I (afamelanotide, coral) bound to the human melanocortin-1 receptor (gray). Also part of the experiment, but not drawn: a G protein and two antibody fragments.

Missing parts

  • The peptide’s first amino acid and the caps on both its ends aren’t in the model, and the second amino acid’s side chain is cut short.
  • A calcium ion that bridges the peptide and the receptor in the experiment isn’t drawn.

7F4H, Ma et al., 2021. Rendered with Mol* (Sehnal et al., 2021) from RCSB PDB data (Berman et al., 2000).

Specs. The facts at a glance.

Length
13 amino acids
Sequence
Ac-S-Y-S-Nle-E-H-f-R-W-G-K-P-V-NH₂
Sold as
  • Melanotan I 10 mg
Regulatory status
FDA-approved as the Scenesse 16 mg implant to increase pain-free light exposure in adults with EPP. The approval does not cover cosmetic tanning or vendor Melanotan-I products.
Also known as
Afamelanotide (Scenesse)

Sources. What this page rests on.

Every source behind this page, with what it says and when it was checked, is in the Source library.

Melanotan I in the Source library

Original overview and research notes · annotated 2026-10-01

Historical collection text. Read alongside the claim corrections above; identity or evidence qualifications may supersede this wording.

Tanning and sun protection

An approved tanning peptide used as medicine for a rare sunlight-sensitivity disease.

The skin hormone α-MSH with two amino acids swapped so it lasts longer. A straight 13-amino-acid chain.

It targets MC1R on pigment cells and increases eumelanin, the dark, protective pigment. It’s more selective than Melanotan II, with fewer effects on sexual function and appetite.

Trials in erythropoietic protoporphyria (EPP), a disease that makes sunlight painful, increased the time patients could spend in light. The approved form is a slow-release implant under the skin.

Original status record: FDA-approved in 2019 as Scenesse (implant) for EPP; approved in the EU since 2014.

More in Skin, hair & tanning.

Glossary

Cryo-EM

Cryo-electron microscopy. Molecules are frozen in a thin layer of ice and photographed thousands of times with an electron microscope; the images are combined into a 3D map.

Glossary

Resolution

How sharp a structure is, measured in ångströms (Å; a ten-billionth of a meter). Smaller is sharper.

Glossary

Protein Data Bank (PDB)

The free worldwide archive of 3D structures of proteins and other molecules measured in experiments. Each entry has a four-character code, like 7KI0.