Educational research reference · Not medical advice · Compounds discussed are research materials, not approved drugs
Home / Protocols / Melanotan-II
Protocol · Research Dosing Guide

Melanotan-II (MT-II) Dosing Protocol: Injection, Nasal Spray & Research (2026)

A research reference for the melanocortin agonist Melanotan-II, with separate injection and nasal-spray protocols, reconstitution math, mechanism, and the safety considerations most consistently flagged in pigmentation research.

Melanotan-II Quick Start

Melanotan-II (MT-II) is a synthetic cyclic analog of alpha-melanocyte-stimulating hormone (α-MSH). It is a non-selective melanocortin-receptor agonist, acting at MC1R (linked to skin pigmentation) and MC4R (linked to sexual response and appetite). It is studied in pigmentation, photoprotection, and sexual-function research models.

Quick reference Preclinical / community
Class
Melanocortin agonist (α-MSH analog)
Formats
Vial (SubQ) · Nasal spray
Targets
MC1R, MC4R
Schedule shape
Loading then maintenance
Vial size
10 mg

This guide is an educational research reference. It does not diagnose, treat, or prescribe, and is not medical advice. Consult a licensed clinician before considering any compound.

Melanotan-II Dosing Protocols

The injectable (subcutaneous) and nasal-spray formats are documented as two separate protocols. Community-derived planning typically uses a low loading phase, then a smaller, less frequent maintenance phase once the target response is reached. These are research-planning references, not personal dosing recommendations.

Injection — Subcutaneous

Reconstituted 10 mg vial, U-100 insulin syringe.
PhasePer doseFrequency
Loading250 mcgOnce daily
Maintenance500 mcg2–3× weekly
10 mg + 2 mL BAC → 5,000 mcg/mL · 250 mcg = 5 units

Nasal Spray

Pre-mixed nasal spray, ready to use.
PhasePer dose# of spraysFrequency
Loading300 mcg3 spraysOnce daily
Maintenance500 mcg5 sprays2–3× weekly
Each 0.1 mL spray delivers 100 mcg
Many research protocols start at the low end and increase slowly, because nausea and flushing are most common early and at higher single doses.

Melanotan-II Reconstitution Guide

MT-II ships as a lyophilized powder. The BAC water volume sets the concentration and draw volume for the injectable vial. Nasal sprays ship pre-mixed and ready to use.

Injection

BACConc.250 mcg
2 mL5,000 mcg/mL0.05 mL · 5 u
1 mL10,000 mcg/mL0.025 mL · 2.5 u

2 mL is the default; units are U-100 syringe units.

Reconstitution steps

  1. Inspect the vial. Confirm label and intact powder.
  2. Wipe the stoppers. Alcohol swab on both vials.
  3. Draw BAC water. 2 mL into the injectable vial.
  4. Inject down the wall. Release water slowly down the inside wall, not onto the powder.
  5. Swirl, do not shake. Roll gently until clear.
  6. Refrigerate. Store at 2–8 °C; do not freeze.

How to use the nasal spray

  1. Prime first use. Pump 2–3 sprays into a tissue until a fine, even mist appears.
  2. Position. Tilt the head slightly forward; insert the tip just inside one nostril, aimed slightly outward toward the ear — not at the septum.
  3. Spray and breathe. Press once while breathing in gently; do not sniff hard, which sends the solution down the throat instead of onto the mucosa.
  4. Alternate nostrils. For multi-spray doses, switch nostrils each spray to spread absorption and limit irritation.
  5. Count per the protocol. Use the sprays-per-dose shown above; if a dose isn't a whole number, round up.
  6. Between uses. Wipe the tip, recap, and refrigerate.

How Melanotan-II Works

MT-II mimics α-MSH and activates melanocortin receptors. At MC1R on melanocytes it stimulates melanogenesis (eumelanin production), the basis for pigmentation research. At MC4R in the central nervous system it influences sexual arousal and appetite — the same MC4R activity underlies the related approved fragment bremelanotide (PT-141).

MC1R → pigmentation

Stimulates melanin synthesis in melanocytes in pigmentation models.

MC4R → arousal/appetite

Central melanocortin activity linked to sexual response and reduced appetite.

Non-selective

Unlike PT-141, MT-II is not MC4R-selective, so it drives both pigmentation and central effects.

Open question

Long-term human safety, especially around melanocytic lesions, is not established.

Who Should Avoid Melanotan-II

Atypical moles / melanoma history

MT-II increases melanocyte activity and can darken moles; a personal/family history of melanoma or many atypical nevi is a key caution.

Pregnancy & lactation

No human reproductive safety data.

Cardiovascular concerns

Melanocortin activity can affect blood pressure; review with a clinician.

Unmonitored skin changes

New or changing pigmented lesions warrant dermatologic evaluation before continuing.

Melanotan-II Side Effects & Safety

Nausea & flushing

The most common short-term effects, typically worse early and at higher single doses.

Pigment changes

Darkening of moles, freckles, and new pigmented spots are commonly reported; dermatologic monitoring is prudent.

Spontaneous erections

A frequently reported MC4R-mediated effect in male users.

Appetite suppression

Reduced appetite is commonly reported.

Timeline & What to Monitor

TimeframeCommonly trackedNotes
Days 1–3Nausea, flushing, injection-site responseEarly-dose tolerability is most prominent here.
Weeks 1–3Pigmentation responsePigment changes build gradually; this drives the loading→maintenance shift.
OngoingMoles and pigmented lesionsTrack any new or changing lesion; seek dermatologic review.

Research Evidence Context

Pigmentation

Early clinical and preclinical work explored melanotan peptides for tanning and photoprotection research.

Sexual function

MC4R activity informed development of the approved related fragment bremelanotide (PT-141).

Safety signals

Case reports describe changing moles and melanoma concerns with unregulated MT-II use.

Open question

MT-II itself is not an approved drug and lacks long-term controlled safety data.

Storage & Handling

StateStorageNotes
Lyophilized (powder)−20 °C long-term; fridge short-termMore stable than reconstituted solution.
Reconstituted (liquid)2–8 °CUse within ~3–4 weeks; do not freeze.
AppearanceClear, colorlessDiscard cloudy or particulate solutions.

Mistakes & Troubleshooting

  1. Strong nausea/flushing. Often dose-related; research protocols typically start low and titrate slowly.
  2. Wrong BAC volume. Recalculate concentration; injection assumes 2 mL, spray assumes 10 mL.
  3. Missed dose. Skip and continue at the next scheduled time; do not double-dose.
  4. New or changing mole. Stop and seek dermatologic evaluation.
  5. Left out overnight. Treat reconstituted solution as compromised and discard.

Melanotan-II vs PT-141

FeatureMelanotan-IIPT-141 (Bremelanotide)
SelectivityNon-selective (MC1R + MC4R)MC4R-selective
Main research focusPigmentation + sexual responseSexual response

Monitoring

There is no peptide-specific lab for MT-II. The most relevant monitoring is dermatologic — periodic skin/mole checks — plus blood-pressure awareness given melanocortin vascular effects.

Frequently Asked Questions

What is Melanotan-II?

A synthetic α-MSH analog and non-selective melanocortin agonist studied in pigmentation and sexual-function research.

How is the injection dosed vs the nasal spray?

Separate protocols. Injection commonly references 250 mcg daily loading then 500 mcg 2–3× weekly. The spray delivers 100 mcg per spray, so loading is 3 sprays and maintenance is 5 sprays.

How is MT-II reconstituted?

For injection, 10 mg in 2 mL BAC water gives 5,000 mcg/mL, so 250 mcg = 0.05 mL = 5 units. The spray ships pre-mixed and delivers 100 mcg per spray.

Why does MT-II cause nausea and darker moles?

MC4R activity drives nausea/flushing (worse early), and MC1R activity increases melanocyte activity, which can darken existing moles and create new pigmented spots. Changing lesions warrant dermatologic review.

Is this page medical advice?

No. It is an educational research reference and does not diagnose, treat, or prescribe. Consult a licensed clinician before considering any compound.

References

  1. Dorr RT, et al. Evaluation of melanotan-II, a superpotent melanotropic peptide, in humans. Life Sci (1996).
  2. Wessells H, et al. Melanocortin receptor agonists and erectile response. Urology / J Urol (1998–2000).
  3. Hadley ME, Dorr RT. Melanocortin peptide therapeutics: melanotan analogs. Peptides (2006).
  4. Langan EA, et al. Melanotropic peptides: safety concerns with unregulated use. Br J Dermatol (review).
  5. King SH, et al. Melanocortin receptors and bremelanotide (PT-141) development. Pharmacology (review).