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Protocols · Cosmetic

Melanotan II: literature-reported ranges

Melanotan II has a small early human literature on melanogenesis from the 1990s, after which development stopped. It is also the compound in this list with the most substantial case-report literature describing harms, and that context belongs alongside any figure.

Read this first

Every figure on this page is a range reported in published literature or in a publicly documented study protocol. It is a record of what researchers used, not a recommendation, a therapeutic protocol, or advice. Peptide Intel Hub is an independent publication, sells nothing, and describes these compounds as in-vitro research reagents only.

Compound at a glance

Class
Cyclic α-MSH analogue
Reported half-life
Approximately 1 hour
Routes used in the literature
Subcutaneous in the published studies
Also written as

What the published studies reported

Each row below describes one body of work. The model and population are part of the figure — a rodent per-kilogram quantity and a human trial quantity are not comparable.

Early human melanogenesis studies

Reported quantity
0.01 mg/kg per administration
Frequency
Once daily
Study duration
10 consecutive days in the published arms

Melanin density was measured by reflectance spectroscopy.

Extended tanning-response arms

Reported quantity
Around 0.025 mg/kg
Frequency
Every other day
Study duration
Up to 4 weeks

Nausea and facial flushing were reported as dose-limiting.

Dosage chart

These figures match the published chart for this compound on peptidedosages.com, including the reconstitution volume, resulting concentration, insulin-syringe units and the staged schedule. Educational reference only — not instructions, and not medical advice.

Melanotan II · 10 mg Vial

Melanotan II is dosed at 250 mcg–1 mg daily via subcutaneous injection in educational protocols. A 10 mg vial reconstituted with bacteriostatic water yields about 3.33 mg/mL. This information is for research and educational use only.

Reconstitute
Add 3.0 mL bacteriostatic water → 3.33 mg/mL concentration.
Typical daily range
250–1000 mcg once daily (gradual titration over 8–12 weeks).
Easy measuring
At 3.33 mg/mL, 1 unit = 0.01 mL ≈ 33.3 mcg on a U-100 insulin syringe.
Storage
Lyophilized: freeze at −20 °C (−4 °F) or below; after reconstitution, refrigerate at 2–8 °C (35.6–46.4 °F); use within 1–2 weeks.

Standard / Gradual Titration (3 mL = 3.33 mg/mL)

Week / PhaseDaily DoseUnits (per injection) (mL)
Week 1250 mcg (0.25 mg)7.5 units (0.075 mL)
Week 2500 mcg (0.5 mg)15 units (0.15 mL)
Week 3750 mcg (0.75 mg)22.5 units (0.225 mL)
Weeks 4–81000 mcg (1 mg)30 units (0.30 mL)
Maintenance<br>(after Week 8)500–1000 mcg<br>(1–2× weekly)15–30 units<br>(0.15–0.30 mL)
Source chart on peptidedosages.com

Mixed with 3 ml of bacteriostatic water

The same arithmetic for every vial size Melanotan II is supplied in, using a fixed 3 ml of bacteriostatic water. One unit on a U-100 insulin syringe is 0.01 ml, so the unit column below is simply the volume that carries the reported amount. Educational arithmetic only — not instructions, and not medical advice.

Melanotan II · 3 ml bacteriostatic water

Vial sizeConcentrationPer 1 unit250 mcg =1 mg =
10 mg3.33 mg/ml33 mcg7.5 units30 units

Unit columns use the range reported for this compound (250 mcg–1 mg). Only the vial sizes this compound is actually supplied in are shown, and every figure assumes exactly 3 ml of bacteriostatic water. For any other volume, use the reconstitution calculator.

Reconstitution maths

A 10 mg vial in 2 mL of bacteriostatic water gives 5 mg/mL.

Open the reconstitution calculator

How to read these figures

  • Published case reports link this compound to changes in melanocytic naevi and to rhabdomyolysis; several regulators have issued warnings.
  • Unregulated supply chains for this compound are widely documented.
  • Melanocortin receptor selectivity is poor compared with PT-141.

Sources and citations

These are the published records the figures on this page are drawn from. Each one describes what researchers administered, in which model or population, and over what period. Quantities reported in a study are specific to that study's design and are not transferable guidance.

  1. [1]
    Synthetic Melanotropic Peptide Initiates Erections in Men With Psychogenic Erectile Dysfunction: Double-Blind, Placebo Controlled Crossover Study

    Wessells H, Fuciarelli K, Hansen J, et al. · J Urol · 1998 · DOI 10.1016/S0022-5347(01)62903-3

    Ten men with psychogenic erectile dysfunction received subcutaneous Melanotan-II at doses of 0.025 mg/kg or 0.5-4 mg per dose in a crossover trial to evaluate erectogenic effects.

    View the record
  2. [2]
    Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study

    Dorr RT, Lines R, Levine N, et al. · Life Sci · 1996 · PMID 8637402

    Phase I dose-escalation study in human volunteers administering subcutaneous Melanotan-II (doses from 0.005 to 0.157 mg/kg) to assess tanning, safety, and pharmacokinetics.

    View the record
  3. [3]
    Melanocortin receptor agonists, penile erection, and sexual motivation: human studies with Melanotan II

    Wessells H, Levine N, Hadley ME, Dorr RT, Hruby V. · Int J Impot Res · 2000 · PMID 11035391

    Review of studies in which Melanotan II was administered subcutaneously to 20 men with erectile dysfunction using double-blind, placebo-controlled crossover designs to assess penile rigidity and sexual motivation.

    View the record

Search the databases yourself

Read the Melanotan II research brief

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© 2026 Peptide Intel Hub · Marbella · Educational research reference · For in-vitro research use only
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