Melanotan II

Melanotan II (MT-II)

A cyclic analog of alpha-MSH that promotes skin tanning, reduces appetite, and enhances sexual function.
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100% 50% · t½ Time → Serum level
Molecular Weight 1024.18 Da
Half-Life ~1–2 hours
Typical Dose 0.5–1 mg
Cycle Length 2–4 weeks loading, then maintenance
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Description

Melanotan II (MT-II) is a synthetic cyclic analog of alpha-melanocyte-stimulating hormone (α-MSH) that was originally developed at the University of Arizona in the 1980s as a potential sunless tanning agent. It activates multiple melanocortin receptors (MC1R, MC3R, MC4R) with broad potency, producing a constellation of effects: increased melanin production (tanning without UV exposure), appetite suppression, enhanced sexual function and libido, and reduced body fat. Melanotan II is the precursor from which PT-141 (bremelanotide) was derived — PT-141 was developed to retain the sexual function benefits while reducing the tanning and other side effects. MT-II has a broader receptor profile than PT-141 and produces more pronounced tanning effects, but also has a higher side effect burden. It is not FDA-approved and is classified as a research chemical.

Key Characteristics

Molecular Formula

C50H69N15O9

Molecular Weight

1024.18 Da

Half-Life

~1–2 hours

Administration Routes

Subcutaneous injection, Intranasal

Typical Dose

0.5–1 mg

Frequency

Daily (loading), then as needed

Investigated Benefits

* Benefits based on preclinical/animal research unless otherwise noted.

Mechanism of Action

“A cyclic analog of alpha-MSH that promotes skin tanning, reduces appetite, and enhances sexual function.”

Melanotan II activates all five melanocortin receptor subtypes with varying potency, with highest affinity for MC1R, MC3R, and MC4R. MC1R activation on melanocytes triggers the cAMP-PKA pathway, stimulating the transcription factor MITF and upregulating the enzymes involved in melanin synthesis (tyrosinase, TRP-1, TRP-2). This produces eumelanin (brown/black pigment) in the skin, providing a tan and some degree of UV protection. MC3R and MC4R activation in the hypothalamus suppresses appetite through NPY/AgRP inhibition and POMC activation, and activates the neural circuits for sexual arousal (similar to PT-141). MC4R activation in the paraventricular nucleus also triggers spontaneous erections in men through a spinal cord mechanism. The broad receptor activation profile of MT-II compared to PT-141 explains its more pronounced tanning effects and higher incidence of nausea and other side effects.

Administration Routes

Subcutaneous injection

Intranasal

Key Characteristics

Typical Dose

0.5–1 mg

Frequency

Daily (loading), then as needed

Cycle Length

2–4 weeks loading, then maintenance

Administration

Subcutaneous injection

Protocol Notes

Start with 0.25 mg to assess tolerance. Nausea is common, especially initially. Tanning effects begin within 1–2 weeks. Use sunscreen despite tanning — MT-II does not fully replace UV protection.

Reconstitution Guide

Add 2 mL bacteriostatic water to 10 mg vial → 5 mg/mL For 0.5 mg dose: draw 0.1 mL (10 units on U-100 syringe)

Storage Information

Lyophilized: refrigerate. Reconstituted: refrigerate and use within 30 days.

Quality & Sourcing Standards

When sourcing Melanotan II for research purposes, the following quality benchmarks should be verified before use.

Documented serious adverse events

FDA’s listing for Melanotan II cites published case reports of melanoma, posterior reversible encephalopathy syndrome, sympathomimetic toxidrome and priapism. DermNet additionally reports rhabdomyolysis and states that its use is not recommended for anybody. FDA placed Melanotan II in Category 2 (significant safety risks) in September 2023.

Purity:

>98% (verified by HPLC)

Certificate of Analysis (COA):

Must be provided by supplier

Endotoxin Testing:

<0.1 EU/mg (prevents bacterial contamination)

GMP Compliance:

Manufactured in cGMP-certified facility

Third-Party Testing:

Independent lab verification preferred

Storage Information

Lyophilized: refrigerate. Reconstituted: refrigerate and use within 30 days.

FDA Disclaimer

The statements made within this website have not been evaluated by the US Food and Drug Administration. The products and information provided are not intended to diagnose, treat, cure, or prevent any disease. This website is intended for educational and research purposes only. Many peptides described on this site are not approved by the FDA for human therapeutic use and are classified as research chemicals. Nothing on this site constitutes medical advice.

Research Highlights

1

Demonstrated tanning effects in multiple human studies

2

Appetite suppression and weight loss in animal models

3

Erectile function improvement in clinical studies

Evidence Level

Multiple animal studies and/or early human trials. Reasonable confidence in mechanism, but human data is limited.

Compatible Peptides

Peptides commonly used alongside Melanotan II for synergistic effects

PT-141

An FDA-approved melanocortin agonist for hypoactive sexual desire disorder with central nervous system mechanism.

Quick Reference

Category

Hormone & GH

Status

Research Only
 

Dose

0.5–1 mg

Frequency

Daily (loading), then as needed

Cycle

2–4 weeks loading, then maintenance