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SKIN/TANNING

Melanotan 2

Melanotan 2 (MT-2)

Non-Selective Melanocortin Peptide for Tanning and Skin Pigmentation

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Overview

What is Melanotan 2?

Melanotan 2 (MT-2) is a synthetic analogue of alpha-melanocyte-stimulating hormone (alpha-MSH), a naturally occurring peptide that regulates skin pigmentation and other physiological processes. Developed originally at the University of Arizona in the 1980s as a potential tool for studying melanogenesis, MT-2 was designed to be a more potent and metabolically stable version of alpha-MSH. Researchers hoped the compound could reduce UV exposure required for tanning, thereby lowering skin cancer risk associated with sun-seeking behavior.

MT-2 acts as a non-selective agonist at multiple melanocortin receptors: MC1R, MC3R, MC4R, and MC5R. Activation of MC1R on melanocytes triggers the upregulation of eumelanin production, the dark brown-black pigment responsible for skin darkening. Because MT-2 binds all four receptor subtypes rather than selectively targeting MC1R, it produces a range of effects beyond pigmentation, including spontaneous erections (via MC4R in the central nervous system), appetite suppression (MC3R and MC4R), and changes in sebaceous gland activity (MC5R).

Early phase I clinical trials demonstrated statistically significant increases in skin reflectance and visual pigmentation scores in subjects receiving subcutaneous MT-2 injections. In one landmark trial published in JAMA Dermatology, subjects experienced measurable tanning after only five low doses administered every other day. The same study documented that 8 of 10 male subjects developed clinically significant penile erections after administration, an unexpected finding that eventually led researchers to develop PT-141 (bremelanotide) as a targeted sexual dysfunction treatment. Despite promising early data, MT-2 has never completed the full FDA approval process for any indication, and it remains unapproved for human therapeutic use in the United States, European Union, and most other jurisdictions.

The compound is available through research peptide vendors and is widely used off-label by individuals seeking accelerated tanning, particularly those who tan poorly due to fair skin phenotypes (Fitzpatrick types I-II). Users must understand that the long-term safety profile of MT-2 is incompletely characterized, that the compound can cause changes to existing moles and nevi that mimic melanoma, and that its use is not endorsed by dermatology or endocrinology professional bodies. Responsible use requires pre-use dermatological evaluation and periodic skin monitoring throughout any course of administration.

Research Supply

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Protocol

Dosage Guide

Route: Subcutaneous injection into lower abdomen or lateral thigh

Dosing Schedule

PeriodDose
Loading (Week 1-2)0.25 mg once daily, evening
Maintenance0.5-1.0 mg, 2-3x weekly
Minimal effective (research)0.025 mg/kg every other day
Maximum studied0.03 mg/kg per study day

Reconstitution

VIAL SIZE10 mg
WATER VOLUME2 mL bacteriostatic water
CONCENTRATION5 mg/mL (5,000 mcg/mL)
Each 0.1 mL (10 units on a U-100 insulin syringe) = 0.5 mg

Injection Volumes

DoseVolumeSyringe Units
0.25 mg0.025 mL2.5 units on insulin syringe
0.5 mg0.05 mL5 units
1.0 mg0.10 mL10 units

Administration Tips

  • Inject the water slowly against the side of the vial; do not shake, swirl gently to avoid denaturing the peptide
  • Injecting in the evening can reduce the impact of nausea, which tends to occur within 1-2 hours of dosing
  • Injections are administered subcutaneously into the lower abdomen or lateral thigh using a 27-31 gauge insulin syringe
  • Store reconstituted vials refrigerated at 2-8 degrees Celsius; use within 4-6 weeks
  • Alternatively, add 2 mL BAC water for a 5 mg/mL solution to make smaller doses easier to measure precisely
Safety

Risks & Side Effects

Commonly Reported

Nausea: the most frequently reported side effect, occurring at nearly all dose levels in clinical trials; typically mild and transient, resolving within 1-2 hoursFlushing and facial redness: occurs shortly after injection due to vasodilatory effects mediated through melanocortin receptors in vascular smooth muscleSpontaneous erections in men: a predictable pharmacological effect of MC4R agonism, often accompanied by a stretching and yawning complex; duration can range from 1-5 hours depending on doseFatigue and lethargy: reported by some users during the loading phase, typically resolving as the body adaptsAppetite suppression: MC3R and MC4R agonism reduces appetite in many users; this effect can be significant at higher dosesChanges in moles and skin lesions: MT-2 stimulates pigmentation broadly, including in pre-existing nevi; moles may darken or increase in size

Serious Risks

Melanoma risk

Current evidence does not establish a direct causal link between MT-2 and melanoma development. However, the peptide stimulates melanocyte proliferation, and any increased cancer risk in users is likely mediated through increased UV-seeking behavior. Pre-use dermatological evaluation and ongoing skin monitoring are strongly advised.

Cardiovascular effects

MT-2 can cause transient increases in blood pressure and heart rate. These effects are generally mild but potentially significant in individuals with pre-existing cardiovascular disease.

Psychiatric effects

Anecdotal reports of mood changes and, rarely, psychiatric symptoms with high-dose use.

FAQ

Frequently Asked Questions

Related Research
Expert Voices

Experts Covering Melanotan 2

LEGAL DISCLAIMER

The information provided on this page is for educational and informational purposes only and is not intended as medical advice. Melanotan 2 has not been approved by the FDA for any medical condition. Always consult with a qualified healthcare professional before starting any peptide therapy. Individual results may vary. Peptides Institute is not responsible for any adverse effects resulting from the use of information provided on this site.