Melanotan II research vial
SwissNova Labs
Melanotan II · 10mg
≥99% Purity · COA Included
Hormonal

Melanotan II

Purity: 99%+
Size: 10mg
Grade: Research
Form: Lyophilized
SwissNova Labs · Research Grade
HormonalNEW!

Melanotan II

Melanocortin agonist for tanning, libido, and appetite research.

Melanogenesis — stimulates UV-independent skin darkening via MC1R activationSexual function — MC3R/MC4R activation enhances arousal (parent of PT-141)Appetite suppression — MC4R agonism reduces food intakeBroad melanocortin activity — research tool for multiple receptor systems
Strength10mg
$25.00
10mg · Research use only
Compound Specifications
Purity99%+
Molecular Weight1024.2 Da
Vial Size10mg
SequenceAc-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
Vial Supply
Duration~10 weeks supply
Week 1Week 10
Why Researchers Choose This Compound

Key Benefits

01
Melanogenesis

stimulates UV-independent skin darkening via MC1R activation

02
Sexual function

MC3R/MC4R activation enhances arousal (parent of PT-141)

03
Appetite suppression

MC4R agonism reduces food intake

04
Broad melanocortin activity

research tool for multiple receptor systems

Mechanism of Action

Active Signaling Pathway

BioHuman Research Dossier
PreclinicalResearch use only — not for human consumption

Investigated Pathways

MC1R / MC4RMelanocortin ReceptorPigmentation Research

Proposed Mechanism

MT-II activates MC1R on melanocytes to stimulate melanin production (tanning), MC3R/MC4R in the hypothalamus for sexual arousal and appetite suppression, and MC5R for exocrine gland regulation. Its broad melanocortin receptor activity produces multiple simultaneous effects.

Research Highlights

  • Shown to produce significant skin darkening without UV exposure in clinical trials
  • Demonstrated erectile function improvement in men with psychogenic ED
  • Appetite suppression via MC4R activation — potential obesity research application
  • Parent compound of PT-141 (bremelanotide) — FDA-approved derivative
PreclinicalEvidence Strength

Evidence is primarily from in vitro cell studies and animal models. Human data is limited or absent.

Research FocusBrain & CNS
Brain & CNS body system research map
Brain & CNS

For laboratory research only

All Research Systems →

For research use only — not for human consumption. No treatment claims.

Full Research Hub →
Supply Calculator

How long will one vial last?

Based on standard research protocols, here's exactly what to expect from a single 10mg vial — and when to plan your next order.

One vial lasts
10
weeks
Approximately 2 months of supply at standard protocol volumes.
Reorder around week 9 to avoid running out
Your supply timeline10mg vial
Start↑ ReorderWeek 10 — empty
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Vial supply estimate is based on standard research protocol volumes. Actual duration will vary based on your specific protocol design.

Research Literature

Scientific Background

Mechanism of Action

MT-II activates MC1R on melanocytes to stimulate melanin production (tanning), MC3R/MC4R in the hypothalamus for sexual arousal and appetite suppression, and MC5R for exocrine gland regulation. Its broad melanocortin receptor activity produces multiple simultaneous effects.

Clinical Context

Melanotan II was developed at the University of Arizona as a potential photoprotective agent. Its broad melanocortin activity makes it a versatile research tool for studying multiple physiological systems.

Research Highlights

  • Shown to produce significant skin darkening without UV exposure in clinical trials
  • Demonstrated erectile function improvement in men with psychogenic ED
  • Appetite suppression via MC4R activation — potential obesity research application
  • Parent compound of PT-141 (bremelanotide) — FDA-approved derivative

Storage & Reconstitution

Store at -20°C. Reconstitute with 2 mL bacteriostatic water → 5 mg/mL. Stable 4 weeks at 2–8°C. Protect from light.

Peer-Reviewed Research

Key Studies

1996Journal of Investigative Dermatology

Melanotan II: a potent melanotropin for photoprotection

Dorr RT et al.

Melanotan II produced significant skin darkening without UV exposure in clinical trials via MC1R activation.

PubMed →
1998Journal of Urology

Melanotan II for erectile dysfunction

Wessells H et al.

Melanotan II produced penile erections in men with psychogenic erectile dysfunction via central melanocortin receptor activation.

PubMed →
2007Journal of Sexual Medicine

Sexual effects of Melanotan II

King SH et al.

Melanotan II demonstrated sexual arousal effects in both males and females via MC3R/MC4R activation.

PubMed →
Absorption & Distribution

Pharmacokinetics

PK Parameters
Bioavailability~80% SubQ
Peak Plasma1–2 hours
Half-life~2–3 hours; broader receptor profile than PT-141 produces more side effects
ClearanceProteolytic degradation; renal clearance
Volume of Distribution~0.4 L/kg
What this means

Bioavailability indicates how much of the compound reaches systemic circulation. Peak plasma is when blood levels are highest. Half-life determines dosing frequency — compounds with short half-lives require more frequent dosing to maintain therapeutic levels.

The volume of distribution reflects how widely the compound distributes into tissues. A higher Vd means the compound concentrates in tissues rather than staying in plasma.

Molecular Targets

Receptor Binding Profile

MC1RAgonist

Stimulates melanin production in melanocytes for UV-independent skin darkening

MC3RAgonist

Energy homeostasis and secondary sexual function effects

MC4RAgonist

Sexual arousal, appetite suppression via hypothalamic pathways

MC5RAgonist

Exocrine gland regulation

Safety Profile

Side Effects & Adverse Events

Common
  • Nausea (50%)
  • Flushing
  • Spontaneous erections (males)
  • Facial flushing
Uncommon
  • Fatigue
  • Yawning
  • Stretching
Serious
  • Hyperpigmentation of existing moles (monitor for changes)
  • Potential melanoma risk with UV exposure
NOTE:Non-selective melanocortin agonist; broader receptor profile than PT-141 means more side effects. Monitor moles and skin lesions regularly.
Research Safety

Contraindications & Interactions

Absolute Contraindications
History of melanoma or atypical molesCardiovascular disease
Relative Contraindications
Fair skin with many moles (monitor closely)Hypertension
Drug Interactions
Antihypertensives (additive BP effects)Dopaminergic drugs (additive)
NOTE:Broader receptor profile than PT-141 means more side effects. PT-141 preferred for sexual function research due to better selectivity.
Stack Protocols

Synergistic Compounds

PT-141

PT-141 is the more selective derivative of Melanotan II for sexual function — use PT-141 for sexual function, Melanotan II when tanning is also desired.

Use Melanotan II 0.5 mg SubQ for tanning protocols; switch to PT-141 1 mg as-needed for sexual function.

View Compound →
Sourcing & Testing

Transparent Global Sourcing

🇨🇳

Manufactured

Sourced through our manufacturing partner in China

🧪

Independent Testing

Analytical reports available from Janoshik Analytical

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Batch Verification

Batch-specific COAs with online verification via janoshik.com

🇺🇸

US Fulfillment

Orders fulfilled from the United States

Testing documentation varies by product and batch. Customers may review available reports and verification information before ordering. COA task numbers and verification keys can be confirmed directly at janoshik.com/verification. For research use only — not for human consumption.
RESEARCH USE ONLY:All products are sold strictly for in vitro research and laboratory use. Not intended for human consumption, clinical use, diagnosis, treatment, or prevention of any disease or condition. By purchasing, you confirm you are a qualified researcher and will use these compounds in accordance with all applicable laws and regulations.