Skin & Hair

Melanotan II 10mg

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$40
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Certificate of Analysis
Most recent lab test
Freedom
99.71%
Purity
10.48 mg
Tested mass · 10 mg labeled · +4.8%
Test panel
Identity confirmed · ConfirmedSterility · No growthMicrobial (PCR) · PassEndotoxin · PassAppearance · White Lyophilized Powder
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Lot 160-710L-DK · Search code Pept2607210477
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Pept2607210477
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For laboratory and research use only. Not for human or veterinary use, not a drug, food, or cosmetic.

Melanocortin Peptide · Broad-Spectrum Agonist

MT2. The potent, broad-spectrum melanotan, the version most researchers actually mean.

A 10mg lyophilized vial of Melanotan 2, a cyclic analog of alpha-MSH researched for rapid pigmentation and a range of melanocortin-driven effects. The more potent of the two melanotans, active across multiple receptors at lower amounts.

High Potency
Stronger pigmentation effect per amount than MT1, generally used at lower research amounts.
Broad-Spectrum
Active across MC1R, MC3R, MC4R and MC5R, not just the pigmentation receptor.
Beyond Tanning
Its MC4R activity is what spun off the libido research that became PT-141.
WHAT YOU'RE WORKING WITH

One peptide. Several receptors. The reason MT2 hits harder than MT1.

Sequence
Cyclic
alpha-MSH Analog
A cyclic, ring-structured analog of alpha-melanocyte-stimulating hormone. The cyclization makes it more stable and longer-acting than the natural hormone.
Targets
MC1R + MC4R
Multi-Receptor
Activates MC1R for pigmentation, plus MC3R, MC4R and MC5R, which is where the appetite and libido effects come from.
Output
Pigment +
And More
Strong eumelanin production for tanning, alongside the broader melanocortin effects MT1 largely stays out of.

MT2 is Melanotan 2, a cyclic analog of the body's own alpha-MSH. Unlike MT1, which is tuned to stay selective for the pigmentation receptor, MT2 is a broad melanocortin agonist. It drives strong pigmentation through MC1R, but it also hits MC3R, MC4R and MC5R, which is the source of both its extra effects and its side effects. That breadth is exactly why MT2 is more potent than MT1, and exactly why it comes with more to manage.

How MT2 Works

MT2 (Melanotan 2) is a synthetic, cyclic analog of alpha-melanocyte-stimulating hormone (alpha-MSH). Where natural alpha-MSH is cleared from the body almost immediately, MT2's ring structure makes it far more stable and longer-acting, so it stays bound to its receptors long enough to produce a strong, sustained effect.

The core pigmentation mechanism is the same one MT1 uses. MT2 binds the melanocortin-1 receptor (MC1R) on melanocytes, raises intracellular cAMP, activates tyrosinase, and drives production of eumelanin, the darker photoprotective pigment. The difference is that MT2 does not stop at MC1R. It is a broad-spectrum agonist that also activates MC3R, MC4R and MC5R.

That breadth is the whole story of MT2. The MC4R activity in particular is responsible for the libido and appetite effects MT2 is known for, and it is the reason a separate compound, bremelanotide (PT-141), was developed out of this research line specifically for sexual function. The same broad activity that makes MT2 more potent than MT1 is also what produces its better-documented side effects: nausea, facial flushing, appetite suppression, and darkening of existing moles and freckles.

ONE PEPTIDE, MULTIPLE RECEPTORS
MC1R→ Pigmentation, eumelanin production, tanning effect
MC3R→ Energy balance and inflammatory signaling roles
MC4R→ Appetite suppression and libido effects
MC5R→ Exocrine gland and sebaceous activity

One molecule across the melanocortin system. The breadth is the potency and the side effects both.

MT2 vs MT1: The Honest Comparison

This is the decision most people are weighing, so here it is straight. MT2 and MT1 reach the same pigmentation endpoint, but MT2 does it harder and brings more along with it.

MT2 (Melanotan 2)
MT1 (Melanotan 1)
Selectivity. Broad agonist. Hits MC1R, MC3R, MC4R and MC5R.
Strongly selective for MC1R, the pigmentation receptor.
Potency. More potent for pigmentation, generally used at lower amounts.
Less potent per amount, usually requires more frequent administration.
Side effects. Better-documented: nausea, flushing, appetite suppression, libido effects, mole darkening.
Researched for a much quieter profile with fewer of those effects.
Extra effects. MC4R activity drives libido and appetite changes beyond tanning.
Activity stays concentrated on pigmentation.
Best fit. Researchers studying maximum pigmentation or the broader melanocortin effects.
Researchers who want pigmentation with minimal systemic activity.

What's in the Vial

One lyophilized vial containing 10mg of MT2 (Melanotan 2) at research-grade purity. Reconstitute with bacteriostatic water. Tested for purity by third-party HPLC analysis. COA available on this product page.

Why Researchers Choose MT2 Over MT1
  • More potent for pigmentation, effective at lower research amounts
  • Broad-spectrum activity across the melanocortin receptor family
  • The version most community research and protocols are built around
  • MC4R activity opens up effects beyond tanning alone
  • Cyclic structure resists breakdown for longer-lasting activity
  • The original research line behind PT-141 (bremelanotide)
  • Single peptide, single reconstitution, straightforward to work with

About the Name

"Melanotan" is a contraction of melanocyte and tan, which is exactly the system the molecule was built to act on. The numbering separates the two analogs that came out of the original University of Arizona research. MT2 is the second and more potent of the pair, a cyclic structure that trades MT1's selectivity for a stronger, broader effect. It became the more widely known of the two melanotans, to the point that when people say "melanotan" without a number, MT2 is usually what they mean.

Research Context

MT2's research history runs in two directions. On the pigmentation side, it is the more potent melanotan and the one most community protocols are based on. On the broader side, its MC4R activity made it the starting point for an entire separate line of research into sexual function, which produced bremelanotide (PT-141), now an approved prescription drug for hypoactive sexual desire disorder. MT2 itself is not an approved drug and is not FDA-approved for human use. Unlike MT1, whose active form afamelanotide reached clinical approval for pigmentation, MT2's clinical legacy lives in the PT-141 derivative rather than in MT2 directly. Researchers using MT2 are working with a well-studied but unapproved compound that has a meaningful side-effect profile.

Stacking Notes

MT2 is most often used on its own, since its potency and breadth already cover a lot of ground. Some researchers pair it with MT1, leaning on MT2 for the heavy pigmentation work while using MT1 to carry part of the load with less systemic burden. Others run MT2 alongside PT-141 in protocols focused on the MC4R-driven effects rather than tanning. No published combination data exists at this level, and any pairing is community-driven rather than formally studied.

Storage

Lyophilized: store refrigerated, away from light. After reconstitution: keep refrigerated, use within 30 days. Do not freeze reconstituted product. Protect from light at all stages.

Product Highlights
  • 10mg MT2 (Melanotan 2) per vial
  • Cyclic alpha-MSH analog
  • Broad-spectrum melanocortin agonist
  • Researched for potent pigmentation and broader effects
  • More potent than MT1, used at lower amounts
  • The research line behind PT-141 (bremelanotide)
  • Third-party HPLC tested
  • COA available on product page
  • Lyophilized for shelf stability
For Research Use Only. MT2 (Melanotan 2) is a research compound. It is not approved by the FDA for human use. Safety and efficacy in this context have not been established. This product is sold strictly for laboratory and research purposes. Not for human consumption.
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