Peptides / Melanotan 2
10 mg Melanocortin research Research use only

Melanotan 2

Melanotan II is a synthetic cyclic analogue of alpha-melanocyte-stimulating hormone, developed at the University of Arizona as a melanocortin receptor research tool. It is supplied strictly for laboratory research into melanocortin signalling.

Melanotan 2 10 mg

What it is

Melanotan II is a cyclic heptapeptide analogue of α-MSH, the hormone that signals melanocytes to produce pigment. It activates multiple melanocortin receptors (MC1R, MC3R, MC4R, MC5R), which is why it has been used in research spanning pigmentation, appetite and other signalling pathways.

Its research history is genuinely notable: an off-target MC4R effect observed during early studies directly led to the development of bremelanotide (PT-141), which became an FDA-approved medicine. Melanotan II itself was never taken through a completed regulatory development programme.

It is an unlicensed compound with well-documented safety concerns in the case literature, and the MHRA has issued standing public warnings about melanotan products marketed for human use. PMR PHARMA supplies it solely as a laboratory reference material for receptor research.

Regulatory note: Melanotan products are the subject of standing MHRA public warnings. Melanotan II is an unlicensed compound with documented safety concerns in the medical case literature. It is supplied strictly as a laboratory reference material for research into melanocortin receptor signalling — not for human use of any kind.
Research highlights

What the studies suggest

Findings from the published literature, with the evidence level stated honestly for every claim.

4
Receptor targets

Binds MC1R, MC3R, MC4R and MC5R — a broad melanocortin receptor probe used across pigmentation and signalling research.

Mechanism
PT-141
Research legacy

An off-target effect observed in Melanotan II studies led directly to bremelanotide — now an FDA-approved drug.

History
α-MSH
Parent hormone

A stabilised cyclic analogue of the body's own melanocyte-stimulating hormone.

Chemistry

Specifications

CompoundMelanotan II (MT-2)
CAS number121062-08-6
Molecular weight~1,024.2 Da
Content10 mg — lyophilised vial
Purity≥99% (HPLC) — batch COA supplied
FormLyophilised powder
Storage2–8 °C, protected from light
Formats: Lyophilised vial. Batch-matched third-party COA supplied with every order — request yours via WhatsApp with your batch number.

Certificate of analysis

Laboratory test report for Melanotan 2 View full certificate
Lab verified
LaboratoryJanoshik Analytical
Report#198520
Purity (HPLC)99.694%
Content measured9.73 mg
Analysis date25 Jul 2026

Client, manufacturer and verification fields are redacted for commercial confidentiality. Results, batch and purity data are unaltered.

Storage & handling

Store lyophilised at 2–8 °C or −20 °C, protected from light. Reconstituted solution should be refrigerated at 2–8 °C.

Questions

What is Melanotan II used for in research?

As a broad melanocortin receptor agonist, it is used to study pigmentation biology and MC receptor signalling pathways in laboratory models.

Is Melanotan II licensed?

No. It is not an approved medicine in any country, and the UK MHRA has issued standing public warnings about melanotan products marketed for human use. It is supplied strictly for laboratory research.

How is it verified?

Independent third-party HPLC purity and mass-spectrometry identity testing per batch, with COAs available on request.

No checkout. No middlemen.

Enquire about Melanotan 2 directly

Message us on WhatsApp for availability, batch COAs and dispatch. A real person replies — usually within the hour.

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All products supplied by PMR PHARMA are intended strictly for laboratory research use only. They are not intended for human or veterinary use, consumption, administration, or any therapeutic purpose. These products are not medicines, supplements, cosmetics or food, and have not been evaluated by the MHRA, EMA or FDA. Nothing on this site is intended to diagnose, treat, cure or prevent any disease.