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For research use only. Not for human or veterinary use.Melanotan II. For research use only. Not for human or veterinary use.

Melanotan II research peptide

$46.00 – $138.00

For research use only. Not for human or veterinary use.

  • ≥98% by HPLC (lot-specific)
  • Canada fulfilment

Size

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Third-party lab verified

HPLC + MS

Independently tested for identity and purity

Batch
MT2-081426
Tested
August 14, 2026
Purity
99.6%

Tested by Testides

Melanotan II

$92.00

Product description

Melanotan II research peptide is supplied to qualified Canadian institutions as a characterized laboratory material for in vitro melanocortin-receptor pharmacology. The compound is a cyclic heptapeptide analogue of α-melanocyte-stimulating hormone (MT-II).

In vitro, the lactam bridge confers conformational rigidity and metabolic stability relative to linear α-MSH. Melanotan II is non-selective across MC1R, MC3R, MC4R, and MC5R, which is why it is used as a reference agonist when an assay must occupy the melanocortin family rather than a single subtype. Typical designs record cAMP or reporter readouts in receptor-expressing cells and compare subtype-selective ligands. This listing describes receptor pharmacology in experimental systems only and does not assign a cosmetic or clinical use.

The material is offered as a lyophilized vial. Identity data (CAS 121062-08-6, formula C50H69N15O9, molecular weight 1024.2 g/mol, sequence Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2, PubChem CID 92432) are listed on the specification table. Store lyophilized at −20 °C, protected from light, and handle under the receiving institution's chemical-hygiene plan.

Lots are sourced from a GMP-aligned peptide manufacturing partner and released against the stated HPLC purity for that lot (≥98% by HPLC, lot-specific). Identity, chromatographic purity, and related analytical results are documented on the lot certificate of analysis (COA). Retain the COA with the inventory record.

This listing is a research-use-only peptide offered to qualified Canadian institutions for in vitro and laboratory use. Purchasing access is limited to verified Canadian research institutions; individual consumer accounts are not accepted. It is not for human or veterinary use, is not intended for diagnostic procedures, and has not been evaluated or authorized by Health Canada as a drug, diagnostic, or medical product.

Material specifications

Fields a receiving desk can paste into an order record.

SKU
NL-MT2-10
Pack
10 mg lyophilized vial
Purity
≥98% by HPLC (lot-specific)
CAS
121062-08-6
Molecular formula
C50H69N15O9
Molecular weight
1024.2 g/mol
Sequence
Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2
PubChem CID
92432

Common questions

No. Melanotan II is not authorised by Health Canada, the FDA, the EMA, the TGA or any other regulator, for any indication. Several regulators have issued warnings about unauthorised supply of it.
It is a non-selective agonist at MC1R, MC3R, MC4R and MC5R, all of which signal through Gs and adenylyl cyclase to raise cAMP. Because one ligand activates all four, pigmentary and central effects cannot be separated.
Yes, at case-report level. Published reports describe eruptive and changing melanocytic naevi following melanotan use, and separate reports describe melanoma in users. Case reports show temporal association rather than causation, and no cohort study of users exists.
No. Bremelanotide (PT-141) is a related but distinct molecule from the same melanocortin lineage, narrowed toward MC4R selectivity. It completed controlled trials and was approved in the United States in 2019; Melanotan II never entered comparable development.
A lactam bridge - an amide bond between an aspartate side chain and a lysine side chain - closes the peptide into a ring. This holds the α-MSH His-Phe-Arg-Trp message sequence in a fixed conformation, increasing potency and metabolic stability without improving receptor selectivity.
Only small early-phase studies, principally from around 2000. There is no published Phase 3 programme, no long-term cohort, no carcinogenicity data and no characterised human pharmacokinetics in the indexed literature.