- Variant
- 10MG
- Lot #
- Pending
- Labeled
- 10MG
- Actual
- Pending
- Tested
- Pending
Documents identity, purity, net peptide content, HPLC conformity, heavy metals, sterility, and endotoxin review for the selected batch.

Research use only. Not for human consumption.
We use third-party testing to give you a clearer look at identity, purity, and batch consistency before a product reaches your lab. Our testing is done by ILS Labs.
Documents identity, purity, net peptide content, HPLC conformity, heavy metals, sterility, and endotoxin review for the selected batch.
Based on the current compound category and related research focus.
Reference details for molecular identification, handling conditions, and storage guidance.
Structural identifiers and catalog-level compound reference data.
Common catalog aliases and related compound naming.
Storage states and handling notes for controlled laboratory workflows.
Scientific context and research-use framing for this catalog material.
Melanotan I is a linear peptide analog of alpha-melanocyte-stimulating hormone. Structurally, it belongs to alpha-MSH analog research and is relevant to laboratory studies involving melanocortin receptor-family biology, peptide-receptor binding models, and ligand design.
Melanocortin systems are studied through receptor subtypes such as MC1R, MC3R, MC4R, and MC5R, with alpha-MSH serving as one of the endogenous melanocortin-related ligands. Melanotan I is often placed in MC1R-associated pathway research and alpha-MSH analog studies. PMC
Researchers may use Melanotan I in controlled workflows involving MC1R-associated pathway models, melanocortin receptor signaling, ligand-receptor binding models, and alpha-MSH analog characterization. The product overview centers on receptor-family research and peptide identity.
For laboratory research use only. Not for human or veterinary use.
Peer-reviewed studies referenced for educational purposes only. Not intended as medical advice or product claims.
Luger TA, Böhm M
Minder EI
Lengweiler S, Kreim S, Barman-Aksözen J, Maurer M, Minder EI
Chang CL, Cai Z, Hsu SYT
Wensink D, Wagenmakers MAEM, Langendonk JG
Kim ES, Garnock-Jones KP


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