MT-1
MT-1 from the Nexus Tanning & Pigmentation catalog, supplied for controlled in-vitro research workflows.
Ships from the US with tracking.
Catalog active: Catalog pricing is active. Live warehouse counts are not published.
- Lot-specific COA
- HPLC + MS fields
- Batch archived
For in-vitro research use only. Not for human consumption.
Melanotan I (afamelanotide) is a linear tridecapeptide analog of α-melanocyte-stimulating hormone. It demonstrates selectivity for the MC1R receptor compared to other melanocortin receptor subtypes, making it a valuable tool for studying melanogenesis signaling specifically through MC1R-mediated pathways.
MT-1 definition
MT-1 is a synthetic 13-amino-acid alpha-melanocyte-stimulating hormone (α-MSH) analog containing nor-leucine at position 4 and D-phenylalanine at position 7. Research models examine its selective agonism at melanocortin receptors (particularly MC1R) and its role as a research-context comparator to MT-2 (melanotan II) for melanocortin selectivity studies. Research use only.
No sequence is listed in the current catalog record for this product.
- CAS
- 75921-69-6
- MW
- 1646.85 g/mol
- Sequence
- Not listed
- Half-life
- Not listed
- Formula
- C78H111N21O19
- Purity
- 99.82%
- Form
- Lyophilized powder
- Class
- MC1R-Selective Melanocortin Agonist
The dossier.
Compound Overview
Melanotan I (afamelanotide), also listed as MT-1, is a linear tridecapeptide analog of α-melanocyte-stimulating hormone. In research literature, it demonstrates selectivity for the MC1R receptor relative to other melanocortin receptor subtypes, which makes it useful for studying melanogenesis signaling through MC1R-mediated pathways.
Research Background & Published Literature
Afamelanotide has been investigated in clinical research settings for erythropoietic protoporphyria (EPP) and is marketed under the brand name Scenesse in certain regions. Those references describe separate regulated clinical contexts; Nexus MT-1 is supplied only as a chemical research reagent and is not offered for human or therapeutic use. Laboratory research focuses on MC1R-selective signaling, eumelanin synthesis, and photoprotection pathways.
Researchers reviewing the literature around this compound can use the peer-reviewed resources below for additional context on mechanism of action, signaling pathways, and controlled laboratory research applications:
- Sawyer et al. (1980) — Proc Natl Acad Sci U S A
- Langendonk et al. (2015) — N Engl J Med
- Minder et al. (2015) — Expert Rev Clin Pharmacol
Storage, Handling & Stability Guidelines
Use the applicable lot/source record for storage of unopened material. Any diluent selection, preparation, temperature, aliquoting, or post-reconstitution hold conditions must be established by a qualified laboratory under a validated SOP; this page does not establish a stability window.
- Keep ambient-temperature exposure as brief as practical during handling to support compound integrity.
- Reseal vials promptly after each withdrawal to limit moisture exposure.
- Use appropriate personal protective equipment and follow institutional chemical safety protocols at all times.
- For traceability, label all aliquots with compound name, concentration, reconstitution date, and operator initials.
Quality Assurance & Lab Verification
A finalized public Certificate of Analysis is available for this catalog item. Review the public COA for the applicable lot. Lot-specific identifiers, assay values, and methods are maintained in that record and are not repeated in this product dossier.
Shipping
Orders ship within the United States via USPS; international orders are not accepted. Laboratories should follow their validated SOP together with any handling fields published for the represented product or lot; no universal prepared-solution condition is inferred here.
Compound details.
- CAS Number
- 75921-69-6
- Molecular Weight
- 1646.85 g/mol
- Class
- Linear alpha-MSH analog
- Sequence length
- 13 residues
- Primary research target
- MC1R (with secondary activity at MC3/4/5)
Research context.
Studied in preclinical research models examining melanocortin-1 receptor pharmacology, melanogenesis pathway research, and receptor-selectivity comparison against MT-2. Research use only.
Verification standard.
Certificate information is lot-specific. A finalized public record shows only the methods, fields, and results present for that named lot. A pending certificate state exposes no assay values and must not be interpreted as analytical verification. Review Nexus lab verification.
Analytical record.
- Reported HPLC purity
- 99.82%
- Retention time
- 11.00 min
- Observed mass
- 1647.01 Da
- Batch
- APX-2026-0313-A
The normalized Certificate of Analysis publishes only the lot-specific fields represented in the public record. It is not an originating laboratory report or raw instrument file.
View certificate of analysis - batch APX-2026-0313-A- Sequence
- Not listed
- Model preview
- Unavailable
Molecular model preview is unavailable for this catalog record.
The chemistry.
Linear 13-amino acid peptide analog of α-MSH (also known as Afamelanotide)
Technical specifications.
- Product Name: Melanotan I 10mg
- Classification: MC1R-Selective Melanocortin Agonist
- Structural Description: Linear 13-amino acid peptide analog of α-MSH (also known as Afamelanotide)
- CAS Number: 75921-69-6
- Molecular Weight: 1646.85 g/mol
- Purity: ≥99% (verified by HPLC and Mass Spectrometry)
- Physical Form: Lyophilized (freeze-dried) powder
- Intended Use: In-vitro research use only — not for human consumption
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MT-1 research FAQ.
What is MT-1 used for in research?
MT-1 is supplied for controlled in-vitro research workflows in the Tanning & Pigmentation category. It is not labeled for human or veterinary use.
Does MT-1 have a finalized analytical record?
MT-1 has a finalized Nexus Lab Verified record that reports 99.82% HPLC area-percent purity for the represented batch. Other fields are shown only where present.
Which MT-1 variants are published?
Published Nexus variants include 10mg.
Does MT-1 include a COA?
Yes. The current Nexus record links MT-1 to finalized batch APX-2026-0313-A.
