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Omni Peptides

Melanotan I

Regular price Dhs. 200.00 AED
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Size
Quantity
Lyophilised & sealed vials
Independent COA · ≥99% purity
Cold-chain dispatch · same day Dubai
Discreet · unbranded outer packaging

Melanotan I (also known as Melanotan-1, Afamelanotide, or [Nle⁴, D-Phe⁷]-α-MSH) is a synthetic linear tridecapeptide analog of alpha-melanocyte-stimulating hormone (α-MSH). This research compound was designed for selective agonism at the melanocortin-1 receptor (MC1R) with improved potency and enzymatic stability compared to native α-MSH. It has attracted significant scientific interest for its potent stimulation of eumelanin synthesis, photoprotection, and potential tissue-protective effects without the strong central melanocortin activity (MC3R/MC4R) that characterizes Melanotan II.

Preliminary and advanced preclinical studies indicate that Melanotan I robustly activates melanocytes to increase melanin production, enhances UV resistance, and may exert anti-inflammatory and cytoprotective actions. Researchers utilize this peptide in laboratory and animal models to investigate mechanisms of melanogenesis, photobiology, skin pigmentation disorders, and melanocortin receptor signaling. As a research-grade compound, Melanotan I is intended exclusively for in vitro and animal studies (note: afamelanotide has received regulatory approval in certain jurisdictions for erythropoietic protoporphyria under the brand Scenesse, but research formulations remain designated for laboratory use). Scientists value its higher MC1R selectivity relative to Melanotan II, linear structure, and utility in studying targeted pigmentation pathways with reduced off-target central effects.

Molecular Formula
C₇₈H₁₁₁N₂₁O₁₉
Molecular Weight
1646.85 g/mol
Sequence
Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH₂ (Nle = norleucine; D-Phe = D-phenylalanine; N-terminal acetylation, C-terminal amidation)
01 Melanogenesis and Photoprotection
Preclinical investigations demonstrate potent MC1R-mediated stimulation of eumelanin production in melanocytes, leading to increased skin pigmentation and enhanced resistance to UV-induced damage. Studies explore its potential in models of photoprotection, sunburn prevention, and pigmentary disorders.
02 Skin and Dermatological Research
Melanotan I is studied for its ability to modulate melanocyte activity, improve barrier function, and reduce oxidative stress in UV-exposed or injured skin models. Research examines applications in vitiligo-like conditions and photodermatoses.
03 Anti-Inflammatory and Cytoprotective Effects
Investigations highlight reductions in pro-inflammatory signaling and cellular damage in models of skin injury, inflammation, and oxidative stress, with mechanisms linked to MC1R activation beyond pure pigmentation.
04 Comparison to Melanotan II
Unlike the cyclic Melanotan II (which strongly activates MC3R/MC4R and produces erectogenic and appetite-suppressant effects), Melanotan I shows preferential MC1R activity with minimal central nervous system or sexual side-effect profiles in research models.
05 Broader Melanocortin Biology
Emerging studies probe its influence on immune modulation, wound healing, and potential systemic effects mediated by peripheral melanocortin receptors.
Storage & Handling

Lyophilised vials are stable at −20°C for up to 2 years unopened. Once reconstituted, refrigerate at 2–8°C and use within 28 days. Avoid repeated freeze-thaw cycles.

Beyond Use Date

Pre-filled formats (cartridge, pen, nasal) carry a beyond-use date of typically 4–8 weeks from receipt. ≥98% purity by HPLC. For in vitro and preclinical research use only — not for human or veterinary use.

Molecular Formula
C₇₈H₁₁₁N₂₁O₁₉
Molecular Weight
1646.85 g/mol
Sequence
Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH₂ (Nle = norleucine; D-Phe = D-phenylalanine; N-terminal acetylation, C-terminal amidation)

— About this compound

Melanotan I is a synthetic α-MSH tridecapeptide analogue.

Melanotan I (also known as Melanotan-1, Afamelanotide, or [Nle⁴, D-Phe⁷]-α-MSH) is a synthetic linear tridecapeptide analog of alpha-melanocyte-stimulating hormone (α-MSH). This research compound was designed for selective agonism at the melanocortin-1 receptor (MC1R) with improved potency and enzymatic stability compared to native α-MSH. It has attracted significant scientific interest for its potent stimulation of eumelanin synthesis, photoprotection, and potential tissue-protective effects without the strong central melanocortin activity (MC3R/MC4R) that characterizes Melanotan II.

Preliminary and advanced preclinical studies indicate that Melanotan I robustly activates melanocytes to increase melanin production, enhances UV resistance, and may exert anti-inflammatory and cytoprotective actions. Researchers utilize this peptide in laboratory and animal models to investigate mechanisms of melanogenesis, photobiology, skin pigmentation disorders, and melanocortin receptor signaling. As a research-grade compound, Melanotan I is intended exclusively for in vitro and animal studies (note: afamelanotide has received regulatory approval in certain jurisdictions for erythropoietic protoporphyria under the brand Scenesse, but research formulations remain designated for laboratory use). Scientists value its higher MC1R selectivity relative to Melanotan II, linear structure, and utility in studying targeted pigmentation pathways with reduced off-target central effects.

VIAL ANATOMY
LYOPHILISED VIAL
Flip-off cap
Tamper-evident seal
Rubber stopper
Bacteriostatic-water compatible
Batch-labelled body
Lot & expiry printed
USP Type I glass
Borosilicate, sealed
Melanotan I vial
Melanotan I
10 MG
DUBAI PEPTIDES
RESEARCH USE ONLY
BLACK RESEARCH SERIES

Research Applications

Where researchers apply it.

01 Melanogenesis and Photoprotection
Preclinical investigations demonstrate potent MC1R-mediated stimulation of eumelanin production in melanocytes, leading to increased skin pigmentation and enhanced resistance to UV-induced damage. Studies explore its potential in models of photoprotection, sunburn prevention, and pigmentary disorders.
02 Skin and Dermatological Research
Melanotan I is studied for its ability to modulate melanocyte activity, improve barrier function, and reduce oxidative stress in UV-exposed or injured skin models. Research examines applications in vitiligo-like conditions and photodermatoses.
03 Anti-Inflammatory and Cytoprotective Effects
Investigations highlight reductions in pro-inflammatory signaling and cellular damage in models of skin injury, inflammation, and oxidative stress, with mechanisms linked to MC1R activation beyond pure pigmentation.
04 Comparison to Melanotan II
Unlike the cyclic Melanotan II (which strongly activates MC3R/MC4R and produces erectogenic and appetite-suppressant effects), Melanotan I shows preferential MC1R activity with minimal central nervous system or sexual side-effect profiles in research models.
05 Broader Melanocortin Biology
Emerging studies probe its influence on immune modulation, wound healing, and potential systemic effects mediated by peripheral melanocortin receptors.

— Verified & Documented

Every vial is backed by a Certificate of Analysis.

Each lot is independently characterised by HPLC and mass spectrometry, with identity, mass and purity documented per batch and available on request.

Additional quality-control testing, including sterility, endotoxin and heavy metals, is conducted periodically across our product range.

>99%
HPLC Purity
MS
Identity Confirmed
Certificate of Analysis
MELANOTAN I · BATCH MT110-0626 · QC RELEASE
PASS
IdentityConfirmed
Mass10.60 mg
Purity99.79%
AppearanceWhite Lyophilised
LabJanoshik Analytical (Independant)
Date24/07/26

Storage & Handling

Storage & Handling

Lyophilised vials are stable at −20°C for up to 2 years unopened. Once reconstituted, refrigerate at 2–8°C and use within 28 days. Avoid repeated freeze-thaw cycles.

Beyond Use Date

Pre-filled formats (cartridge, pen, nasal) carry a beyond-use date of typically 4–8 weeks from receipt. ≥98% purity by HPLC. For in vitro and preclinical research use only — not for human or veterinary use.