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Omni Peptides

Melanotan II

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

MT-2 (Melanotan II, also known as MTII or Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH₂) is a synthetic cyclic heptapeptide analog of alpha-melanocyte-stimulating hormone (α-MSH). This research compound has garnered extensive scientific interest for its potent, non-selective agonism at multiple melanocortin receptors (MC1R, MC3R, MC4R, MC5R), with particularly strong activity at MC1R and MC4R. Preliminary and advanced preclinical studies indicate that MT-2 may robustly stimulate melanogenesis (skin and hair pigmentation), induce erections via central melanocortin pathways, modulate sexual behavior, suppress appetite, and influence energy homeostasis. Researchers utilize MT-2 in laboratory and animal models to investigate mechanisms of melanocortin receptor signaling, pigmentation biology, sexual function, obesity, and neuroendocrine regulation. As a research-grade compound, MT-2 is intended exclusively for in vitro and animal studies. Scientists value its enhanced potency, prolonged duration of action compared to native α-MSH, and its utility in dissecting the pleiotropic effects of melanocortin receptor activation across dermatological, reproductive, and metabolic research domains.

Molecular Formula
C₅₀H₆₉N₁₅O₉
Molecular Weight
1024.2 g/mol
Sequence
Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH₂ (cyclic heptapeptide lactam; N-terminal acetylation, C-terminal amidation)
01 Melanogenesis and Photoprotection
Preclinical investigations demonstrate that MT-2 potently activates MC1R on melanocytes, leading to dose-dependent increases in eumelanin synthesis, skin darkening, and enhanced UV photoprotection. Studies explore its potential in models of UV-induced damage, sunburn prevention, and pigmentary disorders.
02 Sexual Function and Erectile Response
MT-2 induces penile erections and increases sexual desire through central activation of melanocortin pathways (primarily MC4R) in the hypothalamus and other brain regions. Research frequently examines its rapid-onset erectogenic effects in various animal models, including those with vascular or neurogenic erectile dysfunction.
03 Appetite Suppression and Metabolic Regulation
Investigations show MT-2 reduces food intake, decreases body weight, and improves metabolic parameters in obesity models via MC4R-mediated effects in the central nervous system. Studies compare its anorexigenic potency to other melanocortin agonists and explore interactions with leptin and other feeding circuits.
04 Neuroendocrine and Behavioral Effects
MT-2 modulates sexual motivation, partner preference, grooming behavior, and stress-related responses in preclinical models. Research probes its influence on hypothalamic-pituitary-adrenal axis activity, reward pathways, and potential applications in models of hypoactive sexual desire or compulsive behaviors.
05 Broader Physiological and Dermatological Implications
Emerging studies investigate MT-2’s roles in inflammation modulation, cardiovascular effects, neuroprotection, and tissue remodeling, with particular interest in its MC1R-independent actions and potential in models of skin cancer prevention, alopecia, and metabolic syndrome.
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
C₅₀H₆₉N₁₅O₉
Molecular Weight
1024.2 g/mol
Sequence
Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH₂ (cyclic heptapeptide lactam; N-terminal acetylation, C-terminal amidation)

— About this compound

Melanotan II is a synthetic cyclic heptapeptide.

MT-2 (Melanotan II, also known as MTII or Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH₂) is a synthetic cyclic heptapeptide analog of alpha-melanocyte-stimulating hormone (α-MSH). This research compound has garnered extensive scientific interest for its potent, non-selective agonism at multiple melanocortin receptors (MC1R, MC3R, MC4R, MC5R), with particularly strong activity at MC1R and MC4R. Preliminary and advanced preclinical studies indicate that MT-2 may robustly stimulate melanogenesis (skin and hair pigmentation), induce erections via central melanocortin pathways, modulate sexual behavior, suppress appetite, and influence energy homeostasis. Researchers utilize MT-2 in laboratory and animal models to investigate mechanisms of melanocortin receptor signaling, pigmentation biology, sexual function, obesity, and neuroendocrine regulation. As a research-grade compound, MT-2 is intended exclusively for in vitro and animal studies. Scientists value its enhanced potency, prolonged duration of action compared to native α-MSH, and its utility in dissecting the pleiotropic effects of melanocortin receptor activation across dermatological, reproductive, and metabolic research domains.

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 II vial
Melanotan II
10mg
DUBAI PEPTIDES
RESEARCH USE ONLY
BLACK RESEARCH SERIES

Research Applications

Where researchers apply it.

01 Melanogenesis and Photoprotection
Preclinical investigations demonstrate that MT-2 potently activates MC1R on melanocytes, leading to dose-dependent increases in eumelanin synthesis, skin darkening, and enhanced UV photoprotection. Studies explore its potential in models of UV-induced damage, sunburn prevention, and pigmentary disorders.
02 Sexual Function and Erectile Response
MT-2 induces penile erections and increases sexual desire through central activation of melanocortin pathways (primarily MC4R) in the hypothalamus and other brain regions. Research frequently examines its rapid-onset erectogenic effects in various animal models, including those with vascular or neurogenic erectile dysfunction.
03 Appetite Suppression and Metabolic Regulation
Investigations show MT-2 reduces food intake, decreases body weight, and improves metabolic parameters in obesity models via MC4R-mediated effects in the central nervous system. Studies compare its anorexigenic potency to other melanocortin agonists and explore interactions with leptin and other feeding circuits.
04 Neuroendocrine and Behavioral Effects
MT-2 modulates sexual motivation, partner preference, grooming behavior, and stress-related responses in preclinical models. Research probes its influence on hypothalamic-pituitary-adrenal axis activity, reward pathways, and potential applications in models of hypoactive sexual desire or compulsive behaviors.
05 Broader Physiological and Dermatological Implications
Emerging studies investigate MT-2’s roles in inflammation modulation, cardiovascular effects, neuroprotection, and tissue remodeling, with particular interest in its MC1R-independent actions and potential in models of skin cancer prevention, alopecia, and metabolic syndrome.

— 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 II · BATCH MT210-1217 · QC RELEASE
PASS
IdentityConfirmed
Mass11.27 mg
Purity99.82%
AppearanceWhite Lyophilised
LabJanoshik Analytical (Independant)
Date02/01/26

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.