Melanotan II

Melanotan II

20
Protective tanning and libido · α-MSH analog
99% Purity Pigmentation Sexual Health

Melanotan II is a synthetic analog of the α-MSH hormone that activates the melanocortin receptors, stimulating melanin production and generating a protective tan against UV radiation. It also has desirable secondary effects such as increased libido, mild appetite suppression, and improvement of the metabolic profile. Very popular among fair-skinned people who seek to tan with less sun exposure.

Key Benefits
Accelerated natural tanning
Increased UV protection
Improved libido and sexual function
Mild appetite suppression
Less sun exposure required
Uniform and long-lasting tan
Mechanism of Action
Melanotan II activates the melanocortin receptors as an α-MSH analog, stimulating melanin production and generating a protective tan against UV radiation. Its action on central receptors accounts for the secondary effects on libido, mild appetite suppression, and improvement of the metabolic profile.
Protocol

Reconstitution & Usage Protocol

Important: Only chill the water for 3 minutes before reconstituting the peptide. Do not prepare with very cold water, because it may freeze, lose its effect, or become damaged.
1Reconstitution
Materials: 1 vial of Melanotan II 10 mg · 1 vial of bacteriostatic water · U-100 insulin syringe · 3 mL syringe · alcohol wipes.
  1. Let the vial reach room temperature for 10–15 minutes.
  2. Disinfect the rubber caps with an alcohol wipe.
  3. Draw 4 mL of bacteriostatic water with the 3 mL syringe in 2 successive draws.
  4. Inject the water slowly down the inner wall of the vial.
  5. Do not shake. Swirl gently until the solution is clear.
Label with the date and refrigerate (2–8 °C). Stable for 28 days.
2Concentration & Dosing
Reconstituting 10 mg in 4 mL → 2.5 mg/mL = 25 mcg per IU.
Target doseUnitsVolume
250 mcg (initial)10 IU0.10 mL
500 mcg (standard loading)20 IU0.20 mL
1 mg (high maintenance)40 IU0.40 mL
Universal formula: IU = (dose in mcg ÷ 25)
3Application
Route
Subcutaneous in the abdomen.
Frequency
Loading phase: 250–500 mcg daily until the desired tone is reached (2–4 weeks). Maintenance phase: 500 mcg – 1 mg, 1–2 times per week + sun exposure or controlled UV booth.
Cycle
A 2–4 week loading phase until the desired tone is reached, followed by maintenance at 500 mcg – 1 mg, 1–2 times per week.
  • Caution: do not combine with intense sun exposure without protection; monitor moles (annual dermatological review recommended).
  • Before applying: let the drawn dose lose its chill (only the amount to be injected) — hold the syringe in your hand for 2–3 minutes.
  • After applying: gently massage the area for ~40 seconds to disperse the peptide and improve absorption.
Importante: Solo poner a enfriar el agua 3 minutos antes de reconstituir el péptido. No preparar con agua muy fría, porque se puede congelar, perder efecto o dañarse.
1Reconstitución
Materiales: 1 vial de Melanotan II 10 mg · 1 vial de agua bacteriostática · jeringa de insulina U-100 · jeringa de 3 mL · toallitas de alcohol.
  1. Atemperar el vial 10–15 minutos.
  2. Desinfectar las tapas de goma con toallita de alcohol.
  3. Cargar 4 mL de agua bacteriostática con jeringa de 3 mL en 2 cargas sucesivas.
  4. Inyectar el agua lentamente por la pared interior del vial.
  5. No agitar. Girar suavemente hasta solución transparente.
Etiquetar con fecha y refrigerar (2–8 °C). Estable 28 días.
2Concentración y dosis
Reconstituyendo 10 mg en 4 mL → 2,5 mg/mL = 25 mcg por UI.
Dosis objetivoUnidadesVolumen
250 mcg (inicial)10 UI0,10 mL
500 mcg (carga estándar)20 UI0,20 mL
1 mg (mantenimiento alto)40 UI0,40 mL
Fórmula universal: UI = (dosis en mcg ÷ 25)
3Aplicación
Vía
Subcutánea en abdomen.
Frecuencia
Fase de carga: 250–500 mcg diarios hasta alcanzar tono deseado (2–4 semanas). Fase de mantenimiento: 500 mcg – 1 mg, 1–2 veces por semana + exposición solar o cabina UV controlada.
Ciclo
Fase de carga de 2–4 semanas hasta alcanzar el tono deseado, seguida de mantenimiento con 500 mcg – 1 mg, 1–2 veces por semana.
  • Precaución: no combinar con exposición solar intensa sin protector; monitorear lunares (revisión dermatológica anual recomendada).
  • Antes de aplicar: dejar que la dosis cargada pierda el frío (solo la cantidad a inyectar) — sostener la jeringa en la mano 2–3 minutos.
  • Después de aplicar: masaje suave en la zona durante ~40 segundos para dispersar el péptido y mejorar absorción.
Important : Ne mettre l'eau à refroidir que 3 minutes avant de reconstituer le peptide. Ne pas préparer avec de l'eau très froide, car il pourrait geler, perdre son effet ou s'abîmer.
1Reconstitution
Matériel : 1 flacon de Melanotan II 10 mg · 1 flacon d'eau bactériostatique · seringue à insuline U-100 · seringue de 3 mL · lingettes d'alcool.
  1. Laisser le flacon revenir à température ambiante 10–15 minutes.
  2. Désinfecter les bouchons en caoutchouc avec une lingette d'alcool.
  3. Prélever 4 mL d'eau bactériostatique avec la seringue de 3 mL en 2 prélèvements successifs.
  4. Injecter l'eau lentement le long de la paroi intérieure du flacon.
  5. Ne pas secouer. Faire tourner doucement jusqu'à obtenir une solution transparente.
Étiqueter avec la date et réfrigérer (2–8 °C). Stable 28 jours.
2Concentration et dosage
En reconstituant 10 mg dans 4 mL → 2,5 mg/mL = 25 mcg par UI.
Dose cibleUnitésVolume
250 mcg (initiale)10 UI0,10 mL
500 mcg (charge standard)20 UI0,20 mL
1 mg (entretien élevé)40 UI0,40 mL
Formule universelle : UI = (dose en mcg ÷ 25)
3Application
Voie
Sous-cutanée dans l'abdomen.
Fréquence
Phase de charge : 250–500 mcg par jour jusqu'à atteindre la teinte souhaitée (2–4 semaines). Phase d'entretien : 500 mcg – 1 mg, 1–2 fois par semaine + exposition solaire ou cabine UV contrôlée.
Cycle
Phase de charge de 2–4 semaines jusqu'à atteindre la teinte souhaitée, suivie d'un entretien à 500 mcg – 1 mg, 1–2 fois par semaine.
  • Précaution : ne pas combiner avec une exposition solaire intense sans protection ; surveiller les grains de beauté (examen dermatologique annuel recommandé).
  • Avant d'appliquer : laisser la dose prélevée perdre son froid (uniquement la quantité à injecter) — tenir la seringue dans la main 2–3 minutes.
  • Après l'application : masser doucement la zone pendant ~40 secondes pour disperser le peptide et améliorer l'absorption.

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Research Highlights

Research Highlights

FAQ

Frequently Asked Questions

What is Melanotan II and how does it generate a tan in research models?

Melanotan II is a synthetic analog of the α-MSH hormone that activates the melanocortin receptors and, in study models, stimulates melanin production to generate a protective tan against UV radiation. Its action on central receptors also accounts for reported secondary effects on libido, mild appetite suppression, and the metabolic profile. It is supplied strictly for in-vitro and laboratory use.

How is the 10 mg vial reconstituted and what concentration results?

Reconstituting 10 mg in 4 mL of bacteriostatic water yields 2.5 mg/mL, equal to 25 mcg per IU on a U-100 insulin syringe. Chill the water for only 3 minutes before use, inject it slowly down the inner wall, do not shake, and swirl gently until the solution is clear. Label, refrigerate at 2–8 °C, and the solution is stable for 28 days.

What dosing schedule is described in the research protocol?

The protocol describes a subcutaneous abdominal route with a loading phase of 250–500 mcg daily (10–20 IU) until the desired tone is reached over 2–4 weeks, followed by maintenance of 500 mcg – 1 mg, 1–2 times per week, paired with sun exposure or a controlled UV booth. Using the formula IU = (dose in mcg ÷ 25), 250 mcg is 10 IU (0.10 mL), 500 mcg is 20 IU (0.20 mL), and 1 mg is 40 IU (0.40 mL). These figures describe laboratory parameters only and are not human-use instructions.

What handling precautions are noted for Melanotan II?

The reference notes not to combine the compound with intense sun exposure without protection and to monitor moles, with an annual dermatological review recommended. Before applying, let only the drawn amount lose its chill by holding the syringe in hand for 2–3 minutes; after applying, massage the area gently for about 40 seconds to disperse the peptide and improve absorption. All use is strictly for in-vitro and laboratory research, not for human or veterinary administration.

Related Compounds

Related Compounds

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