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Pigmentation research · RESEARCH PROFILE

Melanotan II

A melanocortin analogue discussed in pigmentation and systemic signaling.

1 specification·10 source documents·Source updated Jul 13, 2026

At a glance

A melanocortin analogue discussed in pigmentation and systemic signaling.

This profile separates the compound’s scientific background from specification-specific preparation and source schedules. Begin with the research findings and limitations, then select the formulation you want to examine.

How it works

Melanotan II can engage several melanocortin receptors. This helps explain why pigmentation research also reports effects outside the skin.[1][2][3]

Potential benefits & side effects

Interpret each outcome in the context of the study population, formulation and evidence type. Research findings do not establish a personal treatment outcome.

Potential benefits & research findings

Pigmentation findings should be read together with adverse events and case reports. Increased pigmentation is not evidence of protection from ultraviolet damage or skin cancer.[1][2][3]

Read the original publications to see the measured endpoints, comparator, duration and uncertainty. Mechanistic plausibility and a favorable experimental result are different from demonstrated clinical benefit.

Side effects & evidence limitations

Interpret the reported adverse effects together with the study population, route and observation period. Small or short studies can miss uncommon and delayed harms. Evidence from a related compound does not establish the safety of Melanotan II.

Source-reported adverse effects and cautions

  • Nausea (dose-dependent; most common at higher doses)[1][2].
  • Facial flushing and increased skin warmth[3].
  • Injection site reactions (redness, mild stinging)[7].
  • Sources are available for independent reading. Individual claims and research schedules have not yet undergone an independent clinical review by Pep Science.

    Editorial responsibility
    Pep Science editorial desk
    Last independent review
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    Editorial standards & corrections

    SPECIFICATIONS & SOURCE SCHEDULES

    Explore a vial size

    Select the exact formulation. Vial content, target dose and prepared concentration are different measurements.

    Showing 10 mg · 1 source tables

    Source-derived research information. Table phases retain the source’s actual duration; open-ended phases are not converted into a fixed eight-week course. Review the original study before interpreting a schedule.

    Standard / Gradual Titration (3 mL = 3.33 mg/mL)

    Week 1Week 2Week 3Weeks 4–8Week 8
    Week / PhaseDaily DoseUnits (per injection) (mL)
    Week 1250 mcg (0.25 mg)7.5 units (0.075 mL)
    Week 2500 mcg (0.5 mg)15 units (0.15 mL)
    Week 3750 mcg (0.75 mg)22.5 units (0.225 mL)
    Weeks 4–81000 mcg (1 mg)30 units (0.30 mL)
    Maintenance(after Week 8)500–1000 mcg(1–2× weekly)15–30 units(0.15–0.30 mL)

    Frequency: Inject once daily subcutaneously during the initial 8-week tanning phase; transition to 1–2 injections per week for maintenance dosing to sustain pigmentation[3]. This schedule uses the standard 3.0 mL dilution for consistent unit measurements. For ≤10-unit (≤0.10 mL) administrations, consider 30- or 50-unit insulin syringes for improved readability.

    Additional schedule context & duration

    Concise summary of the once-daily subcutaneous regimen.

    • Goal: Increase skin pigmentation (tanning) through melanocortin receptor activation[1].
    • Schedule: Daily subcutaneous injections for 6–8 weeks during loading phase, then maintenance dosing 1–2× weekly[3].
    • Dose Range: 250–1000 mcg daily with gradual titration to minimize side effects.
    • Reconstitution: 3.0 mL per 10 mg vial (3.33 mg/mL) for accurate unit measurements.
    • Storage: Lyophilized frozen at −20 °C (−4 °F); reconstituted refrigerated at 2–8 °C (35.6–46.4 °F); use within 1–2 weeks[6].

    Suggested daily titration approach based on clinical research.

    • Start: 200–250 mcg daily; increase by 100–250 mcg increments every 1–2 weeks as tolerated[2].
    • Target: 500–1000 mcg daily by Weeks 4–8 (studied effective range is 1–2 mg/day)[1].
    • Frequency: Once per day (subcutaneous) during loading phase.
    • Cycle Length: 6–8 weeks for initial tanning, then switch to maintenance dosing.
    • Maintenance: 500–1000 mcg administered 1–2× per week to sustain pigmentation[3].
    • Timing: Any consistent time; rotate injection sites to reduce irritation.

    Read this source protocol ↗ · View cited documents ↓

    Preparation

    Preparation and stability depend on the formulation, diluent, container and handling. The source-specific notes below apply to the selected record.
    Reconstitution Steps
    1. Draw 3.0 mL bacteriostatic water with a sterile syringe.
    2. Inject slowly down the vial wall to avoid foaming; do not shake vigorously.
    3. Gently roll or swirl the vial until the powder is fully dissolved.
    4. Label the vial with the reconstitution date and store refrigerated at 2–8 °C (35.6–46.4 °F), protected from light.

    Important: This guide is for educational purposes only and is not medical advice. Melanotan II is not an approved medication. For research use only.

    Storage Instructions

    Proper storage preserves peptide stability and potency.

    • Lyophilized: Store at −20 °C (−4 °F) or below in dry, dark conditions; keep desiccated to minimize moisture exposure[6].
    • Reconstituted: Refrigerate at 2–8 °C (35.6–46.4 °F); use within 1–2 weeks with bacteriostatic water preservative[6].
    • Avoid freeze–thaw: Do not refreeze reconstituted solution; prepare aliquots if longer storage needed.
    • Allow vials to reach room temperature before opening to reduce condensation.

    Injection Technique

    Subcutaneous injection guidance from clinical best-practice resources[7][9].

    • Clean the vial stopper and injection site with alcohol swabs; allow both to air dry completely[9].
    • Use a 1 mL insulin syringe (29–31 gauge, ½ inch needle) for subcutaneous administration[7].
    • Pinch a fold of skin approximately 1 inch thick at the injection site (abdomen preferred, at least 2 inches from navel)[8].
    • Insert the needle at 45–90° depending on body composition; release the pinch after needle insertion[8].
    • Do not aspirate for subcutaneous injections; inject slowly and steadily[9].
    • Withdraw the needle at the same angle; apply gentle pressure with clean gauze if needed.
    • Rotate sites systematically to avoid lipohypertrophy or scarring[8].
    • Dispose of used syringes immediately in a proper sharps container; never reuse needles[7].

    Materials & quantity planning

    Source materials checklist · 10 mg

    Plan based on an 8–16 week daily protocol with gradual titration (including transition to maintenance dosing).

    • Peptide Vials (Melanotan II, 10 mg each):

      • 8 weeks ≈ 5 vials (~45–50 mg total)
      • 12 weeks ≈ 8 vials (~70–75 mg total)
      • 16 weeks ≈ 10 vials (~95–100 mg total)
    • Insulin Syringes (U-100, 1 mL):

      • Per week (daily dosing): 7 syringes
      • 8 weeks: 56 syringes
      • 12 weeks: 84 syringes
      • 16 weeks: 112 syringes
    • Bacteriostatic Water (10 mL bottles): Use 3.0 mL per vial for reconstitution.

      • 8 weeks (5 vials): 15 mL2 × 10 mL bottles
      • 12 weeks (8 vials): 24 mL3 × 10 mL bottles
      • 16 weeks (10 vials): 30 mL3 × 10 mL bottles
    • Alcohol Swabs: One for the vial stopper + one for the injection site each day.

      • Per week: 14 swabs (2/day)
      • 8 weeks: 112 swabs → recommend 2 × 100-count boxes
      • 12 weeks: 168 swabs → recommend 2 × 100-count boxes
      • 16 weeks: 224 swabs → recommend 3 × 100-count boxes


    Calculate a phased quantity

    Enter each finite phase from the schedule you are studying. Open-ended phases need an explicit duration. Calculation uses 10 mg per vial and 3 mL per vial.

    Complete each phase to calculate totals.

    Quantity estimates exclude preparation losses and expiry. Follow the formulation’s handling and disposal requirements.

    FOLLOW THE EVIDENCE

    References & further reading

    Original publications and source documents cited across this product’s variants. A listed source is not an independent endorsement of a dosing schedule.