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title: "Melanotan I: Dosing &amp; Vendor Prices — BodyHackGuide"
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5.  Melanotan I 

# Melanotan I

Other FDA Approved 

Download  PDF

Also known as: Afamelanotide, CUV1647, Scenesse, alpha-MSH analog, \[Nle4,D-Phe7\]-alpha-MSH (linear) 

Melanotan I (afamelanotide) is a linear synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH) with the substitution of norleucine at position 4 and D-phenylalanine at position 7. Unlike Melanotan II (which is cyclic), Melanotan I is a linear peptide that is significantly more selective for MC1R over MC4R — making it a tanning/photoprotective agent with substantially less sexual and appetite-stimulating side effects.

Half-Life:  Controlled-release subcutaneous implant (Scenesse): high inter-subject variability; median Tmax ~36 h, mean Cmax ~3.7 ng/mL, apparent terminal half-life ~15 h, with plasma levels measurable to ~96 h post-dose (FDA pharmacokinetics, n=12). Injected/bolus free peptide: peak plasma at ~1-2 h with an elimination half-life of ~30 minutes; the Nle4/D-Phe7 modifications prolong biological (melanogenic) activity well beyond plasma clearance. Route:  Subcutaneous, Intramuscular MW:  1646.85 g/mol (average; molecular formula C78H111N21O19) 

Last reviewed: Sep 3, 2026 

[

Other

Category



](/wiki#cat-other)

FDA Approved

Research Stage

OverviewChemical InfoDosing & ProtocolsInteractionsResearchCompare Prices2 Related

## Overview

### Best Price Available

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1 vial · vial

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### At A Glance

Mechanism 

Melanotan I is afamelanotide, i.e. \[Nle4, D-Phe7\]-alpha-MSH ('NDP-alpha-MSH'), a synthetic 13-amino-acid analog of alpha-melanocyte-stimulating hormone. The Nle4 and D-Phe7 substitutions make it resistant to enzymatic breakdown and roughly 10-100x more potent than native alpha-MS… 

Half-Life 

Controlled-release subcutaneous implant (Scenesse): high inter-subject variability; median Tmax ~36 h, mean Cmax ~3.7 ng/mL, apparent terminal half-life ~15 h, with plasma levels measurable to ~96 h post-dose (FDA pharmacokinetics, n=12). Injected/bolus free peptide: peak plasma at ~1-2 h with an elimination half-life of ~30 minutes; the Nle4/D-Phe7 modifications prolong biological (melanogenic) activity well beyond plasma clearance.

Dosing 

every 1 to 4 weeks

Dose Range 

16000mcg 

Routes 

Subcutaneous Intramuscular 

Common Vials 

5mg 10mg 

Potential Benefits 

Increased melanin (eumelanin) production and skin darkening via MC1R activation, with a reduced UV requirement FDA-approved photoprotection in erythropoietic protoporphyria (EPP) as the Scenesse 16 mg subcutaneous implant \[PMID:26132941\] Reduced phototoxic pain and improved quality of life in EPP patients in randomized controlled trials \[PMID:26132941\] Tends to produce fewer MC4R-type effects (spontaneous erections, strong libido, marked nausea) than the cyclic Melanotan II - attributable to Melanotan II's greater potency and metabolic stability, not to true MC1R selectivity of Melanotan I Investigated in research settings for photoprotection in UV-sensitive populations 

Safety Notes 

Common 

Nausea (typically milder and less frequent than with Melanotan II) Facial flushing Headache Fatigue Skin hyperpigmentation; darkening of existing moles, freckles and nevi 

Serious 

Darkening or change in appearance of moles/nevi - requires baseline and periodic full-skin dermatologic monitoring Long-term safety of chronic melanocortin stimulation, including any effect on melanoma risk, is not established In the pivotal EPP implant trials serious adverse events were not considered drug-related \[PMID:26132941\] 

### Overview

Melanotan I (afamelanotide) is a linear synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH) with the substitution of norleucine at position 4 and D-phenylalanine at position 7. Unlike Melanotan II (which is cyclic), Melanotan I is a linear peptide that is significantly more selective for MC1R over MC4R — making it a tanning/photoprotective agent with substantially less sexual and appetite-stimulating side effects. Afamelanotide was FDA-approved in October 2019 under the brand name Scenesse as an implant for erythropoietic protoporphyria (EPP), a rare photosensitivity disorder. Melanotan I is meaningfully different from Melanotan II in structure, selectivity, and side-effect profile and should not be confused with it.

## Chemical Information

IUPAC Name

Not yet available 

CAS Number

Not yet available 

Molecular Formula

Not yet available 

Molecular Mass

1646.85 Da (C78H111N21O19; PubChem CID 16197727)

Amino Acid Sequence

Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2 (\[Nle4, D-Phe7\]-alpha-MSH / NDP-alpha-MSH; 13-residue analog of alpha-MSH, N-acetylated with a C-terminal amide)

## Dosing & Protocols

### Unlock Dosing Protocols

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## Research

### Unlock Research Data

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-   Access mechanism of action details 

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## Interactions

Interaction and contraindication data is being compiled for Melanotan I. Check back soon.

General Safety Note

Always consult a qualified healthcare professional before combining research compounds. Interactions may exist that are not yet documented.

Best Price 

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up to $35.00

Best $/mg 

$3.5000

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Listings 

2

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![Ion Peptide logo](https://ionpeptide.com/wp-content/uploads/2025/08/ion-peptide-logo-1-300x148.jpg)

[Ion Peptide](/vendor/ion-peptide)

[70 ](/vendor-trust-scorecard)

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Melanotan I 5mg

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1 vial ● Out of Stock 

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![Ion Peptide logo](https://ionpeptide.com/wp-content/uploads/2025/08/ion-peptide-logo-1-300x148.jpg)

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🇺🇸 US 🌍 International 

Melanotan I 10mg

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Current low

$35.00

as of Apr 22, 2026

7-day low

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no 7d data yet

30-day low

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no 30d data yet

30-day change

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baseline building

Tracking since Apr 22, 2026 · 2 data points

### Vendors Selling Melanotan I

[

![Ion Peptide logo](https://ionpeptide.com/wp-content/uploads/2025/08/ion-peptide-logo-1-300x148.jpg)

#### Ion Peptide

4.5 

2 listings · from $19.00 





](/vendor/ion-peptide)

How we score these vendors

Every supplier above is graded 0–100 on COA verification, payment transparency, shipping, reviews, and active listings. Methodology published, no pay-to-rank.

[View Scorecard](/vendors/scorecard)

### Related Compounds

[View All](/wiki)

[

### Aminotadalafil

Other Preclinical 

Aminotadalafil is an unapproved research analog of tadalafil, the PDE5 inhibitor marketed under the brand name Cialis for erectile dysfunction and under Adcirca for pulmonary arterial hypertension.

2.5 mg - 20 mg (oral) 

9 studies View Profile 

](/compound/aminotadalafil)[

### B7-33

Other Preclinical 

B7-33 is a single-chain, 26-amino-acid peptide engineered as a functionally selective agonist of the relaxin family peptide receptor 1 (RXFP1), designed to recapitulate the therapeutic activity of human H2 relaxin — the endogenous peptide hormone that is naturally elevated during pregnancy and has broad cardioprotective, vasodilatory, and anti-fibrotic effects.

t½ In vitro serum-stability half-life is approximately 6 minutes; B7-33 is rapidly degraded (a lipidated analog extended this to ~60 minutes in the same assay). Human in vivo pharmacokinetics are unpublished, and rapid clearance is expected for a small linear peptide (Praveen et al. 2023, PMID 37047588).  500-4000 mcg subcutaneous per injection (community/self-report research doses; most commonly ~1000 mcg / 1 mg once daily). No validated human dose exists - all figures are empirical extrapolations from rodent pharmacology. 

11 studies View Profile 

](/compound/b7-33)[

### Kisspeptin-10 (KSPTN)

Other Clinical (investigational) 

KSPTN is the vendor shorthand for kisspeptin, a naturally occurring peptide encoded by the KISS1 gene and the master upstream regulator of the reproductive (hypothalamic-pituitary-gonadal) hormone axis.

t½ Kisspeptin-10: very short, reported on the order of ~4 minutes (rapid plasma clearance). Kisspeptin-54 is longer-acting (tens of minutes). The brief half-life is why human studies dose it intravenously by bolus or continuous infusion.  20-100 

Preclinical View Profile 

](/compound/ksptn)[

### PNC-27

Other Preclinical 

PNC-27 is a p53-derived peptide that selectively induces membranolysis in cancer cells.

t½ Unknown (no published PK data)  0 

Preclinical View Profile 

](/compound/pnc-27)[

### Prostamax

Other Preclinical 

Prostamax is a short synthetic peptide developed in Russia by Vladimir Khavinson and collaborators at the St.

t½ Not characterized in published pharmacokinetic literature  10 mg oral capsule, 1-2 daily for 10-30 days 

6 studies View Profile 

](/compound/prostamax)[

### RU-58841

Other Preclinical 

RU-58841 (also known as PSK-3841 or HMR-3841, and commonly written simply as RU in hair-loss forums) is a non-steroidal androgen receptor antagonist originally developed by Roussel Uclaf (later absorbed into Sanofi) in the late 1980s and early 1990s.

25 mg - 50 mg topical daily (dissolved in vehicle) 

11 studies View Profile 

](/compound/ru-58841)

### Side-by-Side Comparisons

[All Comparisons](/compare)

[Melanotan I vs Melanotan II](/compare/melanotan-i-vs-melanotan-ii "Melanotan I vs Melanotan Ii")

[

View Full Dosage Guide →

Protocols, calculator & safety for Melanotan I



](/guides/dosage/melanotan-i)

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[All Posts](/blog)

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Evidence-tiered review of 10 peptide nasal sprays — Semax, Selank, Oxytocin (S); PT-141, DSIP, Epithalon (A); Noopept, NAD+, 5-Amino-1MQ (B); Melanotan-II (C). Human-trial counts, PMID citations, safety, dosing, and pre-made vs DIY tradeoffs. Tiers match the live pillar scorecard.

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4/21/2026 ](/blog/complete-peptide-reconstitution-guide-2026)

### Best Price

![Ion Peptide logo](https://ionpeptide.com/wp-content/uploads/2025/08/ion-peptide-logo-1-300x148.jpg)

Ion Peptide

$19.00

[Buy Now](https://ionpeptide.com/product/melanotan-i/?ref=reddit15)

1 vendors · 2 listings

### Research Score

45 

0 PubMed studies

### Quality Indicators

Data Completeness

63% 

Description 

Mechanism of Action 

Chemical Data 

Dosing Protocols 

Safety Profile 

PubMed Studies 

Interactions 

Vendor Listings 

### Quick Facts

Half-Life

Controlled-release subcutaneous implant (Scenesse): high inter-subject variability; median Tmax ~36 h, mean Cmax ~3.7 ng/mL, apparent terminal half-life ~15 h, with plasma levels measurable to ~96 h post-dose (FDA pharmacokinetics, n=12). Injected/bolus free peptide: peak plasma at ~1-2 h with an elimination half-life of ~30 minutes; the Nle4/D-Phe7 modifications prolong biological (melanogenic) activity well beyond plasma clearance.

Molecular Weight

1646.85 Da (C78H111N21O19; PubChem CID 16197727)

Administration

Subcutaneous, Intramuscular

Trial Phase

FDA Approved

### Safety Profile

Common Side Effects

-   •  Nausea (typically milder and less frequent than with Melanotan II)
-   •  Facial flushing
-   •  Headache
-   •  Fatigue
-   •  Skin hyperpigmentation; darkening of existing moles, freckles and nevi

[Full Dosage Guide](/guides/dosage/melanotan-i)[Calculate Your Dose](/tools/reconstitution)

Research Disclaimer

This information is for educational and research purposes only. Not intended as medical advice. Consult a healthcare professional before use.

## Frequently Asked Questions

What is Melanotan I used for in research?

Melanotan I (afamelanotide) is a linear synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH) with the substitution of norleucine at position 4 and D-phenylalanine at position 7. Unlike Melanotan II (which is cyclic), Melanotan I is a linear peptide that is significantly more selective for MC1R over MC4R — making it a tanning/photoprotective agent with substantially less sexual and appetite-stimulating side effects. Afamelanotide was FDA-approved in October 2019 under the brand name Scenesse as an implant for erythropoietic protoporphyria (EPP), a rare photosensitivity disorder. Melanotan I is meaningfully different from Melanotan II in structure, selectivity, and side-effect profile and should not be confused with it.

What forms does Melanotan I come in?

Melanotan I is available in vial form.

How much does Melanotan I cost?

Prices start at $19.00 across 1 verified vendor.

How do I compare Melanotan I vendors?

Compare prices, payment methods, shipping, and COA scores across 1 vendor.

## Research Tools

[

### Peptide Calculator

Reconstitution & syringe units



](/tools/reconstitution)[

### Reconstitution Guide

How to mix, step by step



](/guides/how-to-reconstitute-peptides)[

### Nasal Spray Calc

mL per actuation



](/tools/intranasal)[

### Half-Life Visualizer

Decay curves



](/tools/halflife)

## Related Compounds

[View All](/wiki)

[

### Aminotadalafil

Other Preclinical 

Aminotadalafil is an unapproved research analog of tadalafil, the PDE5 inhibitor marketed under the brand name Cialis for erectile dysfunction and under Adcirca for pulmonary arterial hypertension.

2.5 mg - 20 mg (oral) 

9 studies View Profile 

](/compound/aminotadalafil)[

### B7-33

Other Preclinical 

B7-33 is a single-chain, 26-amino-acid peptide engineered as a functionally selective agonist of the relaxin family peptide receptor 1 (RXFP1), designed to recapitulate the therapeutic activity of human H2 relaxin — the endogenous peptide hormone that is naturally elevated during pregnancy and has broad cardioprotective, vasodilatory, and anti-fibrotic effects.

t½ In vitro serum-stability half-life is approximately 6 minutes; B7-33 is rapidly degraded (a lipidated analog extended this to ~60 minutes in the same assay). Human in vivo pharmacokinetics are unpublished, and rapid clearance is expected for a small linear peptide (Praveen et al. 2023, PMID 37047588).  500-4000 mcg subcutaneous per injection (community/self-report research doses; most commonly ~1000 mcg / 1 mg once daily). No validated human dose exists - all figures are empirical extrapolations from rodent pharmacology. 

11 studies View Profile 

](/compound/b7-33)[

### Kisspeptin-10 (KSPTN)

Other Clinical (investigational) 

KSPTN is the vendor shorthand for kisspeptin, a naturally occurring peptide encoded by the KISS1 gene and the master upstream regulator of the reproductive (hypothalamic-pituitary-gonadal) hormone axis.

t½ Kisspeptin-10: very short, reported on the order of ~4 minutes (rapid plasma clearance). Kisspeptin-54 is longer-acting (tens of minutes). The brief half-life is why human studies dose it intravenously by bolus or continuous infusion.  20-100 

Preclinical View Profile 

](/compound/ksptn)[

### PNC-27

Other Preclinical 

PNC-27 is a p53-derived peptide that selectively induces membranolysis in cancer cells.

t½ Unknown (no published PK data)  0 

Preclinical View Profile 

](/compound/pnc-27)[

### Prostamax

Other Preclinical 

Prostamax is a short synthetic peptide developed in Russia by Vladimir Khavinson and collaborators at the St.

t½ Not characterized in published pharmacokinetic literature  10 mg oral capsule, 1-2 daily for 10-30 days 

6 studies View Profile 

](/compound/prostamax)[

### RU-58841

Other Preclinical 

RU-58841 (also known as PSK-3841 or HMR-3841, and commonly written simply as RU in hair-loss forums) is a non-steroidal androgen receptor antagonist originally developed by Roussel Uclaf (later absorbed into Sanofi) in the late 1980s and early 1990s.

25 mg - 50 mg topical daily (dissolved in vehicle) 

11 studies View Profile 

](/compound/ru-58841)

## Side-by-Side Comparisons

[All Comparisons](/compare)

Compare Melanotan I head-to-head: mechanism, half-life, dosing, safety, and live pricing.

[Melanotan I vs Melanotan II](/compare/melanotan-i-vs-melanotan-ii "Melanotan I vs Melanotan Ii")

Free 2026 Peptide Cheat Sheet — 50 pages, PDF

Reconstitution math, concentration charts, half-lives, and vendor trust tiers. The reference we wish we had on day one.

[Download Free](/guides/peptide-cheat-sheet-download?utm_source=compound-melanotan-i)

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