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For research, development and manufacturing use only. Not for human or veterinary use.

Cosmetic & Skin · Source-reviewed dossier

Melanotan I

Source-Reviewed Research Dossier

Melanotan I is an informal name associated with afamelanotide, a synthetic α-MSH analogue. FDA approval applies to the SCENESSE 16 mg implant for erythropoietic protoporphyria—not to tanning products, research powder or other formulations.

Research use only Lot documents on request
Melanotan I research product family with 1 catalog variants
AI-generated packaging mockup for catalog navigation. It is not a photograph of an actual supplied lot; container, label and presentation may vary.

Product family

Compound overview

Shared values below are consolidated from the current catalog record. They are not independent verification or lot results; the current product specification and lot COA control.

Product identity

Product type
Peptide research compound
Catalog family
Melanotan I
Research category
Cosmetic & Skin
Catalog CAS RN
75921-69-6
Catalog molecular formula
C78H111N21O19
Catalog molecular weight
1646.85 g/mol
Catalog sequence
Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2
Identity boundary
The name Melanotan I is used inconsistently; equivalence to licensed afamelanotide requires exact sequence, formulation and product documentation.
Evidence status
Human pigmentation pharmacology and one product-specific FDA approval; catalog material is not SCENESSE
Intended use
Research, development and manufacturing use only

Literature reference parameters

Compound or material class
Afamelanotide-related α-MSH analogueCatalog-family identity
Evidence scope
Human pigmentation pharmacology and one product-specific FDA approval; catalog material is not SCENESSEDo not generalize beyond the cited model
Source review
Primary or authoritative records linked belowChecked 2026-09-01

Identity safeguard Reference identifiers above describe the literature compound record. The supplied form, formula, molecular weight, purity and storage conditions must be verified against the product-specific specification and lot COA.

Mechanism of action

How Melanotan I is studied

A target-to-pathway view grounded in the linked research records.

Afamelanotide-related α-MSH analogue research basis

Afamelanotide activates melanocortin-1 receptors on melanocytes and increases eumelanin production.

Evidence and material boundary

A validated implant’s formulation, controlled release, indication and risk controls cannot be assigned to a catalog material or tanning use.

Reported research findings

What published studies report about Melanotan I

Reported outcomes are paired with their experimental model and evidence boundary.

Human pharmacology study

Pigmentation and pharmacokinetics were studied in volunteers

An early human study evaluated the synthetic melanotropin analogue now associated with afamelanotide.

Early experimental exposure does not establish safety for unapproved tanning formulations.

Read the primary study
FDA prescribing information

SCENESSE approval is formulation- and indication-specific

The label covers a 16 mg controlled-release implant for adults with erythropoietic protoporphyria.

It does not approve catalog Melanotan I, self-injection or cosmetic tanning.

Read the primary study
Translation boundary: findings are limited to the evidence level stated on each card. Experimental protocol quantities are research details, not usage instructions.

Catalog options

Variant specifications

Pack-level catalog data; lot-level controls remain document-specific.

Catalog no.MT1
Pack size10 mg × 10 vials
Current variant
Specification & documents for MT1

Product specification

Single-component peptide · 10 mg/vial nominal · 10-vial pack · supplied form and release limits controlled by lot specification.

Lot documentation

Request by lot: CoA, HPLC purity and MS identity

Quality system

Quality documentation

Document availability is stated honestly and can vary by catalog variant or lot.

Lot-specific Certificate of AnalysisAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request
Product Specification SheetAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request
Analytical Method SummaryAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request

Analytical interpretation

Interpret the documents, not just the headline number.

Use the source-reviewed guide to separate chromatographic area purity, quantitative assay, LC-MS identity, composition and stability evidence before comparing variants or requesting a lot record.

Open the Quality & Documentation Hub

HPLC area ≠ assayA dominant peak does not establish target mass fraction.

Intact mass ≠ full sequenceIdentity strength depends on resolution and orthogonal evidence.

Counterions affect contentWater, salt form and solvents change the as-is composition.

Storage needs a data basisShipping practice is not the same as stability evidence.

Evidence map

Research context

Published studies and regulatory records, not customer testimonials or usage guidance.

Human pharmacology study

Pigmentation and pharmacokinetics were studied in volunteers

Early experimental exposure does not establish safety for unapproved tanning formulations.

View primary record
FDA prescribing information

SCENESSE approval is formulation- and indication-specific

It does not approve catalog Melanotan I, self-injection or cosmetic tanning.

View primary record
Evidence boundary: each card states its evidence type. Human trials and regulatory records describe the studied or regulated intervention; preclinical records remain model-specific. None verifies the identity, quality, safety or efficacy of this catalog lot or provides usage instructions.

Literature basis

Curated references

Third-party publications selected for direct relevance.

  1. 01 Human pharmacology study
  2. 02 FDA prescribing information

Research FAQ

Melanotan I questions

Concise answers for researchers comparing identity, evidence and catalog variants.

What is Melanotan I?

Melanotan I is an informal name associated with afamelanotide, a synthetic α-MSH analogue. FDA approval applies to the SCENESSE 16 mg implant for erythropoietic protoporphyria—not to tanning products, research powder or other formulations.

What evidence is available for Melanotan I?

Human pigmentation studies and a narrow product approval exist, but no general tanning approval follows.

Does the cited research validate this catalog material?

No. The cited records describe their own intervention, formulation, model and controls. They do not verify the identity, purity, sterility, safety or efficacy of a catalog lot.

Which quality documents can be requested?

A lot-specific COA, product specification sheet and analytical method summary can be requested where applicable.

How should Melanotan I be stored?

Store at -20 °C, protected from light and moisture. After reconstitution, aliquot and avoid repeated freeze-thaw cycles. Confirm the applicable storage statement on the product-specific specification and lot documentation.

Knowledge tools

Continue with structured evidence

Move from this dossier into canonical evidence maps, verified status records, analytical interpretation and laboratory calculations.

Internal technical source review

Claims were checked against the linked primary publication, regulatory label or authoritative compound record. Published findings stay attached to their study model, formulation and route. Catalog identity and lot quality remain controlled by the applicable specification and lot-specific documents.

Editorial status: NHD evidence editorial workflow · 2026-09-01 · Not independent medical review · Review policy

Technical procurement

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Selected: MT1 · 10 mg × 10 vials