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⚠️ FOR RESEARCH PURPOSES ONLY — This compound is not FDA approved. All data presented is from clinical trials for educational reference.

PT-141 – 10MG

Price range: $25.00 through $200.00

PT-141 (Bremelanotide) is a specialized synthetic peptide derived from $\alpha$-MSH. Unlike other melanocortins, it is primarily researched for its unique ability to act directly on the central nervous system through specific receptor pathways, making it a critical tool for neuroendocrine and pharmacological studies.

SKU P41-2122 Category

Certificate of Analysis

Third Party Tested by Freedom Diagnostics

99.97%

Purity
Variant PT-141 – 10mg
Lot # pt10-1640
Labeled 10mg
Actual 10.64
Tested Jun 25, 2026

99.95%

Purity
Variant PT-141 – 10mg
Lot # PT10-1639
Labeled 10mg
Actual 10.49mg
Tested Apr 16, 2026

Compound Information

Technical specifications

What Is PT-141 10MG?

Type Synthetic Cyclic Peptide
CAS Number 189691-06-3
Molecular Weight 1025.2 g/mol
Molecular Weight (Cu) N/A
Amino Acids 7 Amino Acids
Sequence Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys-OH)
Formula C50H68N14O10

Stability Information

Lyophilized Powder

−20°C

Reconstituted

2-8°C

About PT-141 10MG

Information

PT-141 (Bremelanotide) is a specialized synthetic peptide derived from $\alpha$-MSH. Unlike other melanocortins, it is primarily researched for its unique ability to act directly on the central nervous system through specific receptor pathways, making it a critical tool for neuroendocrine and pharmacological studies.

Product

Specifications

Molecular Formula C50H68N14O10
Molecular Weight 1025.16 g/mol
Sequence Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
Purity ≥99% (HPLC verified)
Form Lyophilized powder
Appearance White to off-white powder
Solubility Soluble in water, bacteriostatic water
Storage -20°C (lyophilized), 2-8°C (reconstituted)

FAQ

Frequently asked questions

What is the origin of PT-141?
PT-141 is a synthetic cyclic peptide derived from the naturally occurring alpha-melanocyte-stimulating hormone ($\alpha$-MSH).
It is primarily studied for its activity with MC3R and MC4R receptors involved in central nervous system signaling.
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