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How to Reconstitute PT-141 (Bremelanotide): A Step-by-Step Guide

Reconstituting PT-141 (Bremelanotide) is not identical to reconstituting any other compound in this library. Water-soluble and straightforward to reconstitute.

Cyclic heptapeptide, melanocortin receptor agonistReproductiveMetabolic

In plain English

Straightforward — it dissolves readily in bacteriostatic water. Its ring structure is rigid, so unlike long floppy molecules it is not especially sensitive to agitation. A 10 mg vial in 2 mL gives 5 mg/mL.

What PT-141 (Bremelanotide) actually is

PT-141 has an unusual history. It is a breakdown product of a compound originally developed for research into skin pigmentation, and an unexpected observation during that work redirected attention to the breakdown product, which was then developed as its own line of research.

Supplied for laboratory research use only — not for human or animal use.

Research-grade PT-141 (Bremelanotide)

Third-party tested by HPLC and LC-MS, ≥99% purity, with a Certificate of Analysis on every order. Ships across Canada.

Technical detail below

Diluent selection for PT-141 (Bremelanotide)

PrimaryBacteriostatic water (0.9% benzyl alcohol)
Alternative 1Sterile water (USP grade)

Water-soluble and straightforward to reconstitute. The molecule is cyclic — closed through a lactam bridge rather than a disulfide — which makes it conformationally constrained and notably more rigid than a linear peptide of similar length.

Common reconstitution reference

Vial
10mg
Diluent
2mL
Concentration
5.0mg/mL

A 10 mg vial in 2 mL gives 5 mg/mL. Keep reconstituted material protected from light.

Open the PT-141 (Bremelanotide) calculator

Method notes for this compound

  • Protect from light at all stages.
  • Standard gentle reconstitution; the constrained ring is not agitation-sensitive in the way flexible long chains are.
  • Store refrigerated and aliquot rather than repeatedly sampling one vial.

What PT-141 (Bremelanotide) is studied for

Melanocortin receptor pharmacology

Acts at melanocortin receptors, with MC3R and MC4R the subtypes of research interest.

Central rather than peripheral mechanism

Distinguished in the literature by acting centrally, unlike vascular-mechanism compounds in adjacent research areas.

Melanotan II lineage

Its origin as a metabolite of a pigmentation-research compound is central to understanding its development history.

Cyclic constraint

The lactam bridge restricts conformational freedom, a common strategy for improving receptor selectivity.

Summarizes published preclinical literature. Provided for research reference only; not a claim of efficacy or a description of human use.

More PT-141 (Bremelanotide) reference

Reconstitution reference for other compounds

PT-141 (Bremelanotide) overview PT-141 (Bremelanotide) calculatorPT-141 (Bremelanotide) product details

PT-141 (Bremelanotide) is supplied strictly as a research chemical for in-vitro laboratory and research use only. It is not intended for human or animal consumption, diagnostic, or therapeutic use. This page is educational laboratory-handling reference information — not medical advice, not usage guidance, and not a protocol.