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PT-141 Spray, 10mg, lyophilized research peptide vial, Eppix Labs
Certificate of Analysis — 10mgCertificate of Analysis for PT-141 Spray 10mg
Chemical StructurePT-141 Spray chemical structure
Amino Acid SequencePT-141 Spray amino acid chain
Latest COA

PT-141 Spray10mg

Batch
PT-CA-26A-01
Tested by
Janoshik
Tested on
2026-02-05
Added
2026-08-01
Avg Purity99.864%
Avg Mass11.86 mg
Verify on Janoshik
CAS
189691-06-3
Formula
C50H68N14O10
Mol. weight
1025.19 g/mol
Form
Pre-mixed solution
Storage
Refrigerated, 2–8 °C
Tested by
Janoshik
Low on StockNasal Sprays
BatchPT-CA-26A-01

PT-141 Spray

PT-141 Spray Canada — Nasal Spray

Melanocortin Receptor Research Peptide — Nasal Spray

PT-141, also known as bremelanotide in scientific literature, is a synthetic peptide analogue derived from melanocortin receptor research. It is developed for controlled laboratory investigation involving melanocortin receptor signaling systems.

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Research Use Only

This product is intended strictly for laboratory research use within Canada. It is not approved by Health Canada for the diagnosis, treatment, cure, or prevention of any disease. Not for human or veterinary use.

By purchasing, you confirm the material will be used solely for lawful research purposes in accordance with applicable Canadian regulations.

PT-141, also known as bremelanotide in scientific literature, is a synthetic peptide analogue derived from melanocortin receptor research. It is developed for controlled laboratory investigation involving melanocortin receptor signaling systems.

In experimental models, PT-141 is studied for its interaction with melanocortin receptors and associated neuroendocrine signaling pathways under in vitro and preclinical research conditions.

Purity

Third-party tested for purity, ID, quantity.

Amino Acid Sequence
Amino acid chain diagram
Chemical Structure
Chemical structure diagram
Compound Properties
CAS Number189691-06-3
Molecular FormulaC50H68N14O10
Molecular Weight1025.19 g/mol
PubChem CID9941379

Overview

PT-141 is a synthetic melanocortin receptor agonist evaluated in research focused on melanocortin pathway signaling and neuroendocrine regulatory systems. Experimental studies examine receptor-binding dynamics and downstream signaling frameworks within controlled laboratory environments.

Preclinical and clinical research publications have explored its receptor interaction characteristics and pathway-level signaling mechanisms under structured experimental conditions.

History

PT-141 originated from investigations into melanocortin receptor agonists derived from α-melanocyte–stimulating hormone (α-MSH) analogues. Research into melanocortin signaling pathways led to the development of synthetic peptides designed to selectively interact with melanocortin receptor subtypes.

Subsequent studies documented its receptor-binding profile and neuroendocrine signaling properties in experimental models.

Key Research Areas

Laboratory investigations into PT-141 have focused on melanocortin receptor activation models and neuroendocrine signaling pathways. Research frameworks evaluate receptor-mediated interaction, melanocortin pathway dynamics, and regulatory signaling mechanisms under controlled in vitro and preclinical conditions.

2 of the 4 areas below are addressed directly by a paper cited on this page.

Melanocortin receptor activation models

Addressed on this page by Diamond 2004. The work appeared in Int J Impot Res. Each is linked to its source record in the references below, so what was measured — and in what system — can be read rather than taken on trust.

  • Diamond, L.E. et al. (2004) — Double-blind, placebo-controlled evaluation of the safety, pharmacokinetic properties and pharmacodynamic effects of intranasal PT-141, a melanocortin receptor agonist, in healthy males and patients with mild-to-moderate erectile dysfunction. Int J Impot Res 16(1):51–59.

Neuroendocrine signaling pathway studies

No paper cited on this page reports on neuroendocrine. This heading marks where PT-141 Spray is discussed in the category rather than a question the cited literature answers, and it is worth knowing which of these areas has work behind it and which does not.

α-MSH analogue research frameworks

No paper cited on this page reports on analogue. This heading marks where PT-141 Spray is discussed in the category rather than a question the cited literature answers, and it is worth knowing which of these areas has work behind it and which does not.

Receptor subtype interaction investigations

Addressed on this page by Diamond 2004. The work appeared in Int J Impot Res. Each is linked to its source record in the references below, so what was measured — and in what system — can be read rather than taken on trust.

  • Diamond, L.E. et al. (2004) — Double-blind, placebo-controlled evaluation of the safety, pharmacokinetic properties and pharmacodynamic effects of intranasal PT-141, a melanocortin receptor agonist, in healthy males and patients with mild-to-moderate erectile dysfunction. Int J Impot Res 16(1):51–59.

The references section of this page cites 4 primary papers published between 2004 and 2025 — a limited but non-trivial record. Every citation is linked to its PubMed or DOI record so it can be read rather than taken on trust, and the summaries above describe what those papers report rather than what the compound is claimed to do.

Research compounds attract claims that outrun their evidence. Below are the ones most often encountered for PT-141 Spray, set against what the papers cited on this page actually report. Where the record is thin or contested, that is stated rather than smoothed over.

Also called

PT-141 Spray is also referred to as bremelanotide, PT141.

Approved prescription medicines containing the same active ingredient are sold under the brand name Vyleesi. The material supplied here is not those products and is not interchangeable with them. Those are regulated pharmaceuticals manufactured to a licensed specification and dispensed under medical supervision. This is a research compound, and what is published for it is its measured purity and content per lot.

Human trial data exists

PT-141 Spray is commonly described online in connection with increased libido and sexual function. In the research literature the same compound is filed under melanocortin receptor activation models, neuroendocrine signaling pathway studies and α-MSH analogue research frameworks.

Of the 4 papers cited on this page, published between 2004 and 2025, 3 report work in human participants — Kingsberg 2019, Clayton 2016 and Diamond 2004. Human data for a molecule is not the same as evidence for material supplied as a research compound: published trials use pharmaceutical-grade product under medical supervision at defined doses. What is established for the material sold here is its measured purity and content per lot.

Nothing above is a statement of what this material does. It is a summary of what has been published and what has not. Eppix Labs supplies research materials only and provides no dosing, administration or protocol guidance.

Verification for PT-141 Spray is per lot, not per product. The current 10mg lot PT-CA-26A-01 returned 99.864% purity, 11.86 mg measured, 118.6% of the labelled 10 mg, assayed by Janoshik. Those figures are the laboratory's, published in full rather than reduced to a badge.

The lot code printed on the vial matches the code on the certificate for PT-141 Spray. Matching the two is what confirms the unit in hand came from the batch that was tested — a certificate not tied to a lot code proves nothing about any particular unit.

Researchers who buy PT-141 Spray in Canada through Eppix Labs receive the lot described by the certificate above: the code printed on the vial label is the code on the certificate, and both are searchable on the batch verification page.

Verify a batch code →

Storage
Refrigerated, 2–8 °C
Light
Protect from UV and direct light
Reconstitution
Not applicable — supplied in solution
Format
Pre-mixed solution

PT-141 Spray ships as a prepared solution rather than as lyophilized powder, so it is already past the point at which a powder would be reconstituted. That shortens handling but tightens storage: a compound in solution is less stable than the same compound dry, and refrigeration from arrival onward is the relevant control.

The stability window for a solution is shorter than the shelf life of a sealed lyophilized vial of the same compound. Records for laboratory work in this format should note the date the unit was opened, not only the date it was received.

Vials may appear empty on arrival. Lyophilized material collects at the base of the vial and is often not visible until the vial is inspected under direct light.

Reconstitution calculator →

Included
  • 1 × sealed spray unit in the strength selected (10mL - 100 mcg per spray / Single Vial, 10mL - 250 mcg per spray / Single Vial available), batch-labelled
  • The batch-linked Certificate of Analysis for the exact lot shipped
  • Discreet outer packaging with no product names on the exterior
  • Canada Post Xpresspost, tracked, typically 1–2 business days from Canadian stock
Not included
  • Laboratory consumables of any kind
  • Dosing, administration or protocol guidance of any kind

No. Eppix Labs products are supplied exclusively for laboratory research. We do not provide dosing, administration, or usage guidance.

Each vial contains 10mg of lyophilized PT-141. Independent third-party testing verifies purity, identity, and net content per batch.

The vial contains only the peptide preparation. Any laboratory materials required for experimental procedures must be sourced separately.

Duration depends entirely on research protocol, storage conditions, and laboratory application.

Kingsberg, S.A. et al.(2019)

Bremelanotide for the Treatment of Hypoactive Sexual Desire Disorder: Two Randomized Phase 3 Trials. Obstet Gynecol 134(5):899–908.

PubMed
Clayton, A.H. et al.(2016)

Bremelanotide for female sexual dysfunctions in premenopausal women: a randomized, placebo-controlled dose-finding trial. Womens Health (Lond) 12(3):325–337.

PubMed
Diamond, L.E. et al.(2004)

Double-blind, placebo-controlled evaluation of the safety, pharmacokinetic properties and pharmacodynamic effects of intranasal PT-141, a melanocortin receptor agonist, in healthy males and patients with mild-to-moderate erectile dysfunction. Int J Impot Res 16(1):51–59.

PubMed
Borland, J.M. et al.(2025)

Female Syrian hamster analyses of bremelanotide, a US FDA approved drug for the treatment of female hypoactive sexual desire disorder.

PubMed

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Support

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