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PT-141 (Bremelanotide) 10mg is a high-purity, research-grade melanocortin peptide targeting MC3R and MC4R pathways. Known for its strong CNS activity and rapid blood-brain barrier penetration, this compound is widely utilized in advanced receptor signaling, neurobiology, and reproductive research. Each vial is verified at 99.98% purity and includes third-party COA for laboratory assurance.

Technical Specifications

Peptide PT-141 (Bremelanotide acetate)
Sequence Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-OH
Length 7 AA (cyclic)
Formula C₅₀H₆₈N₁₄O₁₀
Mol. Weight 1,025.20 g/mol
CAS 189691-06-3
Purity 99.98% (HPLC)
Testing HPLC / ESI-MS
COA Included (Batch-Specific)
Amount 10mg per vial
Targets MC3R, MC4R (Primary)
BBB Crosses (CNS-active)
Half-Life ~2–4 hours
Reconstitution 2–5 mL sterile/bacteriostatic water
Storage -20°C (Dry); Avoid Freeze-Thaw
Stability 1–2 months (-20°C, aliquoted)
Applications MC4R signaling, CNS & reproductive research
Dosage (In-Vitro) 1–1000 nM
Dosage (In-Vivo) 0.1–1 mg per administration
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Description

The Premium Melanocortin Receptor Agonist – PT-141 (Bremelanotide) 10mg. Uncompromised Purity for Advanced Receptor Research.

 

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PT-141 is a synthetic cyclic heptapeptide analog of alpha-melanocyte stimulating hormone (α-MSH). It is a potent, non-selective agonist of melanocortin receptors, with primary activity at MC3R and MC4R. Unlike other melanocortin peptides, PT-141 is specifically optimized for central nervous system activity, crossing the blood-brain barrier to activate hypothalamic pathways.

This is receptor grade. This is for serious researchers only. Buy PT-141 Bremelanotide 10mg Online Europe

Introducing the PT-141 (Bremelanotide) 10mg Peptide from buypurepeptideseu.com – the most advanced melanocortin receptor agonist available for European researchers. Ten milligrams of lyophilized, receptor-grade peptide for advanced MC3R, MC4R, and behavioral research. Buy PT-141 Bremelanotide 10mg Online Europe

Whether you are in Berlin studying MC4R signaling pathways in the hypothalamus, in Paris researching the neurobiology of reproductive behavior, or in Milan investigating dose-response relationships of melanocortin agonists, this peptide is your laboratory’s essential tool. We ship discreetly and securely to Albania, Andorra, Austria, Belgium, Bosnia, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Moldova, Monaco, Montenegro, Netherlands, North Macedonia, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Ukraine, Vatican City, and the United Kingdom.

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What Is PT-141 (Bremelanotide)? The Science of Selective Melanocortin Activation

Let us break down the pharmacology. PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide that represents a significant advancement over earlier melanocortin peptides.

Mechanism of action: PT-141 is an agonist at melanocortin receptors, with highest affinity for MC3R and MC4R, and lower affinity for MC1R. Unlike Melanotan 2 (MT2), PT-141 has been structurally optimized to cross the blood-brain barrier efficiently while reducing peripheral MC1R-mediated pigmentation effects. This makes it the preferred tool for studying central melanocortin pathways.

Structural features: PT-141 is a cyclic heptapeptide with the sequence Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-OH. The cyclic structure provides enhanced stability and receptor binding affinity. The C-terminal hydroxyl group (rather than amide found in MT2) alters receptor selectivity, reducing MC1R activity while preserving MC3R/MC4R activity.

Research applications: PT-141 is the reference standard for studying:

  • MC3R and MC4R signaling pathways

  • Central melanocortin system activation

  • Reproductive behavior and sexual function

  • Hypothalamic appetite regulation (MC4R-mediated)

  • Neurobiology of reward and motivation

  • Dose-response relationships of melanocortin agonists

Clinical relevance: Bremelanotide (PT-141) is the active ingredient in Vyleesi, an FDA-approved treatment for hypoactive sexual desire disorder (HSDD) in premenopausal women. This clinical validation makes PT-141 a uniquely valuable research tool.

The Pure Peptides Shop advantage: Our PT-141 (Bremelanotide) 10mg Peptide is manufactured under GMP peptide manufacturer EU standards. Each batch is third party tested with a Certificate of Analysis (COA) verifying 99.98% purity. We do not cut corners. We do not hide our lab testing transparency.

This is analytical grade PT-141 Europe in lyophilized format. For researchers who need the premium melanocortin receptor agonist for central nervous system studies, PT-141 is the essential tool.


Product Deep Dive: PT-141 (Bremelanotide) 10mg Specifications

Peptide Name: PT-141 (Bremelanotide)
Full Name: Bremelanotide acetate (formerly PT-141)
Amino Acid Sequence: Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-OH (cyclic heptapeptide)
Molecular Formula: C₅₀H₆₈N₁₄O₁₀
Molecular Weight: 1,025.20 g/mol (free base)
CAS Number: 189691-06-3 (Bremelanotide)
Purity Guarantee: 99.98% (HPLC verified, COA included)
Amount per Vial: 10mg
Form: Lyophilized powder (white to off-white cake)
Reconstitution: Bacteriostatic water or sterile water (do not use DMSO or alkaline solutions)
Storage (Lyophilized): -20°C (-4°F) for long-term storage; stable for 3 months at 4°C
Storage (Reconstituted): Aliquot and store at -20°C (-4°F); avoid freeze-thaw cycles

Comparison: PT-141 vs MT2 vs MT1

Parameter PT-141 (Bremelanotide) Melanotan 2 (MT2) Melanotan 1 (MT1)
Sequence Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-OH Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-NH₂ Linear 13-aa peptide
C-terminus Hydroxyl (-OH) Amide (-NH₂) Amide (-NH₂)
Primary Targets MC3R, MC4R MC1R, MC3R, MC4R MC1R (selective)
MC1R Activity Low High High (selective)
Blood-Brain Barrier Crosses readily Crosses readily Limited crossing
Primary Research Use CNS melanocortin, behavior Pigmentation + CNS Pigmentation (selective)
Clinical Status Approved (Vyleesi) Research only Approved (Afamelanotide)

Primary Research Applications:

  • MC3R and MC4R signaling and pharmacology

  • Central melanocortin pathway activation

  • Reproductive behavior and sexual function research

  • Hypothalamic appetite and energy balance studies

  • Neurobiology of reward, motivation, and behavior

  • Female sexual dysfunction (FSD) models

  • Dose-response and receptor binding studies

  • Comparative melanocortin receptor pharmacology

Mechanism of Action Summary:

Receptor PT-141 Activity Primary Research Application
MC1R Low (minimal) Pigmentation (not primary)
MC3R High Energy homeostasis, unknown functions
MC4R High (primary) Sexual behavior, appetite, reward
MC5R Minimal Exocrine gland function

Why European Researchers Choose PT-141 10mg

You are an advanced researcher studying melanocortin receptors, particularly MC4R pathways in the central nervous system. You understand that PT-141 offers unique advantages over other melanocortin peptides for CNS research.

The problem with MT2 for MC4R research:

  • MT2 has high MC1R activity, causing pigmentation effects that can confound long-term studies

  • MT2’s C-terminal amide vs PT-141’s C-terminal hydroxyl alters receptor selectivity

  • PT-141 is the clinically approved version (Vyleesi), making it the reference standard

The PT-141 advantage for research:

  • Optimized for CNS research: Crosses blood-brain barrier efficiently

  • Reduced MC1R activity: Minimal pigmentation effects compared to MT2

  • Clinically validated: Active ingredient in FDA-approved Vyleesi

  • Premium purity: 99.98% receptor grade for consistent results

What makes PT-141 unique for research:

  • MC4R selectivity: Preferred tool for studying central melanocortin pathways

  • Behavioral research: Reference standard for sexual behavior studies

  • Receptor pharmacology: Cleaner profile than MT2 for CNS-focused research

  • Dose-response studies: 10mg vial provides material for multiple experiments

Who uses our PT-141 (Bremelanotide) 10mg Peptide?

  • MC3R and MC4R signaling research institutions

  • Neurobiology of behavior and reproductive biology laboratories

  • Hypothalamic appetite and energy balance research centers

  • Female sexual dysfunction (FSD) research programs

  • Receptor pharmacology and dose-response studies

  • Pharmaceutical research institutions

  • Universities studying the premium melanocortin receptor agonist for CNS research


The European Logistics Advantage (Why We Convert)

You are a professional researcher. You do not have time for customs delays or “where can I find a peptide shop in Albania” only to receive low-purity PT-141. Our backend is designed for high-volume eCommerce and high-ticket researchers.

Speed: Orders placed before 14:00 CET ship same-day from our EU hub.

Discretion: Plain boxes. No “PT-141” or “Bremelanotide” labels on outer packaging. Neutral customs declarations. Lyophilized vials are shipped with ice packs for stability.

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Trust Signals:

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  • Discreet delivery guaranteed

  • Third party tested peptides EU with COA included

  • ISO certified peptide supplier Europe standards

  • For research use only – full regulatory compliance

  • Premium receptor grade – highest quality PT-141 available

Urgency Trigger: Our PT-141 (Bremelanotide) 10mg Peptide is manufactured in limited batches. Current stock for Central Europe is at 20% capacity. The next production run has a 8-10 week lead time. When it is gone, it is gone. Bulk deals available for institutional buyers.


FAQ: Your Questions & Answered

1. Q: What is the difference between PT-141 and Melanotan 2 (MT2)?
A: PT-141 (Bremelanotide) has a C-terminal hydroxyl group (-OH) instead of the amide (-NH₂) found in MT2. This structural difference reduces MC1R activity (pigmentation) while preserving MC3R/MC4R activity (CNS effects). PT-141 is the clinically approved version (Vyleesi) and is the preferred tool for studying central melanocortin pathways without pigmentation confounders.

2. Q: What receptors does PT-141 target?
A: PT-141 is a non-selective melanocortin receptor agonist with highest affinity for MC3R and MC4R. It has low activity at MC1R and minimal activity at MC5R. The MC4R pathway is the primary mediator of its CNS effects on sexual behavior and appetite.

3. Q: Does PT-141 cross the blood-brain barrier?
A: Yes. PT-141 readily crosses the blood-brain barrier, allowing it to activate central melanocortin receptors (MC3R, MC4R) in the hypothalamus. This CNS activity is what makes PT-141 valuable for studying reproductive behavior, appetite, and reward pathways.

4. Q: How does PT-141 compare to MT1 for research?
A: PT-141 is CNS-active (crosses blood-brain barrier) and targets MC3R/MC4R. MT1 is MC1R-selective, has limited blood-brain barrier crossing, and is used primarily for pigmentation research without CNS effects. They are tools for different research questions.

5. Q: How do I verify the 99.98% purity claim?
A: Every batch we ship has a unique Certificate of Analysis (COA) . You can scan the QR code on the box to see the HPLC chromatogram and mass spectrometry data. We are a third party tested peptides EU supplier with full lab testing transparency.

6. Q: Do you ship to my specific city (e.g., Vienna, Austria)?
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7. Q: What is the difference between GMP and non-GMP peptides?
A: GMP peptide manufacturer EU standards are for pharmaceutical grade. Our PT-141 is analytical grade (99.98%+), which exceeds many GMP standards for purity but is labeled “For Research Use Only” . This is GMP vs Non-GMP Peptides Explained .

8. Q: How should I reconstitute PT-141?
A: Reconstitute in bacteriostatic water or sterile water. Gently swirl – do not shake. After reconstitution, aliquot immediately and store at -20°C (-4°F) to prevent degradation from freeze-thaw cycles. Do not use DMSO or alkaline solutions.

9. Q: What is the recommended dosage for in vitro research?
A: For cell culture studies, typical concentrations range from 1-1000 nM. Start at 100 nM and optimize based on your specific cell type and receptor expression levels (MC3R, MC4R, or MC1R-expressing cells).

10. Q: Does PT-141 have pigmentation effects that should be considered?
A: PT-141 has reduced MC1R activity compared to MT2, but some minimal MC1R activation may occur at higher concentrations. For research focused specifically on CNS effects without pigmentation confounders, PT-141 is preferred over MT2. However, researchers should still control for potential minor pigmentation effects in long-term studies.

11. Q: How should I store unopened PT-141 vials?
A: Store unopened lyophilized vials at -20°C (-4°F) for long-term storage (up to 12 months). Stable for up to 3 months at 4°C (refrigerated). Do not open vials until ready to reconstitute.

12. Q: Do you offer bulk pricing for institutions?
A: Yes. Visit buypurepeptideseu.com and contact our wholesale division. We supply bulk peptide supply Europe and wholesale research peptides EU for universities and laboratories. Bulk deals available for orders of 10+ vials.

13. Q: Is payment secure?
A: 100%. We use AES-256 encryption and accept secure cryptocurrencies and credit cards. Your privacy is our priority.

14. Q: How long does delivery take to Scandinavia?
A: To buy peptides Stockholmbuy peptides Oslobuy peptides Copenhagen, or buy peptides Helsinki, delivery takes 3-5 business days. Lyophilized vials are shipped with ice packs for stability.  ...........................................

15. Q: Do you sell to the UK post-Brexit?
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The difference between a wasted research cycle and a breakthrough in melanocortin receptor signaling is the quality of your reagents. Do not trust your melanocortin research to a peptide supplier in Bulgaria that lacks a COA. Do not risk buying PT-141 in Spain from a reseller who cannot verify purity or receptor selectivity.

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For research use only. Not for human consumption or therapeutic use. Must be 18+ to purchase. All products are for laboratory research purposes only. By ordering, you confirm you are a qualified researcher. PT-141 (Bremelanotide) is for in vitro and authorized in vivo research only, specifically for studies involving MC3R and MC4R signaling, reproductive behavior, central melanocortin pathways, and female sexual dysfunction (FSD) models.