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  • PT-141 (Neurological Arousal) | 10mg x 10 Vials Kit | >99% Purity

PT-141 (Neurological Arousal) | 10mg x 10 Vials Kit | >99% Purity

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Chemical Specifications
Product Name PT-141 (Bremelanotide Acetate)
CAS Number 189691-06-3
Molecular Formula C50H68N14O10
Protein Structure Cyclic Heptapeptide (Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH)
Molecular Weight 1025.2 g/mol
Purity (HPLC) ≥ 99.0%
Appearance White Lyophilized Powder
Storage Store at -20°C (Protect from light and moisture)
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          Description
          🧠

          What is PT-141 (Bremelanotide)?

          PT-141 (Bremelanotide), supplied in elite 10mg x 10 Vials research kits, is a revolutionary cyclic heptapeptide widely regarded in neuroscience as the “Ultimate Desire Engine.” Unlike traditional compounds (like PDE5 inhibitors) that merely alter localized blood flow and rely on existing physical stimulation, PT-141 operates on a completely different, infinitely more profound level. It bypasses the vascular system entirely, directly crossing the blood-brain barrier to target the Central Nervous System (CNS). By acting as a potent agonist for the melanocortin receptors (specifically MC3R and MC4R) in the hypothalamus, PT-141 artificially ignites the brain’s primitive pathways for sexual arousal, generating true, neurological libido from the source. This makes it a groundbreaking, gender-neutral peptide for researching severe arousal disorders.

          Key Features & Neurological Protocols

          Central Nervous System Targeting

          Bypasses the plumbing, hacks the mainframe. Crosses the blood-brain barrier to directly stimulate the hypothalamus, initiating arousal at the neurological level rather than the cardiovascular level.

          🎯

          MC4R Receptor Agonist

          The key to the ignition. It forcefully binds to and activates the Melanocortin 4 Receptors (MC4R), the specific neuro-pathways responsible for generating intense sexual desire and behavioral drive.

          👫

          Universal Arousal (Men & Women)

          Because it targets the brain’s universal desire centers, it is highly effective in both male and female research models, proving invaluable in studies concerning Hypoactive Sexual Desire Disorder (HSDD).

          🚀

          True Libido Generation

          It doesn’t just enable a physical response; it creates the psychological want. Researchers observe a profound surge in spontaneous desire and anticipation, independent of immediate physical stimulation.

          🛡️

          Bypasses Vascular Limits

          The ultimate solution for non-responders. Because it doesn’t rely on nitric oxide pathways or blood pressure manipulation, it works effectively in models where traditional PDE5 inhibitors completely fail.

          🧬

          Cyclic Heptapeptide Stability

          Engineered with a specific cyclo-structure. This prevents rapid enzymatic degradation in the bloodstream, allowing the molecule sufficient time to penetrate the brain and exert its powerful neurological effects.

          How It Works: Hacking the Arousal Mainframe

          To understand the dimensional superiority of PT-141, you must look at how traditional treatments work. Drugs like Viagra or Cialis are PDE5 inhibitors; they are essentially “vascular mechanics.” They relax smooth muscle to allow more blood flow, but they do absolutely nothing if the brain isn’t sending the signal for arousal in the first place. If the psychological desire is missing, the physical mechanics will not engage.

          PT-141 is a neurological hacker. Originally developed from the tanning peptide Melanotan II, scientists isolated the specific sequence responsible for severe arousal and removed the melanin-stimulating properties. The resulting cyclic heptapeptide, Bremelanotide, is a synthetic analog of alpha-MSH (α-Melanocyte-stimulating hormone).

          When administered, PT-141 enters the bloodstream and easily crosses the blood-brain barrier. It travels directly to the hypothalamus—the primitive control center of the brain—and aggressively binds to the Melanocortin 3 and 4 Receptors (MC3R/MC4R). Activation of these specific neural circuits does not just cause a physical reflex; it actively generates the dopamine-driven sensation of intense sexual anticipation and libido. It sends a cascading “arousal” command down the spinal cord, triggering robust physiological responses in both men and women, driven entirely by a newly ignited, uncontrollable psychological desire. It is the purest form of chemically induced neuro-arousal currently known to science.

          🧪 What’s In The Kit

          • Active Compound: PT-141 (Bremelanotide Acetate)
          • Structure: Cyclic Heptapeptide
          • Format: 10-Vial Professional Kit
          • Net Contents: 10mg per vial (100mg total)
          • Purity: ≥99.0% (HPLC Verified)

          👩‍🔬 Who Uses It

          • Neurological Arousal Investigators
          • HSDD (Hypoactive Sexual Desire Disorder) Researchers
          • Erectile Dysfunction (Non-Responder) Analysts
          • Behavioral Neuroscience Labs
          • Melanocortin Receptor Specialists

          🔗 Best Paired With

          • Sterile Bacteriostatic Water (BAC)
          • Oxytocin (For synergistic emotional bonding & climax intensity)
          • PDE5 Inhibitors (For ultimate dual-pathway research)
          • Calibrated Insulin Syringes