Melanocortin Receptor Agonist | Libido & Arousal Research | For Research Use Only

PT-141 (Bremelanotide) is a synthetic peptide analog of α-MSH (alpha-melanocyte-stimulating hormone) that acts on the melanocortin receptors MC1R and MC4R. It is widely researched for its role in enhancing sexual arousal, libido, and erectile function, particularly in models where these functions are impaired.

Unlike PDE5 inhibitors that act on the vascular system, PT-141 acts directly on the brain’s arousal centres, making it a unique compound for neuroendocrine and sexual health research.

🔍 Key Features

• Enhances Sexual Desire & Arousal – Studied in both male and female models

• Central Nervous System Action – Stimulates MC4R receptors in the hypothalamus

• Non-Hormonal & Non-Vascular Mechanism

• Fast Onset in Preclinical Models – Effects observed within hours of administration

• Research Applications – Sexual dysfunction, libido restoration, neuropeptide signalling

⚙️ Peptide Details

• Peptide Name: PT-141 (Bremelanotide)

• CAS Number: 189691-06-3

• Molecular Formula: C₅₀H₆₈N₁₄O₁₀

• Molecular Weight: ~1025.2 g/mol

• Purity: ≥ 98% (HPLC Verified)

• Form: Lyophilised white powder

• Unit Size: 10mg per vial

🧊 Storage & Handling

• Storage (lyophilised): Store at –20°C, protected from light

• Reconstitution: Use sterile bacteriostatic water

• Post-Reconstitution: Store at 2–8°C and use within 7–10 days

• Avoid: Exposure to heat, moisture, and repeated freeze-thaw cycles

⚠️ For Research Use Only

PT-141 – 10mg is supplied exclusively for research and investigational purposes. It is not intended for human consumption, therapeutic use, or resale. Must be handled by qualified professionals in controlled laboratory settings.