PT-141 (Bremelanotide) — 10mg

PT-141 (Bremelanotide) — 10mg
Product Specifications
Benefits
Personal responsibility notice: By purchasing this product you confirm that you do so entirely on your own initiative and at your own personal responsibility. You are fully aware of the laws and regulations applicable in your country and region regarding research chemicals.
What is PT-141 (Bremelanotide) — 10mg?
PT-141 (Bremelanotide) is a synthetic cyclopeptide that acts as a melanocortin receptor agonist with a unique mechanism of action for sexual function. It is FDA approved as Vyleesi® for hypoactive sexual desire in premenopausal women (2019). Each vial contains 10mg of lyophilized PT-141, ≥99% purity, HPLC tested. PT-141 differs fundamentally from PDE-5 inhibitors (Viagra, Cialis): it works via the central nervous system through activation of melanocortin-3 and -4 receptors in the hypothalamus — not via vasodilation. This makes it effective in forms of sexual dysfunction where vascular interventions are insufficient. PT-141 increases sexual desire and arousal via neurochemical pathways. As a derivative of Melanotan II it was originally researched for skin pigmentation, where the sexual side effect was discovered, leading to targeted therapeutic development. In research protocols: doses of 1–2mg subcutaneous 45–60 minutes before use. The effects last 6–12 hours. Reconstitution with bacteriostatic water required. For laboratory and research purposes only.
Benefits & Mechanism
PCT & Recovery
Post Cycle Therapy (PCT) is not required after PT-141 use. It has no effect on the HPTA axis.
Frequently Asked Questions (FAQ)
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View FAQScientific Research
Bremelanotide (PT-141) is derived from Melanotan II, a cyclic analog of α-MSH. FDA approved in 2019 as Vyleesi for HSDD in premenopausal women. Effective dose in clinical trials: 1.75mg subcutaneous. Acts via MC3R and MC4R in the hypothalamus. Clinical studies (RECONNECT, REVIVE) show significant improvement in sexual desire versus placebo. WADA status: not on the prohibited list.

