Research Use Only - Not for human consumption. 18+ only.
Sexual Health & LibidoSubcutaneous

Bremelanotide

Also known as: PT-141, Vylessi (brand name)

A melanocortin receptor agonist FDA-approved for hypoactive sexual desire disorder in premenopausal women; works centrally to enhance sexual motivation and arousal.

Beginner Basics

Plain-English guide to Bremelanotide

What it does

This peptide works in the brain to increase sexual desire and arousal by activating certain nerve pathways. Researchers study it because it's approved to help women who have low interest in sexual activity.

Typical dose

1.75 mg injected under the skin, used as needed before sexual activity. Maximum once per 24 hours.

When to inject

About 45 minutes before you plan to be sexually active, so it has time to work.

Storage

Keep the dry powder in a cool, dark place at room temperature until you mix it. After mixing with water, refrigerate it and use within 24 hours.

First-timer tip

Plan ahead-set a timer for 45 minutes after injecting so you know when it's reached full effect, rather than guessing.

Research Status

FDA-approved

For research purposes only. Not approved for human use. Not medical advice.

Research Areas

Increases sexual desire and arousal in women
Enhances genital sensation and responsiveness
Improves sexual satisfaction and orgasm frequency
Activates central melanocortin pathways
Non-hormonal mechanism of action

Side Effects

Nausea
CommonMild

Occurs in approximately 40% of users, typically mild and transient. Usually resolves within 30 minutes to 1 hour. Taking the injection with food may reduce incidence. Antiemetics (e.g., ginger, ondansetron) may be considered if severe.

Facial flushing
CommonMild

Reported in 20–30% of users. Characterized by warmth and redness in the face and neck. Self-resolving and typically lasts 15–30 minutes. Not medically concerning but may be socially noticeable.

Headache
UncommonMild

Occurs in approximately 5–10% of users. Usually mild and resolves within 1–2 hours. Standard analgesics (acetaminophen, ibuprofen) may be used if needed.

Injection site reactions
UncommonMild

Mild erythema, bruising, or discomfort at the injection site. Minimize by rotating sites, using proper injection technique, and allowing the solution to reach room temperature before injection.

Darkening of skin or moles
RareModerate

Melanocortin agonists can stimulate melanin production. Rare but documented in clinical trials. Monitor existing moles and report any changes to a dermatologist. Use sunscreen (SPF 30+) during and after treatment.

Hypertension (elevated blood pressure)
UncommonModerate

Transient increases in systolic and diastolic blood pressure have been reported, typically mild and resolving within 1–2 hours. Contraindicated in women with uncontrolled hypertension. Monitor blood pressure before and after injection if history of hypertension.

Dizziness or lightheadedness
UncommonMild

Reported in a small percentage of users. Sit or lie down if experienced. Ensure adequate hydration before injection.

Spontaneous penile erection (in female partners' male partners)
UncommonMild

Melanocortin agonists can affect sexual function in partners exposed to the peptide. Not applicable to the female user but relevant for household safety and storage.

Dosing Reference

ParameterValue
Dose range1.75 mg
Frequency, timing and route - members only

Research disclaimer

Figures drawn from published research literature and community logs. Not clinical recommendations. Consult a qualified professional. Research use only.

Reconstitution Guide

Do not use saline or bacteriostatic saline, use only bacteriostatic water for reconstitution

Do not shake the vial vigorously; gentle swirling prevents peptide degradation

Discard immediately if the solution appears cloudy, discolored, or contains visible particles

Use within 30 days of reconstitution when stored at 2-8°C

Do not freeze the reconstituted solution; freezing may denature the peptide

Use the PeptideVolt reconstitution calculator for your exact concentration

Use the PeptideVolt reconstitution calculator for your exact concentration

Molecular and Pharmacological Data

Molecular weight1025.2 g/mol
Half-lifeApproximately 1–2 hours (plasma); effects persist 24–48 hours due to central nervous system retention
SequenceMembers only

Bremelanotide is a melanocortin-4 receptor (MC4R) agonist that acts centrally in the hypothalamus to enhance sexual motivation and arousal in women. By activating MC4R signaling pathways involved in sexual desire, it increases genital sensation and responsiveness without affecting systemic hormone levels. This non-hormonal mechanism makes it suitable for premenopausal women with hypoactive sexual desire disorder.

Pathways and mechanism detail available to members

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Research Use Only. All content on this page is provided for informational and educational purposes related to scientific research. Bremelanotide is not approved for human use by the FDA or any equivalent regulatory body. This is not medical advice. Do not use any substance discussed here for therapeutic, diagnostic, or preventative purposes. Consult a qualified healthcare professional before making any health-related decisions. The Peptide Volt does not endorse the use of any research chemicals. 18+ only.