Library

PT-141 (Research Grade)

Peptide Index
Research Use
Also known as Palatin precursor

Function

Primary
Sexual dysfunction (men & women) · Libido enhancement
Mechanism
MC3R/MC4R agonist — centrally activates hypothalamic melanocortin pathways; enhances sexual arousal independent of hormonal levels.
Evidence
Pre-clinical / Observational
Research
Phase II/III data led to Vyleesi approval

Dosing

Range
0.5–2 mg PRN
Frequency
As needed (max 1×/24h)
Route
Subcutaneous · Intranasal

Administration & Technique

Subcutaneous
45–60 min before activity.
DeviceInsulin syringe.
TechniqueAbdomen or thigh. Rotate sites.
Intranasal
Research alternative — faster onset (~30 min).
DeviceNasal spray.
Technique1 spray per nostril.

Injection & Application Sites

Front
Back
Subcutaneous
  • Abdomen2 in (5 cm) away from the navel, either side. Fastest, most consistent SubQ absorption.
  • Outer thighUpper outer quadrant, a hand-width below the hip. SubQ pinch at 45°.
Intranasal
  • IntranasalAlternate nostrils, spray on inhalation, do not sniff hard.

Diagram is a general illustration, not a medical instruction. Rotate sites every injection, keep 1 in (2.5 cm) between recent sites, and avoid scars, moles, bruises and the navel area.

Cycling

PRN only.

Timing & Interactions

When to take
SubQ or intranasal 45–60 min before anticipated activity. Max ~1 dose per 24 hrs.
Do not combine with
  • ·Uncontrolled hypertension
  • ·Melanotan II — same class
Complements
  • ·Kisspeptin-10 for research stacks

Storage & Reconstitution

Powder (Pre-Reconstitution)
Refrigerate 2–8°C; freeze for long-term.
After Reconstitution
Refrigerated up to 4 weeks with bacteriostatic water.
Full BAC water & reconstitution guide →

Reconstitution Calculator

Concentration
2.50 mg/mL
Volume per dose
0.100 mL
Insulin syringe
10.0 units (U-100)

1 mL = 100 units on a standard U-100 insulin syringe. Draw to the nearest 0.5 unit and confirm dosing with a clinician before injection.

Your Notes

Your Notes

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Benefits

  • ·On-demand libido enhancement in both sexes
  • ·Centrally mediated, hormone-independent

Risks

  • ·Nausea
  • ·Flushing
  • ·Transient BP elevation
  • ·Compounded purity concerns

Contraindications

  • ·Uncontrolled hypertension
  • ·Cardiovascular disease

Regulatory

Research-grade not FDA-approved; FDA-approved analog = Vyleesi (bremelanotide)

Veterinary Use (Pets)

No established veterinary protocol for PT-141 (Research Grade). Consult a licensed veterinarian before considering off-label use in any species.

Full veterinary reference →

Cited Works

  1. Diamond LE et al. PT-141, a melanocortin agonist for sexual dysfunction. Int J Impot Res. 2004;16:51.
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