For laboratory research use only — not for human or veterinary consumption.
The Peptide Index
Dosing guide

PT-141 Dosage Chart & Schedule

A melanocortin-receptor agonist, FDA-approved as Vyleesi for hypoactive sexual desire disorder in premenopausal women. Studied for arousal via central nervous-system pathways rather than the vascular route.

Route
Subcutaneous
Frequency
As needed
Half-life
Approximately 2
Storage
Refrigerate reconstituted; keep lyophilized cool + dark
The short answer

Used as needed before anticipated activity rather than on a daily schedule. The approved Vyleesi dose is 1.75 mg subcutaneously, with limits of no more than one dose per 24 hours and a monthly cap.

Figures describe how PT-141 is reported in the research literature and research-community references — not a recommendation for human use. For laboratory research only.

Dosage protocols

Commonly referenced research tiers. Start conservative; every compound and study context differs.

Starter
1 mg
per dose
Frequency
As needed
Weekly total
As needed (not daily)
Cycle
Not daily; assess nausea

Lower amount sometimes referenced first to gauge nausea, which is a common labeled effect.

Most commonStandard
1.75 mg
per dose
Frequency
As needed
Weekly total
As needed (not daily)
Cycle
Max 1 dose/24h; monthly cap

Matches the approved Vyleesi single-use dose taken before anticipated activity.

As-needed, with caps

  • Approved as Vyleesi for hypoactive sexual desire disorder in premenopausal women; the labeled dose is 1.75 mg subcutaneously before anticipated activity.
  • Labeling limits use to no more than one dose in 24 hours and no more than eight doses per month.
  • Nausea is a common labeled effect, which is why a lower first dose is sometimes referenced.

Ready to run this protocol?

Dosing is only as good as the vial. PT-141 is third-party tested with published COAs from our top-rated source — reconstitute with confidence and skip the guesswork on identity and purity.

PT-141 reconstitution

Based on a standard 10 mg vial: with 2 mL bacteriostatic water = 5,000 mcg/mL (5 mg/mL); 1 unit ≈ 50 mcg.

Concentration
5,000 mcg/mL
Per syringe unit
50 mcg
Draw for 1.75 mg
35 units
Doses per vial
~5
Open this mix in the calculator →

From vial to injection in 6 steps

1

Wipe both vial tops

Swab the peptide vial and the bacteriostatic-water vial with fresh alcohol and let them dry.

2

Draw the water

Pull the planned amount of bacteriostatic water (2 mL) into the syringe.

3

Add it slowly

Run the water down the inside wall of the vial — don't blast the powder. Swirl gently; never shake.

4

Let it dissolve

Wait until the solution is fully clear, then refrigerate the vial.

5

Draw your dose

Pull the calculated units on a U-100 insulin syringe (~35 units for 1.75 mg).

6

Store between uses

Keep the reconstituted vial refrigerated and use within its stable window.

Handling & storage

  • A 10 mg vial + 2 mL bacteriostatic water = 5 mg/mL, so 1.75 mg draws to about 35 units on a U-100 syringe.
  • It is dosed occasionally, so one reconstituted vial lasts many doses; refrigerate between uses.
  • Keep the lyophilized powder cool and dark before mixing.

PT-141 dosing FAQ

Is PT-141 taken daily?

No. It is used as needed before anticipated activity, and labeling caps it at one dose per 24 hours and eight doses per month.

What is the reference dose?

The approved Vyleesi dose is 1.75 mg subcutaneously; some references start at about 1 mg to gauge nausea, a common labeled effect.

What draws up on a syringe?

From a 10 mg vial in 2 mL (5 mg/mL): 1 mg = about 20 units and 1.75 mg = about 35 units on a U-100 insulin syringe.

Sources

Categories: Sexual Health · Status: Approved (see notes). This page is educational and for laboratory research use only; it is not medical advice.