PT-141 is bremelanotide, and unlike most compounds with a calculator page it has an approved human dose behind it. That makes the dose figure settled and the water volume the only thing left to decide.
Below the calculator: a reconstitution chart, the dose figure at every experience level, the on-demand dosing limits, the health conditions that change the answer, and the references. Every dose figure is read from the Klarovel engine's dose table, never typed into the page.
How many milligrams are in your PT-141 (Bremelanotide) vial?
How much bacteriostatic water are you adding?
Syringe size
Experience with injectable peptides
Selects the dose row the engine would use, which changes the target, the upper bound and the ceiling together.
Body weight
The engine catalog does not flag PT-141 (Bremelanotide) weight sensitive, and the dose calculator applies no generic weight scaling, so this does not change the target. Inventing a per-kilogram rule would be worse than leaving it alone.
Standard dose at the beginner level
35.0 units
1.75 mg
Frequency: as needed, at least 45 minutes before sexual activity; max 1 dose per 24 hours, max 8 doses per month. Timing: On demand. Route: subcutaneous.
The three phases in the order the engine escalates a dose, with the unit mark for each at 10 mg in 2 ml. Change the experience level, weight or age above and the whole table recomputes.
| Phase | Dose | Draw | Doses per vial |
|---|---|---|---|
| Phase 1, opening dose | 1.75 mg | 35.0 units | 5 |
| Phase 2, standard dose | 1.75 mg | 35.0 units | 5 |
| Phase 3, upper dose | 1.75 mg | 35.0 units | 5 |
| Ceiling, not exceeded | 1.75 mg | 35.0 units | 5 |
Doses read from the beginner row of dose_protocols, the engine's dose table. Unit marks are arithmetic over your vial size and water volume.
Every level side by side, unmodified. This is the raw dose table, so the shape of the ramp is visible instead of collapsed into a single recommended number.
| Experience | Opening | Standard | Upper | Ceiling | Frequency |
|---|---|---|---|---|---|
| Never used peptides | 1.75 mg | 1.75 mg | 1.75 mg | 1.75 mg | as needed, at least 45 minutes before sexual activity; max 1 dose per 24 hours, max 8 doses per month |
| Researched, not used | 1.75 mg | 1.75 mg | 1.75 mg | 1.75 mg | as needed, at least 45 minutes before sexual activity; max 1 dose per 24 hours, max 8 doses per month |
| Beginner | 1.75 mg | 1.75 mg | 1.75 mg | 1.75 mg | as needed, at least 45 minutes before sexual activity; max 1 dose per 24 hours, max 8 doses per month |
| Intermediate | 1.75 mg | 1.75 mg | 1.75 mg | 1.75 mg | as needed, at least 45 minutes before sexual activity; max 1 dose per 24 hours, max 8 doses per month |
| Experienced | 1.75 mg | 1.75 mg | 1.75 mg | 1.75 mg | as needed, at least 45 minutes before sexual activity; max 1 dose per 24 hours, max 8 doses per month |
Every cell read verbatim from dose_protocols. Where a level repeats the same figure across columns, that is what the table holds: no ramp has been invented to fill the row.
Pre-calculated syringe units for every water volume against the dose figures this compound actually uses, at your selected vial size of 10 mg. A cell reading "n/a" means the draw exceeds a 100-unit syringe at that concentration.
| BAC water | Conc. | Opening1.75 mg | Standard1.75 mg | Upper1.75 mg | Ceiling1.75 mg |
|---|---|---|---|---|---|
| 1 ml | 10 mg/ml | 17.5 | 17.5 | 17.5 | 17.5 |
| 1.5 ml | 6.67 mg/ml | 26.3 | 26.3 | 26.3 | 26.3 |
| 2 ml | 5 mg/ml | 35 | 35 | 35 | 35 |
| 2.5 ml | 4 mg/ml | 43.8 | 43.8 | 43.8 | 43.8 |
| 3 ml | 3.33 mg/ml | 52.5 | 52.5 | 52.5 | 52.5 |
| 4 ml | 2.5 mg/ml | 70 | 70 | 70 | 70 |
| 5 ml | 2 mg/ml | 87.5 | 87.5 | 87.5 | 87.5 |
Column doses are the beginner row's opening, standard, upper and ceiling figures from dose_protocols. Unit marks are arithmetic.
One on-cycle runs 52 weeks followed by 0 weeks off, from the engine catalog. Multiplied out at the standard dose and your mix, that is what the cycle costs in consumables.
Supplies are not computed for this combination, because the frequency string on this dose row does not map to a fixed number of administrations per week and a supply figure is not worth guessing at.
Cycle length, loading phase and taper from PEPTIDE_CATALOG. Administrations per week derived from the frequency string on the dose row. Counts are arithmetic.
Free founding-member access while spots last. We'll send your reconstitution + a link to claim your slot.
PT-141 is bremelanotide, a melanocortin receptor agonist and a cyclic analogue of the alpha-melanocyte-stimulating hormone family. Unlike most of the catalog it reached approval: the FDA approved it on 21 June 2019 under NDA 210557, marketed as Vyleesi, for premenopausal women with acquired, generalised hypoactive sexual desire disorder. The two RECONNECT phase 3 trials behind that decision were published in Obstetrics and Gynecology in 2019, and a safety analysis across the whole development programme followed in 2022.
Approval is why the dose figure on this page does not move with experience level. The engine dose table carries the labelled figure at every level rather than inventing a ramp to fill the columns, and the frequency string carries the label's own two limits verbatim: no more than one dose in twenty-four hours, and more than eight doses a month is not recommended. Those limits are part of the dose, not advice attached to it.
One honest caveat about what this calculator is for. The approved product is a single-use autoinjector holding a fixed volume, so nobody reconstitutes it. A vial of lyophilised powder is a different presentation, and reconstitution arithmetic is what a reader with a vial actually needs. The dose target the calculator aims at is the sourced one either way, and the reference list below is the clinical literature on the compound rather than a set of dose citations.
| Route | subcutaneous |
|---|---|
| Timing | On demand |
| Catalog frequency | As needed, max 8x/month |
| Cycle | 52 weeks on, 0 weeks off |
| Taper before the off period | Not specified |
| Loading phase | None |
| Weight sensitive | No |
Catalog note: Inject subcutaneously at least 45 minutes before activity. Maximum one dose per 24 hours and no more than 8 doses per month. May cause nausea on first use.
Every row above is read from PEPTIDE_CATALOG, the engine catalog, and the note is quoted verbatim rather than paraphrased.
Klarovel holds two upper bounds for PT-141 (Bremelanotide) in two different places, and they do not agree. The engine dose table puts the highest ceiling at 1.75 mg across the experience levels. The older research row carries 1 mg.
The engine dose table is the one that binds. The dose guard that caps generated protocols reads its ceilings from that table and falls back to the research row only where no dose row exists, because a guard that fights the engine trims legitimately curated doses and trains everyone to ignore its warnings.
Both figures are printed here rather than one, so a reader who finds the lower number elsewhere can see that both exist and which one the software actually uses.
A public page cannot know your health data, so it cannot tell you whether a compound is appropriate. What it can do is list the conditions the engine's contraindication matrix associates with this compound, and what the engine does about each. In a generated protocol these resolve automatically and the reason is shown alongside the exclusion.
| Condition | Engine action | Reason |
|---|---|---|
| Uncontrolled hypertension | Excluded | PT-141 may cause acute blood pressure elevation. Contraindicated with uncontrolled hypertension. |
| Heart condition | Caution | PT-141 may cause transient blood pressure elevation. Cardiological clearance recommended with known heart disease. |
| Mental health | Monitored | PT-141 may affect mood via the melanocortin system. Monitor mood changes with mental health conditions. |
Conditions, severities and reasons read verbatim from CONTRAINDICATION_RULES, the engine's contraindication matrix. This is not the full set of things worth raising with a clinician; it is the set the engine acts on.
These papers cover bremelanotide from mechanism through approval: the melanocortin pharmacology, the early arousal studies, the two RECONNECT phase 3 trials, the pooled safety analysis, and two published critiques of the phase 3 evidence. The critiques are included deliberately. A reference list that carries only the favourable half of a literature is a marketing document.
The dose figures on this page are not sourced from these papers. They are read from the Klarovel engine's own dose table, which is cited inline wherever a number appears. These references cover mechanism, pharmacology and clinical context.
12 references, every identifier resolved against NCBI on 2026-08-03. Per peptide, a relevance-sorted esearch was run and every returned id was resolved through esummary. Any id esummary could not resolve was dropped, and any record carrying the 'Retracted Publication' pubtype was dropped. Titles, journals, years and first authors below are the values esummary returned, not authored text. One retracted record was dropped: PMID 37696839 (thymosin beta 4 query). Regenerated 2026-08-03 for cjc1295_no_dac, ipamorelin, pt141, retatrutide, aod9604 and sermorelin using the same esearch + esummary procedure; no record was added whose esummary payload lacked a title, journal or first author.
Beyond the arithmetic
A calculator converts a dose into syringe units. The Klarovel engine decides the dose: it reads your health data, resolves contraindications, sets the envelope by experience level, removes incompatible pairs and builds the cycling and monitoring schedule. Blood work is optional and sharpens the result. It is never required.