Half-Life Visualizer

See how compounds rise, peak and clear over time.
FREE
For education only - tap to read the full notice
This is an informational tool, not medical advice, and not a substitute for a qualified healthcare professional. It does not diagnose, treat, or recommend anything, and it does not tell you what to take or how much. Curves shown are illustrations based on published pharmacokinetic data and general models; real-world results vary. We do not sell, supply, or help anyone obtain any substance. Talk to a licensed clinician or pharmacist about your health.
Data & references. Anabolic-androgenic compound half-lives, ester behavior and anabolic:androgenic ratings are referenced from William Llewellyn's Anabolics (the standard reference text), alongside peer-reviewed pharmacokinetic literature and approved drug labeling for peptides, GLP-1s and pharmaceuticals. Values are published estimates that vary by individual, formulation and route; curves are illustrative.
Why half-life matters - and how it relates to side-effects - read me

What it is. A compound's half-life is the time it takes for the amount in your blood to fall by half. If something has a 24-hour half-life, half is left after one day, a quarter after two, an eighth after three, and so on. It is the single most useful number for understanding how a compound behaves in the body over time.

Accumulation & steady state. If a dose repeats before the previous one clears, the leftovers stack. With regular dosing, levels climb until the amount going in each interval equals the amount cleared - "steady state." Reaching it takes about 4-5 half-lives. A long half-life builds slowly to a smooth, steady level; a short one is fast-on, fast-off, with much bigger peaks and troughs.

Why stability matters for side-effects. Many side-effects track the extremes, not the average - the peak right after a dose (too much, too fast) and the crash at the trough (levels dropping off). Holding a compound in a steady band, instead of letting it spike and dip, is generally how people try to keep side-effects down. Splitting the same weekly amount into smaller, more frequent doses lowers the peak-to-trough swing without changing the average - the same total, a flatter line.

How fast you can stabilize. Because it takes 4-5 half-lives to settle, a long-half-life compound can take weeks to reach a stable level - which is why some protocols use a larger early "loading" dose to get there sooner instead of waiting for it to build. A short-half-life compound stabilizes quickly but needs frequent dosing to stay there. The moving-average overlay and the peak:trough readout in this tool show how steady any given pattern actually is.

Washout & interactions. Half-life also sets how long a compound lingers after the last dose (~4-5 half-lives to clear), and because it governs timing, it shapes how compounds overlap when combined and how long effects and side-effects persist. Two compounds at the same dose can behave completely differently if their half-lives differ.

Important: published half-lives are estimates that vary with the individual (genetics, body composition, liver and kidney function), the formulation, and the route. Treat every curve here as an illustration, not a precise prediction, and not medical advice.

📱 Turn your phone sideways for a wider view of the charts.

Model fidelity

Half-life data

Simulation window

Add a compound to visualize

What "anabolic : androgenic" means. Anabolic = tissue / muscle-building. Androgenic = masculinizing effects (libido, body/facial hair, prostate, oily skin, aggression). Testosterone is the reference at 100 : 100. A higher first number = more muscle-building relative to androgenic side-effects (in rodents). The Combined A:A card weights each compound's rating by its modeled level, so it reflects the inputs you entered. Ratings come from the 1950s rat (Hershberger) bioassay in Llewellyn's Anabolics and are a rough guide only - the clean split seen in rodents is much weaker in humans, where every AAS is meaningfully androgenic.

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Half-Life Lab community

Compound profiles, half-life explainers, deep dives and member discussion, inside the Skool community.

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Cmax = peak just after a dose; Cmin = trough before the next (at steady state). Solid lines = concentration in relative units: an index proportional to serum level, not real ng/dL - read shapes, ratios and peak:trough, not absolute numbers. All three model modes share one scale (ester-aware also scales by each ester's active-hormone fraction). Right axis: estradiol (E2, pink) and prolactin (PRL, purple), illustrative only.
Estrogen crashed. Ancillary load is driving modeled E2 very low. In reality, excessively low estrogen causes joint pain, low libido, fatigue, mood issues and poor lipids - over-suppression is its own harm. (Illustrative only.)
\u26a0 Hypoglycemia risk. The modeled glucose curve is being driven low by insulin (and any IGF-1). In reality, too much insulin causes rapid, potentially fatal low blood sugar. This is an illustration of timing and interaction only, never a dose. Education and risk literacy, not medical advice.
Set a Stop point on a compound's active-window slider to see how long it takes to clear after the last dose.
iPhone: tap the button and choose Add All when the Calendar sheet appears (open the tool in Safari or Chrome, not an in-app browser). Android: opens in Google Calendar import. Desktop: double-click for Apple Calendar, or Google Calendar → Settings → Import. Each dose becomes a 15-min marker at your start time; twice/thrice-daily orals spread evenly across the day.

Log side effects as they happen. Each entry drops a numbered marker on the charts at the day it occurred, anchored to the Start date and window you set in the Simulation window panel, so you can see what your modeled levels were doing when it showed up. Saved only in this browser, never uploaded.

MildModerateSeveremarkers anchor to the Start date and window in the Simulation window panel
Tracking and education only. This logs what you report and shows its timing next to modeled levels. It does not diagnose anything and does not tell you to change a dose. A pattern you notice here is a reason to talk with a licensed clinician, who can advise on any adjustment, which you can then model in the tool. If you ever feel acutely unwell (for example chest pain, a severe headache, or very high blood pressure), seek medical help now.