A Field Guide · Vol. I · No. 1

The EtG Field Guide

ETHYL GLUCURONIDE
Est. half-life 2.6–3.8 h3
Detectable up to ~80 h11

Urinary EtG over time

EtG left axis · BAC right axis
Urinary EtG (ng/mL) BAC overlay (fixed right axis, g/dL) Drink events
Reading at
(+0.0 h)
showing actual now
EtG Now
ng/mL
BAC Now
g/dL
Peak
ng/mL
Clears 500 ng/mL
h
Clears 100 ng/mL
h

The curve is a model — pharmacokinetics are a probability cloud, not a promise. BAC is overlaid with a fixed visual scale so its shape stays comparable as inputs change.

The four cutoffs

Detection thresholds, and who uses them

A "positive" EtG depends on where somebody drew the line. Different programs draw it in different places.

Field notes

What the curve is actually telling you

EtG is a metabolite, not alcohol.

Your liver conjugates a small fraction of ethanol with glucuronic acid. The result — ethyl glucuronide — is chemically stable, water-soluble, and excreted by the kidneys. It lingers well after the alcohol itself is gone4, which is the whole point of the test.

The "80 hours" number is the outlier, not the rule.

You will see "up to 80 hours" quoted confidently online. That tail comes from heavy, sustained consumption; in detoxification patients, urinary EtG took about 40–130 h to fall below 0.5 mg/L (500 ng/mL)11. One or two drinks typically clear the common 500 ng/mL cutoff in the 24–30 h neighborhood6. The curve above shows both.

Incidental exposure is a real edge case.

Mouthwash, hand sanitizer, kombucha, ripe fruit, and certain communion wines can produce low-positive results at the 100 ng/mL cutoff8. This is why court-adjacent programs often pair EtG with EtS or raise their cutoff.

Why this isn't a test result

Real labs integrate over variable urine volumes, normalize by creatinine, and run two-tier confirmations. The graph above is the shape of what's happening in you, not the number a cup in a bathroom will produce on a Tuesday morning. Treat it as a teacher, not a witness.

Urine concentration changes the number.

The test measures concentration (ng/mL) of EtG, not the total amount of EtG your body has produced. Urine volume and timing can therefore move the measured number around even when the underlying metabolism is unchanged7.

Labs know this. Many programs check creatinine, specific gravity, and other validity markers so a diluted specimen can be reported as dilute or invalid rather than simply negative.

That is why the graph is best read as a concentration model with uncertainty around any real sample, not a guarantee about how a lab will classify one cup of urine.

How the model works

The calculator is intentionally small: a cited set of assumptions feeds one pharmacokinetic model, and the chart renders that result. These are the assumptions currently active in the curve above.

References