Part of the Science & Chemistry suite · 71 calculators

Serial Dilution Calculator

The concentration at every step of a serial dilution — with the total dilution reached and the volumes for each tube.

Each step multiplies the dilution: n steps at a factor of f give a total dilution of fⁿ.

Any unit
Results update as you type
Results
Final concentration
0.000001
Total dilution factor
Concentration at each step
Transfer volume per step (mL)
Diluent per tube (mL)
Total diluent needed (mL)
Total dilution in log₁₀
Reviewed September 2026. Chemistry is the same in every country: SI and laboratory units throughout.
No account required · Google Analytics off unless allowedCalculator arithmetic runs in your browserResults update as you type
All calculations run 100% in your browser. The calculator code does not submit your figures to GlobalCalc to obtain a result.
About serial dilution

How the serial dilution calculator works

Each step multiplies the dilution: n steps at a factor of f give a total dilution of fⁿ. Ten 10-fold steps reach 10¹⁰, which is how a bacterial culture gets to a countable plate.

Serial dilution exists because a single 10,000,000-fold dilution would need a microlitre into ten litres. Splitting it into steps keeps every transfer a pipettable volume, at the cost of compounding any error at each one.

Formula: Cₙ = C₀ / fⁿ

Worked examples

InputsFinal concentrationNote
Six 10-fold steps0.00000110⁻⁶ of the original
Ten 2-fold steps0.00097656251/1024
Three 100-fold steps0.000001a millionth

Frequently asked questions

Why dilute serially instead of all at once?

Because a 10⁶-fold dilution in one step would mean a microlitre into a litre. Serial steps keep every transfer a volume you can pipette accurately.

How many steps do I need?

log(total dilution) ÷ log(step factor). A 10⁶ dilution takes six 10-fold steps or three 100-fold ones.

Does error accumulate?

Yes, and multiplicatively. A 2% error at each of six steps compounds to about 13%. Fewer, larger steps are more accurate if you can pipette them.

What volumes should I use?

For a 10-fold step with 0.9 mL of diluent, transfer 0.1 mL. Mix thoroughly before each transfer — incomplete mixing is the biggest source of error.

Where is this used?

Bacterial plate counts, immunoassay standard curves, and any titration of a potent compound down to a working range.

Where these figures come from

Last checked: September 2026. Atomic masses are the IUPAC conventional values; constants are CODATA 2018; equations are the standard textbook forms.