Dilution Calculator
Calculate concentrations and volumes for simple dilutions and serial dilutions.
Why the Equation Works in Any Units
C1V1 = C2V2 states that the amount of solute is unchanged by adding solvent. Because both sides express the same quantity, the units cancel — molarity, mg/mL, percent or ppm all work, provided both concentrations use the same one.
The most frequent practical error is treating V2 as the volume of solvent to add. It is the final total volume. Making 100 mL from 10 mL of stock means adding solvent up to the 100 mL mark — about 90 mL, not 100.
Serial Dilution and Error Accumulation
| 1:10 steps | Total factor | From 1 mg/mL |
|---|---|---|
| 1 | 10× | 100 μg/mL |
| 3 | 1,000× | 1 μg/mL |
| 6 | 106× | 1 ng/mL |
| 9 | 109× | 1 pg/mL |
Reaching a millionfold dilution in one step would mean pipetting 1 μL into a litre, where measurement error dominates. Serial dilution replaces one impossible measurement with several manageable ones — but errors accumulate.
A random 2% pipetting error over six steps compounds to about 5%, growing as √n. A systematic 2% bias — a miscalibrated pipette used throughout — compounds to about 12%, growing as n. This is why calibration matters more than technique in serial work.
Worked Examples
Common Mistakes
V2 is the final total volume. Solvent to add is V2 minus V1, which is why volumetric flasks are filled to a mark rather than by measuring solvent.
Both concentrations must use the same unit. Converting between molarity and mg/mL requires molar mass, which the equation itself cannot supply.
A systematic calibration error compounds linearly across steps. Alternating pipettes or verifying calibration reduces accumulated bias.
Each dilution must be homogeneous before the next aliquot is drawn. Incomplete mixing is a large and often invisible source of error.
Frequently Asked Questions
Formula Explorer connections
Interpretation: This formula connects solute amount and solution volume, mass or particle count to concentration and colligative behavior. Assumption: Distinguish solution volume from solvent volume, use the stated temperature, and account for dissociation or nonideal activity when required.