Dilution Calculator

Apply C₁V₁ = C₂V₂ to plan any dilution: find final volume, final concentration, stock concentration, or a full serial dilution table.

🧪 Dilution Calculator - C₁V₁ = C₂V₂

Find the final volume V₂ required to reach target concentration C₂.

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Find the final concentration C₂ when V₁ of stock is diluted to total volume V₂.

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Back-calculate the stock concentration C₁ from the diluted solution.

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Generate a serial dilution table. Each step dilutes by the same factor.

Final volume V₂
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Solvent to add
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Dilution factor
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Step-by-step working
Final concentration C₂
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Dilution factor
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Step-by-step working
Stock concentration C₁
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Step-by-step working

📊 What is Dilution?

Dilution is the process of reducing the concentration of a solute in a solution by adding more solvent. When you dilute a solution, the amount of solute stays constant - you only add solvent. This is captured by the fundamental equation:

C₁V₁ = C₂V₂

where C₁ is the initial concentration of the stock solution, V₁ is the volume of stock taken, C₂ is the desired final concentration, and V₂ is the total final volume. The equation simply states that moles of solute are conserved: C₁ × V₁ = moles in stock taken = C₂ × V₂ = moles in final solution.

Dilution calculations are essential in chemistry, biology, pharmacology, and food science. A laboratory routinely prepares working solutions from concentrated stock reagents. A pharmacist dilutes concentrated drug solutions to clinical dosage concentrations. Microbiologists serially dilute samples by factors of 10 to count colony-forming units.

The dilution factor (V₂/V₁) describes how many times more dilute the final solution is compared to the stock. A 1:10 dilution (dilution factor = 10) means 1 part stock in 10 parts total (9 parts solvent added).

📐 Formula

Dilution equation (C₁V₁ = C₂V₂):

Solve for any unknown:

  • V₂ = C₁ × V₁ / C₂ (find total volume needed)
  • C₂ = C₁ × V₁ / V₂ (find final concentration)
  • C₁ = C₂ × V₂ / V₁ (find stock concentration)
  • V₁ = C₂ × V₂ / C₁ (find volume of stock to use)

Dilution factor: DF = V₂ / V₁ = C₁ / C₂

Solvent to add: V_solvent = V₂ − V₁

Serial dilution (n steps, factor f each): Cₙ = C₀ / f^n

Variables:

  • C₁, C₂ - concentrations (any consistent unit: M, %, mg/mL, ppm)
  • V₁ - volume of stock solution taken
  • V₂ - final total volume of diluted solution
  • f - dilution factor per serial dilution step
  • n - number of serial dilution steps

📖 How to Use

Steps to Calculate

1
Find V₂ - enter stock concentration C₁, volume V₁ to take, and target concentration C₂. The calculator returns the required total volume V₂, the volume of solvent to add, and the dilution factor.
2
Find C₂ - enter stock concentration C₁, volume V₁, and final volume V₂. Returns the resulting concentration after dilution.
3
Find C₁ - enter the diluted concentration C₂, the volume of stock taken V₁, and the final volume V₂. Returns the original stock concentration.
4
Serial Dilution - enter stock concentration, dilution factor per step, and number of steps (1–12). A table shows the concentration after every step and the cumulative dilution factor.
5
Volume of solvent - in Find V₂ mode, the calculator always shows both the final volume V₂ and the amount of solvent to add (V₂ − V₁) for practical lab use.

💡 Example Calculations

Example 1 — Preparing 500 mL of 0.1 M NaCl from 5 M Stock

C₁ = 5 M, C₂ = 0.1 M, V₂ = 0.5 L → find V₁

1
C₁V₁ = C₂V₂ → V₁ = C₂ × V₂ / C₁ = 0.1 × 0.5 / 5 = 0.01 L = 10 mL
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Solvent to add = V₂ − V₁ = 500 − 10 = 490 mL
Measure 10 mL of 5 M stock, add to a 500 mL flask, fill with distilled water to the 500 mL mark. Dilution factor = 50×.
Try this example →

Example 2 — Finding Concentration After Dilution

50 mL of 2 M HCl diluted to 200 mL → find C₂

1
C₂ = C₁ × V₁ / V₂ = 2 × 0.05 / 0.2 = 0.5 M
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Dilution factor = V₂ / V₁ = 200 / 50 =
Final concentration = 0.5 M HCl. Moles check: 2 M × 0.05 L = 0.1 mol = 0.5 M × 0.2 L ✓
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Example 3 — Serial 10× Dilution (6 steps)

Stock 1 M, dilution factor 10×, 6 steps

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Step 1: 1 M / 10 = 0.1 M (10× dilution)
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Step 2: 0.1 M / 10 = 0.01 M (100× overall)
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Steps 3–6 continue: 10⁻³, 10⁻⁴, 10⁻⁵, 10⁻⁶ M
After 6 serial 10× dilutions: final concentration = 10⁻⁶ M (1 µM). Overall factor = 10⁶.
Try this example →

❓ Frequently Asked Questions

What is the dilution formula C₁V₁ = C₂V₂?+
C₁V₁ = C₂V₂ expresses conservation of solute: the moles of solute in the stock volume (C₁ × V₁) equal the moles in the diluted solution (C₂ × V₂). Since you only add solvent (not more solute), the total moles remain constant. Rearrange to find any one unknown: V₂ = C₁V₁/C₂, C₂ = C₁V₁/V₂, C₁ = C₂V₂/V₁, V₁ = C₂V₂/C₁.
What is a dilution factor?+
The dilution factor (DF) = V₂ / V₁ = C₁ / C₂. It tells you how much more dilute the final solution is than the stock. A DF of 10 means the final concentration is 1/10 of the stock. A 1:10 dilution (in ratio notation) adds 1 part sample to 9 parts solvent (total 10 parts), giving DF = 10. A 1:2 dilution (DF = 2) takes 1 part sample and 1 part solvent.
How do you perform a serial dilution?+
A serial dilution applies the same dilution factor repeatedly. For a 10× series: take 1 mL of stock into 9 mL of diluent (tube 1, now 10× diluted). Take 1 mL from tube 1 into 9 mL (tube 2, now 100× diluted). Continue for n steps: final concentration = C₀ / 10^n. Serial dilutions are used when you need to span many orders of magnitude in concentration.
What units can C₁ and C₂ use?+
Any concentration unit works in C₁V₁ = C₂V₂ as long as C₁ and C₂ use the same unit. Common choices: molarity (M = mol/L), percent (w/v: g/100 mL; v/v: mL/100 mL), mg/mL, ppm, ppb. Similarly, V₁ and V₂ must use the same volume unit (both mL, both L, etc.) - but the volume unit does not need to match the concentration unit.
How do you prepare a 1:5 dilution?+
A 1:5 dilution (DF = 5) means the final volume is 5× the stock volume taken. Example: take 10 mL of stock and add diluent to reach a total of 50 mL (add 40 mL of diluent). The final concentration is C₁ / 5. Note: 1:5 in US lab notation usually means 1 part sample + 4 parts diluent = 5 parts total (DF = 5). Some sources define 1:5 as 1 part sample + 5 parts diluent (DF = 6) - always clarify which convention is used.
Can you dilute a solution below zero concentration?+
No - concentration cannot go below zero, and you cannot concentrate a solution by diluting it (C₂ cannot exceed C₁). The dilution equation always gives C₂ ≤ C₁. If you need a higher concentration, evaporate solvent (rotary evaporation, lyophilization) or start with a more concentrated stock. The calculator flags it as an error if C₂ > C₁.
What is the difference between a dilution and a solution preparation?+
A solution preparation starts from a pure solid or liquid solute: weigh out the required mass, dissolve, and make up to volume. A dilution starts from an existing solution (the stock) and adds solvent. Use the Molarity Calculator to compute mass for a solution preparation; use this Dilution Calculator once you have the stock. Combining both: first prepare a concentrated stock from solid, then dilute to working concentrations.
How do you calculate the number of moles in a diluted solution?+
Moles = concentration × volume. For the diluted solution: moles = C₂ × V₂. Since C₁V₁ = C₂V₂, the moles in the diluted solution equal C₁ × V₁ - exactly the moles taken from the stock. Example: 10 mL of 5 M stock gives 5 × 0.01 = 0.05 mol. Whether diluted to 100 mL (0.5 M) or 500 mL (0.1 M), the sample still contains 0.05 mol.
What is the significance of the 10-fold dilution series in microbiology?+
In microbiology, 10× serial dilutions allow counting of bacteria or fungi at manageable concentrations. A sample might have 10⁸ CFU/mL (colony-forming units per mL). After 6 serial 10× dilutions, a 100 µL aliquot plated gives about 10 colonies - countable by eye. The original count is then 10 × 10⁶ = 10⁷ CFU/mL. This technique underlies the standard plate count method for food safety, water quality testing, and fermentation monitoring.
How accurate is a dilution in practice?+
Accuracy depends on measuring equipment. Volumetric glassware (volumetric flasks, Grade A pipettes): ±0.01–0.05% error. Graduated cylinders: ±0.5–1%. Plastic transfer pipettes: ±2–5%. For analytical-grade work, use volumetric flasks and calibrated pipettes. For serial dilutions, errors compound: a 2% error per step becomes a 12% error after 6 steps. Calibrate pipettes regularly and use certified reference materials for critical applications.

What is the dilution formula?

The dilution formula is C₁V₁ = C₂V₂, where C₁ is the initial concentration of the stock solution, V₁ is the volume of stock taken, C₂ is the target (final) concentration, and V₂ is the total final volume. The equation expresses conservation of moles: the number of moles of solute is the same before and after dilution (you add solvent, not more solute).

How do you prepare a diluted solution from a stock?

Example: prepare 500 mL of 0.1 M NaCl from a 5 M stock. Use C₁V₁ = C₂V₂: 5 × V₁ = 0.1 × 0.5, so V₁ = 0.05 / 5 = 0.01 L = 10 mL. Measure 10 mL of the 5 M stock, transfer it to a 500 mL volumetric flask, and add distilled water to the 500 mL mark. The volume of solvent added is 500 − 10 = 490 mL.

What is a dilution factor?

The dilution factor (DF) is the ratio of final volume to initial volume: DF = V₂ / V₁. A 1:10 dilution has DF = 10 (1 part sample in 10 parts total, adding 9 parts solvent). A 1:5 dilution has DF = 5. For a series of dilutions with the same DF, the overall factor after n steps is DF^n. The final concentration equals C₁ / DF^n.

What is a serial dilution?

A serial dilution is a stepwise series of dilutions, each by the same factor (typically 2× or 10×). Each step dilutes the previous diluted solution, not the original stock. After n steps of factor f, the concentration is C₀ / f^n. Serial dilutions are used in microbiology (bacterial counting), pharmacology (dose-response curves), and serology (antibody titration) to create a geometric progression of concentrations.

Can C1V1 = C2V2 be used for percent concentrations?

Yes - C₁V₁ = C₂V₂ applies to any concentration unit, as long as C₁ and C₂ use the same unit. It works for molarity (M), percent (w/v, v/v), mg/mL, ppm, ppb, or any other concentration expression. The equation simply says that the total amount of solute is conserved. The volumes must also use the same unit (both mL, both L, etc.).

How do you calculate the volume of solvent to add?

After computing V₂ using C₁V₁ = C₂V₂, the volume of solvent to add is simply V_solvent = V₂ − V₁. Example: if V₁ = 10 mL (stock volume taken) and V₂ = 500 mL (required final volume), add 500 − 10 = 490 mL of solvent. Note: always add stock to solvent (especially for concentrated acids) to control heat of mixing safely.

What is the difference between dilution factor and concentration factor?

Dilution factor (DF = V₂/V₁) is always ≥ 1 and describes how many times more dilute the solution becomes. Concentration factor is its inverse (V₁/V₂ ≤ 1). A DF of 10 means the final concentration is 1/10 of the stock. A concentration factor of 5 (not a dilution) would mean the final concentration is 5× the stock - achieved by evaporation, not by adding solvent.

How does serial dilution apply to antibody titration?

In a titration ELISA or agglutination assay, a serum sample is diluted serially (e.g., 2× steps: 1:2, 1:4, 1:8, 1:16, ...). The titer is reported as the highest dilution that still gives a positive result. If a sample is positive at 1:128 but negative at 1:256, the titer is 1:128 (DF = 128). This calculator's serial dilution table shows all concentrations so you can plan your dilution scheme.

What is the molarity of a diluted solution?

Molarity (M) is moles of solute per litre of solution. When you dilute from C₁ to C₂: C₂ = C₁ × V₁ / V₂. Example: 50 mL of 2 M HCl diluted to 200 mL: C₂ = 2 × 50/200 = 0.5 M. Use the Molarity Calculator to first find C₁ if you only know the mass and molar mass of your solute.

What safety precautions apply when diluting concentrated acids?

Always add acid to water, never water to acid. Concentrated sulfuric acid (H₂SO₄) releases significant heat when mixed with water - adding water to concentrated acid can cause violent spattering. Procedure: fill the container partly with water, then slowly add acid while stirring. Allow to cool between additions. This applies to H₂SO₄, HCl, HNO₃, and other concentrated acids.

How accurate is the C1V1 = C2V2 equation?

The equation assumes ideal behavior: no volume contraction or expansion when mixing, and no chemical reaction between solute and solvent. For most dilutions with water (especially dilute solutions), the approximation is excellent. For concentrated solutions of strong electrolytes or alcohols, there can be slight volume changes (e.g., ethanol + water contracts by up to 3%). For high-precision work, prepare dilutions gravimetrically (by mass) and measure density.