Beer-Lambert Law Calculator

Enter any three of the four Beer-Lambert Law variables — extinction coefficient (ε), path length (l), concentration (c), and absorbance (A) — and the calculator solves for the missing one. Leave exactly one field blank to get your result, or fill in all four to verify the relationship A = ε × l × c.

M⁻¹ cm⁻¹

Molar absorptivity — leave blank to calculate this value

cm

Optical path length through the sample — typically 1 cm for standard cuvettes

M

Molar concentration of the solution in mol/L (M)

Dimensionless measure of light attenuation — leave blank to calculate

Results

Calculated Result

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Solved For

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Absorbance (A)

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Transmittance (T)

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Extinction Coefficient (ε)

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Path Length (l)

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Concentration (c)

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Light Absorbed vs Transmitted

Frequently Asked Questions

What is the Beer-Lambert Law?

The Beer-Lambert Law (also called Beer's Law) describes how light is absorbed as it passes through a solution. It states that absorbance (A) equals the product of the molar extinction coefficient (ε), the path length (l), and the concentration (c): A = ε × l × c. The law is fundamental in spectrophotometry and analytical chemistry.

What is the unit of absorbance in Beer's Law?

Absorbance is dimensionless — it has no units. It is defined as the negative logarithm (base 10) of transmittance: A = −log₁₀(T). Because it is a ratio of intensities, the units cancel out. Typical absorbance values in laboratory work range from 0.1 to 2.0 for reliable measurements.

How do I calculate molar absorptivity (extinction coefficient) from Beer's Law?

Rearrange the Beer-Lambert equation to isolate ε: ε = A / (l × c). You need the measured absorbance, the known path length (usually 1 cm), and the known concentration in mol/L. The result is expressed in units of M⁻¹ cm⁻¹.

How do I calculate concentration from absorbance using Beer's Law?

Rearrange the formula to c = A / (ε × l). Measure the absorbance of your sample spectrophotometrically, then divide by the product of the known extinction coefficient and path length. This is one of the most common uses of Beer's Law in laboratory settings — for example, determining protein or DNA concentration.

How do I convert absorbance to transmittance?

Transmittance (T) and absorbance (A) are related by: T = 10^(−A), and expressed as a percentage: %T = 10^(−A) × 100. For example, an absorbance of 1.0 corresponds to 10% transmittance, meaning 90% of the incident light was absorbed by the sample.

What are the limitations of the Beer-Lambert Law?

Beer's Law assumes a linear relationship between absorbance and concentration, which holds true only at relatively low concentrations (typically below 0.01 M). At high concentrations, interactions between solute molecules, stray light effects, and non-monochromatic radiation can cause deviations. The law also assumes the solution is homogeneous and the solute does not fluoresce or scatter light significantly.

What is a typical path length used in Beer-Lambert calculations?

Most standard laboratory cuvettes have a path length of 1 cm, which simplifies the equation to A = ε × c. However, micro-cuvettes, flow cells, and fiber-optic probes can have different path lengths. Always confirm your cuvette's path length before performing calculations, especially for non-standard setups.

What are common applications of the Beer-Lambert Law?

Beer's Law is widely used in UV-Vis spectrophotometry to determine the concentration of solutions such as DNA, RNA, proteins, and small molecules. It is also applied in environmental monitoring (measuring pollutant concentrations in water), pharmaceutical quality control, food and beverage analysis, and clinical diagnostics such as hemoglobin measurement in blood.

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