Beer-Lambert Law Calculator

Enter three known Beer-Lambert values to calculate absorbance, concentration, molar absorptivity, or path length using absorbance or transmittance readings.

Light reading

Known sample values

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How to use our Beer-Lambert Law Calculator

  1. Choose the quantity you need to find under "Calculate which quantity?".
  2. If absorbance is a known value, choose the reading form, then enter the number exactly as reported: absorbance, transmittance fraction, or percent transmittance.
  3. Enter the remaining known values and select the unit printed beside each one in your lab record, reference source, or cuvette specification.
  4. Click Calculate to see the requested quantity, the absorbance used in the equation, percent light transmitted, and the rearranged relationship.
  5. Sanity-check the reading form and units. A transmittance fraction of 0.25 equals 25%T, but an absorbance of 0.25 is a different measurement.
Example inputs for Beer-Lambert Law Calculator
Example inputs for Beer-Lambert Law Calculator

Definitions

Absorbance (A): A unitless measure of how much light a sample absorbs. Higher absorbance means less light passes through.

Transmittance (T): The fraction of incoming light that passes through a sample. In this calculator, it must be greater than 0 and no more than 1.

Percent transmittance (%T): Transmittance written as a percent. For example, T = 0.25 is 25%T.

Molar absorptivity (ε): A coefficient describing how strongly a dissolved substance absorbs light at a particular wavelength and set of conditions.

Path length (l): The distance light travels through the sample, usually the width of liquid inside a cuvette or sample cell.

Concentration (c): The amount of absorbing substance per volume of solution, often reported as mol/L, mmol/L, or umol/L.

Beer-Lambert law: The relationship A = εlc, which links absorbance with molar absorptivity, path length, and concentration. [1]


Absorbance and Light TransmittedPercent transmittance falls by a factor of 10 for each 1.0 increase in absorbance. Use this reference to distinguish absorbance from transmittance readings.Absorbance and Light TransmittedPercent transmittance falls by a factor of 10 for each 1.0 increase in absorbance.A = 0100 %TA = 0.531.6 %TA = 1.010 %TA = 2.01 %TAbsorbance (A)
Absorbance and Light Transmitted
Use this reference to distinguish absorbance from transmittance readings.

Common mistakes and quick fixes

Mistake: Entering 25 as a transmittance fraction.
Fix: Choose "Percent transmittance" for 25%T, or choose "Transmittance fraction" and enter 0.25.

Mistake: Using a molar absorptivity value from a different wavelength or solvent.
Fix: Use a coefficient for the same substance, wavelength, solvent, and relevant lab conditions.

Mistake: Treating a 10 mm cuvette as 10 cm.
Fix: Select millimeters for a value reported in mm. A 10 mm path length equals 1 cm.

Mistake: Entering a value in mM while mol/L is selected.
Fix: Select mmol/L for a value in mM, or convert 0.050 mM to 0.000050 mol/L before entering it.

Mistake: Entering zero transmittance.
Fix: Use a positive transmittance reading. Zero transmittance would require infinite absorbance, so it cannot produce a finite answer.


Limitations & Key Assumptions / Boundary Conditions

  • The calculation assumes absorbance changes linearly with concentration at the selected wavelength.
  • Molar absorptivity must match the substance, wavelength, solvent, and relevant experimental conditions used for the sample.
  • Cloudiness, particles, bubbles, fingerprints, and dirty cuvettes can scatter or block light and change the measured reading.
  • Chemical changes, fluorescence, stray light, and highly concentrated samples can make measurements differ from the simple Beer-Lambert relationship.
  • Known path length must be greater than zero. Known molar absorptivity and concentration may be zero, but division by a zero factor can produce no solution or infinitely many solutions instead of one numeric answer.
  • The result uses the values entered. It does not replace a calibration curve or laboratory quality checks when those are required.

Methodology

Equation and unit conversion

The calculator applies the Beer-Lambert relationship to values in compatible units. [1]

A = εlc

It converts path length to cm, concentration to mol/L, and molar absorptivity to L mol^-1 cm^-1 before solving. A value in mm is multiplied by 0.1. A value in mmol/L is multiplied by 0.001, and a value in umol/L is multiplied by 0.000001. A coefficient in L mmol^-1 cm^-1 is multiplied by 1,000.

Reading conversion

For a transmittance entry, the calculator first finds absorbance. For a percent-transmittance entry, it divides the percent by 100 to obtain T.

A = -log10(T)

%T = 100 x 10^(-A)

Rearranging the equation

The selected missing quantity determines which version of the relationship is used.

c = A / (εl)

ε = A / (lc)

l = A / (εc)

Worked example

With A = 0.600, ε = 15,000 L mol^-1 cm^-1, and l = 1.00 cm, concentration is 0.600 / (15,000 x 1.00) = 0.000040 mol/L. The matching light transmitted is about 25.12%T.

Zero-factor results

When solving by division, the calculator checks the original denominator. A zero denominator with positive absorbance has no solution. A zero denominator with zero absorbance has infinitely many solutions in the calculator's nonnegative domain. A zero concentration can still produce an absorbance of exactly zero when molar absorptivity and path length are positive.


Sources