Solve Beer-Lambert variables from optical data easily. Compare absorbance trends, review examples, and download reports. Built for fast calibration checks and dependable concentration estimates.
Enter any known values, choose what to solve, and submit. The page calculates the missing Beer-Lambert variable and plots absorbance versus concentration.
Absorbance is dimensionless. Concentration is usually entered in mol/L, path length in cm, and molar absorptivity in L·mol⁻¹·cm⁻¹. The plotted line uses the slope εl, which represents the calibration sensitivity.
| Sample | Absorbance (A) | Molar Absorptivity | Path Length (cm) | Concentration (mol/L) | Wavelength (nm) |
|---|---|---|---|---|---|
| Blue Dye A | 0.300 | 15000 | 1.00 | 2.00e-5 | 610 |
| Blue Dye B | 0.450 | 15000 | 1.00 | 3.00e-5 | 610 |
| Food Color C | 0.620 | 15500 | 1.00 | 4.00e-5 | 540 |
| Reference Solution | 0.180 | 12000 | 1.00 | 1.50e-5 | 520 |
It applies the Beer-Lambert law to relate absorbance, concentration, path length, and molar absorptivity. It also estimates transmittance and plots the absorbance-concentration trend for quick interpretation.
Use absorbance as a unitless value, concentration in mol/L, path length in centimeters, and molar absorptivity in L·mol⁻¹·cm⁻¹. Keeping units consistent is essential for correct results.
Small concentrations are common when molar absorptivity is large or absorbance is modest. The page automatically formats tiny values in scientific notation so they remain readable and accurate.
Yes. Change the solve mode at the top of the form. The calculator can solve for concentration, absorbance, molar absorptivity, or path length using the same Beer-Lambert relationship.
The graph shows the theoretical linear relationship between concentration and absorbance for the current slope εl. Your calculated sample point is added to the chart for context.
Negative absorbance usually indicates measurement or baseline issues rather than a valid sample result. This calculator blocks negative absorbance because standard Beer-Lambert analysis expects nonnegative values.
Transmittance is derived from absorbance using T = 10-A. Percent transmittance is simply that fraction multiplied by 100, which gives a more familiar laboratory reporting format.
Wavelength is optional and does not change the math directly. It is useful for documentation because molar absorptivity depends on wavelength, and many laboratories track readings by wavelength.
Important Note: All the Calculators listed in this site are for educational purpose only and we do not guarentee the accuracy of results. Please do consult with other sources as well.