Wavenumber to Wavelength Converter
Common Conversions
| cm⁻¹ | nm |
|---|---|
| 100 | 100000 |
| 250 | 40000 |
| 500 | 20000 |
| 1000 | 10000 |
| 1500 | 6666.7 |
| 2000 | 5000 |
| 2500 | 4000 |
| 3000 | 3333.3 |
| 3500 | 2857.1 |
| 4000 | 2500 |
| 5000 | 2000 |
| 10000 | 1000 |
Why this conversion matters in chemistry
IR spectra are almost always plotted against wavenumber, but the wavelength form still matters when you're choosing sample cells or sample-preparation windows — a 1650 cm⁻¹ amide-I band in a protein spectrum corresponds to 6.06 µm, which is well inside the transparency range of CaF₂ windows but outside that of common glass. A C–H stretch at 3000 cm⁻¹ is 3.33 µm; a C=O at 1700 cm⁻¹ is 5.88 µm. Dividing 10⁷ by the wavenumber in cm⁻¹ gives you the wavelength in nm, and shifting the decimal by three converts to µm — the native unit of IR optics specifications.
Formula
Worked Examples
10 µm — solidly in the mid-IR fingerprint region, where most diagnostic bands live.
3.33 µm. The C–H stretching region — almost any aliphatic organic spectrum shows peaks here.
5.88 µm. The carbonyl C=O region — one of the most diagnostic features of organic IR spectra.
20 µm — far-IR territory, where lattice vibrations and some metal-ligand modes appear.