Quantification of methanol in contaminated spirits
AN-RS-056
2026-03
en
Protecting consumers from contaminated beverages
Raman spectroscopy is ideally suited to rapidly screen for methanol contamination in spirits.
An alarming global trend highlights the serious harm that can result from ingesting illegal, improperly distilled alcohol. Home-distilled spirits prepared using industrial solvents (i.e., wood alcohol) and presented as legitimate alcoholic beverages often contain methanol. Methanol causes blindness and can lead to death when ingested. This has led to fatal consequences around the world [1–3].
The breaking point for the Czech Republic came in September 2012. The sale of hard liquor was temporarily banned after 20 people died from the consumption of spirits with dangerous levels of methanol [2]. After an exhaustive study using various screening tools, the Czech Republic adopted Raman spectroscopy as the method of choice for identifying and quantifying methanol in contaminated spirits.
This Application Note demonstrates how Raman spectroscopy can be employed as an efficient and rapid screening method for samples of rum contaminated with methanol.
Raman spectroscopy is a fast and easy analytical tool for quantifying the amount of methanol contamination present in alcoholic beverages. It is an ideal method for the discrimination of very similar molecules like ethanol (CH3CH2OH) and methanol (CH3OH), as shown in Figure 1.
The ability of Raman spectrometers to measure through containers and the lack of sensitivity to water make them better suited to measure methanol in beverage samples. These two key properties enable accurate detection of methanol down to approximately 1% by volume in the field with no need to open the bottles for testing. In the lab, the i-Raman NxG and SpecSuite software elevate the detection capabilities of Raman spectroscopy by adding the ability to quantify adulterants. (Figure 2)
This example study measures commercially available coconut rum that is spiked with methanol in concentrations between 0.33% and 5.36%. The i-Raman NxG 785H with a fiber-optic probe is used to collect Raman spectra of the mixtures (Figure 3). Table 1 lists the relevant equipment and instrument settings used for this application study.
The peak at around 1000 cm-1 (highlighted by the inlay of Figure 3) visibly increases with increasing concentration of methanol, becoming significant at approximately 1%.
| Equipment | Acquisition settings | |
|---|---|---|
| i-Raman NxG 785H | Laser Power | 100 |
| Vial holder | Int. time | 1 s |
| SpecSuite Software | Average | 1 |
This data is analyzed with SpecSuite software, and a partial least squares (PLS) regression model is developed on normalized data. The two-factor model developed over the range from 980–1040 cm-1 gives the calibration curve shown in Figure 4, which has an error of cross-validation (SECV) of 0.0794 (Table 2). The R2 value of 0.9980 shown in Table 2 means that the Raman method used here can be used to confidently quantify the amount of methanol in a mixed alcohol sample.
| Parameter | Value |
|---|---|
| Spectral processing | Mean centering Savitzky-Golay derivative |
| R2 | 0.9980 |
| SEC | 0.0681 |
| SECV | 0.0794 |
These results validate that Raman spectroscopy can be used for rapid, quantitative screening of dangerous adulterants in alcoholic beverages. This technique can be expanded to investigate adulteration in other media such as food, petroleum, and pharmaceutical drugs [4].
- Lachenmeier, D. W.; Schoeberl, K.; Kanteres, F.; Is Contaminated Unrecorded Alcohol a Health Problem in the European Union? A Review of Existing and Methodological Outline for Future Studies. Addiction 2011, 106 (s1), 20–30. https://doi.org/10.1111/j.1360-0443.2010.03322.x.
- Spritzer, D.; Bilefsky, D. Czechs See Peril in a Bootleg Bottle. The New York Times. USA September 17, 2012.
- Collins, B. Methanol Poisoning: The Dangers of Distilling Spirits at Home. ABC. Australia June 13, 2013.
- Gryniewicz-Ruzicka, C. M.; Arzhantsev, S.; Pelster, L. N.; et al. Multivariate Calibration and Instrument Standardization for the Rapid Detection of Diethylene Glycol in Glycerin by Raman Spectroscopy. Appl Spectrosc 2011, 65 (3), 334–341. https://doi.org/10.1366/10-05976.