Sensitive Liquids: Reversible Dye-Based Redox Reactions
Polish version is here |
The following article was originally published in the journal for educators Chemia w Szkole (eng. Chemistry in School) (1/2015):

Chemical color-change reactions invariably capture the interest of chemistry enthusiasts. Undeniably spectacular, they can provide a certain aesthetic pleasure. However, it is important to remember that without deeper reflection, these displays have limited educational value. In such cases, they function merely as a form of advertisement, intended to encourage viewers to ask questions [1].
The experiment presented here will undoubtedly prompt every observer to wonder about the nature of these so-called sensitive liquids. They possess a fascinating property: when left undisturbed, they become colorless, yet with each shake, they reveal fleeting — yet undeniably beautiful — colors.
[…]
Preparation
The following chemical substances are required for the experiment:
- sodium hydroxide NaOH
- glucose or fructose C6H12O6 or lactose C12H22O11
- methylene blue C16H18ClN3S
- resazurin C12H7NO4
When preparing the experiment, remember that sodium hydroxide is highly corrosive — contact with skin or eyes can result in severe chemical burns. The dyes used in this experiment (their structural formulas are shown in Fig. 1) can be harmful, so avoid direct skin contact and do not inhale any dust. Keep in mind that methylene blue and resazurin can leave particularly stubborn stains on skin or fabrics.

[…]
First, it is a good idea to prepare the dye solutions:
- methylene blue solution: 0.20 g (0.007 oz) of C16H18ClN3S in 50 cm3 (1.69 fl oz) of water,
- resazurin solution: 0.15 g (0.005 oz) of C12H7NO4 in 50 cm3 (1.69 fl oz) of water.
These solutions are relatively stable and can be stored for an extended period.
The next step of the experiment is to prepare the base solution. In 100 cm3 (3.38 fl oz) of water, dissolve 2 g (0.07 oz) of sodium hydroxide and about 3 g (0.11 oz) of one of the previously mentioned sugars, such as glucose (Photo 1). This solution is unstable and should be used as soon as possible!
At the start of the demonstration, pour approximately 10 cm3 (0.34 fl oz) of the base solution into each of two small bottles, and then add a few drops of one of the dye solutions to each. […]
If you simply leave the liquids undisturbed, after some time (ranging from a few seconds to several minutes) their color begins to fade. Eventually, both solutions become completely colorless and clear (Photo 2).
However, upon shaking the bottles, the solutions regain their intense, characteristic colors (Photo 3). When left undisturbed, they spontaneously become colorless again. Shaking the bottles re-oxidizes the dye back to its blue form, and with continued shaking, this color-change cycle can be repeated many times. […]
Explanation
The color changes observed in this experiment are the result of two opposing reactions taking place in the solution: the reduction and oxidation of the respective dyes — in this case, methylene blue and resazurin [2].
[…]
Glucose (or another reducing sugar) is oxidized to gluconate at the expense of the dye (methylene blue or resazurin). As a result, the dyes themselves are reduced to their colorless leuco forms, which we observe as decolorization [3].
Shaking introduces oxygen from the air into the solution, rapidly oxidizing the leuco dyes back to their colored forms, while the oxygen is reduced to hydrogen peroxide (H2O2) or water (H2O) [4]. However, this state is not permanent because they are once again reduced by glucose.
References:
- [1] Orlińska I., Chemia na wesoło, Chemia w Szkole (eng. Chemistry in School), 4 (2014), Wydawnictwo Edupress, pp. 27-28 back
- [2] Bueno C., Villegas M. L., Bertolotti S. G., Previtali C. M., Neumann M. G., Encinas M. V., The Excited-State Interaction of Resazurin and Resorufin with Aminesin Aqueous Solutions. Photophysics and Photochemical Reaction, Photochemistry and Photobiology 76 (4), 2002, pp. 385–390 back
- [3] Sienko M., Plane R., Chemia. Podstawy i zastosowania, PWN, Warszawa, 1999 back
- [4] Pluciński T., Doświadczenia chemiczne, Wydawnictwo Adamantan, Warszawa, 1997 back
All photographs and illustrations were created by the author.
Marek Ples