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Bromothymol blue is synthesized by addition of elemental bromine to thymol blue in a solution in glacial acetic acid. [ 6 ] To prepare a solution for use as pH indicator, dissolve 0.10 g in 8.0 cm 3 N/50 (a.k.a. 0.02 Normal ) NaOH and dilute with water to 250 cm 3 .
Solution: The main components of a universal indicator, in the form of a solution, are thymol blue, methyl red, bromothymol blue, and phenolphthalein. This mixture is important because each component loses or gains protons depending upon the acidity or alkalinity of the solution being tested. It is beneficial to use this type of universal ...
The observed spectrum (green) is the sum of the spectra of HA (gold) and of A − (blue), weighted for the concentration of the two species. When a single indicator is used, this method is limited to measurements in the pH range p K a ± 1, but this range can be extended by using mixtures of two or more indicators.
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The increase in pH then causes color change in the bromothymol blue indicator, turning it blue. Under neutral conditions the medium remains a green color. The color change to blue is useful because growth on Simmons' citrate agar is often limited and would be hard to observe if it were not for the color change.
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Bromothymol blue is the indicator used in the agar, it changes to yellow in case of acid production during fermentation of lactose or changes to deep blue in case of alkalinization. Lactose-positive bacteria build yellow colonies. Bacteria which decarboxylate L-cystine cause an alkaline reaction and build deep blue colonies. [1]
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