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Bromothymol blue (also known as bromothymol sulfone phthalein and BTB) is a . It is mostly used in applications that require measuring substances that would have a relatively neutral pH (near 7). A common use is for measuring the presence of in a liquid. It is typically sold in solid form as the salt of the acid indicator.


Structure and properties

The protonated form of bromothymol blue has its peak absorption at 427 nm thus transmitting yellow light in acidic solutions, while the deprotonated form has its peak absorption at 602 nm thus transmitting blue light in more basic solutions. In contrast, highly acidic bromothymol blue is magenta in color.

The general carbon skeleton of bromothymol blue is common to many indicators including , , and bromocresol green.

The presence of one moderate electron-withdrawing group ( atom) and two moderate donating groups (alkyl substituents) are responsible for bromothymol blue's active indication range from a pH of 6.0 to 7.6. While the conjugation is responsible for the length and nature of the color change range, these substituent groups are ultimately responsible for the indicator's active range.

Bromothymol blue is sparingly soluble in oil, but soluble in water, , and aqueous solutions of alkalis. It is less soluble in nonpolar solvents such as , , and , and practically insoluble in .

(2025). 9780911910001, Merck Research Laboratory.


Synthesis and preparation
Bromothymol blue is synthesized by addition of elemental bromine to in a solution in glacial acetic acid.

To prepare a solution for use as pH indicator, dissolve 0.10 g in 8.0 cm3 N/50 (a.k.a. 0.02 Normal) NaOH and dilute with water to 250 cm3. To prepare a solution for use as indicator in volumetric work, dissolve 0.1 g in 100 cm3 of 50% (v/v) .


Uses
Bromothymol blue may be used for observing activities, or as a respiratory indicator (turns yellow as is added).
(2025). 9780849382185, .
(2025). 9780470407530, Wiley.
A common demonstration of BTB's pH indicator properties involves exhaling through a tube into a neutral solution of BTB. As CO2 is absorbed from the breath into the solution, carbonic acid forms and change the solution color from green to yellow. Thus, BTB is commonly used in science classes to demonstrate that the more that muscles are used, the greater the CO2 output.

Bromothymol blue has been used in conjunction with to monitor the fungal enzyme activity with phenol red turning pink and bromothymol blue turning blue signalling an increase in pH and therefore enzyme activity. However, a recent study suggests that is more useful in determining activity due to the bright yellow ring formed in the zone of enzyme activity.

It may also be used in the laboratory as a biological slide . At this point, the bromothymol is already blue, and a few drops of BTB are used on a water slide. The specimen is mixed with blue BTB solution and fixed to a slide by a . It is sometimes used to determine or nuclei under the microscope.

Bromothymol is used in for detecting premature rupture of membranes. typically has a pH > 7.2, bromothymol will therefore turn blue when brought in contact with fluid leaking from the amnion. As vaginal pH normally is acidic, the blue color indicates the presence of amniotic fluid. The test may be false-positive in the presence of other alkaline substances such as or , or in the presence of bacterial vaginosis.


See also


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