Bromothymol blue
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| Names | |
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| Preferred IUPAC name
3,3-Bis[3-bromo-4-hydroxy-2-methyl-5-(propan-2-yl)phenyl]-2,1λ6-benzoxathiole-1,1(3H)-dione | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.884 |
| EC Number |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C27H28Br2O5S | |
| Molar mass | 624.38 g·mol−1 |
| Density | 1.25 g/cm3 |
| Melting point | 202 °C (396 °F; 475 K) |
| Sparingly soluble in water[1] | |
| Acidity (pKa) | 7.0 |
| Hazards | |
| GHS labelling: | |
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| Warning | |
| H302, H315, H319 | |
| P264, P270, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P501 | |
| NFPA 704 (fire diamond) | |
| Safety data sheet (SDS) | http://www.sciencelab.com/msds.php?msdsId=9927468 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Bromothymol blue (also known as bromothymol sulfone phthalein and BTB) is a pH indicator. 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 carbonic acid in a liquid. It is typically sold in solid form as the sodium salt of the acid indicator.
Structure and properties
| Bromothymol blue (pH indicator) | ||
| below pH 6.0 | above pH 7.6 | |
| 6.0 | ⇌ | 7.6 |
Bromothymol blue acts as a weak acid in a solution. It can thus be in protonated or deprotonated form, appearing yellow or blue, respectively. It is bright aquamarine by itself, and greenish-blue in a neutral solution. The deprotonation of the neutral form results in a highly conjugated structure, accounting for the difference in color. An intermediate of the deprotonation mechanism is responsible for the greenish color in neutral solution.[2]
The protonated form of bromothymol blue has its peak absorption at 427 nm thus transmitting yellow light in acidic solutions, and the deprotonated form has its peak absorption at 602 nm thus transmitting blue light in more basic solutions.[3] Highly acidic Bromothymol blue is magenta in color.
The general carbon skeleton of bromothymol blue is common to many indicators including chlorophenol red, thymol blue, and bromocresol green.[2]
The presence of one moderate electron-withdrawing group (bromine 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.[2]
Bromothymol blue is sparingly soluble in oil, but soluble in water, ether, and aqueous solutions of alkalis. It is less soluble in nonpolar solvents such as benzene, toluene, and xylene, and practically insoluble in petroleum ether.[4]
Synthesis and preparation
Bromothymol blue is synthesized by addition of elemental bromine to thymol blue in a solution in glacial acetic acid.[5]
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) ethanol.[4]
Uses
Bromothymol blue may be used for observing photosynthetic activities, or as a respiratory indicator (turns yellow as CO2 is added).[6][7] 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, forming carbonic acid, the solution changes 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 phenol red to monitor the fungal asparaginase enzyme activity with phenol red turning pink and bromothymol blue turning blue indicating an increase in pH and therefore enzyme activity.[8] However, a recent study suggests that methyl red is more useful in determining activity due to the bright yellow ring form in the zone of enzyme activity.[9]
It may also be used in the laboratory as a biological slide stain. 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 cover slip. It is sometimes used to define cell walls or nuclei under the microscope.
Bromothymol is used in obstetrics for detecting premature rupture of membranes.[10] Amniotic fluid 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 blood or semen, or in the presence of bacterial vaginosis.
See also
References
- ^ "Archived copy". Archived from the original on 2015-11-26. Retrieved 2015-12-11.
{{cite web}}: CS1 maint: archived copy as title (link) - ^ a b c De Meyer, Thierry (March 2014). "Substituent effects on absorption spectra of pH indicators: An experimental and computational study of sulfonphthaleine dyes". Dyes and Pigments. 102: 241–250. doi:10.1016/j.dyepig.2013.10.048. hdl:1854/LU-4353650. Archived from the original on 2020-07-29. Retrieved 2020-03-16.
- ^ Nahhal; et al. (18 July 2012). "Thin film optical BTB pH sensors using sol–gel method in presence of surfactants" (PDF). International Nano Letters. 2 (16): 3. Bibcode:2012INL.....2...16E. doi:10.1186/2228-5326-2-16. Archived (PDF) from the original on 2014-11-29. Retrieved 18 November 2014.
- ^ a b O'Neil, Maryadele J (2006). The Merck Index. Merck Research Laboratory. p. 1445. ISBN 978-0-911910-00-1.
- ^ "Bromothymol blue" (PDF). Archived (PDF) from the original on 27 November 2020. Retrieved 4 April 2020.
- ^ Sabnis R. W. (2007). Handbook of Acid-Base Indicators. CRC Press. ISBN 978-0-8493-8218-5.
- ^ Sabnis R. W. (2010). Handbook of Biological Dyes and Stains: Synthesis and Industrial Applications (1st ed.). Wiley. ISBN 978-0-470-40753-0.
- ^ "Isolation and screening of L-asparaginase free of glutaminase and urease from fungal sp". researchgate.net. 22 August 2016.
{{cite web}}: CS1 maint: url-status (link) - ^ Dhale, Mohan (July 2014). "A comparative rapid and sensitive method to screen l-asparaginase producing fungi". Journal of Microbiological Methods. 102: 66–68. doi:10.1016/j.mimet.2014.04.010. PMID 24794733.
- ^ King, Arthur G. (1935-12-01). "The determination of rupture of the membranes". American Journal of Obstetrics & Gynecology. 30 (6): 860–862. doi:10.1016/S0002-9378(35)90429-X. ISSN 0002-9378.