Phenol red
From Wikipedia, the free encyclopedia
| Phenol red | |
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| Identifiers | |
| CAS number | [143-74-8] |
| SMILES | Oc1ccc(cc1)C(=C2C=CC(=[OH+])C=C2)c3ccccc3S(=O)([O-])=O |
| Properties | |
| Molecular formula | C19H14O5S |
| Molar mass | 354.377 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Phenol red (also known as phenolsulfonphthalein or PSP) is a pH indicator that is frequently used in cell biology laboratories.
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[edit] Chemical structure and properties
Phenol red exists as a red crystal that is stable in air. Its solubility is 0.77 grams per liter (g/L) in water and 2.9 g/L in ethanol.[1] It is a weak acid with pKa = 8.00 at 20°C.
A solution of phenol red is used as a pH indicator: its color exhibits a gradual transition from yellow to red over the pH range 6.6 to 8.0. Above pH 8.1, phenol red turns a bright pink (fuchsia) color.
| Phenol red (pH indicator) | ||
| below pH 6.6 | above pH 8.0 | |
| 6.6 | ↔ | 8.0 |
This observed color change is because phenol red loses protons (and changes color) as the pH increases. In crystalline form, and in solution under very acidic conditions (low pH), the compound exists as a zwitterion as in the structure shown above, with the sulfate group negatively charged, and the ketone group carrying an additional proton. This form is sometimes symbolically written as H2+PS− and is orange-red. If the pH is increased (pKa = 1.2), the proton from the ketone group is lost, resulting in the yellow negatively charged ion HPS−. At still higher pH (pKa = 7.7), the phenol's hydroxide group loses its proton, resulting in the red ion PS2−.[2]
In several sources, the structure of phenol red is shown with the sulfur atom being part of a cyclic group, similar to the structure of phenolphthalein.[1][3] However, this cyclic structure could not be confirmed by X-ray crystallography.[4]
Several indicators share a similar structure to phenol red, including bromothymol blue, thymol blue, bromocresol purple, thymolphthalein, and phenolphthalein. (A table of other common chemical indicators is available in the article on pH indicators.)
[edit] Phenolsulfonphthalein test
Phenol red was used in the phenolsulfonphthalein test, also known as the PSP test. This test was used to estimate the overall blood flow through the kidney and is now obsolete.
The test is based on the fact that phenol red is excreted almost entirely in the urine. By measuring the amount of phenol red excreted colorimetrically, kidney function can be determined.[5] Phenol red solution is administered intravenously, all of the urine produced is collected and the phenol red present determined.[6]
[edit] Indicator for cell cultures
Most living tissues prosper at a near-neutral pH; that is, a pH close to 7. The pH of blood ranges from 7.35 to 7.45, for instance. When cells are grown in tissue culture, the medium in which they grow is held close to this physiological pH. A small amount of phenol red added to this growth medium will have a pink-red color under normal conditions. Typically 15 mg / 1 L is used for cell culture.
In the event of problems, waste products produced by dying cells or overgrowth of contaminants will cause a change in pH, leading to a change in indicator color. For example, a culture of relatively slowly-dividing mammalian cells can be quickly overgrown by bacterial contamination. This usually results in an acidification of the medium, turning it yellow. Many biologists find this a convenient way to rapidly check on the health of tissue cultures. In addition, the waste products produced by the mammalian cells themselves will slowly decrease the pH, gradually turning the solution orange and then yellow. This color change is an indication that even in the absence of contamination, the medium needs to be replaced (generally, this should be done before the medium has turned completely orange).
Since the color of phenol red can interfere with some spectrophotometric and fluorescent assays, many types of tissue culture media are also available without phenol red.
[edit] Estrogen mimic
Phenol red is a weak estrogen mimic, and in cell cultures can enhance the growth of cells that express the estrogen receptor.[7]
An important breakthrough in biotechnology was reported in the scientific literature on May 5th, 2005. Using phenol red as a differentiation factor, scientists at the University of Tennessee produced human oocytes (eggs) from cells scraped from the surface of adult ovaries. These cells on the outer ovarian surface are known as ovarian surface epithelial cells. Such cells had been taken from five women aged 39 to 52 and were cultured in the presence of phenol red, inducing oogenesis.[8]
Previously, human eggs had only been produced in vitro from totipotent, blastomeric embryonic stem cells. One of the significant aspects of this experiment is that it demonstrated viable human egg cells can easily be produced from an adult cell that already has some degree of specialization. Furthermore, it lessens the implications associated with the fact that women are born with all of the egg cells they will ever have throughout their lives. While this breakthrough was not without controversy, it provides hope for infertile women wishing to undergo in vitro fertilization, and hints at the possibility of new options for post-menopausal women as well. It also suggests that the future of stem cell research may not have to rely as heavily on human embryos as a source of unspecialized, totipotent cells for research.
[edit] Use in swimming pool test kits
Phenol red, sometimes labelled with a different name, such as "Guardex Solution #2", is used as a pH indicator in home swimming pool test kits.[9]
[edit] References
- ^ a b Merck Index, 11th ed., 7213 Phenolsulfonphtalein
- ^ Tamura Z, Maeda M. Differences between phthaleins and sulfonphthaleins. Yakugaku Zasshi. 1997 Nov;117(10-11):764-70. (Japanese) PMID 9414589
- ^ Phenolsulfonphthalein, from the PubChem Compound database
- ^ Yamaguchi K., Tamura Z., Maeda M. Molecular structure of the zwitterionic form of phenolsulfonphthalein. Analytical Sciences 1997, vol. 13, no3, pp. 521-522
- ^ Encyclopedia Britannica, Phenolsulfonphthalein Test, accessed 1 October 2006.
- ^ MedlinePlus, Phenolsulfonphthalein (Diagnostic), accessed 1 October 2006.
- ^ Berthois Y. et al. (1986) Phenol red in tissue culture media is a weak estrogen: implications concerning the study of estrogen-responsive cells in culture. Proc. Nat. Acad. Sci. 83(8):2496-500.
- ^ Bukovsky, A., Oogenesis in Cultures Derived from Adult Human Ovaries, Reproductive Biology and Endocrinology, 2005, 3:17. doi:10.1186/1477-7827-3-17
- ^ Guardex Solution 2 - Phenol Red Material Safety Data Sheet
