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| Names | |
|---|---|
| Preferred IUPAC name
3,3-Bis(3-chloro-4-hydroxyphenyl)-2,1λ6-benzoxathiole-1,1(3H)-dione | |
| Other names
3′,3′-Dichlorophenolsulfonaphthalein
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.022.382 |
| EC Number |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C19H12Cl2O5S | |
| Molar mass | 423.26 g·mol−1 |
| Melting point | 261 °C (502 °F; 534 K)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Chlorophenol red (pH indicator) | ||
| below pH 5.4 | above pH 6.8 | |
| 5.4 | ⇌ | 6.8 |
Chlorophenol red is an indicator dye that changes color from yellow to violet in the pH range 5.4 to 6.8.[2] The pH of a substance is determined by taking the negative logarithm of the Hydronium ion concentration and the indictor changes color due to the dissociation of H+ ions.[3] The lambda max is at 572 nm.[4]
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แผนฉุกเฉินและการป้องกันการหกรั่วไหลของสารเคมี คลอโรฟีนอล เรด (Chlorophenol Red )
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Transcription
Properties and uses
The dissociation mechanism of chlorophenol red is similar to that of phenolphthalein meaning it can be used as a color indicator. The dissociation of hydroxyl and hydrogen atoms creates the dissociate scheme of chlorophenol red to change color from yellow to red.[5] The pH properties of chlorophenol red are used to selectively determine the amount of chlorine dioxide in drinking water. Chlorophenol red selectively reacts with 0.1–1.9 mg/L chlorine dioxide at pH 7.[6] The electrochemical properties of Chlorophenol red allows it to be a chromogenic label and can undergo oxidation creating several phenolic intermediates. The bacterial hydrolysis of a chlorophenol red labelled substrate produces chlorine retaining intermediates on electrodes.[7]
References
- ^ Haynes, p. 3.116
- ^ Haynes, p. 8.88
- ^ "pH Indicators". Chemistry LibreTexts. 2013-10-02. Retrieved 2021-03-14.
- ^ "Chlorophenol Red".
- ^ Hanai, Toshihiko (2016). "Quantitative Evaluation of Dissociation Mechanisms in Phenolphthalein and the Related Compounds". Journal of Computer Chemistry. 15: 13–21. doi:10.2477/jccj.2015-0055.
- ^ Sweetin, Deborah L.; Sullivan, Elizabeth; Gordon, Gilbert (1996-01-01). "The use of chlorophenol red for the selective determination of chlorine dioxide in drinking water". Talanta. 43 (1): 103–108. doi:10.1016/0039-9140(95)01721-6. PMID 18966469.
- ^ Casimero, Charnete; Bigham, Teri; McGlynn, Ruairi J.; Dooley, James S. G.; Ternan, Nigel G.; Snelling, William J.; Critchley, Megan E.; Zinkel, Cameron L.; Smith, Robert B.; Sabogal-Paz, Lyda P.; Davis, James (2019-12-01). "Electroanalytical properties of chlorophenol red at disposable carbon electrodes: Implications for Escherichia coli detection" (PDF). Bioelectrochemistry. 130: 107321. doi:10.1016/j.bioelechem.2019.06.006. PMID 31306878. S2CID 196813601.
Cited sources
- Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. ISBN 9781498754293.
This page was last edited on 10 April 2024, at 18:46