≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht
2,4,6-Trifluorophenol is a trihalogenated phenol, which is a substrate for the enzyme, dehaloperoxidase (DHP). It is known that DHP is a dual-function protein that displays elements of both hemoglobins and peroxidases. Studies indicate that DHP has a role in oxygen transport, oxidizing halogenated phenols in the presence of hydrogen peroxide. These studies reveal that 2,4,6-Trifluorophenol alters the stereochemistry of the enzyme binding site. Furthermore, 2,4,6-Trifluorophenol can be used to determine the mechanism of DHP and the role of all the intermediates formed during turnover. Another application of this product is that 2,4,6-Trifluorophenol may be used in an indirect enzyme-linked immunosorbent assay (ELISA) for the biological monitoring of 2,4,6-trichlorophenol. Additionally, association of phenol and 2,4,6-trifluorophenol has been investigated by 1H- and 19F-NMR spectroscopy. A trihalogenated phenol, which is a substrate for the enzyme, dehaloperoxidase (DHP)
This compound belongs to the class of organic compounds known as p-fluorophenols. These are fluorophenols carrying a iodine at the C4 position of the benzene ring.
External Descriptors
Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
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