2,4,6-triiodophenol
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | 2,4,6-triiodophenol | |||||||||||||||
other names |
TIP |
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Molecular formula | C 6 H 2 OHI 3 | |||||||||||||||
Brief description |
yellowish solid |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 471.80 g mol −1 | |||||||||||||||
Physical state |
firmly |
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Melting point |
157-159 ° C |
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solubility |
practically insoluble in water |
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safety instructions | ||||||||||||||||
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Toxicological data | ||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
2,4,6-Triiodophenol is an aromatic compound that is derived from both phenol and iodobenzene . The structure consists of a benzene ring with an attached hydroxyl group (-OH) and three iodine atoms (-I) as substituents .
Extraction and presentation
2,4,6-Triiodophenol can be obtained by reacting an alcoholic solution of iodine and phenol with hydrogen peroxide .
properties
2,4,6-triiodophenol is a yellowish solid that is practically insoluble in water.
use
2,4,6-Triiodophenol is used as an iodinated disinfectant in the treatment of wastewater. It is also used for biochemical studies.
Individual evidence
- ^ A b Google Patents: US4677124A - Process for preparing and therapeutical applications of the "2,4,6-triiodophenol" , accessed March 7, 2018
- ↑ a b c d e data sheet 2,4,6-triiodophenol, 97% from Sigma-Aldrich , accessed on March 7, 2018 ( PDF ).
- ↑ a b c data sheet 2,4,6-triiodophenol, 98% from AlfaAesar, accessed on March 7, 2018 ( PDF )(JavaScript required) .
- ↑ Jurd, L .: The Iodination of Aromatic Compounds. III. Halogenation of Aromatic Ethers in the Presence of Hydrogen Peroxide , Australian Journal of Scientific Research , Series A: Physical Sciences, vol. 2, p. 595, accessed March 7, 2018.
- ↑ Rafael DC Gallo, Karimi S. Gebara, Rozanna M. Muzzi, Cristiano Raminelli: Efficient and selective iodination of phenols promoted by iodine and hydrogen peroxide in water. In: Journal of the Brazilian Chemical Society . 21, 2010, p. 770, doi : 10.1590 / S0103-50532010000400026 .
- ↑ FAO: Characterization of plasma triiodophenol binding proteins in vertebrates and tissue distribution of triiodophenol in Rana catesbeiana tadpoles , accessed on March 7, 2018.