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About This Item
Linear Formula:
F3C6H2OH
CAS Number:
Molecular Weight:
148.08
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
form
solid
mp
49-51 °C (lit.)
SMILES string
Oc1c(F)cc(F)cc1F
InChI
1S/C6H3F3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H
InChI key
QQFWMPUXPLBWTG-UHFFFAOYSA-N
General description
2,4,6-Trifluorophenol is a halogen-substituted phenol. Peroxidase oxidation of 2,4,6-trifluorophenol has been reported. Association of phenol and 2,4,6-trifluorophenol has been investigated by 1H- and 19F-NMR spectroscopy.
Application
2,4,6-Trifluorophenol may be used in an indirect enzyme-linked immunosorbent assay (ELISA) for the biological monitoring of 2,4,6-trichlorophenol.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Revisiting the peroxidase oxidation of 2,4,6-trihalophenols: ESR detection of radical intermediates.
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Chemical research in toxicology, 24(11), 1862-1868 (2011-09-29)
The peroxidase oxidation of 2,4,6-trichlorophenol (TCP) has been clearly shown to result in 2,6-dichloro-1,4-benzoquinone (DCQ). DCQ is a 2-electron oxidation product of TCP that has undergone para dechlorination. Many peroxidases show similar oxidation of the substrate, TCP, to yield the
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Environmental science & technology, 43(14), 5377-5382 (2009-08-28)
1H- and 19F-NMR measurements of spin-lattice (T1) and spin-spin (T2) relaxationtimes and diffusion ordered spectroscopy (DOSY) were applied to investigate the association of nonsubstituted (phenol (P)) and halogen-substituted (2,4-dichlorophenol (DCP); 2,4,6-trichlorophenol (TCP), and 2,4,6-trifluorophenol (TFP) phenols with a dissolved humic
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