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345806

Sigma-Aldrich

2,4,6-Trifluorophenol

99%

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About This Item

Linear Formula:
F3C6H2OH
CAS Number:
2268-17-9
Molecular Weight:
148.08
MDL number:
MFCD00061216
UNSPSC Code:
12352100
PubChem Substance ID:
24861350
NACRES:
NA.22

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.[1] Association of phenol and 2,4,6-trifluorophenol has been investigated by 1H- and 19F-NMR spectroscopy.[2]

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.[3]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBZ9555
BCBR0543V
BCBP4995V
BCBM0802V
BCBG4107V

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Bradley E Sturgeon et al.
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
Daniela Smejkalová et al.
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
Roger Galve et al.
Analytical chemistry, 74(2), 468-478 (2002-01-29)
Trichlorophenols (TCP) eliminated by the urine can be considered as potential biomarkers of exposure of many chemicals (chlorophenols, chlorophenoxy acid herbicides, prochloraz, lindane, hexachlorobenzene, etc). High-throughput screening methods are necessary to carry out efficient monitoring programs that may help to
Erin M Kollitz et al.
Toxicological sciences : an official journal of the Society of Toxicology, 163(1), 226-239 (2018-02-07)
Brominated phenolic compounds (BPCs) are found in the environment, and in human and wildlife tissues, and some are considered to have endocrine disrupting activities. The goal of this study was to determine how structural differences of 3 BPC classes impact
Marie A Colucci et al.
Journal of medicinal chemistry, 50(23), 5780-5789 (2007-10-20)
NAD(P)H:quinone oxidoreductase 1 is a proposed target in pancreatic cancer. We describe the synthesis of a series of indolequinones, based on the 5- and 6-methoxy-1,2-dimethylindole-4,7-dione chromophores with a range of phenolic leaving groups at the (indol-3-yl)methyl position. The ability of

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