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Merck

345806

Sigma-Aldrich

2,4,6-Trifluorophenol

99%

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About This Item

Wzór liniowy:
F3C6H2OH
Numer CAS:
Masa cząsteczkowa:
148.08
Numer MDL:
Kod UNSPSC:
12352100
Identyfikator substancji w PubChem:
NACRES:
NA.22

Próba

99%

Postać

solid

mp

49-51 °C (lit.)

ciąg SMILES

Oc1c(F)cc(F)cc1F

InChI

1S/C6H3F3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H

Klucz InChI

QQFWMPUXPLBWTG-UHFFFAOYSA-N

Opis ogólny

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.

Zastosowanie

2,4,6-Trifluorophenol may be used in an indirect enzyme-linked immunosorbent assay (ELISA) for the biological monitoring of 2,4,6-trichlorophenol.
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Piktogramy

Exclamation mark

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Organy docelowe

Respiratory system

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

dust mask type N95 (US), Eyeshields, Gloves


Certyfikaty analizy (CoA)

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Odwiedź Bibliotekę dokumentów

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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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