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F13002

Sigma-Aldrich

3-Fluorophenol

98%

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About This Item

Fórmula lineal:
FC6H4OH
Número de CAS:
372-20-3
Peso molecular:
112.10
Beilstein/REAXYS Number:
1904536
EC Number:
206-748-6
MDL number:
MFCD00002254
UNSPSC Code:
12352100
PubChem Substance ID:
24894758
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.514 (lit.)

bp

178 °C (lit.)

mp

8-12 °C (lit.)

density

1.238 g/mL at 25 °C (lit.)

SMILES string

Oc1cccc(F)c1

InChI

1S/C6H5FO/c7-5-2-1-3-6(8)4-5/h1-4,8H

InChI key

SJTBRFHBXDZMPS-UHFFFAOYSA-N

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Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

159.8 °F - closed cup

flash_point_c

71 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Chao-jie Zhang et al.
Huan jing ke xue= Huanjing kexue, 27(9), 1841-1845 (2006-11-30)
An acclimated activated sludge was examined for its ability to degrade 3-fluorophenol in aerobic batch cultures. The result indicated that the organism degrades up to 100 mg/L 3-fluorophenol completely with approximately 100% fluoride anion release within 16 h. 3-Fluorophenol can
Zhang Chaojie et al.
Journal of hazardous materials, 141(1), 295-300 (2006-08-16)
An acclimated activated sludge was examined for its ability to degrade meta-fluorophenol as sole carbon source in aerobic batch cultures. The mechanism study revealed that the initial step in the aerobic biodegradation of meta-fluorophenol was their transformation to fluorocatechol. Following
S Peelen et al.
European journal of biochemistry, 218(2), 345-353 (1993-12-01)
The regioselectivity and rate of the ortho-hydroxylation of 3-fluorophenol by phenol hydroxylase from Trichosporon cutaneum (EC 1.14.13.7) was studied using 19F-NMR. The regioselective hydroxylation as well as the rate of ortho-hydroxylation are pH dependent with a pKa of 6.5. At
Alessandro Granata et al.
Biomacromolecules, 8(10), 3214-3223 (2007-09-22)
The present study describes the pattern of protein modification undergone by human holo-myoglobin by reactive fluoroquinones enzymatically produced by oxidation of 3-fluorophenol in mild conditions (pH 7.4, 25 degrees C). The fluoroquinones react with a number of histidine residues. Surface
Norihiro Tsuji et al.
Physical chemistry chemical physics : PCCP, 8(1), 114-121 (2006-02-17)
Two-color (1 + 1') REMPI mass spectra of o-, m- and p-fluorophenol.ammonia (1 ration) clusters were measured with a long delay time between excitation and ionization lasers. The appearance of NH(4)(NH(3))(n-1)(+) with 100 ns delay after exciting the S(1) state
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