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F13207

Sigma-Aldrich

4-Fluorophenol

99%

Synonym(s):

4-Hydroxyphenyl fluoride, p-Fluorophenol

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About This Item

Linear Formula:
FC6H4OH
CAS Number:
371-41-5
Molecular Weight:
112.10
Beilstein:
1362752
EC Number:
206-736-0
MDL number:
MFCD00002316
UNSPSC Code:
12352100
PubChem Substance ID:
24894759
NACRES:
NA.22

Assay

99%

bp

185 °C (lit.)

mp

43-46 °C (lit.)

SMILES string

Oc1ccc(F)cc1

InChI

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

InChI key

RHMPLDJJXGPMEX-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

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 Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

154.4 °F - closed cup

Flash Point(C)

68 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Maria Isabel M Ferreira et al.
Applied and environmental microbiology, 75(24), 7767-7773 (2009-10-20)
Arthrobacter sp. strain IF1 is able to grow on 4-fluorophenol (4-FP) as a sole source of carbon and energy. To clone the 4-FP degradation genes, DNA libraries were constructed and screened with a probe obtained by PCR using primers designed
Maria Isabel M Ferreira et al.
Applied microbiology and biotechnology, 78(4), 709-717 (2008-01-30)
A Gram-positive bacterial strain capable of aerobic biodegradation of 4-fluorophenol (4-FP) as the sole source of carbon and energy was isolated by selective enrichment from soil samples collected near an industrial site. The organism, designated strain IF1, was identified as
Tobias L Ross et al.
Molecules (Basel, Switzerland), 16(9), 7621-7626 (2011-09-09)
4-[(18)F]Fluorophenol is a versatile synthon for the synthesis of more complex radiopharmaceuticals bearing a 4-[(18)F]fluorophenoxy moiety. In order to prepare 4-[(18)F]fluorophenol in no-carrier-added (n.c.a.) form only a nucleophilic labelling method starting from [(18)F]fluoride is suitable. In this paper a new
Lydie Coulombel et al.
Applied microbiology and biotechnology, 89(6), 1867-1875 (2010-11-09)
Escherichia coli cells, expressing 4-hydroxyphenylacetate 3-hydroxylase, fully transformed 4-halogenated phenols to their equivalent catechols as single products in shaken flasks. 4-Fluorophenol was transformed at a rate 1.6, 1.8, and 3.4-fold higher than the biotransformation of 4-chloro-, 4-bromo-, and 4-iodo-phenol, respectively.
Louise C Nolan et al.
Analytical biochemistry, 344(2), 224-231 (2005-08-03)
A spectrophotometric method for the quantitative determination of an enzyme activity resulting in the accumulation of 4-substituted phenols is described in this article. Toluene-4-monooxygenase (T4MO) activity in whole cells of Pseudomonas mendocina KR1 is used to demonstrate this method. This
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