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553638

Sigma-Aldrich

4-Fluorobiphenyl

95%

Synonym(s):

(4-Fluorophenyl)benzene, 1-Fluoro-4-phenylbenzene, 4-Fluorbiphenyl, 4-Fluoro-1,1′-biphenyl, 4′-Fluoro-1,1′-biphenyl, 4′-Fluorobiphenyl, p-Fluorobiphenyl, p-Fluorodiphenyl

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About This Item

Linear Formula:
C6H5C6H4F
CAS Number:
324-74-3
Molecular Weight:
172.20
EC Number:
206-304-1
MDL number:
MFCD00011650
UNSPSC Code:
12352100
PubChem Substance ID:
24879341
NACRES:
NA.22

Assay

95%

form

solid

refractive index

n20/D 1.5200 (lit.)

bp

283-284 °C (lit.)

mp

75-79 °C (lit.)

density

1.288 g/mL (lit.)

functional group

fluoro
phenyl

SMILES string

Fc1ccc(cc1)-c2ccccc2

InChI

1S/C12H9F/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H

InChI key

RUYZJEIKQYLEGZ-UHFFFAOYSA-N

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General description

4-Fluorobiphenyl is a fluorinated biphenyl compound. It undergoes biochemical degradation in the presence of various mycorrhizal fungi to afford 4-fluorobiphen-4′-ol and 4-fluorobiphen-3′-ol as major products.

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW3218
MKCV6227
MKCV1269
MKCT3836
MKCS2105

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Cormac D Murphy
Omics : a journal of integrative biology, 11(3), 314-324 (2007-09-22)
Fluorinated organic compounds, although rare in nature, are significant environmental contaminants owing to the numerous applications for which this class of compounds is employed. It is important that biodegradation of these compounds can be readily assessed in order to provide
N A Green et al.
Applied and environmental microbiology, 65(9), 4021-4027 (1999-09-03)
The pathways of biotransformation of 4-fluorobiphenyl (4FBP) by the ectomycorrhizal fungus Tylospora fibrilosa and several other mycorrhizal fungi were investigated by using (19)F nuclear magnetic resonance (NMR) spectroscopy in combination with (14)C radioisotope-detected high-performance liquid chromatography ((14)C-HPLC). Under the conditions
N A Green et al.
Chemosphere, 38(5), 1085-1101 (1999-02-24)
The incubation of the model pollutant [U-14C]'-4-fluorobiphenyl (4FBP) in soil, in the presence and absence of biphenyl (a co-substrate), was carried out in order to study the qualitative disposition and fate of the compound using 14C-HPLC and 19F NMR spectroscopy.
Jessica Amadio et al.
Applied microbiology and biotechnology, 86(1), 345-351 (2009-12-04)
The fungus Cunninghamella elegans is a useful model of human catabolism of xenobiotics. In this paper, the biotransformation of fluorinated biphenyls by C. elegans was investigated by analysis of the culture supernatants with a variety of analytical techniques. 4-Fluorobiphenyl was
J G Bundy et al.
Xenobiotica; the fate of foreign compounds in biological systems, 32(6), 479-490 (2002-08-06)
1. Little is known about metabolism of xenobiotics by earthworms, despite their importance in soil ecotoxicity testing. Normal earthworms and earthworms treated with antibiotics to ensure inhibition of gut microflora were exposed to two model xenobiotic compounds, 4-fluoroaniline and 4-fluorobiphenyl
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