553638
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:
Molecular Weight:
172.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
206-304-1
MDL number:
Assay:
95%
Form:
solid
Quality Level
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
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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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.
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.