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553638

Sigma-Aldrich

4-Fluorbiphenyl

95%

Synonym(e):

(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

Lineare Formel:
C6H5C6H4F
CAS-Nummer:
324-74-3
Molekulargewicht:
172.20
EG-Nummer:
206-304-1
MDL-Nummer:
MFCD00011650
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24879341
NACRES:
NA.22

Qualitätsniveau

100

Assay

95%

Form

solid

Brechungsindex

n20/D 1.5200 (lit.)

bp

283-284 °C (lit.)

mp (Schmelzpunkt)

75-79 °C (lit.)

Dichte

1.288 g/mL (lit.)

Funktionelle Gruppe

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

InChIKey

RUYZJEIKQYLEGZ-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCW3218
MKCV6227
MKCV1269
MKCT3836
MKCS2105

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Sigma-Aldrich

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Sigma-Aldrich

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Biphenyl

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.
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
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
Drazenka Selesi et al.
FEMS microbiology ecology, 68(1), 86-93 (2009-02-04)
The aromatic hydrocarbon biphenyl is a widely distributed environmental pollutant. Whereas the aerobic degradation of biphenyl has been extensively studied, knowledge of the anaerobic biphenyl-oxidizing bacteria and their biochemical degradation pathway is scarce. Here, we report on an enrichment culture
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