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553638

Sigma-Aldrich

4-Fluorobiphenyl

95%

Synonyme(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

Formule linéaire :
C6H5C6H4F
Numéro CAS:
324-74-3
Poids moléculaire :
172.20
Numéro CE :
206-304-1
Numéro MDL:
MFCD00011650
Code UNSPSC :
12352100
ID de substance PubChem :
24879341
Nomenclature NACRES :
NA.22

Pureté

95%

Forme

solid

Indice de réfraction

n20/D 1.5200 (lit.)

Point d'ébullition

283-284 °C (lit.)

Pf

75-79 °C (lit.)

Densité

1.288 g/mL (lit.)

Chaîne SMILES 

Fc1ccc(cc1)-c2ccccc2

InChI

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

Clé InChI

RUYZJEIKQYLEGZ-UHFFFAOYSA-N

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Description générale

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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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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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