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Merck

51411

Supelco

Fluorobenzene

analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C6H5F
Número de CAS:
Peso molecular:
96.10
Beilstein/REAXYS Number:
1236623
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥99.7% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.465 (lit.)
n20/D 1.465

bp

85 °C (lit.)

mp

−42 °C (lit.)

density

1.024 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

Fc1ccccc1

InChI

1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H

InChI key

PYLWMHQQBFSUBP-UHFFFAOYSA-N

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General description

Fluorobenzene is a colorless liquid, which can find applications as a reagent for resin or plastic polymers and also as an insecticide. It also plays the role of a capping agent in the synthesis of a non-fullerene electron acceptor like SF(DPPFB)4 comprising of a spirobifluorene core and four diketopyrrolopyrrole (DPP) arms that can find applications in designing organic solar cells.

Application

Fluorobenzene may be used as an analytical reference standard for the determination of the analyte in cell suspensions of Rhizobiales strain F11, and water samples by liquid chromatography (LC) based techniques. It may also be used as an internal standard for the determination of volatile aromatic compounds in gasoline by comprehensive two-dimensional gas chromatography (GC x GC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

5.0 °F - closed cup

flash_point_c

-15 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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The aerobic metabolism of fluorobenzene by Rhizobiales sp. strain F11 was investigated. Liquid chromatography-mass spectrometry analysis showed that 4-fluorocatechol and catechol were formed as intermediates during fluorobenzene degradation by cell suspensions. Both these compounds, unlike 3-fluorocatechol, supported growth and oxygen
A non-fullerene electron acceptor with a spirobifluorene core and four diketopyrrolopyrrole arms end capped by 4-fluorobenzene
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