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About This Item
Empirical Formula (Hill Notation):
C6H5F
CAS Number:
Molecular Weight:
96.10
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
207-321-7
Beilstein/REAXYS Number:
1236623
MDL number:
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
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
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.
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
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
Regulatory Information
危险化学品
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Maria F Carvalho et al.
Applied and environmental microbiology, 72(11), 7413-7417 (2006-09-19)
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
Yuan C, et al.
Dyes and Pigments, 143, 217-222 (2017)
Sittig's Handbook of Toxic and Hazardous Chemicals and Carcinogens, Volume 1 (2017)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 51411-5ML-F | 04061836958954 |


