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33001

Supelco

pentafluorobenzyl bromide (PFB-Br)

analytical standard

Synonym(s):

2,3,4,5,6-Pentafluorobenzyl bromide, α-Bromo-2,3,4,5,6-pentafluorotoluene, (Bromomethyl)pentafluorobenzene

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About This Item

Linear Formula:
C6F5CH2Br
CAS Number:
Molecular Weight:
260.99
Beilstein:
647808
EC Number:
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:

grade

analytical standard
for GC derivatization

description

Alkylation reagent

reaction suitability

reagent type: derivatization reagent
reaction type: Alkylations

reagent type: derivatization reagent
reaction type: Esterifications

packaging

ampule of 5 g

technique(s)

gas chromatography (GC): suitable (ECD)

refractive index

n20/D 1.471 (lit.)

bp

174-175 °C (lit.)

mp

19-20 °C (lit.)

density

1.728 g/mL at 25 °C (lit.)

SMILES string

Fc1c(F)c(F)c(CBr)c(F)c1F

InChI

1S/C7H2BrF5/c8-1-2-3(9)5(11)7(13)6(12)4(2)10/h1H2

InChI key

XDEPVFFKOVDUNO-UHFFFAOYSA-N

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General description

Pentafluorobenzyl bromide (PFB-Br) is a derivatization reagent. Excess reagent may be removed by reaction with an aminophenol. It is an alkylation reagent suitable for electron capture detector (ECD) detection. It is also a lachrymator.

Application

It is used for the analysis of D2/E2-isoprostanes using negative ion chemical ionization-gas chromatography/mass spectrometry (NICI-GC/MS). Fatty acids may be converted to pentafluorobenzyl esters using PFG-Br and diisopropylethylamine during determination of fatty acids using NICI-GC/MS.

Other Notes

Reagent for pentafluorobenzyl ester.

related product

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

181.4 °F - closed cup

Flash Point(C)

83 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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J D Morrow et al.
The Journal of biological chemistry, 269(6), 4317-4326 (1994-02-11)
We recently reported the discovery that a series of novel prostaglandin (PG)F2-like compounds (F2-isoprostanes) are produced in vivo independent of the cyclooxygenase as products of free radical-catalyzed lipid peroxidation. F2-isoprostanes are initially formed in situ from arachidonic acid esterified to
J B Barham et al.
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Previous studies reveal that supplementation of human diets with gamma-linolenic acid (GLA) reduces the generation of lipid mediators of inflammation and attenuates clinical symptoms of chronic inflammatory disorders such as rheumatoid arthritis. However, we have shown that supplementation with this
P O Edlumd et al.
Acta pharmacologica et toxicologica, 40(1), 145-152 (1977-01-01)
A highly sensitive gas-liquid chromatographic method with electron capture detection of clonidine in plasma is described. The alkaline samples (100-200mul) are extracted into cyclohexane-butanol (9:1), re-extracted into 0.1 N sulphuric acid, made alkaline and back-extracted into cyclohexane-butanol. The pentafluorobenzyl derivatives
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