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446882

Sigma-Aldrich

Perfluorohexyl bromide

98%

Synonym(s):

1-Bromotridecafluorohexane

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10 G
$82.00

About This Item

Linear Formula:
CF3(CF2)5Br
CAS Number:
Molecular Weight:
398.95
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

$82.00

List Price$164.00Save 50%

In StockDetails


Request a Bulk Order

Quality Level

assay

98%

form

liquid

refractive index

n20/D 1.3 (lit.)

bp

97 °C (lit.)

density

1.871 g/mL at 25 °C (lit.)

functional group

bromo
fluoro

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)Br

InChI

1S/C6BrF13/c7-5(16,17)3(12,13)1(8,9)2(10,11)4(14,15)6(18,19)20

InChI key

JTYRBFORUCBNHJ-UHFFFAOYSA-N

Application

Employed in the preparation of perfluorononanal by hydroformylation.[1][2]

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Journal of Fluorine Chemistry, 61, 217-217 (1993)
Journal of Fluorine Chemistry, 67, 189-189 (1994)
R F Mattrey et al.
AJR. American journal of roentgenology, 148(6), 1259-1263 (1987-06-01)
The ability to distinguish bowel from other intraabdominal structures is essential for the accurate diagnosis of intraabdominal disease with MR. Because perfluorochemicals have no protons, they cause no MR signal. Since they are immiscible with water, they create a signal
S L Wootton et al.
AJR. American journal of roentgenology, 161(2), 409-416 (1993-08-01)
The disadvantages of water-soluble gastrointestinal contrast agents include high osmolality, contrast dilution, and severe toxicity if aspirated. Perfluorocarbons are nontoxic in the lung and peritoneal cavity. Because perfluorocarbons are immiscible with water, they have no osmotic effect and cannot be
Douglass et al.
The Journal of organic chemistry, 65(5), 1434-1441 (2000-05-18)
A triphenylsilyl group is used as an auxiliary in the synthesis of heterodisubstituted p-carboranes via triphenylsilyl-p-carborane (1). The preparation of 1 is statistical, but with recovery of the starting p-carborane, the effective conversion to 1 is about 90%. Carborane 1

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