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446882

Sigma-Aldrich

Perfluorohexyl bromide

98%

Synonym(s):

1-Bromotridecafluorohexane

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About This Item

Linear Formula:
CF3(CF2)5Br
CAS Number:
335-56-8
Molecular Weight:
398.95
EC Number:
206-391-6
MDL number:
MFCD00042349
UNSPSC Code:
12352100
PubChem Substance ID:
24868303
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.3 (lit.)

bp

97 °C (lit.)

density

1.871 g/mL at 25 °C (lit.)

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

Related Categories

Application

Employed in the preparation of perfluorononanal by hydroformylation.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Journal of Fluorine Chemistry, 61, 217-217 (1993)
Zhang Feng et al.
Angewandte Chemie (International ed. in English), 54(4), 1270-1274 (2014-12-04)
An efficient palladium-catalyzed Heck-type reaction of fluoroalkyl halides, including perfluoroalkyl bromides, trifluoromethyl iodides, and difluoroalkyl bromides, has been developed. The reaction proceeds under mild reaction conditions with high efficiency and broad substrate scope, and provides a general and straightforward access
M Scrime et al.
Journal of pharmaceutical sciences, 70(11), 1199-1201 (1981-11-01)
Beagle dogs received single perfluorohexyl bromide doses, either 30.2 g/kg po or 3.8 g/kg intratracheally. The apparent first-order plasma half-life during the terminal elimination phase was approximately 8 hr after oral treatment and greater than 8 hr after intratracheal administration.
D R Enzmann et al.
Investigative radiology, 16(1), 46-49 (1981-01-01)
The neat liquid and an emulsion of two perfluorocarbon compounds were injected into the knee joints of dogs and a human cadaver to investigate their applicability for arthrography. Excellent delineation of joint structures was observed for as long as 24
Journal of Fluorine Chemistry, 67, 189-189 (1994)
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