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Merck

446882

Sigma-Aldrich

Perfluorhexylbromid

98%

Synonym(e):

1-Bromtridecafluorhexan

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About This Item

Lineare Formel:
CF3(CF2)5Br
CAS-Nummer:
Molekulargewicht:
398.95
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.3 (lit.)

bp

97 °C (lit.)

Dichte

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

InChIKey

JTYRBFORUCBNHJ-UHFFFAOYSA-N

Anwendung

Employed in the preparation of perfluorononanal by hydroformylation.

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Intra-abdominal sepsis and perfluorocarbons: mechanism of protection.
D B Hoyt et al.
Current surgery, 39(3), 165-167 (1982-05-01)
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
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
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.

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