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Merck
CN

446882

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
NACRES:
NA.22
PubChem Substance ID:
24868303
UNSPSC Code:
12352100
EC Number:
206-391-6
MDL number:
MFCD00042349
Assay:
98%
Form:
liquid

Key Documents

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Product Name

Perfluorohexyl bromide, 98%

InChI key

JTYRBFORUCBNHJ-UHFFFAOYSA-N

InChI

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

SMILES string

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

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

Quality Level

100

Related Categories

Application

Employed in the preparation of perfluorononanal by hydroformylation.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV4976
MKCB9978
MKCB0283V
MKBR8755V
MKBR2281V

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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
Intra-abdominal sepsis and perfluorocarbons: mechanism of protection.
D B Hoyt et al.
Current surgery, 39(3), 165-167 (1982-05-01)
Journal of Fluorine Chemistry, 61, 217-217 (1993)
Journal of Fluorine Chemistry, 67, 189-189 (1994)
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