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Merck
CN

467642

11-Bromo-1-undecene

95%

Synonym(s):

1-Bromo-10-undecene, 10-Undecenyl bromide

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About This Item

Linear Formula:
Br(CH2)9CHCH2
CAS Number:
7766-50-9
Molecular Weight:
233.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24870428
MDL number:
MFCD00040825
Beilstein/REAXYS Number:
1753231

Key Documents

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Product Name

11-Bromo-1-undecene, 95%

InChI

1S/C11H21Br/c1-2-3-4-5-6-7-8-9-10-11-12/h2H,1,3-11H2

SMILES string

BrCCCCCCCCCC=C

InChI key

YPLVPFUSXYSHJD-UHFFFAOYSA-N

assay

95%

refractive index

n20/D 1.468 (lit.)

bp

149-150 °C/35 mmHg (lit.)

density

1.063 g/mL at 25 °C (lit.)

functional group

alkyl halide
allyl
bromo

Quality Level

100

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Application

11-Bromo-1-undecene to synthesize brominated polyethylene (PE) via metallocene-catalyzed copolymerization with ethylene. It is also used to prepare poly(olefin)-based anion exchange membranes (AEMs) for practical alkaline fuel cell applications.

General description

11-Bromo-1-undecene is a halogenated hydrocarbon. It can be synthesized by employing alkenyl esters or dibromides as starting materials.

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

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCBV8458
BCBV5538
BCBQ3929V
SHBD9311V
SHBD7875V

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Covalent and Non-covalent Attachment and Patterning of Polypyrrole at Silicon Surfaces.
Pike AR, et al.
Advanced Materials, 15(3), 254-257 (2003)
Marrani AG, et al.
Electrochimica Acta, 53(11), 3903-3909 (2008)
Synthesis of epoxy-terminated dialkyl disulfides for polymerizable self-assembled monolayers.
Yeager LJ, et al.
Tetrahedron Letters, 39(46), 8409-8412 (1998)
Polymer Preprints (American Chemical Society, Division of Polymer Chemistry), 45, 931-932 (2004)
The facile preparation of alkenyl metathesis synthons.
Baughman TW, et al.
Tetrahedron, 60(48), 10943-10948 (2004)

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