Skip to Content
MilliporeSigma
All Photos(1)

Documents

232467

Sigma-Aldrich

1,11-Dibromoundecane

≥98%

Synonym(s):

Undecamethylene dibromide

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
Br(CH2)11Br
CAS Number:
16696-65-4
Molecular Weight:
314.10
Beilstein/REAXYS Number:
1740980
EC Number:
240-745-0
MDL number:
MFCD00000224
UNSPSC Code:
12352100
PubChem Substance ID:
24853902
NACRES:
NA.22

assay

≥98%

form

liquid

refractive index

n20/D 1.491 (lit.)

bp

190-192 °C/18 mmHg (lit.)

mp

−10.6 °C (lit.)

density

1.335 g/mL at 25 °C (lit.)

SMILES string

BrCCCCCCCCCCCBr

InChI

1S/C11H22Br2/c12-10-8-6-4-2-1-3-5-7-9-11-13/h1-11H2

InChI key

SIBVHGAPHVRHMJ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

1,11-Dibromoundecane was used in preparation of:
  • thermotropic main-chain polyether and has been studied by variable-temperature solid-state 13C NMR spectroscopy
  • discotic side group liquid crystal polymer based on poly(methyl methacrylate)
  • self-assembled monolayer (SAM) substrate, 11-(mercaptoundecyl)triethylene glycol
  • SAM of a ferrocene (Fc)-porphyrin (P)-C60 triad on a gold electrode

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Convenient synthesis of a discotic side group liquid crystal polymer.
Mchattie GS and Imrie CT.
Journal of Materials Chemistry, 8(1), 47-51 (1998)
The chain conformations of a polyether based on bis (4-hydroxyphenoxy)-p-xylylene and 1, 11-dibromoundecane (HPX-c11) in its mesophase states, derived from 13C NMR.
Cheng J, et al.
Journal of Polymer Science. Part B, Polymer Letters, 32(4), 721-736 (1994)
Synthesis and photoelectrochemical properties of a self-assembled monolayer of a ferrocene-porphyrin-fullerene triad on a gold electrode.
Imahori H, et al.
Chemical Communications (Cambridge, England), 13, 1165-1166 (1999)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service