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Sigma-Aldrich

1,2-Bis(2-iodoethoxy)ethane

96%

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5 G
$41.30

About This Item

Linear Formula:
ICH2CH2OCH2CH2OCH2CH2I
CAS Number:
36839-55-1
Molecular Weight:
369.97
MDL number:
MFCD00075008
UNSPSC Code:
12352100
PubChem Substance ID:
24860131
NACRES:
NA.22
form:
liquid
assay:
96%

$41.30

List Price$59.00Save 30%

In StockDetails

Request a Bulk Order

Quality Level

100

assay

96%

form

liquid

refractive index

n20/D 1.572 (lit.)

density

2.028 g/mL at 25 °C (lit.)

functional group

ether
iodo

SMILES string

ICCOCCOCCI

InChI

1S/C6H12I2O2/c7-1-3-9-5-6-10-4-2-8/h1-6H2

InChI key

BCAGFJXMCZSAHD-UHFFFAOYSA-N

Application

1,2- Bis (2-iodoethoxy)ethane was used as crosslinking reagent for synthesis of:
  • zirconia-based, alkali-stable strong anion-exchange stationary phase[1]
  • silica-coated nanoparticles[2]
  • novel shell cross-linked (SCL) micelles with pH-responsive poly(2-(diethylamino)ethyl methacrylate) cores and thermoresponsive poly(N-isopropylacrylamide) coronas[3]

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_germany

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
MKCM2902
MKCK7205
05415DBV
05415DB
19228DB

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C McNeff et al.
Analytical biochemistry, 274(2), 181-187 (1999-10-21)
The synthesis and use of a zirconia-based, alkali-stable strong anion-exchange stationary phase are described for the removal of pyrogenic lipopolysaccharides (LPS) from insulin. The strong anion-exchange material is produced by deposition of polyethyleneimine (PEI) onto porous zirconia particles, followed by
Yuting Li et al.
Macromolecular rapid communications, 30(6), 464-468 (2009-03-19)
The mean diameter of poly[2-(dimethylamino)ethyl methacrylate]-block-poly[2-(diisopropylamino)ethyl methacrylate] (PDMA-PDPA) diblock copolymer micelles can be easily adjusted from 27-155 nm (as measured by DLS) by either selective quaternisation of the PDMA block or by adding PDPA homopolymer prior to micellisation; these self-assembled
Xiaoze Jiang et al.
Biomacromolecules, 8(10), 3184-3192 (2007-09-25)
A double hydrophilic ABC triblock copolymer, poly(2-(diethylamino)ethyl methacrylate)-b-poly(2-(dimethylamino)ethyl methacrylate)-b-poly(N-isopropylacrylamide) (PDEA-b-PDMA-b-PNIPAM), containing the well-known pH-responsive PDEA block and thermoresponsive PNIPAM block, was synthesized by atom transfer radical polymerization via sequential monomer addition using ethyl 2-chloropropionate as the initiator. The obtained triblock
Yueyuan Mao et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(46), 16623-16630 (2015-09-30)
Two large conjugated naphthalimide derivatives with or without three-methane-bridged thiazole orange (TO3; i.e., compounds 1 a and 2 a, respectively) were designed and synthesized. The fluorescence of the naphthalimide group in compound 1 a at λ=532 nm initially decreased and that for the TO3

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