333433
1,2-Bis(2-iodoethoxy)ethane
96%
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About This Item
Produits recommandés
Pureté
96%
Forme
liquid
Indice de réfraction
n20/D 1.572 (lit.)
Densité
2.028 g/mL at 25 °C (lit.)
Groupe fonctionnel
ether
iodo
Chaîne SMILES
ICCOCCOCCI
InChI
1S/C6H12I2O2/c7-1-3-9-5-6-10-4-2-8/h1-6H2
Clé InChI
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
- silica-coated nanoparticles
- novel shell cross-linked (SCL) micelles with pH-responsive poly(2-(diethylamino)ethyl methacrylate) cores and thermoresponsive poly(N-isopropylacrylamide) coronas
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
10 - Combustible liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
235.4 °F - closed cup
Point d'éclair (°C)
113 °C - closed cup
Équipement de protection individuelle
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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
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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
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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
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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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