900652
2-Aminoethylmethacrylamide hydrochloride
≥98%
Synonym(s):
N-(2-Aminoethyl) methacrylamide hydrochloride, AEMA
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About This Item
Application
Monomer for polymerization reactions, may be used to synthesize polymers for nucleic acid complexation and polyplex formation.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Bioconjugate chemistry, 22(6), 1228-1238 (2011-05-05)
The facile synthesis of biocompatible and nontoxic gene delivery vectors has been the focus of research in recent years due to the high potential in treating genetic diseases. 2-Methacryloxyethyl phosphorylcholine (MPC) copolymers were recently studied for their ability to produce
Langmuir : the ACS journal of surfaces and colloids, 30(42), 12619-12626 (2014-09-30)
We report two new amino acid based antifouling zwitterionic polymers, poly(N(4)-(2-methacrylamidoethyl)asparagine) (pAspAA) and poly(N(5)-(2-methacrylamidoethyl)glutamine) (pGluAA). The vinyl monomers were developed from aspartic acid and glutamic acid. Surface-initiated photoiniferter-mediated polymerization was employed to graft polymer brushes from gold surfaces. Different thickness
Diblock glycopolymers promote colloidal stability of polyplexes and effective pDNA and siRNA delivery under physicological salt and serum conditions.
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Chemistry (Weinheim an der Bergstrasse, Germany), 13(27), 7701-7707 (2007-06-30)
Linear copolymers have been developed which carry binding sites tailored for sulfated sugars. All binding monomers are based on the methacrylamide skeleton and ensure statistical radical copolymerization. They are decorated with o-aminomethylphenylboronates for covalent ester formation and/or alkylammonium ions for
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