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900652

Sigma-Aldrich

2-Aminoethylmethacrylamide hydrochloride

≥98%

Synonym(s):

N-(2-Aminoethyl) methacrylamide hydrochloride, AEMA

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About This Item

Empirical Formula (Hill Notation):
C6H13ClN2O
CAS Number:
76259-32-0
Molecular Weight:
164.63
MDL number:
MFCD09264233
UNSPSC Code:
12162002
NACRES:
NA.23

Quality Level

100

assay

≥98%

form

powder or chunks

mp

120-125 °C

storage temp.

−20°C

Application

Monomer for polymerization reactions, may be used to synthesize polymers for nucleic acid complexation and polyplex formation.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCC7473

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Marya Ahmed et al.
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
Wenchen Li et al.
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.
Smith AE, et al.
Biomacromolecules, 12, 3015-3022 (2011)
Wei Sun et al.
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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