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Merck
CN

900652

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:
Molecular Weight:
164.63
UNSPSC Code:
12162002
NACRES:
NA.23
MDL number:
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Quality Level

assay

≥98%

form

powder or chunks

mp

120-125 °C

storage temp.

−20°C

SMILES string

Cl.N(CCN)C(=O)C(=C)C

InChI key

RUSMHXACRXXLKQ-UHFFFAOYSA-N

Application

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


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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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
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)



Global Trade Item Number

SKUGTIN
900652-1G04061823759663