900652
2-Aminoethylmethacrylamide hydrochloride
≥98%
Sinonimo/i:
N-(2-Aminoethyl) methacrylamide hydrochloride, AEMA
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About This Item
Formula empirica (notazione di Hill):
C6H13ClN2O
Numero CAS:
Peso molecolare:
164.63
Numero MDL:
Codice UNSPSC:
12162002
NACRES:
NA.23
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Livello qualitativo
Saggio
≥98%
Stato
powder or chunks
Punto di fusione
120-125 °C
Temperatura di conservazione
−20°C
Stringa SMILE
Cl.N(CCN)C(=O)C(=C)C
InChI
RUSMHXACRXXLKQ-UHFFFAOYSA-N
Applicazioni
Monomer for polymerization reactions, may be used to synthesize polymers for nucleic acid complexation and polyplex formation.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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I clienti hanno visto anche
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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