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408980

Sigma-Aldrich

2-(Diethylamino)ethyl methacrylate

contains 1500 ppm MEHQ as inhibitor, 99%

Sinônimo(s):

β-(Diethylamino)ethyl methacrylate, 2-(N ,N -Diethylamino)ethyl methacrylate

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About This Item

Fórmula linear:
H2C=C(CH3)CO2CH2CH2N(C2H5)2
Número CAS:
105-16-8
Peso molecular:
185.26
Número MDL:
MFCD00038314
Código UNSPSC:
12162002
ID de substância PubChem:
24865612
NACRES:
NA.23

Nível de qualidade

100

Ensaio

99%

forma

liquid

contém

1500 ppm MEHQ as inhibitor

índice de refração

n20/D 1.444 (lit.)

pb

80 °C/10 mmHg (lit.)

densidade

0.922 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCN(CC)CCOC(=O)C(C)=C

InChI

1S/C10H19NO2/c1-5-11(6-2)7-8-13-10(12)9(3)4/h3,5-8H2,1-2,4H3

chave InChI

SJIXRGNQPBQWMK-UHFFFAOYSA-N

Aplicação

2-(Diethylamino)ethyl methacrylate can be used as a precursor in the preparation of:
  • Polymeric mediator containing ferrocene moieties which are applicable in electrochemical biosensors.
  • Sepiolite-based nanocomposites by (cryo)polymerization method.
  • Thermoresponsive triblock copolymers via group transfer polymerization (GTP).

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H317,H319,H332

Classificações de perigo

Acute Tox. 4 Inhalation - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

170.6 °F - closed cup

Ponto de fulgor (°C)

77 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
MKCQ5846
MKCM4170
MKCL1860
MKCH6355
MKCD1231

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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Daniel Shae et al.
Nature nanotechnology, 14(3), 269-278 (2019-01-22)
Cyclic dinucleotide (CDN) agonists of stimulator of interferon genes (STING) are a promising class of immunotherapeutics that activate innate immunity to increase tumour immunogenicity. However, the efficacy of CDNs is limited by drug delivery barriers, including poor cellular targeting, rapid
Akifumi Kawamura et al.
Colloids and surfaces. B, Biointerfaces, 99, 74-81 (2011-11-15)
Bioconjugated gel particles that have complexes composed of lectin concanavalin A (ConA) and 2-glucosyloxyethyl methacrylate (GEMA) were synthesized by the surfactant-free emulsion copolymerization of N,N-diethylaminoethyl methacrylate (DEAEMA), poly(ethylene glycol) dimethacrylate (PEGDMA), GEMA, and modified-ConA with polymerizable groups. The resultant gel
Dave J Adams et al.
Journal of controlled release : official journal of the Controlled Release Society, 128(2), 165-170 (2008-04-26)
Vesicles prepared from block copolymers have been mooted for the encapsulation of water-soluble molecules. This is because the membranes of polymer vesicles have been shown to be more stable than those in vesicles formed from lipids, with the membrane properties
Melissa DiazDuarte-Rodriguez et al.
Polymers, 11(6) (2019-06-04)
In the present study, poly(ethylene glycol)-b-poly(N,N-diethylaminoethyl methacrylate) (PEG-b-PDEAEM) amphiphilic block copolymers were synthetized by reversible addition-fragmentation chain transfer (RAFT) polymerization using two different macro chain transfer agents containing PEG of 2000 and 5000 g/mol and varying the length of the
Feng Qian et al.
Biomacromolecules, 7(10), 2722-2727 (2006-10-10)
Several novel functionalized graft copolymer nanoparticles consisting of chitosan (CS) and the monomer methyl methacrylate (MMA), N-dimethylaminoethyl methacrylate hydrochloride (DMAEMC), and N-trimethylaminoethyl methacrylate chloride (TMAEMC), which show a higher solubility than chitosan in a broader pH range, have been prepared
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