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Merck

408980

2-(Diethylamino)ethyl methacrylate

contains 1500 ppm MEHQ as inhibitor, 99%

Synonym(s):

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

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About This Item

Linear Formula:
H2C=C(CH3)CO2CH2CH2N(C2H5)2
CAS Number:
105-16-8
Molecular Weight:
185.26
NACRES:
NA.23
PubChem Substance ID:
24865612
UNSPSC Code:
12162002
MDL number:
MFCD00038314

Key Documents

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InChI

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

SMILES string

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

InChI key

SJIXRGNQPBQWMK-UHFFFAOYSA-N

assay

99%

form

liquid

contains

1500 ppm MEHQ as inhibitor

refractive index

n20/D 1.444 (lit.)

bp

80 °C/10 mmHg (lit.)

density

0.922 g/mL at 25 °C (lit.)

Quality Level

100

Related Categories

Application

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).

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKDB2171
MKCZ7373
MKCX2856
MKCV9743
MKCW0438

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K Podual et al.
Journal of controlled release : official journal of the Controlled Release Society, 67(1), 9-17 (2000-04-25)
Glucose oxidase and catalase were immobilized on poly(diethylaminoethyl methacrylate-g-ethylene glycol) gels by copolymerization of the constituent monomers and the functionalized enzyme solutions. The hydrogels were prepared in the form of discs and microparticles. The amount and the activity of enzymes
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
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
Sumon Ganguli et al.
Macromolecular bioscience, 10(8), 853-859 (2010-03-20)
Poly(N,N-diethylaminoethyl methacrylate)-graft-poly(ethylene glycol) (PEAMA-g-PEG) has previously been used as a novel additive to improve the heat resistance of lysozyme, which has a positive net charge and a negatively charged active site. In the present study, we show that PEAMA-g-PEG prevents
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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