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408980

Sigma-Aldrich

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
MDL number:
MFCD00038314
UNSPSC Code:
12162002
PubChem Substance ID:
24865612
NACRES:
NA.23

Quality Level

100

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.)

SMILES string

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

InChI key

SJIXRGNQPBQWMK-UHFFFAOYSA-N

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

Signal Word

Warning

Hazard Statements

H315,H317,H319,H332

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

170.6 °F - closed cup

Flash Point(C)

77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV9743
MKCW0438
MKCV2310
MKCQ5846
MKCM4170

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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
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
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
J M Cornejo-Bravo et al.
Biomaterials, 17(12), 1187-1193 (1996-06-01)
Copolymers of N, N-diethylaminoethyl methacrylate (DEA) and methyl methacrylate (MMA) were synthesized in ethanolic solution and characterized in terms of reactivity ratios, densities and water vapour sorption. For the reaction conditions studied the copolymerization is essentially random. Polymer densities, determined
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
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