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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
MKCQ5846
MKCM4170
MKCL1860
MKCH6355
MKCD1231

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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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