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408980

Sigma-Aldrich

2-(Diethylamino)ethyl methacrylate

contains 1500 ppm MEHQ as inhibitor, 99%

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Synonym(s):
β-(Diethylamino)ethyl methacrylate, 2-(N ,N -Diethylamino)ethyl methacrylate
Linear Formula:
H2C=C(CH3)CO2CH2CH2N(C2H5)2
CAS Number:
Molecular Weight:
185.26
MDL number:
PubChem Substance ID:
NACRES:
NA.23

Quality Level

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

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This Item
444332408972347485
2-(Diethylamino)ethyl methacrylate contains 1500 ppm MEHQ as inhibitor, 99%

408980

2-(Diethylamino)ethyl methacrylate

2-(Diethylamino)ethyl acrylate 95%, contains 25 ppm monomethyl ether hydroquinone as inhibitor

408972

2-(Diethylamino)ethyl acrylate

density

0.922 g/mL at 25 °C (lit.)

density

0.914 g/mL at 25 °C (lit.)

density

0.922 g/mL at 25 °C (lit.)

density

0.928 g/mL at 25 °C (lit.)

refractive index

n20/D 1.444 (lit.)

refractive index

n20/D 1.442 (lit.)

refractive index

n20/D 1.443 (lit.)

refractive index

n20/D 1.428 (lit.)

bp

80 °C/10 mmHg (lit.)

bp

82 °C/10 mmHg (lit.)

bp

199 °C (lit.)

bp

-

contains

1500 ppm MEHQ as inhibitor

contains

~1000 ppm monomethyl ether hydroquinone (MEHQ) as inhibitor

contains

25 ppm monomethyl ether hydroquinone as inhibitor

contains

≤100 ppm BHT as inhibitor

form

liquid

form

liquid

form

-

form

liquid

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

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk_germany

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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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
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
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
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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