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408972

2-(Diethylamino)ethyl acrylate

95%, contains 25 ppm monomethyl ether hydroquinone as inhibitor

Synonym(s):

(N ,N -Diethylamino)ethyl acrylate, [2-(Acryloyloxy)ethyl]diethylamine

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100 ML

$170.00

$170.00

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About This Item

Linear Formula:
CH2=CHCOOCH2CH2N(C2H5)2
CAS Number:
2426-54-2
Molecular Weight:
171.24
EC Number:
219-378-5
MDL number:
MFCD00042882
UNSPSC Code:
12162002
PubChem Substance ID:
24865611
NACRES:
NA.23

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vapor pressure

0.77 psi ( 20 °C)

assay

95%

contains

25 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.443 (lit.)

bp

199 °C (lit.)

density

0.922 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C9H17NO2/c1-4-9(11)12-8-7-10(5-2)6-3/h4H,1,5-8H2,2-3H3

InChI key

QHVBLSNVXDSMEB-UHFFFAOYSA-N

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1 of 4

This Item
408980415650496952
2-(Diethylamino)ethyl acrylate 95%, contains 25 ppm monomethyl ether hydroquinone as inhibitor

Sigma-Aldrich

408972

2-(Diethylamino)ethyl acrylate

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

Sigma-Aldrich

408980

2-(Diethylamino)ethyl methacrylate

3-(Dimethylamino)propyl acrylate 95%

Sigma-Aldrich

415650

3-(Dimethylamino)propyl acrylate

2-[[(Butylamino)carbonyl]oxy]ethyl acrylate

Sigma-Aldrich

496952

2-[[(Butylamino)carbonyl]oxy]ethyl acrylate

assay

95%

assay

99%

assay

95%

assay

-

density

0.922 g/mL at 25 °C (lit.)

density

0.922 g/mL at 25 °C (lit.)

density

0.928 g/mL at 25 °C (lit.)

density

1.06 g/mL at 25 °C (lit.)

contains

25 ppm monomethyl ether hydroquinone as inhibitor

contains

1500 ppm MEHQ as inhibitor

contains

-

contains

-

refractive index

n20/D 1.443 (lit.)

refractive index

n20/D 1.444 (lit.)

refractive index

n20/D 1.44 (lit.)

refractive index

n20/D 1.46 (lit.)

bp

199 °C (lit.)

bp

80 °C/10 mmHg (lit.)

bp

167 °C (lit.)

bp

-

vapor pressure

0.77 psi ( 20 °C)

vapor pressure

-

vapor pressure

-

vapor pressure

-

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 2

flash_point_f

165.0 °F - closed cup

flash_point_c

73.9 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW2250
MKCT8070
MKCR3478
MKCR3536
MKCM5512

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Yujing You et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 107(6), 1786-1791 (2018-11-16)
Cell growth and release from the hydrogel scaffolds are critical steps in cell culture and cell therapies. Herein a double network hydrogel with one thermosensitive P(AEtMA-Cl-DEAEA) network and the other polyacrylamide network is reported. The diad hydrogel is elastic and
Mayra Eliana Valencia Zapata et al.
Polymers, 12(7) (2020-07-28)
Despite the potential of acrylic bone cement (ABC) loaded with chitosan (CS) for orthopedic applications, there are only a few in vitro studies of this composite with CS loading ≤ 15 wt.% evaluated in bioactivity tests in simulated body fluid
Nasha Qiu et al.
Biomacromolecules, 19(6), 2308-2319 (2018-05-09)
Gene therapy has demonstrated effectiveness in many genetic diseases, as evidenced by recent clinical applications. Viral vectors have been extensively tested in clinical gene-therapy trials, but nonviral vectors such as cationic polymers or lipids are much less used due to
Robert Löwe et al.
Molecules (Basel, Switzerland), 24(2) (2019-01-20)
Eight new polymerizable ammonium-TFSI ionic liquids were synthesized and characterized with respect to an application in energy storage devices. The ionic liquids feature methacrylate or acrylate termination as polymerizable groups. The preparation was optimized to obtain the precursors and ionic
Lucia Cenci et al.
Journal of nanobiotechnology, 13, 51-51 (2015-08-28)
Molecularly imprinted polymer (MIP) technique is a powerful mean to produce tailor made synthetic recognition sites. Here precipitation polymerization was exploited to produce a library of MIP nanoparticles (NPs) targeting the N terminus of the hormone Hepcidin-25, whose serum levels

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