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Merck

408980

Sigma-Aldrich

2-(Diethylamino)ethylmethacrylat

contains 1500 ppm MEHQ as inhibitor, 99%

Synonym(e):

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

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About This Item

Lineare Formel:
H2C=C(CH3)CO2CH2CH2N(C2H5)2
CAS-Nummer:
Molekulargewicht:
185.26
MDL-Nummer:
UNSPSC-Code:
12162002
PubChem Substanz-ID:
NACRES:
NA.23

Qualitätsniveau

Assay

99%

Form

liquid

Enthält

1500 ppm MEHQ as inhibitor

Brechungsindex

n20/D 1.444 (lit.)

bp

80 °C/10 mmHg (lit.)

Dichte

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

InChIKey

SJIXRGNQPBQWMK-UHFFFAOYSA-N

Anwendung

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).

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

170.6 °F - closed cup

Flammpunkt (°C)

77 °C - closed cup

Persönliche Schutzausrüstung

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


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Die Dokumentenbibliothek aufrufen

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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