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415332

Sigma-Aldrich

Ethylene glycol methyl ether methacrylate

99%

Synonym(s):

2-Methoxyethyl methacrylate

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About This Item

Linear Formula:
H2C=C(CH3)CO2CH2CH2OCH3
CAS Number:
6976-93-8
Molecular Weight:
144.17
EC Number:
230-241-9
MDL number:
MFCD00048122
UNSPSC Code:
12162002
PubChem Substance ID:
24865993
NACRES:
NA.23

Quality Level

200

Assay

99%

form

liquid

refractive index

n20/D 1.431 (lit.)

bp

65 °C/12 mmHg (lit.)

density

0.993 g/mL at 25 °C (lit.)

SMILES string

COCCOC(=O)C(C)=C

InChI

1S/C7H12O3/c1-6(2)7(8)10-5-4-9-3/h1,4-5H2,2-3H3

InChI key

YXYJVFYWCLAXHO-UHFFFAOYSA-N

General description

Polymers prepared from this monomer may have uses in polyelectrolytes and may be biocompatible.

Application

Used in the synthesis of copolymers of styrene and 2-methoxyethyl methacrylate.

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H360FD

Hazard Classifications

Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Separation of stat-copoly (styrene/2-methoxyethyl methacrylate) samples according to composition by gradient high-performance liquid chromatography.
Glockner G, et al.
Journal of Applied Polymer Science, 37(11), 3147-3161 (1989)
Priyanshi Agnihotri et al.
Soft matter, 16(33), 7845-7859 (2020-08-07)
Herein, we report synthesis of thermoresponsive poly(N-isopropylaccrylamide) (PNIPAM) microgels with short oligo(ethylene glycol) (OEG) chain comonomers (1 to 4/5 repeating unit) by surfactant-free precipitation copolymerization. The efficient incorporation of the comonomers was confirmed by a complete set of characterization methods
Caroline R Szczepanski et al.
European polymer journal, 67, 314-325 (2015-05-09)
This work presents an approach to extend the period for phase separation, independent of temperature, in ambient phase-separating photopolymerizations based on the copolymerization of structurally similar mono- and di-vinyl monomers. Copolymer resins composed of triethylene glycol dimethacrylate (TEGDMA) and ethylene
Vitalii Rosiuk et al.
Langmuir : the ACS journal of surfaces and colloids, 35(21), 7009-7017 (2019-05-14)
Nanoprecipitation is a straightforward yet powerful technique to synthesize polymer nanoparticles loaded with various biologically active compounds or contrast agents. Particle formation in this approach is kinetically controlled, and various assembly parameters have been used to control the size distribution

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