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408913

Sigma-Aldrich

Ethylene glycol methyl ether acrylate

contains 50-100 ppm MEHQ as inhibitor, 98%

Synonym(s):

2-Methoxyethyl acrylate

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About This Item

Linear Formula:
H2C=CHCO2CH2CH2OCH3
CAS Number:
3121-61-7
Molecular Weight:
130.14
EC Number:
221-499-3
MDL number:
MFCD00048149
UNSPSC Code:
12162002
PubChem Substance ID:
24865607
NACRES:
NA.23

Assay

98%

form

liquid

contains

50-100 ppm MEHQ as inhibitor

refractive index

n20/D 1.427 (lit.)

bp

56 °C/12 mmHg (lit.)

density

1.012 g/mL at 25 °C (lit.)

SMILES string

COCCOC(=O)C=C

InChI

1S/C6H10O3/c1-3-6(7)9-5-4-8-2/h3H,1,4-5H2,2H3

InChI key

HFCUBKYHMMPGBY-UHFFFAOYSA-N

Related Categories

General description

2-methoxyethyl acrylate can undergo RAFT copolymerization with itaconic anhydride.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Muta. 2 - Repr. 1B - Skin Corr. 1C - Skin Sens. 1 - STOT RE 2

Supplementary Hazards

EUH071

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

140.0 °F

Flash Point(C)

60 °C

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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RAFT copolymerization of itaconic anhydride and 2-methoxyethyl acrylate: a multifunctional scaffold for preparation of ?clickable? gold nanoparticles.
Javakhishvili I, et al.
Chemical Communications (Cambridge, England), 49, 4803-4805 (2013)
Daisuke Sato et al.
Physical chemistry chemical physics : PCCP, 22(38), 21672-21677 (2020-09-12)
Periodic patterns are ubiquitous in nature and spontaneously form on molecular to cosmic scales by the interplay between reaction and diffusion. Understanding how these patterns form is important to understand the construction rules of nature and apply them in the
Yanzhao Nie et al.
Molecules (Basel, Switzerland), 23(4) (2018-03-29)
Despite notable progress, the fabrication of well-defined polypeptides via controlled ring-opening polymerization (ROP) of α-amino acid N-carboxyanhydrides (NCAs) using convenient catalysts under mild conditions in a relatively short polymerization time is still challenging. Herein, an easily obtained catalyst system composed
Shunsuke Tazawa et al.
Macromolecular rapid communications, 41(19), e2000346-e2000346 (2020-08-19)
Thermoplastic solid poly(2-methoxyethyl acrylate) (PMEA)-based polyurethane (PU) is synthesized through the reversible addition-fragmentation chain transfer (RAFT) polymerization and the condensation polymerization, using hydroxyl-terminated RAFT reagents and diisocyanate, respectively. Neat PMEA is a promising antithrombogenic liquid used in the medical fields.
Takuma Kureha et al.
Colloids and surfaces. B, Biointerfaces, 155, 166-172 (2017-04-19)
Poly(2-methoxyethyl acrylate) (pMEA) microspheres are prepared through facile free-radical polymerization in water without additives and impurities, such as surfactants, other polymers, and organic solvents, which are usually used to synthesize pMEA chains. Clean and pure (non-factionalized and non-cross-linking) pMEA microspheres
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