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Merck

408913

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
NACRES:
NA.23
PubChem Substance ID:
24865607
UNSPSC Code:
12162002
EC Number:
221-499-3
MDL number:
MFCD00048149

Key Documents

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InChI key

HFCUBKYHMMPGBY-UHFFFAOYSA-N

InChI

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

SMILES string

COCCOC(=O)C=C

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.)

Quality Level

100

Related Categories

General description

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

signalword

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

supp_hazards

EUH071

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

140.0 °F

flash_point_c

60 °C

ppe

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Group 4: Flammable liquids + Type 2 petroleums + Hazardous rank III + Water insoluble liquid

fsl

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

408913-250ML: + 408913-BULK: + 408913-1L: + 408913-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
STBK3050
STBJ5588
STBJ0989
STBH8855
STBG3798V

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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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