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Oligo ethylene glycol methyl ether methacrylate

Manufactured by Merck Group
Sourced in United States

Oligo (ethylene glycol) methyl ether methacrylate is a chemical compound used in the manufacture of various laboratory equipment and materials. It serves as a key component in the production processes of these items. The core function of this product is to facilitate the manufacturing of laboratory equipment and related products.

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5 protocols using oligo ethylene glycol methyl ether methacrylate

1

Nanofibrillated Cellulose Hydrogel Preparation

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Nanofibrillated cellulose hydrogel (2%) was prepared as previously reported using a mechanical homogenization method [37 ,38 (link)]. Nanocrystalline cellulose hydrogel (11.9%) was purchased from the Process Development Center, University of Maine. m-Cresol, lithium chloride, N,N-dimethylacetamide, chlorobenzene, phenol, polyethylenimine (PEI) (number average molecular mass Mn = 60 kg/mol), maleic acid (MA), sodium hypophosphite, glycidyl methacrylate (GMA, 97%), azoisobutyronitrile (AIBN), oligo (ethylene glycol) methyl ether methacrylate (OEGMA, Mn = 950 g/mol, stabilized with inhibitors), and inhibitor removers (kits for removing hydroquinone and monomethyl ether hydroquinone (MEHQ) and tert-butylcatechol (BHT)) were purchased from Sigma-Aldrich (St. Louis, MO, USA).
Silicon wafers (100 crystal plane) with a native oxide layer were purchased from University Wafer (South Boston, MA, USA). A polyethylene terephthalate (PET) film (0.50 mm thick) and a nylon 6,6 (PA 6,6) film (0.5 mm thick) were purchased from GoodFellow, Coraopolis, PA, USA. A cellophane film (regenerated cellulose) 0.03 mm thick was provided by Thermetrics. Cotton (100%, plain weave), nylon 6,6 (100%, spun, plain weave), cotton/polyester, PET (50%/50%, plain weave), polyester, and PET (100%, spun, plain weave) fabrics were purchased from Testafabrics, Inc., West Pittston, PA, USA.
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2

Synthesis of Stimuli-Responsive Polymers

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Methacrylic anhydride,
1,6-hexanediol, triethylamine (TEA), 4-(dimethylamino)pyridine (DMAP), p-toluenesulfonic acid monohydrate, pyrrolidine 99%, oligo(ethylene
glycol)methyl ether methacrylate (OEGMA, number-average molecular
weight Mn = 500 and 300
g/mol), di(ethylene glycol)methyl ether methacrylate (Mn = 188.22 g/mol, 95%), and 2,2′-azobis(2-methylpropionitrile)
(AIBN) were purchased from Sigma-Aldrich. Ferric chloride hexahydrate
(FeCl3·6H2O) was purchased from Acros Organics.
The sulfur trioxide–pyridine complex (SO3-Pyr) was
purchased from TCI Chemicals Europe. Sodium nitrite, ACS reagent grade,
was purchased from Carlo Erba Reagents S.r.l., Italy. 2-Cyanopropan-2-yl
dithiobenzoate (CPDB) chain-transfer agent was purchased from STREM
Chemicals, Inc., BISCHHEIM, France. All solvents were purchased from
Sigma-Aldrich except dimethylformamide and THF, which were procured
from VWR International, Milan, Italy. Water used for cloud-point determinations
was of Milli-Q grade. Chloroform-d was obtained from
Acros Organics and dimethylsulfoxide-d6 (DMSO-d6; glass ampules) from VWR International.
OEGMA and MEO2MA were passed through a basic alumina column
to remove the inhibitor and stored at −20 °C until use.
DMSO was dried over 4 Å molecular sieves and stored under argon.
0.1 M HCl was standardized using anhydrous CaCO3 and then
used to titrate 0.1 M sodium hydroxide immediately before use.
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3

Synthesis of POEGMA-Coated Magnetic Nanoparticles

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The BPE coated particles were used for growing poly (oligo (ethylene glycol) methyl ether methacrylate) (POEGMA) brushes from the MNPs’ surface through ATRP technique. 60 mg of BPE coated MNPs were suspended in 616 mmol THF. 0.134 mmol of copper chloride (Sigma-Aldrich) was added to the nanoparticle solution and the contents were sonicated until the solution was well dispersed and uniform. 2.8 kmol of oligo (ethylene glycol) methyl ether methacrylate (300 Da MW, Sigma-Aldrich) were added to the reaction. Prior to use, the monomer was purified to remove inhibitors using a prepacked inhibitor column (Sigma-Aldrich) for hydroquinone and monomethyl ether hydroquinone. The flask was sealed, set in an oil bath maintained at 60 °C, and N2 gas was flushed while the reaction was continuously stirred. Once the solution had reached 60 °C, 0.4 mmol of 4–4’dinonyl-2–2’bipyridine (Sigma-Aldrich) were added to the reaction and the flask was again sealed and flushed with N2 gas for 30 minutes. The reaction was let to run for overnight at 60 °C. On next day, the reaction was cool down and the MNPs were precipitated by centrifugation, and washed 3X with THF, 3X with acetone and 3X with Millipore water. Finally, the POEGMA coated MNPs (MNPs-POEGMA) were lyophilized and stored as powder for further experiments. The obtained MNPs-POEGMA are water soluble (Figure S1).
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4

ATRP of Functionalized Methacrylates

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Ethyl 2-bromo-2-methylpropionate (EBiB, 98%), 2-hydroxyethyl methacrylate (HEMA, ≥99%), oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn = 300 g mol−1), copper(i) bromide (CuBr, 98%), benzyl alcohol (BA, ≥99%) and tris[2-(dimethylamino)ethyl]amine (Me6TREN, ≥99%) were purchased from Sigma-Aldrich. HEMA and OEGMA were purified by passing over a short column of activated basic alumina (Sigma-Aldrich) to remove the inhibitor and stored at −27 °C. Copper bromide was purified according to methods described in ref. 49 and 50 (link) and stored under argon at 4 °C. Dimethyl sulfoxide (DMSO, ≥99.5%, for HPLC) purchased from POCH S.A. (Gliwice, Poland) and water (HPLC Plus) purchased from Sigma-Aldrich were purged with argon before use. Concentrated phosphate-buffered saline (PBS, BioUltra) from Sigma-Aldrich was used after tenfold dilution with filtered, deionized water.
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5

Synthesis of Functional Copolymers

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D,L-Lactide (Sigma Aldrich), (2-(2-methoxyethoxy)ethyl methacrylate) (DEGMA, average M n ca. 188, Sigma Aldrich), oligo(ethylene glycol) methyl ether methacrylate (OEGMA, average M n ca. 500, Sigma Aldrich), copper(II) bromide (Alfa Aesar, 99%), N,N,N 0 ,N 00 ,N 00pentamethyldiethylenetriamine (PMDTA) (Sigma Aldrich, 99%), tin(II)2-ethylhexanoate (Sn(Oct) 2 ) (Sigma Aldrich, 95%), 2-butanone (Sigma Aldrich, 99%) were used as received.
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