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1 on a copolymer of glycidyl methacrylate and ethylene dimethacrylate.
2 droxyethyl methacrylate and the cross-linker ethylene dimethacrylate (3 mol %) to form stable hydroge
3 erization of mixtures of butyl methacrylate, ethylene dimethacrylate, and 2-acrylamido-2-methyl-1-pro
4 consisting of 2-vinyl-4,4-dimethylazlactone, ethylene dimethacrylate, and acrylamide or 2-hydroxyethy
5 oxy)ethylcarbamoyl]-10,11-dihydroquinidine , ethylene dimethacrylate, and glycidyl methacrylate or 2-
6 rization of a mixture of butyl methacrylate, ethylene dimethacrylate, and porogens at different tempe
8 hydrolysis of poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads affords an efficiency of
9 -microm porous poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads prepared by the staged te
10 nce of monolithic poly(butyl methacrylate-co-ethylene dimethacrylate-co-2-acrylamido-2-methyl-1-propa
11 )-ethylcarbamoyl]-10,11-dihydroqui nidine-co-ethylene dimethacrylate-co-2-hydroxyethyl methacrylate)
13 ynthesized using COC as a template molecule, ethylene dimethacrylate (EDMA) as a functional monomer,
14 th containing vinylbenzyl chloride (VBC) and ethylene dimethacrylate (EDMA) to form a novel monolithi
15 yethyl-N-(3-sulfopropyl)ammonium betaine and ethylene dimethacrylate inside a 100-mum-i.d. capillary.
16 neric hydrophobic poly(butyl methacrylate-co-ethylene dimethacrylate) layer with no ionizable functio
17 he 50 microm thin poly(butyl methacrylate-co-ethylene dimethacrylate) layers supported onto 4.0 x 3.3
18 into the poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate) monolith by simply admixing the
19 25-mm-long porous poly(butyl methacrylate-co-ethylene dimethacrylate) monolith prepared within a 50-m
20 repared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith through reaction of it
21 repared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith through reaction of so
22 the hydrolyzed poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith was not sufficient to
23 peptides using a poly(lauryl methacrylate-co-ethylene dimethacrylate) monolithic column, and ESI/TOF
24 copolymerization of butyl methacrylate with ethylene dimethacrylate, or 2-hydroxyethyl methacrylate
26 ity substrate, poly(glycidyl methacrylate-co-ethylene dimethacrylate) porous polymer monolith (GMA-ED
28 ted polymerization of butyl methacrylate and ethylene dimethacrylate, was tested for solid-phase extr
29 copolymerization of propargyl acrylate with ethylene dimethacrylate were allowed to react with azido
30 on a copolymer of glycidyl methacrylate and ethylene dimethacrylate were developed for ultrafast imm
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