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Merck

410896

Sigma-Aldrich

2-Hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone

98%

Sinónimos:

1-[4-(2-Hydroxyethoxy)phenyl]-2-hydroxy-2-methyl-1-propan-1-one, 2-Hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methyl-1-propanone, 2-Hydroxy-2-methyl-1-[4-(2-hydroxyethoxy)phenyl]propan-1-one, 4-(2-Hydroxyethoxy)phenyl 2-hydroxy-2-propyl ketone

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About This Item

Fórmula lineal:
HOCH2CH2OC6H4COC(CH3)2OH
Número de CAS:
Peso molecular:
224.25
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

Quality Level

assay

98%

mp

88-90 °C (lit.)

SMILES string

CC(C)(O)C(=O)c1ccc(OCCO)cc1

InChI

1S/C12H16O4/c1-12(2,15)11(14)9-3-5-10(6-4-9)16-8-7-13/h3-6,13,15H,7-8H2,1-2H3

InChI key

GJKGAPPUXSSCFI-UHFFFAOYSA-N

Application

2-Hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone can be used as a photo-initiator to synthesize:
  • Polyacrylamide-grafted chitosan nanoparticles by copolymerization of acrylamide and chitosan nanoparticles.
  • Hydrophobic polyurethane sponge through thiol–ene Click reaction.

pictograms

Environment

hcodes

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

not determined

flash_point_c

not determined

ppe

Eyeshields, Gloves, type N95 (US)


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Carbohydrate polymers, 151, 565-575 (2016-07-31)
In the present work, a new flocculant, polyacrylamide-grafted chitosan nanoparticles (NCS-g-PAM), was synthesized by the copolymerization of acrylamide (AM) and chitosan nanoparticle (NCS) under ultraviolet irradiation using 2-hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone as photo-initiator. The NCS was prepared by the ionic gelation between chitosan
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