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Merck

196118

2,2-Dimethoxy-2-phenylacetophenone

99%

Synonyme(s) :

α,α-Dimethoxy-α-phenylacetophenone, Benzil α,α-dimethyl acetal

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A propos de cet article

Formule linéaire :
C6H5COC(OCH3)2C6H5
Numéro CAS:
Poids moléculaire :
256.30
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
246-386-6
Beilstein/REAXYS Number:
2054295
MDL number:
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InChI key

KWVGIHKZDCUPEU-UHFFFAOYSA-N

InChI

1S/C16H16O3/c1-18-16(19-2,14-11-7-4-8-12-14)15(17)13-9-5-3-6-10-13/h3-12H,1-2H3

SMILES string

COC(OC)(C(=O)c1ccccc1)c2ccccc2

assay

99%

mp

67-70 °C (lit.)

Quality Level

Gene Information

Application

2,2-Dimethoxy-2-phenylacetophenone (DMPA) can be used as a photoinitiator:
  • For the photopolymerization of methacrylate monomers in thick sections(~2mm).
  • In the preparation of UV-curing silicone rubber with excellent mechanical properties and thermal stability via thiol-ene reaction.
It can also be used as a starting material to prepare a water-soluble supramolecular-structured photoinitiator which is more efficient than DMPA.

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - STOT RE 2

target_organs

oral cavity

Classe de stockage

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Marta Goliszek et al.
Polymers, 12(5) (2020-05-23)
The preparation and the thermal and mechanical characteristics of lignin-containing polymer biocomposites were studied. Bisphenol A glycerolate (1 glycerol/phenol) diacrylate (BPA.GDA) was used as the main monomer, and butyl acrylate (BA), 2-ethylhexyl acrylate (EHA) or styrene (St) was used as
Lin-Ping Yu et al.
Biomacromolecules, 20(9), 3233-3241 (2019-01-10)
Fluorescent materials play an important role in biomedical fields. However, the main types of fluorescent materials suffer from several disadvantages especially the biotoxicity, which largely restrict its wider applications in biological fields. In this study, a highly efficient rare-earth-modified fluorescent
Huier Gao et al.
ACS applied materials & interfaces, 8(47), 32504-32511 (2016-11-05)
Conjugated polymers containing long-chain alkyl side groups for solubility are generally unstretchable: large strain induces crack formation, fracture, or plastic deformation. When the polymers are stretched to reorient the conjugated chains along the stretching direction, high dichroic ratio is observed
H Wada et al.
Journal of dental research, 83(3), 222-226 (2004-02-26)
Previously, we have reported that sealants incorporating bisphenol A dimethacrylate showed estrogenicity by a reporter gene assay. This study tested the hypothesis that commercial composites, which contain various monomers and additives, exhibit estrogenic activity in vitro. The estrogenic activities of
Xiuzhong Zhu et al.
Polymers, 11(5) (2019-05-19)
In this study, a new pH-tunable thermoresponsive hydroxyl-terminated hyperbranched polyether (HTHP 2) was successfully prepared via a one-pot cationic polymerization technique and postmodification. In the first step, hydroxyl-terminated hyperbranched polyether containing double bonds (HTHP 1) were synthesized. Then, through thiol-ene

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