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Merck

196118

2,2-Dimethoxy-2-phenylacetophenone

99%

Synonym(s):

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

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About This Item

Linear Formula:
C6H5COC(OCH3)2C6H5
CAS Number:
24650-42-8
Molecular Weight:
256.30
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24851736
EC Number:
246-386-6
Beilstein/REAXYS Number:
2054295
MDL number:
MFCD00008475

Key Documents

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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

200

Gene Information

human ... ACHE(43), BCHE(590), CES1(1066)

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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
GHS08,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

oral cavity

Storage Class

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ8331
MKCW2526
MKCW2521
MKCT1097
MKCT7946

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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
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
Franziska D Zitzmann et al.
Lab on a chip, 17(24), 4294-4302 (2017-11-10)
Lab-on-a-chip devices that combine, e.g. chemical synthesis with integrated on-chip analytics and multi-compartment organ-on-a-chip approaches, are a fast and attractive evolving research area. While integration of appropriate cell models in microfluidic setups for monitoring the biological activity of synthesis products
Haisong Lin et al.
Nature communications, 11(1), 4405-4405 (2020-09-04)
Active biofluid management is central to the realization of wearable bioanalytical platforms that are poised to autonomously provide frequent, real-time, and accurate measures of biomarkers in epidermally-retrievable biofluids (e.g., sweat). Accordingly, here, a programmable epidermal microfluidic valving system is devised
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
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