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196118

Sigma-Aldrich

2,2-Dimethoxy-2-phenylacetophenone

99%

Sinônimo(s):

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

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About This Item

Fórmula linear:
C6H5COC(OCH3)2C6H5
Número CAS:
24650-42-8
Peso molecular:
256.30
Beilstein:
2054295
Número CE:
246-386-6
Número MDL:
MFCD00008475
Código UNSPSC:
12162002
ID de substância PubChem:
24851736
NACRES:
NA.23

Ensaio

99%

pf

67-70 °C (lit.)

cadeia de caracteres SMILES

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

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

chave InChI

KWVGIHKZDCUPEU-UHFFFAOYSA-N

Informações sobre genes

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

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Categorias relacionadas

Aplicação

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.

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Warning

Frases de perigo

H302,H373,H412

Classificações de perigo

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

Órgãos-alvo

oral cavity

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

Certificados de análise (COA)

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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
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
Huan Zhang et al.
Advanced materials (Deerfield Beach, Fla.), 31(44), e1904029-e1904029 (2019-09-07)
Superstretchable materials have many applications in advanced technological fields but are difficult to stretch to more than 1000× their original length. A superstretchable dynamic polymer network that can be stretched to 13 000× its original length is designed. It is
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
Henrike Niederholtmeyer et al.
Nature communications, 9(1), 5027-5027 (2018-11-30)
Cells in tissues or biofilms communicate with one another through chemical and mechanical signals to coordinate collective behaviors. Non-living cell mimics provide simplified models of natural systems; however, it has remained challenging to implement communication capabilities comparable to living cells.
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