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Key Documents

196118

Sigma-Aldrich

2,2-Dimethoxy-2-phenylacetophenone

99%

Synonyme(s) :

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

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About This Item

Formule linéaire :
C6H5COC(OCH3)2C6H5
Numéro CAS:
Poids moléculaire :
256.30
Numéro Beilstein :
2054295
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Pureté

99%

Pf

67-70 °C (lit.)

Chaîne 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

Clé InChI

KWVGIHKZDCUPEU-UHFFFAOYSA-N

Informations sur le gène

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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.

Pictogrammes

Health hazardExclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Organes cibles

oral cavity

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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


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Consulter la Bibliothèque de documents

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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