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124893 Aldrich

Camphorquinone

97%

Synonym: (±)-Camphorquinone, 2,3-Bornanedione

  • CAS Number 10373-78-1

  • Empirical Formula (Hill Notation) C10H14O2

  • Molecular Weight 166.22

  •  Beilstein Registry Number 1909463

  •  EC Number 233-814-1

  •  MDL number MFCD00064160

  •  PubChem Substance ID 24847632

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Properties

Related Categories Materials Science, Miscellaneous, Organic Photoinitiators, Polymer Science, Polymerization Initiators,
InChI Key   VNQXSTWCDUXYEZ-LDWIPMOCSA-N
assay   97%
mp   197-203 °C(lit.)

Description

Packaging

5, 10, 50 g in glass bottle

Application

CQ-amines are used as a photo initiators for free radical polymerization. CQ was used as an initiator in the preparation of silver nanoparticle/silica/ polymer nanocomposites. Photopolymerization kinetics of dimethacrylates were studied using the CQ/amine initiator system.

General description

Camphorquinone (CQ) absorbs UV radiation in the region of 200-300nm due to the Π−Π* transition and visible light (400-500nm) due to the n, Π* transition of the α-dicarbonyl chromophore.

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

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Protocols & Articles

Articles

The Progress in Development of Dental Restorative Materials

With dentists placing nearly 100 million dental fillings into patients′ teeth annually in the U.S. alone, polymeric composite restoratives account for a very large share of the biomaterials market. T...
Jeffrey Stansbury1* and Christopher Bowman2
Material Matters 2010, 5.3, 73.
Keywords: Adhesion, Applications, Biomaterials, Infrared spectroscopy, Methods, Nanomaterials, Polymerization reactions, Reductions, Separation, Sol-gel, Spectroscopy

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Peer-Reviewed Papers
15

References

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