Skip to Content
Merck
CN
All Photos(2)

Documents

124893

Sigma-Aldrich

Camphorquinone

97%

Synonym(s):

(±)-Camphorquinone, 2,3-Bornanedione

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H14O2
CAS Number:
Molecular Weight:
166.22
Beilstein:
1909463
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

Quality Level

Assay

97%

form

solid

mp

197-203 °C (lit.)

SMILES string

[H][C@@]12CC[C@@](C)(C(=O)C1=O)C2(C)C

InChI

1S/C10H14O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6H,4-5H2,1-3H3/t6-,10+/m1/s1

InChI key

VNQXSTWCDUXYEZ-LDWIPMOCSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

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.

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.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Camphorquinone-amines photoinitating systems for the initiation of free radical polymerization.
Jakubiak J, et al.
Polymer, 44(18), 5219-5226 (2003)
Yin-Chu Chen et al.
Dental materials : official publication of the Academy of Dental Materials, 23(6), 655-664 (2006-07-25)
The primary absorber in dental resins is the photoinitiator, which starts the photo polymerization process. We studied the quantum yield of conversion of camphorquinone (CQ), a blue light photoinitiator, in dental resin composites using a LED lamp (3M FreeLight) and
The role of oxygen in camphorquinone initiated photopolmerization
Andrzejewska E, et al.
Macromolecular Chemistry and Physics, 199(3), 441-449 (1998)
Mohammad Joulaei et al.
Journal of dental research, dental clinics, dental prospects, 6(4), 131-137 (2013-01-02)
Effect of surface treatments on repair bond strength of aged composite resins might be different due to their dissimilar fillers. The aim was to evaluate the effect of different surface treatments on repair micro-shear bond strength (µSBS) of silica- (Spectrum
Photopolymerization kinetics of dimethacrylates using the camphorquinone/amine initiator system
Cook WD
Polymer, 33(3), 600-609 (1992)

Articles

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service