Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

124893

Sigma-Aldrich

Camphorquinone

97%

Synonym(s):

(±)-Camphorquinone, 2,3-Bornanedione

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C10H14O2
CAS Number:
10373-78-1
Molecular Weight:
166.22
Beilstein/REAXYS Number:
1909463
EC Number:
233-814-1
MDL number:
MFCD00064160
UNSPSC Code:
12162002
PubChem Substance ID:
24847632
NACRES:
NA.23

Quality Level

100

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

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SDBB2067
STBL4372
SDBB0428
09003AQV
09003AQ

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

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)
Fabrication and characterization of gold/acrylic polymer nanocomposites.
Burunkova J, et al.
European Polymer Journal null
Photopolymerization kinetics of dimethacrylates using the camphorquinone/amine initiator system
Cook WD
Polymer, 33(3), 600-609 (1992)
View All Related Papers

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.

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