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Thermo Scientific Chemicals
(+/-)-Camphorquinone, 99%
CAS: 10373-78-1 | C10H14O2 | 166.22 g/mol
化学物質識別子
CAS10373-78-1
IUPAC Name1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
Molecular FormulaC10H14O2
InChI KeyVNQXSTWCDUXYEZ-UHFFFAOYNA-N
SMILESCC1(C)C2CCC1(C)C(=O)C2=O
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Yellow
FormCrystals or powder or crystalline powder
Melting Point (clear melt)199-206?C
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Camphorquinone derivative (i.e. carboxylated camphorquinone) is used as visible-light photoinitiator in biomedical applications. It is also used in dentistry and is often used in conjunction with hydrogen donating amine.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Camphorquinone derivative (i.e. carboxylated camphorquinone) is used as visible-light photoinitiator in biomedical applications. It is also used in dentistry and is often used in conjunction with hydrogen donating amine.
Solubility
Soluble in ethanol, ethyl ether and benzene.
Notes
Incompatible with strong oxidizing agents.
Camphorquinone derivative (i.e. carboxylated camphorquinone) is used as visible-light photoinitiator in biomedical applications. It is also used in dentistry and is often used in conjunction with hydrogen donating amine.
Solubility
Soluble in ethanol, ethyl ether and benzene.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Ratanajanchai, M.; Tanwilai, D.; Sunintaboon, P. Visible light-induced surfactant-free emulsion polymerization using camphorquinone/tertiary amine as the initiating system for the synthesis of amine-functionalized colloidal nanoparticles. J. Colloid Interface Sci. 2013, 409, 25-31.
- Wessels, M.; Leyhausen, G.; Volk, J.; Geurtsen, W. Oxidative stress is responsible for genotoxicity of camphorquinone in primary human gingival fibroblasts. Clin.Oral.Invest. 2014, 18 (6), 1705-1710.