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(+/-)-Camphorquinone, 99%
CAS: 10373-78-1 | C10H14O2 | 166.22 g/mol
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Catalog number ALFA14967.14
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Quantity:
25 g
Specifications
Chemical Name or Material(+/-)-Camphorquinone
CAS10373-78-1
Melting Point198°C to 202°C
Recommended StorageAmbient temperatures
EINECS Number233-814-1
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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.