Oxidation reactions of alcohols (aldehydes, ketones, carboxylic acids)
At Kanto Chemical, we sell iridium catalysts developed by Professor Emeritus Ryohei Yamaguchi and Professor Kenichi Fujita of Kyoto University, which can oxidize primary and secondary alcohols into the corresponding aldehydes, ketones, and carboxylic acid compounds with high efficiency without using oxidants. Please utilize them as one of the synthetic tools in product development. 【Features】 ■ Cp*Ir cat. 1 For ketone synthesis, reacts under neutral conditions, cost-effective ■ Cp*Ir cat. 2 For ketone and aldehyde synthesis, reacts under neutral conditions and in air atmosphere, reusable catalyst ■ Cp*Ir cat. 3 For ketone and aldehyde synthesis, reacts under neutral conditions and in air atmosphere, higher activity compared to Cp*Ir cat. 1 and 2 ■ Cp*Ir cat. 4 For carboxylic acid synthesis, under basic, aqueous conditions For more details, please download the catalog or feel free to contact us.
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basic information
The oxidation reaction of alcohols is one of the most important reactions in organic synthesis chemistry, and there is a demand for mild and low-toxicity reaction systems.
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For more details, please refer to the catalog below or feel free to contact us.
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Company information
Since its establishment in 1944, Kanto Chemical has continued to develop competitive products in four fields: reagents, electronic materials, clinical diagnostic reagents, and chemical products, under a strict quality control system as a comprehensive reagent manufacturer.