表单
powder
质量水平
反应适用性
reagent type: catalyst
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: catalyst
core: palladium
reaction type: Heck Reaction
reagent type: catalyst
core: palladium
reaction type: Hiyama Coupling
reagent type: catalyst
core: palladium
reaction type: Negishi Coupling
reagent type: catalyst
core: palladium
reaction type: Sonogashira Coupling
reagent type: catalyst
core: palladium
reaction type: Stille Coupling
reagent type: catalyst
core: palladium
reaction type: Suzuki-Miyaura Coupling
标记范围
5 wt. % loading
mp
1552 °C (lit.)
SMILES字符串
[Pd]
InChI
1S/Pd
InChI key
KDLHZDBZIXYQEI-UHFFFAOYSA-N
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一般描述
Palladium on alumina (Pd/Al2O3) (5 wt % loading, powder) is a widely utilized catalyst that can be prepared by wet impregnation of alumina pellets with palladium chloride. It can also be prepared by flame spray pyrolysis (FSP) by utilizing the precursor solution of aluminum sec-butoxide and palladium acetylacetonate.
应用
Pd/Al2O3 can be used as a catalyst in the enantioselective hydrogenation reaction. It can also be potentially used in the formation of an automotive catalytic converter to improve the air quality of urban environments.
其他说明
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.
法规信息
新产品
此项目有
Flame spray synthesis of Pd/Al2O3 catalysts and their behavior in enantioselective hydrogenation
Strobel R, et al.
J. Catal., 222(2), 307-314 (2004)
Aqueous bromate reduction by catalytic hydrogenation over Pd/Al2O3 catalysts
Chen H, et al.
Applied Catalysis. B, Environmental, 96(3-4), 307-313 (2010)
Catalytic activity of Pd/Al2O3 toward the combustion of methane
Gao D, et al.
Catalysis Communications, 9(15), 2583-2587 (2008)
Natsuki Kondo et al.
Nature communications, 5, 5338-5338 (2014-10-28)
The long-chain base phytosphingosine is a component of sphingolipids and exists in yeast, plants and some mammalian tissues. Phytosphingosine is unique in that it possesses an additional hydroxyl group compared with other long-chain bases. However, its metabolism is unknown. Here
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