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化驗
99.95% trace metals basis
形狀
solid
反應適用性
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
環保替代產品特色
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
表面積
40-60 m2/g
環保替代類別
SMILES 字串
[Pd]
InChI
1S/Pd
InChI 密鑰
KDLHZDBZIXYQEI-UHFFFAOYSA-N
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一般說明
我们致力于为您提供更环保的替代产品，以符合“绿色化学的12项原则”的一项或多项原则要求。该产品为增强型，提高了能源效率。点击此处，查看更多详情。
應用
钯黑（以痕量金属计纯度为99.95％）可用作多种可持续应用中的催化剂，其表面积高，约为47 m2g−1。它可用作具有良好性能的阳极催化剂，并可用于聚合物交换膜（PEM）燃料电池。它也可用作氢解反应中钯炭催化剂的替代催化剂。
訊號詞
Danger
危險分類
Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
4.1B - Flammable solid hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
Freestanding palladium nanosheets with plasmonic and catalytic properties
Huang X, et al.
Nature Nanotechnology, 6(1), 28-28 (2011)
Palladium black as model catalyst in the hydrogenolysis of CCl2F2 (CFC-12) into CH2F2 (HFC-32)
Van de Sandt E, et al.
Applied Catalysis A: General, 155(1), 59-73 (1997)
The behavior of palladium catalysts in direct formic acid fuel cells
Zhu Y, et al.
Journal of Power Sources, 139(1-2), 15-20 (2005)
Stefano Nicolai et al.
The Journal of organic chemistry, 78(8), 3783-3801 (2013-03-21)
Tetrahydrofurans and pyrrolidines are among the most important heterocycles found in bioactive compounds. Cyclization-functionalization domino reactions of alcohols or amines onto olefins constitute one of the most efficient methods to access them. In this context, oxy- and aminoalkynylation are especially
Meng Wang et al.
Organic & biomolecular chemistry, 11(16), 2574-2577 (2013-03-15)
A novel Pd/Cu catalyzed domino reaction for the synthesis of functionalized pyrrolo[1,2-b]pyridazines from readily accessible (hetero)aryl propargyl alcohols and 1-amino-2-bromopyrroles was developed. This cascade process involves a Sonogashira cross-coupling reaction, an isomerization and an intramolecular condensation.
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