CAS-Nr.
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Products
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Molecular Structure
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13965-03-2
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Bis(triphenylphosphine)palladium(II) chloride
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palladium(II)%20chloride.jpg)
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14592-56-4
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Bis(acetonitrile)palladium(II) chloride
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palladium(II)%20chloride%20.jpg)
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14220-64-5
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Bis(benzonitrile)palladium chloride
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palladium%20chloride.jpg)
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12317-46-3
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Dichloro(norbornadiene)palladium(II)
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palladium(II)%20.jpg)
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12012-95-2
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Allylpalladium chloride dimer
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12131-44-1
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Di-μ-chlorobis[(1,2,3-η)-1-phenyl-2-propenyl]dipalladium(II)
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![Di-μ-chlorobis[(1,2,3-η)-1-phenyl-2-propenyl]dipalladium(II) Di-μ-chlorobis[(1,2,3-η)-1-phenyl-2-propenyl]dipalladium(II)](https://www.samaterials.de/img/cms/Pd%20%20%20Palladium%20compounds/Di-μ-chlorobis[(1,2,3-η)-1-phenyl-2-propenyl]dipalladium(II).jpg)
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12081-18-4
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Bis(2-methyllallyl)palladium chloride dimer
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palladium%20Chloride%20Dimer.jpg)
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14871-92-2
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(2,2'-Bipyridine)dichloropalladium(II)
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dichloropalladium(II)%20.jpg)
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12107-56-1
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Dichloro(1,5-cyclooctadiene)palladium(II)
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palladium(II)%20.jpg)
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14267-08-4
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DICHLORO(N,N,N’,N’-TETRAMETHYLETHYLENEDIAMINE)PALLADIUM(II)
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PALLADIUM(II)%20.jpg)
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29934-17-6
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Bis(tricyclohexylphosphine)palladium(II) dichloride
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palladium(II)%20Dichloride.jpg)
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40691-33-6
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Trans-dichlorobis(tri-o-tolylphosphine)palladium(II)
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palladium(Ⅱ)%20.jpg) |
14024-61-4
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Bis(2,4-pentanedionato-O,O')palladium(II)
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palladium(II).jpg)
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19978-61-1
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[1,2-Bis(diphenylphosphino)ethane]dichlorpalladium(II)
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![[1,2-Bis(diphenylphosphino)ethane]dichlorpalladium(II) [1,2-Bis(diphenylphosphino)ethane]dichloropalladium(II)](https://www.samaterials.de/img/cms/Pd%20%20%20Palladium%20compounds/[1,2-Bis(diphenylphosphino)ethane]dichloropalladium(II)%20.jpg)
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59831-02-6
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Dichloro[1,3-bis(diphenylphosphino)propane] palladium(II)
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![Dichloro[1,3-bis(diphenylphosphino)propane] palladium(II) Dichloro[1,3-bis(diphenylphosphino)propane] palladium(II)](https://www.samaterials.de/img/cms/Pd%20%20%20Palladium%20compounds/Dichloro[1,3-bis(diphenylphosphino)propane]%20palladium(ii)%20.jpg)
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33309-88-5
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Bis(tericlohexylphosphine)palladium
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palladium.jpg)
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53199-31-8
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Bis(tri-tert-butylphosphine)palladium(0)
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palladium(0)%20.jpg)
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14221-01-3
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Tetrakis(triphenylphosphine)palladium
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palladium%20.jpg)
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32005-36-0
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Bis(dibenzylideneacetone)palladium
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palladium.jpg)
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51364-51-3,52409-22-0
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Tris(dibenzylideneacetone)dipalladium(0)
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dipalladium(0).JPG)
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72287-26-4
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Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II)
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![Dichloro[1,1’-bis(diphenylphosphino)ferrocene]palladium(II) Dichloro[1,1’-bis(diphenylphosphino)ferrocene]palladium(II)](https://www.samaterials.de/img/cms/Pd%20%20%20Palladium%20compounds/Dichloro[1,1’-bis(diphenylphosphino)ferrocene]palladium(II),.jpg)
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7790-38-7
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Palladium(II) iodide
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iodide%20.jpg)
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3375-31-3
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Palladium diacetate
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14588-08-0
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Bis(triphenylphosphinepalladium) acetate
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%20acetate%20.jpg) |
42196-31-6
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Palladium(II) trifluoroacetate
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%20trifluoroacetate,.jpg)
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31277-98-2
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Bis[1,2-bis(diphenylphosphino)ethane]palladium(0)
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![Bis[1,2-bis(diphenylphosphino)ethane]palladium(0) Bis[1,2-bis(diphenylphosphino)ethane]palladium(0)](https://www.samaterials.de/img/cms/Pd%20%20%20Palladium%20compounds/Bis[1,2-bis(diphenylphosphino)ethane]palladium%20(0).jpg)
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7647-10-1
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Palladium chloride
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Palladium (Pd) Catalyst Features:
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Palladium Purity: Palladium is used at 99.9%+ purity. It is incorporated in our organometallic catalysts to deliver reproducible results in organic transformations.
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Catalytic Performance: The catalysts mediate reactions such as C–C coupling, hydrogenation and cross-coupling. This is achieved by utilising palladium’s catalytic function.
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Defined Composition: Catalyst composition is well specified. Customised ligands ensure reproducibility and selectivity in organic synthesis.
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Optimised Reactivity: Reactivity is optimised to produce improved reaction rates and selectivity. This facilitates complex transformations.
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Ease of Handling: The catalysts are designed for simple handling. They are compatible with various solvents and reaction conditions.
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Manufacturing Process: The catalysts are prepared by experts in catalysis and organometallic chemistry. Standard procedures are consistently applied.
Palladium (Pd) Catalyst Applications:
The catalysts are used for various organic transformations. They are applicable in cross-coupling, hydrogenation, Suzuki–Miyaura and Heck reactions.
Cross-coupling reactions: These reactions form C–C and C–N bonds.
Hydrogenation: This reaction adds hydrogen to unsaturated compounds.
Suzuki–Miyaura reactions: These reactions synthesise biaryl compounds for pharmaceutical and materials chemistry.
Heck reactions: These reactions couple aryl halides and olefins. They represent a key process in organic synthesis.
Why choose our Palladium (Pd) catalyst?
Quality Assurance: The catalyst is produced with 99.9%+ purity, defined composition and reproducible performance.
Technical Support: Support is available from experienced chemists and technical experts.
Customised Solutions: Catalysts can be tailored to specific research or production requirements.
Competitive Pricing: The catalysts are offered at competitive prices.
Global Availability: The products are available globally.
Enhance your organic synthesis and catalysis experiments with palladium (Pd) catalysts. Research and production benefit from reproducible performance. Order your catalyst today!
Palladium (Pd) Catalyst Specifications:
- Palladium Purity: 99.9%+
- Ligand Type: Customisable
- Particle Size: Specified according to requirements
- Packaging: Securely sealed to maintain catalyst integrity
- Storage: Store in a cool, dry place away from moisture and air
Palladium (Pd) Catalyst Safety Instructions:
Handle palladium catalysts with care. Follow all safety guidelines when working with chemicals. Please consult the Safety Data Sheet (SDS) for detailed safety information and instructions.