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Palladium Sulfate
PdSO4
Product
Product Code
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99% Palladium Sulfate
PD-S-02
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99.9% Palladium Sulfate
PD-S-03
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99.99% Palladium Sulfate
PD-S-04
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99.999% Palladium Sulfate
PD-S-05
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Palladium Sulfate is a moderately water and acid soluble Palladium source for uses compatible with sulfates. Sulfate compounds are salts or esters of sulfuric acid formed by replacing one or both of the hydrogens with a metal. Most metal sulfate compounds are readily soluble in water for uses such as water treatment, unlike fluorides and oxides which tend to be insoluble. Organometallic forms are soluble in organic solutions and sometimes in both aqueous and organic solutions. Metallic ions can also be dispersed utilizing suspended or coated nanoparticles (See also application discussion at Nanotechnology Information and at Quantum Dots) and deposited utilizing sputtering targets and evaporation materials for uses such as solar energy materials and fuel cells. Palladium Sulfate is generally immediately available in most volumes. High purity, submicron and nanopowder forms may be considered. We also produce Palladium Sulfate Solution. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement.

Palladium is a Block D, Group 10, Period 5 element. The electronic configuration is [Kr] 4d10. In its elemental form palladium's CAS number is 7440-05-3. The palladium atom has a radius of 137.6.pm and it's Van der Waals radius is 163.pm. Palladium is a member of the platinum group of metals. It is an excellent hydrogenation and dehydrogenation catalyst and available in many Organo-metallic forms for this purpose. It is alloyed with gold, silver, iridium and other platinum group elements and used in jewelry. The metal is used in dentistry, watch making, and in making surgical instruments and electrical contacts.

Formula CAS No. Appearance Molecular Weight
PdSO4 13566-03-5 Brown Powder 202.484
PRODUCT CATALOG Submicron & Nanopowder Tolling Ultra High Purity Sputtering Target Crystal Growth Rod, Plate, Powder, etc.
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Recent Research & Development for Palladium

  • The synthesis of 17-alkoxycarbonyl- and 17-carboxamido-13alpha-estra-1,3,5(10),16-tetraene derivatives via palladium-catalyzed carbonylation reactions. Steroids. 2008 Jul;73(6):669-75. Epub 2008 Feb 16.

  • Adsorption of gold(III), platinum(IV) and palladium(II) onto glycine modified crosslinked chitosan resin. Bioresour Technol. 2008 Jun;99(9):3801-9. Epub 2007 Aug 14.

  • Palladium-catalyzed three-component coupling of arynes with allylic acetates or halides and terminal alkynes promoted by cuprous iodide. Chem Commun (Camb). 2008 May 14;(18):2158-60. Epub 2008 Mar 3.

  • Isolation and characterization of stable, distinctly bent, trans-chelated bisphosphine palladium(0) species. Dalton Trans. 2008 May 7;(17):2238-40. Epub 2008 Mar 11.

  • Tetra-2,3-pyrazinoporphyrazines with Externally Appended Pyridine Rings. 5. Synthesis, Physicochemical and Theoretical Studies of a Novel Pentanuclear Palladium(II) Complex and Related Mononuclear Species. Inorg Chem. 2008 May 5;47(9):3903-19.

  • Palladium-catalyzed thiocarbonylation of iodoarenes with thiols in phosphonium salt ionic liquids. J Org Chem. 2008 May 2;73(9):3530-4. Epub 2008 Apr 3.

  • Palladium-Catalyzed Intramolecular C-Arylation of Benzylic Carbon: Synthesis of 3-Benzoxazolylisoindolinones by a Sequence of Ugi-4CR/Postfunctionalization. J Org Chem. 2008 May 2;73(9):3600-3. Epub 2008 Apr 2.

  • A general synthetic entry to the pentacyclic strychnos alkaloid family, using a [4 + 2]-cycloaddition/rearrangement cascade sequence. J Org Chem. 2008 May 2;73(9):3539-50. Epub 2008 Apr 1.

  • Cyclization reactions involving palladium-catalyzed carbene insertion into aryl halides. J Org Chem. 2008 May 2;73(9):3585-8. Epub 2008 Mar 28.

  • Palladium-catalyzed cyclization/heck- and cyclization/conjugate-addition-type sequences in the preparation of polysubstituted furans. J Org Chem. 2008 May 2;73(9):3650-3. Epub 2008 Mar 26.

  • Palladium-catalyzed cross-coupling reaction of tricyclopropylbismuth with aryl halides and triflates. J Org Chem. 2008 May 2;73(9):3604-7. Epub 2008 Mar 26.

  • An Expedient Synthesis of the Fibril Binding Compound FSB via Sequential Pd-Catalyzed Coupling Reactions. J Org Chem. 2008 May 2;73(9):3570-3. Epub 2008 Mar 26.

  • Measurement of excitation functions of helion-induced reactions on enriched Ru targets for production of medically important (103)Pd and (101m)Rh and some other radionuclides. Appl Radiat Isot. 2008 May;66(5):653-67. Epub 2007 Dec 5.

  • Cellular and molecular characterization of an embryonic cell line (BME26) from the tick Rhipicephalus (Boophilus) microplus. Insect Biochem Mol Biol. 2008 May;38(5):568-80. Epub 2008 Feb 9.

  • A New Class of Easily Activated Palladium Precatalysts for Facile C-N Cross-Coupling Reactions and the Low Temperature Oxidative Addition of Aryl Chlorides. J Am Chem Soc. 2008 May 1. [Epub ahead of print] No abstract available.

  • Sulphur poisoning of palladium catalysts used for methane combustion: effect of the support. J Hazard Mater. 2008 May 1;153(1-2):742-50. Epub 2007 Sep 8.

  • Stereoselective Synthesis of 3,3-Diarylacrylonitriles as Tubulin Polymerization Inhibitors. J Org Chem. 2008 May 1. [Epub ahead of print]

  • Enantioselective Baeyer-Villiger Oxidation Catalyzed by Palladium(II) Complexes with Chiral P,N-Ligands. J Org Chem. 2008 May 1. [Epub ahead of print]

  • Novel pathway for N1-acetyl-5-methoxykynuramine: UVB-induced liberation of carbon monoxide from precursor N1-acetyl-N2-formyl-5-methoxykynuramine. J Pineal Res. 2008 May;44(4):450-5. Epub 2008 Jan 9.

  • Palladium-catalyzed perarylation of 3-thiophene- and 3-furancarboxylic acids accompanied by C-h bond cleavage and decarboxylation. Org Lett. 2008 May 1;10(9):1851-4. Epub 2008 Apr 9.

 

 

 

 

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