Skip to Page Content

Palladium Crucibles

High Purity Pd Crucibles
CAS 7440-05-3


Product Product Code Request Quote
(2N) 99% Palladium Crucibles PD-M-02-CR Request Quote
(3N) 99.9% Palladium Crucibles PD-M-03-CR Request Quote
(3N5) 99.95% Palladium Crucibles PD-M-35-CR Request Quote

CHEMICAL
IDENTIFIER
Formula CAS No. PubChem SID PubChem CID MDL No. EC No Beilstein
Re. No.
SMILES
Identifier
InChI
Identifier
InChI
Key
Pd 7440-05-3 24861601 23938 MFCD00011167 231-115-6 N/A [Pd] InChI=1S/Pd KDLHZDBZIXYQEI-UHFFFAOYSA-N

PROPERTIES Mol. Wt. Appearance Density Tensile Strength Melting Point Boiling Point Thermal Conductivity Electrical Resistivity Eletronegativity Specific Heat Heat of Vaporization Heat of Fusion MSDS
106.42 Gray Powder 12.02 gm/cc N/A 1554 °C 2970 °C 0.718 W/cm/K @ 298.2 K 10.54 microhm-cm @ 20°C 2.2 Paulings 0.0584 Cal/g/K @ 25°C 90 K-cal/gm atom at 2970°C 4.12 Cal/gm mole Safety Data Sheet

American Elements specializes in supplying Palladium Crucibles Crucible Packaging, Lab Quantitywith a variety of dimensions including round, in numerous standard diameters and wall thicknesses. Custom configurations are available. Materials include most metals including most transition, refractory and precious metals and other advanced materials. Crucibles can also be produced from custom materials and alloys for commercial and research applications and for new proprietary technologies. Other available shapes include tubes, bar or plate form, as well as custom machined shapes and through other processes such as nanoparticles (See also application discussion at Nanotechnology Information and at Quantum Dots ) and in the form of solutions and organometallics . See research below. We also produce Palladium as rod, pellets, powder, pieces, granules, ingot, wire, and in compound forms, such as oxide. Other shapes are available by request.

Palladium Bohr ModelPalladium (Pd) atomic and molecular weight, atomic number and elemental symbolPalladium (atomic symbol: Pd, atomic number: 46) is a Block D, Group 10, Period 5 element with an atomic weight of 106.42. The number of electrons in each of palladium's shells is 2, 8, 18, 18 and its electron configuration is [Kr] 4d10. The palladium atom has a radius of 137 pm and a Van der Waals radius of 202 pm. In its elemental form, palladium has a silvery white appearance. Palladium is a member of the platinum group of metals (along with platinum, rhodium, ruthenium, iridium and osmium).Elemental Palladium Palladium has the lowest melting point and is the least dense of the group. Palladium can be found as a free metal and alloyed with other platinum-group metals. Nickel-copper deposits are the main commercial source of palladium. Palladium was discovered and first isolated by William Hyde Wollaston in 1803. Its name is derived from the asteroid Pallas. For more information on palladium, including properties, safety data, research, and American Elements' catalog of palladium products, visit the Palladium element page.


HEALTH, SAFETY & TRANSPORTATION INFORMATION
N/A
N/A
N/A
N/A
N/A
N/A
N/A
nwg
N/A        

CUSTOMERS FOR PALLADIUM CRUCIBLES HAVE ALSO LOOKED AT
Palladium Sulfate Palladium Powder Palladium Oxide Pellets Palladium Sputtering Target Palladium Chloride
Palladium Fluoride Palladium Acetate Palladium Silver Silicon Alloy Palladium Wire Palladium Pellets
Palladium Foil Palladium Nanoparticles Chromium Manganese Palladium Alloy Palladium Acetylacetonate Palladium Metal
Show Me MORE Forms of Palladium

PACKAGING SPECIFICATIONS FOR BULK & RESEARCH QUANTITIES
Typical bulk packaging includes palletized plastic 5 gallon/25 kg. pails, fiber and steel drums to 1 ton super sacks in full container (FCL) or truck load (T/L) quantities. Research and sample quantities and hygroscopic, oxidizing or other air sensitive materials may be packaged under argon or vacuum. Shipping documentation includes a Certificate of Analysis and Material Safety Data Sheet (MSDS). Solutions are packaged in polypropylene, plastic or glass jars up to palletized 440 gallon liquid totes.


Have a Question? Ask a Chemical Engineer or Material Scientist
Request an MSDS or Certificate of Analysis

Recent Research & Development for Palladium

  • Palladium-Catalyzed Intramolecular Cyclization of Ynamides: Synthesis of 4-Halo-oxazolones. Huang H, He G, Zhu G, Zhu X, Qiu S, Zhu H. J Org Chem. 2015 Mar 16.
  • Monocarboxylation and Intramolecular Coupling of Butenylated Arenes via Palladium-Catalyzed C-H Activation Process. Liu R, Lu ZH, Hu XH, Li JL, Yang XJ. Org Lett. 2015 Mar 12.
  • Palladium-Catalyzed Cycloisomerization and Aerobic Oxidative Cycloisomerization of Homoallenyl Amides: A Facile and Divergent Approach to 2-Aminofurans. Cheng C, Liu S, Zhu G. Org Lett. 2015 Mar 12.
  • Exhibition of the Brønsted acid-base character of a Schiff base in palladium(ii) complex formation: lithium complexation, fluxional properties and catalysis of Suzuki reactions in water. Kumar R, Mani G. Dalton Trans. 2015 Mar 16.
  • Highly selective detection of palladium and picric acid by a luminescent MOF: a dual functional fluorescent sensor. Sanda S, Parshamoni S, Biswas S, Konar S. Chem Commun (Camb). 2015 Mar 16.
  • Palladium-Catalyzed Cs2CO3-Promoted Arylation of Unactivated C(sp3)-H Bonds by (Diacetoxyiodo)arenes: Shifting the Reactivity of (Diacetoxyiodo)arenes from Acetoxylation to Arylation. Gou Q, Zhang ZF, Liu ZC, Qin J. J Org Chem. 2015 Mar 12.
  • Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3. Cui P, Comanescu CC, Iluc VM. Chem Commun (Camb). 2015 Mar 10.
  • New palladium(ii) and platinum(ii) 5,5-diethylbarbiturate complexes with 2-phenylpyridine, 2,2'-bipyridine and 2,2'-dipyridylamine: synthesis, structures, DNA binding, molecular docking, cellular uptake, antioxidant activity and cytotoxicity. Icsel C, Yilmaz VT, Kaya Y, Samli H, Harrison WT, Buyukgungor O. Dalton Trans. 2015 Mar 16.
  • A Tris(triazolate) Ligand for a Highly Active and Magnetically Recoverable Palladium Catalyst of Selective Alcohol Oxidation Using Air at Atmospheric Pressure. Wang D, Deraedt C, Salmon L, Labrugère C, Etienne L, Ruiz J, Astruc D. Chemistry. 2015 Mar 9.
  • One pot synthesis of diarylfurans from aryl esters and PhI(OAc)2via palladium-associated iodonium ylides. Bao YS, Agula B, Zhaorigetu B, Jia M, Baiyin M. Org Biomol Chem. 2015 Mar 11.
  • A novel water-soluble ESIPT fluorescent probe with high quantum yield and red emission for ratiometric detectionto inorganic and organic palladium. Gao T, Xu P, Liu M, Bi A, Zeng W. Chem Asian J. 2015 Mar 10.
  • Reactions of phenylacetylene with nickel POCOP-pincer hydride complexes resulting in different outcomes from their palladium analogues. Wilson GL, Abraha M, Krause JA, Guan H. Dalton Trans. 2015 Mar 16.
  • Insights into the reaction mechanism of CO oxidative coupling to dimethyl oxalate over palladium: a combined DFT and IR study. Li Q, Zhou Z, Chen R, Sun B, Qiao L, Yao Y, Wu K. Phys Chem Chem Phys. 2015 Mar 11.
  • Palladium-catalyzed oxidative C-H/C-H cross-coupling of 1-substituted 1,2,3-triazoles with furans and thiophenes. Yu X, Huang Z, Liu W, Shi S, Kuang C. Org Biomol Chem. 2015 Mar 13.
  • Chemical Remodeling of Cell-Surface Sialic Acids through a Palladium-Triggered Bioorthogonal Elimination Reaction. Wang J, Cheng B, Li J, Zhang Z, Hong W, Chen X, Chen PR. Angew Chem Int Ed Engl. 2015 Mar 12.
  • Palladium Nanotubes Formed by Lipid Tubule Templating and Their Application in Ethanol Electrocatalysis. Wang Y, Ma S, Su Y, Han X. Chemistry. 2015 Mar 12.
  • Host-Guest Behavior of a Heavy-Atom Heterocycle Re4(CO)16(μ-SbPh2)2(μ-H)2 Obtained from a Palladium-Assisted Ring Opening Dimerization of Re2(CO)8(μ-SbPh2)(μ-H). Adams RD, Pearl WC Jr, Wong YO, Hall MB, Walensky JR. Inorg Chem. 2015 Mar 10.
  • Tackling poison and leach: catalysis by dangling thiol-palladium functions within a porous metal-organic solid. Gui B, Yee KK, Wong YL, Yiu SM, Zeller M, Wang C, Xu Z. Chem Commun (Camb). 2015 Mar 11.
  • Palladium-meta-Terarylphosphine Catalyst for the Mizoroki-Heck Reaction of (Hetero-)Aryl Bromides and Functional Olefins. Tay DW, Jong H, Lim YH, Wu W, Chew X, Robins EG, Johannes CW. J Org Chem. 2015 Mar 13.
  • Palladium(ii)-1-phenylthio-2-arylchalcogenoethane complexes: palladium phosphide nano-peanut and ribbon formation controlled by chalcogen and Suzuki coupling activation. Kumar Rao G, Kumar A, Saleem F, Singh MP, Kumar S, Kumar B, Mukherjee G, Singh AK. Dalton Trans. 2015 Mar 11.