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Palladium hydroxide on carbon (CAS 12135-22-7)

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Alternate Names:
Pearlman′s catalyst
Application:
Palladium hydroxide on carbon is a catalyst for arylation reactions
CAS Number:
12135-22-7
Molecular Weight:
140.43
Molecular Formula:
H2O2Pd
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Palladium hydroxide on carbon catalyzes the direct arylation reactions of aryl iodides and bromides in both intra- and intermolecular processes. The addition of Pd/C to Pd(OH)2/C improves the efficiency of N- or O-debenzylation. Particularly active for hydrogenolysis of benzyl-nitrogen bonds, and has proved successful where other palladium-on-carbon catalysts have failed.


Palladium hydroxide on carbon (CAS 12135-22-7) References

  1. Facile and efficient total synthesis of (+)-preussin.  |  Lee, KY., et al. 2000. Org Lett. 2: 4041-2. PMID: 11112638
  2. De novo synthesis of a methylene-bridged Neu5Ac-alpha-(2,3)-gal C-disaccharide.  |  Notz, W., et al. 2001. J Org Chem. 66: 4250-60. PMID: 11397161
  3. Efficient Synthesis of Ephedra Alkaloid Analogues Using an Enantiomerically Pure N-[(R)-(+)-alpha-Methylbenzyl]aziridine-2-carboxaldehyde.  |  Hwang, GI., et al. 1996. J Org Chem. 61: 6183-6188. PMID: 11667453
  4. Pd(OH)2/C (Pearlman's catalyst): a highly active catalyst for Fukuyama, Sonogashira, and Suzuki coupling reactions.  |  Mori, Y. and Seki, M. 2003. J Org Chem. 68: 1571-4. PMID: 12585906
  5. Golgi endomannosidase inhibitor, alpha-D-glucopyranosyl-(1 --> 3)-1-deoxymannojirimycin: a five-step synthesis from maltulose and examples of N-modified derivatives.  |  Spreitz, J. and Stütz, AE. 2004. Carbohydr Res. 339: 1823-7. PMID: 15220094
  6. Direct arylation reactions catalyzed by Pd(OH)2/C: evidence for a soluble palladium catalyst.  |  Parisien, M., et al. 2005. J Org Chem. 70: 7578-84. PMID: 16149786
  7. Simultaneous removal of benzyl and benzyloxycarbonyl protective groups in 5'-O-(2-deoxy-alpha-D-glucopyranosyl)uridine by catalytic transfer hydrogenolysis.  |  Wandzik, I., et al. 2008. Nucleosides Nucleotides Nucleic Acids. 27: 1250-6. PMID: 19003570
  8. S(N)1-type substitution reactions of N-protected β-hydroxytyrosine esters: stereoselective synthesis of β-aryl and β-alkyltyrosines.  |  Wilcke, D., et al. 2012. Chem Asian J. 7: 1372-82. PMID: 22407877
  9. The fine structure of Pearlman's catalyst.  |  Albers, PW., et al. 2015. Phys Chem Chem Phys. 17: 5274-8. PMID: 25607379
  10. 4-Alkylated Silver-N-Heterocyclic Carbene (NHC) Complexes with Cytotoxic Effects in Leukemia Cells.  |  Sandtorv, AH., et al. 2015. ChemMedChem. 10: 1522-7. PMID: 26250720
  11. The first total synthesis of gobichelin B: a mixed-ligand siderophore of Streptomyces sp. NRRL F-4415.  |  Sridhar, PR., et al. 2018. Org Biomol Chem. 16: 3732-3740. PMID: 29565443
  12. Facile Access to Optically Active 2,6-Dialkyl-1,5-Diazacyclooctanes.  |  Chulakova, DR., et al. 2019. Chem Asian J. 14: 4048-4054. PMID: 31381243
  13. Palladium Hydroxide (Pearlman's Catalyst) Doped MXene (Ti3C2Tx) Composite Modified Electrode for Selective Detection of Nicotine in Human Sweat.  |  Magesh, V., et al. 2022. Biosensors (Basel). 13: PMID: 36671889

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Palladium hydroxide on carbon, 1 g

sc-250642
1 g
$62.00

Palladium hydroxide on carbon, 10 g

sc-250642A
10 g
$327.00

Palladium hydroxide on carbon, 500 g

sc-250642B
500 g
$12839.00

Palladium hydroxide on carbon, 1 kg

sc-250642C
1 kg
$20808.00