Rhodium, 5% on carbon, dry, Thermo Scientific Chemicals
Thermo Scientific Chemicals
Rhodium, 5% on carbon, dry, Thermo Scientific Chemicals
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Quantity:
25 g
1 g
5 g
Catalog number A15965.14
also known as A15965-14
Price (USD)/ Each
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Quantity:
25 g
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Chemical Identifiers
CAS7440-16-6
IUPAC Namerhodium
Molecular FormulaRh
InChI KeyMHOVAHRLVXNVSD-UHFFFAOYSA-N
SMILES[Rh]
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Black
Elemental Analysis(Rhodium) : 4.50-5.50%
FormPowder
Loss on Drying≤5.0%

Rhodium, 5% on carbon is a useful reagent for the conversation of nitriles to primary amines and the hydrogenation of aromatic rings, pyridines, aldehydes and sugars. It is also used for the reduction of oximes to amines and for the reduction of nitrobenzene to phenylhydroxylamine using hydrazine hydrate as the hydrogen source.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Rhodium, 5% on carbon is a useful reagent for the conversation of nitriles to primary amines and the hydrogenation of aromatic rings, pyridines, aldehydes and sugars. It is also used for the reduction of oximes to amines and for the reduction of nitrobenzene to phenylhydroxylamine using hydrazine hydrate as the hydrogen source.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents, halogens, chlorine trifluoride and oxygen difluoride.
RUO – Research Use Only

General References:

  1. Joseph J. Mrowca.; Thomas J. Katz. Catalysis of a Cycloaddition Reaction by Rhodium on Carbon. J. Am. Chem. Soc. 1966, 88 (17), 4012-4015 .
  2. Morris Freifelder.; Ralph M. Robinson.; George R. Stone. Hydrogenation of Substituted Pyridines with Rhodium on Carbon Catalyst. J. Org. Chem. 1962, 27 (1), 284-286.
  3. Rhodium catalysts are especially useful for the hydrogenation of aromatic rings under mild conditions. For details for the hydrogenation of 4-aminobenzoic acid to its hexahydro derivative under modest pressure, see: Org. Synth. Coll., 5, 670 (1973).
  4. Rhodium catalysts have also been used for the reduction of oximes to amines.
  5. For a monograph on catalytic hydrogenation, see: P. N. Rylander, Hydrogenation Methods, Academic Press, N.Y. (1985).
  6. For the reduction of nitrobenzene to phenylhydroxylamine using hydrazine hydrate as the hydrogen source, see: Org. Synth. Coll., 8, 16 (1993).