The average particle size for this product is 19um. The cumulative particle size distribution is as follows:
1% >70um
6% > 60um
17% > 50um
24% > 40um
34% > 30um
49% > 20um
74% > 10um
94% > 5um
98.5% > 3um
100% > 2um
75990
Palladium on activated charcoal
10% Pd basis
Synonym(s):
Pd/C
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All Photos(3)
About This Item
Linear Formula:
Pd
MDL number:
UNSPSC Code:
12141733
eCl@ss:
38191001
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.
Recommended Products
Quality Level
form
powder
reaction suitability
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
greener alternative product characteristics
Designing Safer Chemicals
Catalysis
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sustainability
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concentration
10% Pd
greener alternative category
SMILES string
[Pd]
InChI
1S/Pd
InChI key
KDLHZDBZIXYQEI-UHFFFAOYSA-N
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General description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
Application
Palladium on activated charcoal has been used for the reduction of trimesic acid to form a mixture of cis,cis and cis,trans isomers of 1,3,5-cyclohexanetricarboxylic acid.[1] It can also be used for the conversion of benzylic and allylic alcohols into the corresponding carbonyl compounds in the presence of olefins as hydrogen acceptors.[2]
Other Notes
Catalyst for dehydrogenations[3]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Iida, H.; Watanabe, Y.; Kibayashi, C.
Journal of the American Chemical Society, 107, 5534-5534 (1985)
Effenberger, F.; Muller, W.et al.
The Journal of Organic Chemistry, 55, 3064-3064 (1990)
Variable gelation time and stiffness of low-molecular-weight hydrogels through catalytic control over self-assembly.
Poolman JM, et al.
Nature Protocols, 9(4), 977-977 (2014)
Orlek, B. S.; Wadsworth, H. et al.
Tetrahedron Letters, 32, 1241-1241 (1991)
Brown, H. C.; Rangaishenvi, M. V.
Tetrahedron Letters, 31, 7115-7115 (1990)
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