Skip to Content
Merck
All Photos(3)

Documents

Safety Information

205737

Sigma-Aldrich

Palladium on calcium carbonate

greener alternative

extent of labeling: 5 wt. % loading, poisoned with lead

Synonym(s):

Pd

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
Pd
MDL number:
MFCD03427452
UNSPSC Code:
12141733
eCl@ss:
38191001
PubChem Substance ID:
24852343
NACRES:
NA.22

form

powder

autoignition temp.

>1120 °F

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

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

extent of labeling

5 wt. % loading

greener alternative category

Enabling,

SMILES string

[Ca++].[Pd++].[O-]C([O-])=O.[O-]C([O-])=O

InChI

1S/2CH2O3.Ca.Pd/c2*2-1(3)4;;/h2*(H2,2,3,4);;/q;;2*+2/p-4

InChI key

XGLHAVVVUOEGIO-UHFFFAOYSA-J

Looking for similar products? Visit Product Comparison Guide

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 energy efficiency. Find details here.

Application

Catalyst for:
  • Aqueous Heck coupling and hydroarylation
  • Reduction reactions
  • Hydrogenation reactions
Palladium on calcium carbonate (Pd/CaCO3) can be used as a green catalyst for a variety of applications such as:
  • formation of an efficient catalytic system for Heck coupling reaction and hydroarylation reaction
  • synthesis of Lindlar catalyst for selective hydrogenation of alkynes
  • a catalytic reservoir in Miyaura-Suzuki cross-coupling reactions
  • Stille cross-coupling reactions

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Danger

Hazard Statements

H360FD,H362,H373,H410

Hazard Classifications

Aquatic Chronic 1 - Lact. - Repr. 1A - STOT RE 2

Target Organs

Central nervous system,Blood,Immune system,Kidney

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Specified Class I Designated Chemical Substances

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

205737-1G:4548173930701
205737-10G:4548173930695
205737-BULK:
205737-VAR:
205737-50G:4548173930718

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ligand-free Stille cross-coupling reaction using Pd/CaCO3 as catalyst reservoir
Coelho AV, et al.
Tetrahedron Letters, 48(43), 7671-7674 (2007)
Palladium on Calcium Carbonate Combined to 2-Hydroxypropyl-alpha/beta-cyclodextrins: A Selective Catalytic System for Aqueous Heck Coupling and Hydroarylation
Senra JD, et al.
advanced synthesis and catalysis, 350(16), 2551-2558 (2008)
Palladium on Calcium Carbonate Combined to 2-Hydroxypropyl-alpha/beta-cyclodextrins: A Selective Catalytic System for Aqueous Heck Coupling and Hydroarylation
Senra JD, et al.
Advanced Synthesis & Catalysis, 350(16), 2551-2558 (2008)
Miyaura-Suzuki cross-coupling reactions: the role of Pd/CaCO3 as catalyst reservoir
Oliveira BL and Antunes OAC
Letters in Organic Chemistry, 4(1), 13-15 (2007)
Chun Wong Aaron Chan et al.
Nature communications, 5, 5787-5787 (2014-12-20)
Lindlar catalysts comprising of palladium/calcium carbonate modified with lead acetate and quinoline are widely employed industrially for the partial hydrogenation of alkynes. However, their use is restricted, particularly for food, cosmetic and drug manufacture, due to the extremely toxic nature

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service