di-μ-chloro-bis(η-allyl)palladium

Independent reference data for di-μ-chloro-bis(η-allyl)palladium (CAS 12012-95-2), compiled from public chemistry databases.

Registry identifiers across databases

Computed descriptors

Documented uses on record

• Allylpalladium(II) chloride dimer is an important catalyst used in organic synthesis. (A27)
• Palladium may be absorbed through oral, dermal, and inhalation exposure. Once in the body it distributes to the kidney, liver, spleen, lymph nodes, adrenal gland, lung and bone. Palladium's ability to form complexes allows it the bind to amino acids, proteins, DNA, and other macromolecules. Palladium and its metabolites are excreted in the urine and faeces. (A21)

Synonyms and trade names

Palladium, di-mu-chlorobis(eta3-2-propenyl)di-; RefChem:858349; Palladium, di-.mu.-chlorobis(.eta.3-2-propenyl)di-; Palladium, di-mu-chlorobis(eta3-2-propenyl)di-(9CI); Allyl palladium (II) chloride dimer; 12012-95-2; Allylpalladium chloride dimer; Allylpalladium(II) chloride dimer; allylpalladium(II) chloride; Palladium allyl chloride dimer; [Pd(allyl)Cl]2; Bis(allyl(mu-chloro)palladium); Bis(eta3-allyl)dichlorodipalladium; Bis((eta3-allyl)(chloro)palladium); Bis((mu-chloro)(2-propenyl)palladium); Di-mu-chloro-bis(eta-allyl)palladium

GHS hazard classification

What the public record says

di-μ-chloro-bis(η-allyl)palladium · CAS 12012-95-2 · C6H10Cl2Pd2.

Source: PubChem / Wikidata; the batch COA governs where values differ.