Palladium acetate - 99.98% metals basis, high purity , CAS No.3375-31-3

  • ≥99.98% metals basis
Item Number
P111486
Grouped product items
SKUSizeAvailabilityPrice Qty
P111486-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$146.90
P111486-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$576.90
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Biochemical Assay Reagents (0)

Basic Description

SynonymsPalladium (II) acetate | SR-01000389719 | EU-0040175 | BCP05504 | Palladium(II) acetate | palladium-(II) acetate | UNII-0LTG3460Y5 | Bis(acetato)palladium | Acetic Acid Palladium(II) Salt | AMY1789 | AC-677 | Diacetatopalladium | Acetic acid palladium sal
Specifications & Purity≥99.98% metals basis
Legal InformationProduct of Umicore
Shipped InNormal
Product Description

Product class
M-O, Homogeneous Catalysts, Acetate Ligands


Reaction type
Cross Coupling Reactions with Arenes, CH-Activation, Carbonylation, Mizoroki Heck Coupling Reaction, Sonogashira-Hagihara Coupling Reaction, Suzuki-Miyaura Coupling Reaction, Oxidation


Chemical properties

Chemical formula

C12H18O12Pd3

Empirical formula

[Pd(OAc)2]3

Molecular weight

673.53

Metal

Pd

Theoretical metal content

47

Physical state

powder

Color

red brown

Applications & references

Synthesis of 2-(4-{2-[(2R)-2-Cyclopentyl-5-(5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-4-hydroxy-6-oxo-3,6-dihydro-2H-pyran-2-yl]-ethyl}-2-fluoro-phenyl)-2-methyl-propionitrile on multikilogram scale using a merging Heck coupling reaction. Compound is an inhibitor of the hepatitis C viral polymerase (HCVP) enzyme.


Reference: Org. Proc. Res. Dev. 2006, 10, 814. (DOI: 10.1021/op0600761)


Reductive carbonylation of aryl halides as an alternative and mild route for the introduction of aldehyde functionality, which is mostly desired for fine chemical and pharmaceutical intermediates to open up the wide range of further possible transformations.


Reference: Org. Proc. Res. Dev. 2007, 11, 39. (DOI: 10.1021/op060193w)


Synthesis of the pyrazolopyridinone-based p38 mitogen-activated protein kinase inhibitor including a Suzuki coupling reaction. p38 MAP kinases are intercellular serine/threonine kinases which certainly regulate the production and action of several pro-inflammatory mediators. They are also involved in disease states such as rheumatoid arthritis, Crohn’s diseases and psoriasis.


Reference: Org. Proc. Res. Dev. 2011, 15, 31. (DOI: 10.1021/op100205s)


Efficient hydroformylation of aryl triflates.

Reference: Synthesis 1996, 470 (DOI: 10.1055/s-1996-4246)


Deacetylation-Diazotation-Heck-Sequence: Carbon-Carbon bond formation with acetanilides as formal leaving groups


Reference: Adv. Synth. Catal. 2013, 355, 463 (DOI: 10.1002/adsc.201200929)


Deacetylation-Diazotation-Suzuki-Sequence: Carbon-Carbon bond formation with acetanilides as formal leaving groups.


Reference: Adv. Synth. Catal. 2013, 355, 463 (DOI: 10.1002/adsc.201200929)


Deacetylation-Diazotation-[2+2+1]-Cycloaddition:


Reference: Adv. Synth. Catal. 2013, 355, 463 (DOI: 10.1002/adsc.201200929)

AI Insight

Names and Identifiers

IUPAC Name palladium(2+);diacetate
INCHI InChI=1S/2C2H4O2.Pd/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
InChi Key YJVFFLUZDVXJQI-UHFFFAOYSA-L
Canonical SMILES CC(=O)[O-].CC(=O)[O-].[Pd+2]
Isomeric SMILES CC(=O)[O-].CC(=O)[O-].[Pd+2]
WGK Germany 3
RTECS AJ1900000
PubChem CID 167845
UN Number 3077
Packing Group III
Molecular Weight 224.51
Beilstein 6086766

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDateItem
K2208405Certificate of AnalysisOct 17, 2022 P111486
K2208465Certificate of AnalysisOct 17, 2022 P111486
F2215226Certificate of AnalysisMay 31, 2022 P111486
F2215238Certificate of AnalysisMay 31, 2022 P111486

Safety and Hazards(GHS)

Pictogram(s) GHS09,   GHS05,   GHS07
Signal Danger
Hazard Statements

H302:Harmful if swallowed

H318:Causes serious eye damage

H317:May cause an allergic skin reaction

H400:Very toxic to aquatic life

H410:Very toxic to aquatic life with long lasting effects

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P273:Avoid release to the environment.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P272:Contaminated work clothing should not be allowed out of the workplace.

P333+P313:IF SKIN irritation or rash occurs: Get medical advice/attention.

P362+P364:Take off contaminated clothing and wash it before reuse.

P391:Collect spillage.

P330:Rinse mouth.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P301+P317:IF SWALLOWED: Get medical help.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P317:Get emergency medical help.

WGK Germany 3
RTECS AJ1900000
Class 9
Merck Index 6991

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Solution Calculators