Ordering
Available Variants1 g
CHA.36229-1g
Price
€110.40
Available – Dispatch in 14 days
5 g
CHA.36229-5g
Price
€415.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.36229-1g | €110.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.36229-5g | €415.20 |
99.98% trace metals basis
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | Pd(OCOCH3)2 |
|---|---|
| CAS Number | 3375-31-3 |
| Molecular Weight | 224.51 |
| UNSPSC Code | 12352103 |
| NACRES | NA.23 |
| PubChem Substance ID | 24863696 |
| EC Number | 222-164-4 |
| Beilstein/REAXYS Number | 6086766 |
| MDL number | MFCD00012453 |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
GHS09
   GHS05,GHS07,GHS09
|
|---|---|
| signalword | Danger |
| hcodes | H317,H318,H410 |
| pcodes | P261 - P272 - P273 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Sens. 1A |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 2 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
Palladium(II) acetate, with the CAS number 53189-26-7, is a versatile organopalladium compound that has been widely utilized in various organic synthesis reactions. It is a palladium(II) salt of acetic acid, often employed as a catalyst or reagent in numerous transformations, including cross-coupling reactions, hydrogenation, and oxidation processes. The compound exhibits a rich chemistry, allowing it to participate in the formation of carbon-carbon and carbon-heteroatom bonds, thereby making it a valuable tool in the synthesis of complex molecules. Palladium(II) acetate is commonly used in the presence of other ligands or co-catalysts to enhance its reactivity and selectivity, and its applications have been extended to the synthesis of pharmaceuticals, agrochemicals, and materials science. Its unique properties and reactivity profile make palladium(II) acetate a highly sought-after reagent in modern organic synthesis.
