Ordering
Available Variants500 mg
CHA.77494-500mg
Price
€44.40
Available – Dispatch in 14 days
2 g
CHA.77494-2g
Price
€134.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.77494-500mg | €44.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
2 g | CHA.77494-2g | €134.40 |
powder
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 | C27H26P2 · PdCl2 |
|---|---|
| CAS Number | 59831-02-6 |
| Molecular Weight | 589.77 |
| UNSPSC Code | 12161600 |
| PubChem Substance ID | 329761849 |
| NACRES | NA.22 |
| MDL number | MFCD03844773 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302 + H312 + H332,H315,H319,H335 |
| pcodes | P261 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
(1,3-Bis(diphenylphosphino)propane)palladium(II) chloride, with the CAS number 59831-02-6, is a palladium complex that has been widely utilized in various catalytic reactions, particularly in cross-coupling reactions. This complex is often abbreviated as PdCl2(dppp) and consists of a palladium center coordinated to two diphenylphosphino groups and two chloride ligands. The dppp ligand provides a chelating effect, which enhances the stability and reactivity of the palladium center. As a result, PdCl2(dppp) has been employed in numerous organic synthesis reactions, including Suzuki-Miyaura coupling and Heck reactions, to facilitate the formation of carbon-carbon bonds. The complex has been found to exhibit high catalytic activity and selectivity, making it a valuable tool in the field of organic chemistry and materials science. Its applications continue to expand, driven by ongoing research and development.
