Ordering
Available Variants250 mg
CHA.95388-250mg
Price
€51.52
Available – Dispatch in 14 days
1 g
CHA.95388-1g
Price
€184.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
250 mg | CHA.95388-250mg | €51.52 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.95388-1g | €184.00 |
solid
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
| Empirical Formula (Hill Notation) | C37H55ClNPPd |
|---|---|
| CAS Number | 1142811-12-8 |
| Molecular Weight | 686.69 |
| UNSPSC Code | 12161600 |
| PubChem Substance ID | 329762821 |
| NACRES | NA.22 |
| MDL number | MFCD12911909 |
Safety Information Handling visibility
| pictograms |
GHS08
GHS07
  GHS08,GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335,H351 |
| pcodes | P202 - P261 - P264 - P302 + P352 - P305 + P351 + P338 - P308 + P313 |
| Hazard Classifications | Carc. 2 - 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
tBuXPhos Pd G1, with the CAS number 1142811-12-8, is a palladium-based catalyst utilized in various organic reactions, particularly in cross-coupling reactions. This complex features a phosphine ligand, which plays a crucial role in stabilizing the palladium center and facilitating the catalytic process. The tBuXPhos ligand is known for its high steric hindrance and strong electron-donating properties, allowing for efficient catalysis in a range of reactions, including Suzuki-Miyaura and Buchwald-Hartwig aminations. The catalysts high activity and selectivity make it a valuable tool in modern organic synthesis, enabling the formation of complex molecules with high precision and yield. Its applications are diverse, spanning from pharmaceuticals to materials science, and its use continues to expand as researchers explore new reaction methodologies and substrates.
