Molecular Formula | C72H60P4Pd |
Molar Mass | 1155.561844 |
Melting Point | 103-107 °C |
Boling Point | 360℃ at 760 mmHg |
Water Solubility | insoluble |
Solubility | Soluble in 1% Toluene. |
Appearance | Yellow crystal |
Color | Bright yellow to khaki |
BRN | 6704828 |
Storage Condition | 2-8°C |
Stability | Light Sensitive, Moisture Sensitive |
Sensitive | 7: reacts slowly with moisture/water |
MDL | MFCD00010012 |
Physical and Chemical Properties | Yellow crystal, soluble in benzene and toluene, insoluble in ether and alcohol, sensitive to air, protected from light and refrigerated. As an important transition metal catalyst, tetra (triphenylphosphine) palladium can be used for catalytic coupling, oxidation, reduction, elimination, rearrangement, isomerization and other reactions. Its catalytic efficiency is very high, and it can catalyze many reactions that are difficult to occur under the action of similar catalysts. This reagent is obtained by reducing PdCl2(Ph3P)2 with hydrazine, or prepared by reacting Pd2(DBA)3 with PPh3. Tetra (triphenylphosphine) palladium is sensitive to light and air and needs to be stored in inert gas away from light. When using this reagent, it can be operated in air for a short time, but it is best to operate under nitrogen or argon protection in vacuum equipment. |
Risk Codes | R20/22 - Harmful by inhalation and if swallowed. R40 - Limited evidence of a carcinogenic effect R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36/37 - Wear suitable protective clothing and gloves. S37/39 - Wear suitable gloves and eye/face protection S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
FLUKA BRAND F CODES | 8-10-23 |
TSCA | No |
HS Code | 28439090 |
Hazard Note | Air sensitive/Light sensitive/Irritant |
Hazard Class | MOISTURE SENSITIVE, |
chemical properties | yellow crystal, soluble in benzene, toluene, insoluble in ether and alcohol, sensitive to air, cold storage in the dark. As an important transition metal catalyst, tetra (triphenylphosphine) palladium can be used for catalytic coupling, oxidation, reduction, elimination, rearrangement, isomerization and other reactions. Its catalytic efficiency is very high, and it can catalyze many reactions that are difficult to occur under the action of similar catalysts. This reagent is obtained by reducing PdCl2(Ph3P)2 with hydrazine, or prepared by reacting Pd2(DBA)3 with PPh3. Tetra (triphenylphosphine) palladium is sensitive to light and air and needs to be stored in inert gas away from light. When using this reagent, it can be operated in air for a short time, but it is best to operate under nitrogen or argon protection in vacuum equipment. |
use | special catalyst for synthesis of medicine and pesticide (methylamine abamectin benzoate). widely used in important isomerization reactions, lateral coupling reaction catalysts hydrosilylation, isomerization, carbonylation, oxidation, C- C bond formation and other reactions. Used for coupling reaction, Heck reaction, Sonogashira reaction, Stille reaction, Suzuki reaction. Terakis(triphenylphosphine)palladium(0) Negishi coupling, Suzuki coupling, Stille coupling and Sonogashira coupling reaction catalysts; Buchwald-Hartwig amination reaction catalyst; Vinyl iodide carbonylation reaction catalyst; Aryl bromide reduction reaction catalyst; Carbon-tin bonding reaction catalyst as a catalyst, used in coupling reactions such as Suzuki, Kumada, Negishi, etc. |
EPA chemical substance information | The information is: offered by ofmpub.epa.gov (external link) |