DI-TERT-BUTYLNEOPENTYLPHOSPHINE
Di-t-butylneopentylphosphine
CAS: 60633-21-8
Molecular Formula: C13H29P
DI-TERT-BUTYLNEOPENTYLPHOSPHINE - Names and Identifiers
DI-TERT-BUTYLNEOPENTYLPHOSPHINE - Physico-chemical Properties
| Molecular Formula | C13H29P |
| Molar Mass | 216.34 |
| Density | 0.839g/mLat 25°C |
| Boling Point | 40°C/0.1mmHg |
| Storage Condition | -20°C |
| Refractive Index | n20/D 1.478 |
DI-TERT-BUTYLNEOPENTYLPHOSPHINE - Risk and Safety
| Risk Codes | R17 - Spontaneously flammable in air R21/22 - Harmful in contact with skin and if swallowed. R34 - Causes burns |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 2845 4.2/PG 1 |
| WGK Germany | 3 |
DI-TERT-BUTYLNEOPENTYLPHOSPHINE - Introduction
Di-t-butylneopentylphosphine(Di-t-butylneopentylphosphine) is an organophosphorus compound with the chemical formula C14H31P. It is a colorless liquid with a pungent odor. The following is a description of the nature, use, preparation and safety information of the Di-t-butylneopentylphosphine:
Nature:
Di-t-butylneopentylphosphine is a colorless liquid at room temperature, soluble in some organic solvents such as ether and dichloromethane. It is easily oxidized in air, so it should be stored under inert gas. It is a strong reducing agent that reacts with oxygen, halogens or other oxidants.
Use:
Di-t-butylneopentylphosphine is widely used in organic synthesis. It can be used as a ligand to form complexes with transition metals for catalytic reactions. It can also be used for reduction reactions, coupling reactions and the synthesis of compounds such as glyphosate.
Preparation Method:
Di-t-butylneopentylphosphine are usually prepared by means of acid catalysis. First, di-tert-butylchlorophosphine is reacted with neopentyl lithium to form a Di-t-butylneopentylphosphine lithium salt. Then, it is reacted with an acid to produce the target product Di-t-butylneopentylphosphine.
Safety Information:
Use Di-t-butylneopentylphosphine should pay attention to its toxicity and irritation. Avoid contact with skin and eyes, and make sure to operate in a well-ventilated area. Personal protective equipment such as gloves and glasses should be worn during use. In addition, correct operating methods should be followed, and chemicals should be stored and handled properly to ensure safety. If an accident occurs, immediately take appropriate first aid measures and seek medical help.
Nature:
Di-t-butylneopentylphosphine is a colorless liquid at room temperature, soluble in some organic solvents such as ether and dichloromethane. It is easily oxidized in air, so it should be stored under inert gas. It is a strong reducing agent that reacts with oxygen, halogens or other oxidants.
Use:
Di-t-butylneopentylphosphine is widely used in organic synthesis. It can be used as a ligand to form complexes with transition metals for catalytic reactions. It can also be used for reduction reactions, coupling reactions and the synthesis of compounds such as glyphosate.
Preparation Method:
Di-t-butylneopentylphosphine are usually prepared by means of acid catalysis. First, di-tert-butylchlorophosphine is reacted with neopentyl lithium to form a Di-t-butylneopentylphosphine lithium salt. Then, it is reacted with an acid to produce the target product Di-t-butylneopentylphosphine.
Safety Information:
Use Di-t-butylneopentylphosphine should pay attention to its toxicity and irritation. Avoid contact with skin and eyes, and make sure to operate in a well-ventilated area. Personal protective equipment such as gloves and glasses should be worn during use. In addition, correct operating methods should be followed, and chemicals should be stored and handled properly to ensure safety. If an accident occurs, immediately take appropriate first aid measures and seek medical help.
Last Update：2024-04-10 22:29:15
