DI-P-TOLYLPHOSPHINE
DI-P-TOLYLPHOSPHINE
CAS: 1017-60-3
Molecular Formula: C14H15P
DI-P-TOLYLPHOSPHINE - Names and Identifiers
| Name | DI-P-TOLYLPHOSPHINE |
| Synonyms | DI-P-TOLYLPHOSPHINE DI(4-TOLYL)PHOSPHINE Di(p-tolyl)phosphine BIS(4-METHYLPHENYL)PHOSPHINE |
| CAS | 1017-60-3 |
DI-P-TOLYLPHOSPHINE - Physico-chemical Properties
| Molecular Formula | C14H15P |
| Molar Mass | 214.24 |
| Boling Point | 122-124 °C(Press: 2 Torr) |
| Appearance | liquid |
| Color | colorless |
| Storage Condition | Room Temprature |
| Sensitive | air sensitive |
DI-P-TOLYLPHOSPHINE - Risk and Safety
| Risk Codes | R17 - Spontaneously flammable in air R34 - Causes burns |
| Safety Description | S16 - Keep away from sources of ignition. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S27 - Take off immediately all contaminated clothing. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| UN IDs | 2845 |
DI-P-TOLYLPHOSPHINE - Introduction
P-xylene phosphorus chloride (PDC) is an organic compound with the chemical formula C8H9ClP. It is a colorless and transparent liquid with a pungent odor.
P-xylene phosphorus chloride is widely used as an efficient dehydration reagent and chlorination reagent in organic synthesis. It can be used to convert alcohols, ketones and ethers into the corresponding halogenated derivatives. In addition, it can also be used to prepare specific organophosphites and organophosphite acid chlorides.
P-xylene phosphorus chloride is generally prepared by reacting xylene with phosphorus pentachloride in a reaction solvent. Among them, the addition of phosphorus pentachloride will affect the control of yield and selectivity.
When using P-xylene phosphorus chloride, it is necessary to pay attention to its high irritation and toxicity. Contact with the skin or inhalation of its vapors may cause irritation, burns and damage to the respiratory tract. Therefore, it is necessary to wear appropriate protective equipment during operation and ensure that it is carried out in a well-ventilated environment. In addition, be careful to avoid contact with water and strong oxidants to avoid dangerous chemical reactions.
Please note that P-xylene phosphorus chloride is an organic phosphorus compound, and its use and handling should be carried out in strict accordance with the safety operation procedures of relevant chemicals to ensure personal safety and environmental protection.
P-xylene phosphorus chloride is widely used as an efficient dehydration reagent and chlorination reagent in organic synthesis. It can be used to convert alcohols, ketones and ethers into the corresponding halogenated derivatives. In addition, it can also be used to prepare specific organophosphites and organophosphite acid chlorides.
P-xylene phosphorus chloride is generally prepared by reacting xylene with phosphorus pentachloride in a reaction solvent. Among them, the addition of phosphorus pentachloride will affect the control of yield and selectivity.
When using P-xylene phosphorus chloride, it is necessary to pay attention to its high irritation and toxicity. Contact with the skin or inhalation of its vapors may cause irritation, burns and damage to the respiratory tract. Therefore, it is necessary to wear appropriate protective equipment during operation and ensure that it is carried out in a well-ventilated environment. In addition, be careful to avoid contact with water and strong oxidants to avoid dangerous chemical reactions.
Please note that P-xylene phosphorus chloride is an organic phosphorus compound, and its use and handling should be carried out in strict accordance with the safety operation procedures of relevant chemicals to ensure personal safety and environmental protection.
Last Update：2024-04-10 22:29:15
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View History
DI-P-TOLYLPHOSPHINE
COPPER FLUORIDE, DIHYDRATE
PHENYLTHIOMETHYL AZIDE
decafluorobenzhydrol
BUTYLISOVALERIANAT
809282-20-0
D-aspartic
COPPER FLUORIDE, DIHYDRATE
PHENYLTHIOMETHYL AZIDE
decafluorobenzhydrol
BUTYLISOVALERIANAT
809282-20-0
D-aspartic