Dimethylchlorophosphine
Dimethylchlorophosphine
CAS: 811-62-1
Molecular Formula: C2H6ClP
Dimethylchlorophosphine - Names and Identifiers
| Name | Dimethylchlorophosphine |
| Synonyms | (CH3)2PCl Dimethylchlorophosphine Chlorodimethylphosphine CHLORO(DIMETHYL)PHOSPHINE dimethylphosphinous chloride Phosphinous chloride, dimethyl- |
| CAS | 811-62-1 |
| EINECS | 212-372-3 |
| InChI | InChI=1/C2H6ClP/c1-4(2)3/h1-2H3 |
Dimethylchlorophosphine - Physico-chemical Properties
| Molecular Formula | C2H6ClP |
| Molar Mass | 96.4958 |
| Density | 1,22 g/cm3 |
| Melting Point | -4-0℃ |
| Boling Point | 43.6°C at 760 mmHg |
| Flash Point | -18°C |
| Vapor Presure | 387mmHg at 25°C |
| Appearance | Morphological Liquid |
| Color | Colorless |
| Sensitive | Air & Moisture Sensitive |
Dimethylchlorophosphine - 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. 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 | 2845 |
| Hazard Class | 4.2 |
| Packing Group | I |
Dimethylchlorophosphine - Introduction
Dimethylchlorophosphine, the chemical formula is C2H6ClP, is an organic phosphorus compound. It is a colorless liquid with a pungent odor. Dimethylchlorophosphine can react with water vapor in the air to produce hydrogen chloride, a dangerous corrosive gas.
Dimethylchlorophosphine are widely used in organic synthesis. It can be used as a reagent, as a source of ligands in transition metal catalyzed reactions, and participate in the selective addition and oxidation of olefins. In addition, it can also be used in the preparation of catalysts and pyrotechnics for free radical reactions.
There are two main methods of preparing Dimethylchlorophosphine. One is obtained by reacting trimethylphosphine with a chlorine atom binding agent, and the other is obtained by reacting phosphorous chloride with a methylating agent. The preparation process requires attention to personal protective measures and operating conditions to avoid harmful gases and chemical reactions.
Due to the irritating and corrosive nature of Dimethylchlorophosphine, proper safety precautions must be taken when using them. Protective gloves, safety glasses and protective clothing should be worn to avoid contact with skin and eyes. Operate in a well-ventilated environment and away from flammable and explosive materials. In case of accidental exposure or inhalation, medical attention should be sought immediately.
Dimethylchlorophosphine are widely used in organic synthesis. It can be used as a reagent, as a source of ligands in transition metal catalyzed reactions, and participate in the selective addition and oxidation of olefins. In addition, it can also be used in the preparation of catalysts and pyrotechnics for free radical reactions.
There are two main methods of preparing Dimethylchlorophosphine. One is obtained by reacting trimethylphosphine with a chlorine atom binding agent, and the other is obtained by reacting phosphorous chloride with a methylating agent. The preparation process requires attention to personal protective measures and operating conditions to avoid harmful gases and chemical reactions.
Due to the irritating and corrosive nature of Dimethylchlorophosphine, proper safety precautions must be taken when using them. Protective gloves, safety glasses and protective clothing should be worn to avoid contact with skin and eyes. Operate in a well-ventilated environment and away from flammable and explosive materials. In case of accidental exposure or inhalation, medical attention should be sought immediately.
Last Update：2024-04-10 22:29:15
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