| Chloromethane | |
|---|---|
| General | |
| Systematic name | chloromethane |
| Other names | methyl chloride, monochloromethane |
| Molecular formula | CH3Cl |
| SMILES | CCl |
| Molar mass | 50.49 g/mol |
| Appearance | colorless gas with a faint sweet odor |
| CAS number | * |
| Properties | |
| Density and phase | 0.915 g/ml, gas |
| Solubility in water | 0.5325 g/100 ml |
| Melting point | −97 °C (176 K) |
| Boiling point | −24 °C (249 K) |
| Structure | |
| Molecular shape | tetrahedral |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | Extremely Flammable (F+) Harmful (Xn) |
| NFPA 704 | |
| Flash point | Flammable Gas |
| R/S statement | R: , , S: , , |
| RTECS number | PA6300000 |
| Supplementary data page | |
| Structure and properties | n, εr, etc. |
| Thermodynamic data | Phase behaviour Solid, liquid, gas |
| Spectral data | UV, IR, NMR, MS |
| Related compounds | |
| Related Haloforms | Fluoromethane Iodomethane |
| Related Chloromethanes | Dichloromethane Chloroform Carbon tetrachloride |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Chemical infobox | |
Chloromethane, also called Methyl chloride, or simply R-40 or HCC 40, is a chemical compound once widely used as a refrigerant. It is a colorless flammable gas with a slightly sweet odor. Due to concerns about its toxicity, it is no longer present in consumer products.
Methyl chloride was first synthesized by the French chemists Jean-Baptiste Dumas and Eugene Peligot in 1835 by boiling a mixture of methanol, sulfuric acid, and sodium chloride. This method is similar to that used today.
Most methyl chloride is prepared by reacting methanol with hydrogen chloride, according to the chemical equation
This can be carried out either by bubbling hydrogen chloride gas through boiling methanol with or without a zinc chloride catalyst, or by passing combined methanol and hydrogen chloride vapors over an alumina catalyst at 350 °C.
A smaller amount of methyl chloride is produced by heating a mixture of methane and chlorine to over 400 °C. However, this method also results in more highly chlorinated compounds such as methylene chloride and chloroform and is usually only used when these other products are also desired.
The most important use of methyl chloride today is as a chemical intermediate in the production of silicone polymers. Smaller quantities are used in the manufacture of artificial rubber.
Methyl chloride is also employed as a methylating and chlorinating agent in organic chemistry. It is also used in a variety of other fields: as an extractant for greases, oils and resins, as a propellant and blowing agent in polystyrene foam production, as a local anesthetic, as an intermediate in drug manufacturing, as a catalyst carrier in low temperature polymerization, as a fluid for thermometric and thermostatic equipment and as a herbicide.
In case of ingestion nausea and vomiting may result. Skin contact when in the form of a refrigerated liquid may result in frostbite. Contact with eyes may result in dim vision, widely dilated pupils that react slowly to changes in light.
Chronic exposure to methyl chloride has been linked to birth defects in mice. In humans, exposure to methyl chloride during pregnancy may cause the fetus' lower spinal column, pelvis, and legs to form incorrectly, but this has not been conclusively proven.
In 1997, a re-investigation of Boston's Cocoanut Grove nightclub fire cited a methyl chloride leak from a refrigerator as a major cause of that disaster.
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"Chloromethane".
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