Welcome to the MedLibrary.org Wikipedia Supplement on Chloromethane -- Please Click to Return to Front Page

Chloromethane
IUPAC name	Chloromethane
Other names	Monochloromethane, Methyl chloride, Artic, Freon 40, R 40, UN 1063
Identifiers
CAS number	[74-87-3]
PubChem	6327
EINECS number	200-817-4
ChEBI	36014
RTECS number	PA6300000
SMILES	CCl
InChI	1/CH3Cl/c1-2/h1H3
Properties
Molecular formula	CH3Cl
Molar mass	50.49 g/mol
Appearance	Colorless gas with a faint sweet odor
Density	2.22 kg/m3 (0 °C)
Melting point	−97.7 °C (176 K)
Boiling point	-24.2 °C (249 K)
Solubility in water	5.325 g/l
log P	0.91
Vapor pressure	490 kPa (20 °C)
Structure
Molecular shape	Tetrahedral
Hazards
MSDS	External MSDS
EU classification	Extremely flammable (F+), Harmful (Xn), Carc. Cat. 3
NFPA 704	4 2 0
R-phrases	R10, R40, R48/20
S-phrases	S9, S16, S33
Flash point	-46 °C
Autoignition temperature	625 °C
Supplementary data page
Structure and properties	n, εr, etc.
Thermodynamic data	Phase behaviour Solid, liquid, gas
Spectral data	UV, IR, NMR, MS
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references

Chloromethane, also called Methyl chloride, R-40 or HCC 40, is a chemical compound of the group of organic compounds called haloalkanes. It was once widely used as a refrigerant. It is a colorless extremely flammable gas with a slightly sweet odor, which is, however, detected at possibly toxic levels. 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.

Production

Large amounts of chloromethane are produced naturally in the oceans by the action of sunlight on biomass and chlorine in sea foam. However, all chloromethane that is used in industry is produced synthetically.

Most chloromethane is prepared by reacting methanol with hydrogen chloride, according to the chemical equation

CH₃OH + HCl → CH₃Cl + H₂O

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 chloromethane 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.

Further reaction of chloromethane with hydrochloric acid can produce dichloromethane, trichloromethane (known as chloroform) and tetrachloromethane (also known as carbon tetrachloride).

Uses

Chloromethane was a widely-used refrigerant, but its use has been discontinued due to its toxicity and flammability. Chloromethane was also once used for producing lead-based gasoline additives, but leaded gasoline has been phased out in most of the industrialized world (an important exception being the former Soviet Union).

The most important use of chloromethane today is as a chemical intermediate in the production of silicone polymers. Smaller quantities are used as a solvent in the manufacture of butyl rubber and in petroleum refining.

Chloromethane is 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.

Safety

Inhalation of methyl chloride gas produces central nervous system effects similar to intoxication. Victims may feel drowsy, dizzy, or confused and have difficulty breathing, with gasping and choking, walking or speaking. At higher concentrations, paralysis, seizures, and coma may result.

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.

See also

• Halomethane
• Fluoromethane
• Bromomethane
• Iodomethane

External links

• International Chemical Safety Card 0419
• NIOSH Pocket Guide to Chemical Hazards 0403
• MSDS at Oxford University
• Data sheet at inchem.org
• Toxicological information
• Information about chloromethane
• Concise International Chemical Assessment Document 28 on chloromethane
• IARC Summaries & Evaluations Vol. 71 (1999)

Wikipedia content modification information:

• This page was last modified on 10 October 2008, at 00:13.

Wikipedia Authorship and Review

Wikipedia content provided here is not reviewed directly by MedLibrary.org. Wikipedia content is authored by an open community of volunteers and is not produced by or in any way affiliated with MedLibrary.org.

Wikipedia Usage Guidelines

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article on "Chloromethane".

The URL for this specific entry is:

• http://medlibrary.org/medwiki/Chloromethane

All Wikipedia text is available under the terms of the GNU Free Documentation License. (See Copyrights for details). Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc.