Chloroform, trichlorinated
methane, is a clear, colorless, sweat
smelling, heavy and volatile liquid haloform.
Other haloforms
are fluoroform, CHF3, bromoform,
CHBr3, and iodoform,
CHI3.
It is slightly
soluble in water and is miscible with ethanol, ether, and other organic
solvents. Chloroform is
produced by direct heating of methyl chloride with
chlorine to 500 C. This heating process produces spontaneously a series of chloromethanes, chloromethane,
dichloromethane, trichloromethane(chloroform), and tetrachloromethane which are then separated by distillation.
Chloroform is broken down to phosgene, hydrochloric acid,
and chlorine upon exposure to air,
light, and heat. This compound violently reacts with acetone in the presence of potassium
hydroxide or
strong caustics. It may react explosively with fluorine, N2O4, and methanol. It may also react explosively with chemically
active metals such as aluminum,
lithium sodium, or potassium. It will attack some forms
of plastics, rubber and coatings. Chloroform was an effective anaesthetic but can cause carcinogenic effects.
It has been replaced entirely by other less toxic, more easily controlled
halogenated hydrocarbons. It is
used primarily in the manufacture of chlorofluorocarbon, CFC-22. Chloroform reacts with a strong base (sodium hydroxide) to form dichlorocarbene
in the presence of a phase transfer catalysts. This is an reactive intermediate
during organic synthesis and effects in very different forms. It is a major raw material
in the
production of plastics, especially vinyl chloride. It is also used as an industrial
solvent for lacquers, resins, rubber, fats, greases, gums, waxes, adhesives,
oils, and dry cleaning. It is a useful
heat transfer medium in fire extinguishers. Other uses include fumigants, insecticides, manufacture
of anesthetics and pharmaceuticals, primary source for chlorodifluoromethane
and many other chemical compounds. It is sometimes used as a biocide in preventing public disease as chlorination
is effective to kill almost all bacteria and viruses. But this compound has been prohibited by the FDA to
use in drugs, cosmetics
and food packaging, cough medicines and toothpastes and etc.
|
COMPOUND
|
CAS
#
|
FORMULA
(MOL WT.)
|
BOILING
POINT C
|
DENSITY
|
VAPOR
DENSITY
|
Methyl chloride |
74-87-3 |
CH3Cl
(50.49) |
-24.2
|
0.915
|
1.74
|
Methylene chloride |
75-09-2 |
CH2Cl2
(84.93) |
39.8 |
1.3 |
2.9 |
Chloroacetic Acid |
79-11-8 |
ClCH2COOH
(94.50) |
188
|
1.58
|
3.3
|
1,1-Dichloroethene |
75-35-4 |
CH2=CCl2
(96.94) |
31.7 |
1.213 |
3.4
|
1,2-Dichloroethylene
(isomer mixture) |
540-59-0 |
ClCH=CHCl
(96.94) |
48 - 60 |
1.3 |
3.4 |
1,1-Dichloroethane
|
75-34-3 |
CH3CHCl2
(98.96) |
57.3 |
1.2 |
3.4 |
Ethylene dichloride |
107-06-2 |
ClCH2CH2Cl
(98.96) |
83.5 |
1.2 |
3.4 |
Chloroacetic Chloride |
79-04-9 |
ClCH2COCl
(112.94) |
105
|
1.42
|
3.9
|
1,2-Dichloropropane |
78-87-5 |
CH3CHClCH2Cl
(112.99) |
96.8 |
1.2 |
3.9 |
Chloroform
(Trichloromethane) |
67-66-3 |
CHCl3
(119.38) |
61.7 |
1.5 |
4.1 |
Trichloroethylene |
79-01-6 |
ClCH=CCl2
(131.39) |
86.7 |
1.5 |
4.5 |
1,1,1-Trichloroethane
(Methyl Chloroform) |
71-55-6 |
Cl3CCH3
(133.40) |
74.1 |
1.3 |
4.6 |
1,1,2-Trichloroethane |
79-00-5 |
ClCH2CHCl2
(133.40) |
113.8 |
1.4 |
4.6 |
1,2,3-Trichloropropane |
96-18-4 |
CH2ClCHClCH2Cl
(147.43) |
156 |
1.4 |
5.1 |
Carbon Tetrachloride |
56-23-5 |
CCl4
(153.82) |
76.7 |
1.6 |
5.3 |
1,1,2,2-Tetrachloroethylene |
127-18-4 |
CCl2=CCl2
(165.83) |
121.1 |
1.6 |
5.8 |
1,1,2,2-Tetrachloroethane |
79-34-5 |
CHCl2CHCl2
(167.85) |
146.3 |
1.6 |
5.8 |
The
production and use of 1,1,1-trichloroethane and carbon tetrachloride
have been phased out throughout the world because of suspected harm to the earth's ozone layer.
|