Carbon tetrachloride

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Carbon tetrachloride
Structural formula of carbon tetrachloride Space-filling model carbon tetrachloride
Identifiers
CAS number 56-23-5 YesY
PubChem 5943
ChemSpider 5730 YesY
UNII CL2T97X0V0 YesY
EC number 200-262-8
UN number 1846
KEGG C07561 YesY
ChEBI CHEBI:27385 YesY
ChEMBL CHEMBL44814 YesY
RTECS number FG4900000
Jmol-3D images Image 1
Properties
Molecular formula CCl4
Molar mass 153.82 g mol−1
Appearance colourless liquid
Odor ether-like odor
Density 1.5867 g cm−3 (liquid)

1.831 g cm−3 at −186 °C (solid)
1.809 g cm−3 at −80 °C (solid)

Melting point −22.92 °C (−9.26 °F; 250.23 K)
Boiling point 76.72 °C (170.10 °F; 349.87 K)
Solubility in water 0.081 g/100 mL (25 °C)
Solubility soluble in alcohol, ether, chloroform, benzene, naphtha, CS2
log P 2.64
Vapor pressure 11.94 kPa at 20 °C
kH 2.76x10−2 atm-cu m/mol
Refractive index (nD) 1.4601
Structure
Crystal structure Monoclinic
Molecular shape Tetrahedral
Hazards
MSDS External MSDS
EU Index 602-008-00-5
EU classification Toxic T Dangerous for the Environment (Nature) N
R-phrases R23/24/25, R40, R48/23, R59, R52/53
S-phrases (S1/2), S23, S36/37, S45, S59, S61
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 3: Short exposure could cause serious temporary or residual injury. E.g., chlorine gas Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point Non-flammable
LD50 2350 mg/kg
Thermochemistry
Std molar
entropy
So298
216 J·mol−1·K−1 (liq)
Std enthalpy of
formation
ΔfHo298
−135.4 kJ·mol−1 (liq)
Related compounds
Other cations Silicon tetrachloride
Germanium tetrachloride
Tin tetrachloride
Lead tetrachloride
Related chloromethanes Chloromethane
Dichloromethane
Chloroform
Related compounds Tetrafluoromethane
Tetrabromomethane
Tetraiodomethane
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 (77 °F), 100 kPa)
 YesY (verify) (what is: YesY/N?)
Infobox references

Carbon tetrachloride, also known by many other names (the most notable being carbon tet in the cleaning industry, and as Halon 104 or Freon 10 in HVAC; see Table for others), is the inorganic compound with the formula CCl4. It was formerly widely used in fire extinguishers, as a precursor to refrigerants, and as a cleaning agent. It is a colourless liquid with a "sweet" smell that can be detected at low levels.

Both carbon tetrachloride and tetrachloromethane are acceptable names under IUPAC nomenclature.

History and synthesis

Carbon tetrachloride was originally synthesized by the French chemist Henri Victor Regnault in 1839 by the reaction of chloroform with chlorine,1 but now it is mainly produced from methane:

CH4 + 4 Cl2 → CCl4 + 4 HCl

The production often utilizes by-products of other chlorination reactions, such as from the syntheses of dichloromethane and chloroform. Higher chlorocarbons are also subjected to "chlorinolysis:"

C2Cl6 + Cl2 → 2 CCl4

Prior to the 1950s, carbon tetrachloride was manufactured by the chlorination of carbon disulfide at 105 to 130 °C:2

CS2 + 3Cl2 → CCl4 + S2Cl2

The production of carbon tetrachloride has steeply declined since the 1980s due to environmental concerns and the decreased demand for CFCs, which were derived from carbon tetrachloride. In 1992, production in the U.S.-Europe-Japan was estimated at 720,000 tonnes.2

Properties

In the carbon tetrachloride molecule, four chlorine atoms are positioned symmetrically as corners in a tetrahedral configuration joined to a central carbon atom by single covalent bonds. Because of this symmetrical geometry, CCl4 is non-polar. Methane gas has the same structure, making carbon tetrachloride a halomethane. As a solvent, it is well suited to dissolving other non-polar compounds, fats, and oils. It can also dissolve iodine. It is somewhat volatile, giving off vapors with a smell characteristic of other chlorinated solvents, somewhat similar to the tetrachloroethylene smell reminiscent of dry cleaners' shops.

Solid tetrachloromethane has 2 polymorphs: crystalline II below −47.5 °C (225.6 K) and crystalline I above −47.5 °C.3

At −47.3 °C it has monoclinic crystal structure with space group C2/c and lattice constants a = 20.3, b = 11.6, c = 19.9 (.10−1 nm), β = 111°.4 With a specific gravity greater than 1, carbon tetrachloride will be present as a dense nonaqueous phase liquid if sufficient quantities are spilled in the environment.

Uses

A brass, Pyrene carbon-tetrachloride, fire extinguisher.

In the 20th century, carbon tetrachloride was widely used as a dry cleaning solvent, as a refrigerant, and in lava lamps.5

In 1910, The Pyrene Manufacturing Company of Delaware filed a patent to use carbon tetrachloride to extinguish fires.6 The liquid vaporized and extinguished the flames by inhibiting the chemical chain reaction of the combustion process (it was an early 20th-century presupposition that the fire suppression ability of carbon tetrachloride relied on oxygen removal.) In 1911, they patented a small, portable extinguisher that used the chemical.7 This consisted of a brass bottle with an integrated handpump that was used to expel a jet of liquid toward the fire. As the container was unpressurized, it could be easily refilled after use.8 Carbon tetrachloride was suitable for liquid and electrical fires and the extinguishers were often carried on aircraft or motor vehicles.

One specialty use of carbon tetrachloride was in stamp collecting, to reveal watermarks on postage stamps without damaging them. A small amount of the liquid was placed on the back of a stamp, sitting in a black glass or obsidian tray. The letters or design of the watermark could then be clearly seen.

However, once it became apparent that carbon tetrachloride exposure had severe adverse health effects, such as causing fulminant hepatic necrosis, safer alternatives such as tetrachloroethylene were found for these applications, and its use in these roles declined from about 1940 onward. The fact that high temperatures cause it to react to produce phosgene made it especially hazardous when used against fires. This reaction also caused a rapid depletion of oxygen. Carbon tetrachloride persisted as a pesticide to kill insects in stored grain, but in 1970 it was banned in consumer products in the United States.

Prior to the Montreal Protocol, large quantities of carbon tetrachloride were used to produce the freon refrigerants R-11 (trichlorofluoromethane) and R-12 (dichlorodifluoromethane). However, these refrigerants play a role in ozone depletion and have been phased out. Carbon tetrachloride is still used to manufacture less destructive refrigerants. Carbon tetrachloride has also been used in the detection of neutrinos.

Carbon tetrachloride is one of the most potent hepatotoxins (toxic to the liver), and is widely used in scientific research to evaluate hepatoprotective agents.910

Reactivity

Carbon tetrachloride has practically no flammability at lower temperatures. Under high temperatures in air, it forms poisonous phosgene.

Because it has no C-H bonds, carbon tetrachloride does not easily undergo free-radical reactions. Hence, it is a useful solvent for halogenations either by the elemental halogen or by a halogenation reagent such as N-bromosuccinimide (these conditions are known as Wohl-Ziegler Bromination).

In organic chemistry, carbon tetrachloride serves as a source of chlorine in the Appel reaction.

Solvent

It is used as a solvent in synthetic chemistry research, but, because of its adverse health effects, it is no longer commonly used, and in general chemists try to replace it with other solvents.9 It is sometimes useful as a solvent for infrared spectroscopy, because there are no significant absorption bands > 1600 cm−1. Because carbon tetrachloride does not have any hydrogen atoms, it was historically used in proton NMR spectroscopy. However, carbon tetrachloride is toxic, and its dissolving power is low.11 Its use has been largely superseded by deuterated solvents. Use of carbon tetrachloride in determination of oil has been replaced by various other solvents, such as tetrachloroethylene.9

Safety

Time-series of atmospheric concentrations of CCl4 (Walker et al., 2000).

Exposure to high concentrations of carbon tetrachloride (including vapor) can affect the central nervous system, degenerate the liver10 and kidneys12 and may result (after prolonged exposure) in coma and even death.13 Chronic exposure to carbon tetrachloride can cause liver1415 and kidney damage and could result in cancer.16 See material safety data sheets.17

In 2008, a study of common cleaning products found the presence of carbon tetrachloride in "very high concentrations" (up to 101 mg/m3) as a result of manufacturers' mixing of surfactants or soap with sodium hypochlorite (bleach).18

Like many other volatile substances, carbon tetrachloride is prone to misuse by inhalation, due to its possible depressant and/or dissociative effect upon the central nervous system. Use of carbon tetrachloride in this manner presents serious health risks, and may result in toxic effects described above.

Carbon tetrachloride is also both ozone-depleting19 and a greenhouse gas.20 However, since 199221 its atmospheric concentrations have been in decline for the reasons described above (see also the atmospheric time-series figure). CCl4 has an atmospheric lifetime of 85 years.22

References

  1. ^ V. Regnault (1839) "Sur les chlorures de carbone CCl et CCl2 " (On the chlorides of carbon CCl and CCl2 ), Annales de Chimie et de Physique, vol. 70, pages 104-107. Reprinted in German as: V. Regnault (1839). "Ueber die Chlorverbindungen des Kohlenstoffs, C2Cl2 und CCl2 (On the chlorine compounds of carbon, C2Cl2 und CCl2)". Annalen der Pharmacie 30 (3): 350–352. doi:10.1002/jlac.18390300310. 
  2. ^ a b Manfred Rossberg, Wilhelm Lendle, Gerhard Pfleiderer, Adolf Tögel, Eberhard-Ludwig Dreher, Ernst Langer, Heinz Jaerts, Peter Kleinschmidt, Heinz Strack, Richard Cook, Uwe Beck, Karl-August Lipper, Theodore R. Torkelson, Eckhard Löser, Klaus K. Beutel, “Chlorinated Hydrocarbons” in Ullmann's Encyclopedia of Industrial Chemistry, 2006 Wiley-VCH, Weinheim.doi:10.1002/14356007.a06_233.pub2
  3. ^ Carbon tetrachloride
  4. ^ F. Brezina, J. Mollin, R. Pastorek, Z. Sindelar. Chemicke tabulky anorganickych sloucenin (Chemical tables of inorganic compounds). SNTL, 1986.
  5. ^ Doherty RE (2000). "A History of the Production and Use of Carbon Tetrachloride, Tetrachloroethylene, Trichloroethylene and 1,1,1-Trichloroethane in the United States: Part 1—Historical Background; Carbon Tetrachloride and Tetrachloroethylene". Environmental Forensics 1 (1): 69–81. doi:10.1006/enfo.2000.0010. 
  6. ^ U.S. Patent 1,010,870, filed April 5, 1910.
  7. ^ U.S. Patent 1,105,263, filed Jan 7, 1911.
  8. ^ "Pyrene Fire Extinguishers". Vintage Fire Extinguishers. Retrieved 23 December 2009. 
  9. ^ a b c Use of Ozone Depleting Substances in Laboratories. TemaNord 516/2003.
  10. ^ a b Seifert WF, Bosma A, Brouwer A, et al (January 1994). "Vitamin A deficiency potentiates carbon tetrachloride-induced liver fibrosis in rats". Hepatology 19 (1): 193–201. doi:10.1002/hep.1840190129. PMID 8276355. 
  11. ^ W. Reusch. "Introduction to Nuclear Magnetic Resonance Spectroscopy". Virtual Textbook of Organic Chemistry. Michigan State University. 
  12. ^ Liu KX, Kato Y, Yamazaki M, Higuchi O, Nakamura T, Sugiyama Y (April 1993). "Decrease in the hepatic clearance of hepatocyte growth factor in carbon tetrachloride-intoxicated rats". Hepatology 17 (4): 651–60. doi:10.1002/hep.1840170420. PMID 8477970. 
  13. ^ Recknagel R.O., Glende E.A., Dolak J.A., Waller R.L. (1989). "Mechanism of Carbon-tetrachloride Toxicity". Pharmacology Therapeutics 43 (43): 139–154. doi:10.1016/0163-7258(89)90050-8. 
  14. ^ Recknagel RO (June 1967). "Carbon tetrachloride hepatotoxicity". Pharmacol. Rev. 19 (2): 145–208. PMID 4859860. 
  15. ^ Masuda Y (October 2006). "[Learning toxicology from carbon tetrachloride-induced hepatotoxicity]". Yakugaku Zasshi (in Japanese) 126 (10): 885–99. doi:10.1248/yakushi.126.885. PMID 17016019. dead link
  16. ^ Rood AS, McGavran PD, Aanenson JW, Till JE (August 2001). "Stochastic estimates of exposure and cancer risk from carbon tetrachloride released to the air from the rocky flats plant". Risk Anal. 21 (4): 675–95. doi:10.1111/0272-4332.214143. PMID 11726020. 
  17. ^ Material Safety Data Sheet, Carbon tetrachloride at Fisher Scientific
  18. ^ Odabasi M (2008). "Halogenated Volatile Organic Compounds from the Use of Chlorine-Bleach-Containing Household Products". Environmental Science & Technology 42 (5): 1445–51. Bibcode:2008EnST...42.1445O. doi:10.1021/es702355u. 
  19. ^ Fraser P. (1997). "Chemistry of stratospheric ozone and ozone depletion". Australian Meteorological Magazine 46 (3): 185–193. 
  20. ^ Evans WFJ, Puckrin E (1996). "A measurement of the greenhouse radiation associated with carbon tetrachloride (CCl4)". Geophysical Research Letters 23 (14): 1769–72. Bibcode:1996GeoRL..23.1769E. doi:10.1029/96GL01258. 
  21. ^ Walker, S. J., R. F. Weiss & P. K. Salameh (2000). "Reconstructed histories of the annual mean atmospheric mole fractions for the halocarbons CFC-11, CFC-12, CFC-113 and carbon tetrachloride". Journal of Geophysical Research 105: 14285–96. Bibcode:2000JGR...10514285W. doi:10.1029/1999JC900273. 
  22. ^ The Atlas of Climate Change (2006) by Kirstin Dow and Thomas E. Downing ISBN 978-0-520-25558-6

External links