Carbon tetrachloride

Source: Wikipedia, the free encyclopedia.
For the chemokine, see CCL4.
Carbon tetrachloride
Structural formula of tetrachloride
Space-filling model carbon tetrachloride
Carbon tetrachloride
Names
Preferred IUPAC name
Tetrachloromethane
Other names
Benziform
benzinoform
carbon(+4) chloride
carbon tet
carbon(IV) chloride
Freon-10
Refrigerant-10
Halon-104
methane tetrachloride
methyl tetrachloride
perchloromethane, PCM
Tetraform
Tetrasol
TCM, trematocide
Identifiers
3D model (
JSmol
)
1098295
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard
 100.000.239 Edit this at Wikidata
EC Number
  • 200-262-8
2347
KEGG
RTECS number
  • FG4900000
UNII
UN number 1846
  • InChI=1S/CCl4/c2-1(3,4)5 checkY
    Key: VZGDMQKNWNREIO-UHFFFAOYSA-N checkY
  • InChI=1/CCl4/c2-1(3,4)5
    Key: VZGDMQKNWNREIO-UHFFFAOYAV
  • ClC(Cl)(Cl)Cl
Properties
CCl4
Molar mass 153.81 g/mol
Appearance Colourless liquid
Odor Sweet, chloroform-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)
  • 0.097 g/100 mL (0 °C)
  • 0.081 g/100 mL (25 °C)
Solubility Soluble in alcohol, ether, chloroform, benzene, naphtha, CS2, formic acid
log P 2.64
Vapor pressure 11.94 kPa at 20 °C
2.76×10−2 atm·m3/mol
−66.60×10−6 cm3/mol
Thermal conductivity 0.1036 W/m·K (300 K)[1]
1.4607
Viscosity 0.86 mPa·s[2]
0 D
Structure
Monoclinic
Tetragonal
Tetrahedral
0 D
Thermochemistry
132.6 J/mol·K
214.39 J/mol·K
Std enthalpy of
formation
(ΔfH⦵298)
 −95.6 kJ/mol
−87.34 kJ/mol[3]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 potential occupational carcinogen
GHS labelling:
GHS08: Health hazard
Danger
H301, H302, H311, H331, H351, H372, H412, H420
P201, P202, P260, P261, P264, P270, P271, P273, P280, P281, P301+P310, P302+P352, P304+P340, P308+P313, P311, P312, P314, P321, P322, P330, P361, P363, P403+P233, P405, P501, P502
NFPA 704 (fire diamond)
3
0
0
982 °C (1,800 °F; 1,255 K)
Lethal dose or concentration (LD, LC):
250 mg/kg
  • 5400 ppm (mammal)
  • 8000 ppm (rat, 4 hr)
  • 9526 ppm (mouse, 8 hr)[5]
  • 1000 ppm (human)
  • 20,000 ppm (guinea pig, 2 hr)
  • 38,110 ppm (cat, 2 hr)
  • 50,000 ppm (human, 5 min)
  • 14,620 ppm (dog, 8 hr)[5]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 10 ppm C 25 ppm 200 ppm (5-minute maximum peak in any 4 hours)[4]
REL (Recommended)
 Ca ST 2 ppm (12.6 mg/m3) [60-minute][4]
IDLH
(Immediate danger)
 200 ppm[4]
Safety data sheet (SDS) ICSC 0024
Related compounds
Other anions
 Carbon tetrafluoride
Carbon tetrabromide
Carbon tetraiodide
Other cations
Lead tetrachloride
Related chloromethanes
 Chloromethane
Dichloromethane
Chloroform
Supplementary data page
Carbon tetrachloride (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Carbon tetrachloride, also known by many other names (such as tetrachloromethane, also

HVACR) is a chemical compound with the chemical formula CCl4. It is a colourless liquid with a "sweet" smell that can be detected at low levels. It is practically incombustible at lower temperatures. It was formerly widely used in fire extinguishers, as a precursor to refrigerants and as a cleaning agent, but has since been phased out because of environmental and safety concerns. Exposure to high concentrations of carbon tetrachloride (including vapor) can affect the central nervous system
and degenerate the liver and kidneys. Prolonged exposure can be fatal.

Properties

In the carbon tetrachloride

dry cleaners
' shops.

Solid tetrachloromethane has two

lattice constants a = 20.3, b = 11.6, c = 19.9 (.10−1 nm), β = 111°.[7]

With a

dense nonaqueous phase liquid
if sufficient quantities are spilled in the environment.

History and synthesis

Carbon tetrachloride was originally synthesized by Michael Faraday who named it "protochloride of carbon" in 1820 via decomposition of hexachloroethane ("perchloride of carbon") which he synthesized by chlorination of ethylene[8] 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 this process named "chlorinolysis":

C2Cl6 + Cl2 → 2 CCl4

Prior to the 1950s, carbon tetrachloride was manufactured by the chlorination of carbon disulfide at 105 to 130 °C:[9]

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.[9]

Safety

Carbon tetrachloride is one of the most potent hepatotoxins (toxic to the liver), so much so that it is widely used in scientific research to evaluate hepatoprotective agents.[10][11] Exposure to high concentrations of carbon tetrachloride (including vapor) can affect the central nervous system and degenerate the liver[11] and kidneys,[12] and prolonged exposure may lead to coma or death.[13] Chronic exposure to carbon tetrachloride can cause liver[14][15] and kidney damage and could result in cancer.[16] See safety data sheets.[17]

The effects of carbon tetrachloride on human health and the environment have been assessed under REACH in 2012 in the context of the substance evaluation by France.[18]

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).[19]

Carbon tetrachloride is also both

atmospheric lifetime of 85 years.[23]

At high temperatures in air, it decomposes or burns to produce poisonous phosgene.

Toxicological studies

Carbon tetrachloride is a suspected human

Group 2B, "possibly carcinogenic to humans".[26]

Uses

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

Carbon tetrachloride made from heavy chlorine-37 has been used in the detection of neutrinos.

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

Historical uses

Carbon tetrachloride was widely used as a dry cleaning solvent, as a refrigerant, and in lava lamps.[27] In the last case, carbon tetrachloride is a key ingredient that adds weight to the otherwise buoyant wax.

Solvent

It once was a popular

deuterated solvents. Use of carbon tetrachloride in determination of oil has been replaced by various other solvents, such as tetrachloroethylene.[10] Because it has no C–H bonds, carbon tetrachloride does not easily undergo free-radical reactions. 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
).

Fire suppression

A brass Pyrene carbon tetrachloride fire extinguisher
A Red Comet brand glass globe ("fire grenade") containing carbon tetrachloride

In 1910, the Pyrene Manufacturing Company of Delaware filed a patent to use carbon tetrachloride to extinguish fires.[29] The liquid was vaporized by the heat of combustion and extinguished flames, an early form of gaseous fire suppression. At the time it was believed the gas simply displaced oxygen in the area near the fire, but later research found that the gas actually inhibits the chemical chain reaction of the combustion process.[citation needed]

In 1911, Pyrene patented a small, portable extinguisher that used the chemical.[30] The extinguisher consisted of a brass bottle with an integrated hand-pump that was used to expel a jet of liquid toward the fire. As the container was unpressurized, it could easily be refilled after use.[31] Carbon tetrachloride was suitable for liquid and electrical fires and the extinguishers were often carried on aircraft or motor vehicles. However as early as 1920, there were reports of fatalities caused by the chemical when used to fight a fire in a confined space.[32]

In the first half of the 20th century, another common fire extinguisher was a single-use, sealed glass globe known as a "fire grenade", filled with either carbon tetrachloride or salt water. The bulb could be thrown at the base of the flames to quench the fire. The carbon tetrachloride type could also be installed in a spring-loaded wall fixture with a solder-based restraint. When the solder melted by high heat, the spring would either break the globe or launch it out of the bracket, allowing the extinguishing agent to be automatically dispersed into the fire.[33]

A well-known brand of fire grenade was the "Red Comet", which was variously manufactured with other fire-fighting equipment in the Denver, Colorado area by the Red Comet Manufacturing Company from its founding in 1919 until manufacturing operations were closed in the early 1980s.[34]

Refrigerants

Prior to the Montreal Protocol, large quantities of carbon tetrachloride were used to produce the chlorofluorocarbon 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.

Fumigant

Carbon tetrachloride was widely used as a

fumigant to kill insect pests in stored grain.[35] It was employed in a mixture known as 80/20, that was 80% carbon tetrachloride and 20% Carbon disulfide.[36] The United States Environmental Protection Agency banned its use in 1985.[37]

Gallery

References

  1. ^ Touloukian, Y.S., Liley, P.E., and Saxena, S.C. Thermophysical properties of matter - the TPRC data series. Volume 3. Thermal conductivity - nonmetallic liquids and gases. Data book. 1970.
  2. ISBN 0-07-051799-1
  3. ^ "Carbon tetrachloride" (PDF). Cheméo. Retrieved 14 Jun 2022.{{cite web}}: CS1 maint: url-status (link)
  4. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0107". National Institute for Occupational Safety and Health (NIOSH).
  5. ^ a b "Carbon tetrachloride". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  6. ^ "Carbon Tetrachloride". webbook.nist.gov. Archived from the original on 30 June 2017. Retrieved 28 April 2018.
  7. ^ F. Brezina, J. Mollin, R. Pastorek, Z. Sindelar. Chemicke tabulky anorganickych sloucenin (Chemical tables of inorganic compounds). SNTL, 1986.
  8. ^ Searches in Chemistry and Physics, Michael Faraday (1859)
  9. ^
    doi:10.1002/14356007.a06_233.pub2
  10. ^ a b c Use of Ozone Depleting Substances in Laboratories. TemaNord 516/2003. Archived February 27, 2008, at the Wayback Machine
  11. ^ a b Seifert W. F., Bosma A., Brouwer A. et al. (January 1994). "Vitamin A deficiency potentiates carbon tetrachloride-induced liver fibrosis in rats". Hepatology. 19 (1): 193–201.
    S2CID 205863459.{{cite journal}}: CS1 maint: uses authors parameter (link
    )
  12. ^ Liu K. X., 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.
    S2CID 25794501.{{cite journal}}: CS1 maint: uses authors parameter (link
    )
  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.
    PMID 2675128
    .
  14. ^ Recknagel R. O. (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.
    PMID 17016019
    .
  16. S2CID 31797685.{{cite journal}}: CS1 maint: uses authors parameter (link
    )
  17. ^ Material Safety Data Sheet, Carbon tetrachloride Archived 2010-09-13 at the Wayback Machine at Fisher Scientific.
  18. ^ "Substance evaluation - CoRAP - ECHA". echa.europa.eu. Archived from the original on 20 August 2016. Retrieved 28 April 2018.
  19. ^ Odabasi M. (2008). "Halogenated Volatile Organic Compounds from the Use of Chlorine-Bleach-Containing Household Products". Environmental Science & Technology. 42 (5): 1445–51.
    PMID 18441786
    .
  20. ^ Fraser P. (1997). "Chemistry of stratospheric ozone and ozone depletion". Australian Meteorological Magazine. 46 (3): 185–193.
  21. doi:10.1029/96GL01258.{{cite journal}}: CS1 maint: uses authors parameter (link
    )
  22. doi:10.1029/1999JC900273
    .
  23. ISBN 978-0-520-25558-6
  24. ^ "Report on Carcinogens, Fourteenth Edition - Carbon Tetrachloride" (PDF). ntp.niehs.nih.gov.
  25. ^ "Environmental Health Criteria 208: CARBON TETRACHLORIDE" (PDF). who.int.
  26. ^ "Public Health Statement for Carbon Tetrachloride (Tetracloruro de Carbono)". atsdr.cdc.gov.
  27. S2CID 97680726
    .
  28. ^ W. Reusch. "Introduction to Nuclear Magnetic Resonance Spectroscopy". Virtual Textbook of Organic Chemistry. Michigan State University. Archived from the original on August 31, 2006.
  29. ^ U.S. Patent 1,010,870, filed April 5, 1910.
  30. ^ U.S. Patent 1,105,263, filed Jan 7, 1911.
  31. ^ "Pyrene Fire Extinguishers". Vintage Fire Extinguishers. Archived from the original on 25 March 2010. Retrieved 23 December 2009.
  32. doi:10.1016/S0016-0032(20)91494-1
    . Retrieved 2022-02-03.
  33. ISBN 978-0-203-48499-9
    .
  34. ^ "Red Comet Manufacturing Company". City of Littleton, CO. Archived from the original on 1 October 2016. Retrieved 30 September 2016.
  35. ^ "ACSH Explains: What's The Story On Carbon Tetrachloride?". American Council on Science and Health. 2018-08-09. Retrieved 2022-02-03.
  36. PMID 3535379
    . Retrieved 2022-02-03.
  37. ^ Darst, Guy (1985-02-12). "Manufacturers Take Grain Fumigant Off Market in Face of EPA Testing". AP News. Retrieved 2022-02-03.

External links

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