3D model (JSmol)
|Molar mass||76.13 g·mol-1|
|Density||1.539 g/cm3 (-186°C)
1.2927 g/cm3 (0 °C)
1.266 g/cm3 (25 °C)
|Melting point||-111.61 °C (-168.90 °F; 161.54 K)|
|Boiling point||46.24 °C (115.23 °F; 319.39 K)|
|2.58 g/L (0 °C)
2.39 g/L (10 °C)
2.17 g/L (20 °C)
0.14 g/L (50 °C)
|Solubility||Soluble in alcohol, ether, benzene, oil, CHCl3, CCl4|
|Solubility in formic acid||4.66 g/100 g|
|Solubility in dimethyl sulfoxide||45 g/100 g (20.3 °C)|
|Vapor pressure||48.1 kPa (25 °C)
82.4 kPa (40 °C)
Refractive index (nD)
|Viscosity||0.436 cP (0 °C)
0.363 cP (20 °C)
|0 D (20 °C)|
Std enthalpy of
Gibbs free energy (?fG?)
Std enthalpy of
|Safety data sheet||See: data page|
|GHS signal word||Danger|
|H225, H315, H319, H361, H372|
|P210, P281, P305+351+338, P314
|Flash point||-43 °C (-45 °F; 230 K)|
|102 °C (216 °F; 375 K)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|3188 mg/kg (rat, oral)|
LC50 (median concentration)
|>1670 ppm (rat, 1 h)
15500 ppm (rat, 1 h)
3000 ppm (rat, 4 h)
3500 ppm (rat, 4 h)
7911 ppm (rat, 2 h)
3165 ppm (mouse, 2 h)
LCLo (lowest published)
|4000 ppm (human, 30 min)|
|US health exposure limits (NIOSH):|
|TWA 20 ppm C 30 ppm 100 ppm (30-minute maximum peak)|
|TWA 1 ppm (3 mg/m3) ST 10 ppm (30 mg/m3) [skin]|
IDLH (Immediate danger)
|Supplementary data page|
|Refractive index (n),
Dielectric constant (?r), etc.
|UV, IR, NMR, MS|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Carbon disulfide is a colorless volatile liquid with the formula CS2. The compound is used frequently as a building block in organic chemistry as well as an industrial and chemical non-polar solvent. It has an "ether-like" odor, but commercial samples are typically contaminated with foul-smelling impurities.
The reaction is analogous to the combustion of methane.
Global production/consumption of carbon disulfide is approximately one million tonnes, with China consuming 49%, followed by India at 13%, mostly for the production of rayon fiber. United States production in 2007 was 56,000 tonnes.
CS2 is highly flammable:
It is isoelectronic with carbon dioxide but it is more reactive toward nucleophiles and more easily reduced. These differences in reactivity can be attributed to the weaker ? donor-ability of the sulfido centers, which renders the carbon more electrophilic. Amines afford dithiocarbamates:
This reaction is the basis of the manufacture of regenerated cellulose, the main ingredient of viscose, rayon and cellophane. Both xanthates and the related thioxanthates (derived from treatment of CS2 with sodium thiolates) are used as flotation agents in mineral processing.
Sodium sulfide affords trithiocarbonate:
Carbon disulfide does not hydrolyze readily, although the process is catalyzed by an enzyme carbon disulfide hydrolase.
This conversion proceeds via the intermediacy of thiophosgene, CSCl2.
CS2 polymerizes upon photolysis or under high pressure to give an insoluble material called "Bridgman's black", named after the discoverer of the polymer, Percy Williams Bridgman. Trithiocarbonate (-S-C(S)-S-) linkages comprise, in part, the backbone of the polymer, which is a semiconductor.
It is also a valued intermediate in chemical synthesis of carbon tetrachloride. It is widely used in the synthesis of organosulfur compounds such as metam sodium, xanthates, dithiocarbamates, which are used in extractive metallurgy and rubber chemistry.
It can be used in fumigation of airtight storage warehouses, airtight flat storages, bins, grain elevators, railroad box cars, shipholds, barges and cereal mills. Carbon disulfide is also used as an insecticide for the fumigation of grains, nursery stock, in fresh fruit conservation and as a soil disinfectant against insects and nematodes.
Carbon disulfide is highly toxic. Typical recommended TLV is 30 mg/m3, 10 ppm. Symptoms include tingling or numbness, "cramps, muscle weakness, pain, distal sensory loss, and neurophysiological impairment".