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Carbon Disulfide

CS2 inorganic

Properties

StateLiquid (colorless to pale yellow, volatile, with sweet odor when pure)
ColorColorless (pure); pale yellow (commercial grade)
SolubilitySlightly soluble in water (2.2 g/L at 20°C); miscible with ethanol, ether, benzene, and chloroform
Melting Point-111°C
Boiling Point46°C

About Carbon Disulfide

Carbon disulfide is the sulfur analog of CO2 — same linear S=C=S geometry, sp-hybridized carbon, zero molecular dipole — but the chemistry could not be more different. Where CO2 sublimes at −78.5 °C, CS2 is a volatile liquid (bp 46 °C) because the larger, more polarizable sulfur atoms throw far stronger London dispersion forces between molecules. CS2 has a flash point of −30 °C and an autoignition temperature of just 90 °C, lower than any other common solvent — a hot steam pipe is enough to ignite the vapor — which is why every safety induction for CS2 work emphasizes that there are essentially no acceptable ignition sources in the same room. As a solvent, CS2 dissolves elemental sulfur and white phosphorus better than almost anything else, which makes it indispensable when those allotropes need to be handled in solution. Its largest industrial use, however, is the viscose process: alkali cellulose (wood pulp slurried in NaOH) reacts with CS2 to form sodium cellulose xanthate, which is dissolved in dilute caustic to give the orange viscose dope, then extruded through a spinneret into an acid bath where the xanthate hydrolyzes back to cellulose as rayon fiber. World rayon production still consumes hundreds of thousands of tonnes of CS2 per year. CS2 is also the precursor for dithiocarbamate fungicides — maneb, mancozeb, ziram — made by reaction with primary amines and base, and it is the historical route to CCl4 and tetraethylthiuram disulfide (Antabuse). The catch is severe neurotoxicity: chronic exposure causes peripheral neuropathy, parkinsonism, and accelerated atherosclerosis, and the viscose industry has the documented occupational-disease history to prove it.

Where you'll encounter it

Every viscose rayon plant in the world is essentially a CS2 facility, and the orange-yellow tint of fresh viscose dope on a textile floor is unmistakable. In an organic teaching lab, the small bottle of CS2 in the flammables cabinet is what you reach for when you need to dissolve a few hundred milligrams of S8 for a sulfur transfer reaction or a bromonium-ion trapping experiment, and you handle it in a fume hood with no hot plates running and the bench cleared of friable material. In rubber chemistry, CS2 is the synthetic root of the entire dithiocarbamate accelerator family that makes tire vulcanization possible at industrial scale. Pure CS2 has a sweet, ethereal odor — almost pleasant — but technical grades stink of carbonyl sulfide and H2S impurities, which is the warning that something has gone off.

Common Uses

  • Cellulose xanthate intermediate in viscose rayon and cellophane manufacture (largest single use)
  • Solvent for elemental sulfur and white phosphorus in laboratory work
  • Synthesis of dithiocarbamate fungicides (maneb, mancozeb, ziram) and rubber accelerators
  • Precursor for carbon tetrachloride and tetraethylthiuram disulfide (Antabuse)
  • Flotation collector in nonferrous mining for differential separation of sulfide ores

Safety Information

Extreme fire hazard: flash point −30 °C, autoignition 90 °C, explosive limits 1 to 50 percent in air — among the widest of any common solvent. Vapors are 2.6 times denser than air and pool at floor level. Treat steam pipes, light bulbs, and electrical contacts as ignition sources. Chronic neurotoxicity is the dominant occupational concern: ACGIH TLV-TWA 1 ppm, OSHA PEL 20 ppm (8-hour TWA), with documented peripheral neuropathy, parkinsonism, accelerated atherosclerosis, and reproductive toxicity from long-term low-level exposure in viscose-rayon workers. GHS: H225 (extremely flammable), H315/H319/H336, H361 (reproductive toxicity Cat. 2), H372 (target-organ toxicity, repeated exposure). Use only in a hood with explosion-rated equipment.

This safety summary is for educational reference only and may not be complete. It is not a substitute for Safety Data Sheets (SDS), medical advice, or professional chemical safety guidance. Always consult appropriate SDS and qualified professionals before handling chemicals.

Constituent Elements

Frequently Asked Questions

What is the molar mass of carbon disulfide?
CS2 is 76.141 g/mol: one carbon at 12.011 and two sulfurs at 2 × 32.06 = 64.12. The density of liquid CS2 is 1.26 g/mL at 20 °C, so a 100 mL bottle weighs 126 g and contains about 1.66 mol — relevant when you are scaling a Friedel–Crafts thiation or a sulfur-dissolution prep where stoichiometry is tight.
Why is carbon disulfide important for rayon production?
The viscose process needs to get cellulose into solution without degrading it, and free cellulose dissolves in essentially nothing benign. The trick is to derivatize: alkali cellulose (cellulose-OH treated with NaOH) reacts with CS2 to form the cellulose xanthate, R-O-CS2⁻ Na⁺, which is soluble in dilute caustic. The orange xanthate solution is the viscose. Extrude that through a spinneret into a sulfuric acid / sodium sulfate bath and the xanthate hydrolyzes back to cellulose as fine rayon filaments. CS2 is the only practical reagent that does this transformation at industrial scale.
How is carbon disulfide structurally related to carbon dioxide?
CS2 (S=C=S) and CO2 (O=C=O) share the same linear geometry, sp-hybridized central carbon, and zero net dipole. The huge difference in physical state — CO2 sublimes at −78.5 °C, CS2 boils at +46 °C — comes down to London dispersion. Sulfur is much more polarizable than oxygen, the electron clouds distort more easily, and the resulting instantaneous-dipole interactions hold CS2 molecules together in a liquid phase well above room temperature. Same shape, very different intermolecular forces.