| Weight | 120.173 g/mol |
|---|---|
| Formula | C4H8O2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
SULFOLANE (126-33-0)
Score:
#746 in Physics
,
#2168 in Chemistry
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- Liquidliquid equilibria of multi-component systems including n-hexane, n-octane, benzene, toluene, xylene and sulfolane at 298.15 K and atmospheric pressure (Fluid Phase Equilibria, 2000)
- LiquidLiquid Equilibria of Ternary and Quaternary Systems Including Cyclohexane, 1-Heptene, Benzene, Toluene, and Sulfolane at 298.15 K (Journal of Chemical & Engineering Data, 2000)
- Measurement of Activity Coefficients at Infinite Dilution Using GasLiquid Chromatography. 5. Results for N-Methylacetamide, N,N-Dimethylacetamide, N,N-Dibutylformamide, and Sulfolane as Stationary Phases (Journal of Chemical & Engineering Data, 1997)
- Liquid-liquid equilibria of the ternary mixtures with sulfolane at 303.15 K (Journal of Chemical & Engineering Data, 1996)
- Catalytic pyrolysis of cellulose in sulfolane with some acidic catalysts (Journal of Wood Science, 2007)
- Excess Molar Volumes and Viscosities of Binary Mixtures of Sulfolane with Benzene, Toluene, Ethylbenzene, p-Xylene, o-Xylene, and m-Xylene at 303.15 and 323.15 K and Atmospheric Pressure (Journal of Chemical & Engineering Data, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B -
SMILESC1CCS(=O)(=O)C1
-
InChIKeyHXJUTPCZVOIRIF-UHFFFAOYSA-N
- Pubchem - SULFOLANE
- Wikipedia - sulfolane
Sulfolane (also tetramethylene sulfone, systematic name: 2,3,4,5-tetrahydrothiophene-1,1-dioxide) is an organosulfur compound, formally a cyclic sulfone, with the formula (CH2)4SO2. It is a colorless liquid commonly used in the chemical industry as a solvent for extractive distillation and chemical reactions. Sulfolane was originally developed by the Shell Oil Company in the 1960s as a solvent to purify butadiene.
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