Sulfolane Chemical Properties

Melting point:

20-26 °C (lit.)

Boiling point:

104 °C/0.2 mmHg (lit.) 285 °C (lit.)

Density 

1.261 g/mL at 25 °C (lit.)

vapor density 

4.2 (vs air)

vapor pressure 

0.01 mm Hg ( 20 °C)

refractive index 

n20/D 1.484(lit.)

Flash point:

330 °F

storage temp. 

Store below +30°C.

solubility 

>=100g/l soluble

form 

Liquid After Melting

color 

Clear yellow

Water Solubility 

soluble

FreezingPoint 

26℃

Sensitive 

Hygroscopic

Merck 

14,8955

BRN 

107765

Dielectric constant

44.0

Stability:

Stable. Combustible. Incompatible with strong oxidizing agents.

InChIKey

HXJUTPCZVOIRIF-UHFFFAOYSA-N

LogP

0 at 20℃

CAS DataBase Reference

126-33-0(CAS DataBase Reference)

NIST Chemistry Reference

Thiophene, tetrahydro-, 1,1-dioxide(126-33-0)

EPA Substance Registry System

Sulfolane (126-33-0)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

Safety Statements 

23-25

WGK Germany 

1

RTECS 

XN0700000

TSCA 

Yes

HS Code 

29349990

Hazardous Substances Data

126-33-0(Hazardous Substances Data)

Toxicity

LD50 orally in rats: 1.54 ml/kg (Smyth)

MSDS

• Language:English Provider:Sulfolane
• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Sulfolane Usage And Synthesis

Uses

Sulfolane is widely used as an industrial solvent, especially in the extraction of aromatic hydrocarbons from hydrocarbon mixtures and to purify natural gas. The first large scale commercial use of sulfolane, the sulfinol process, was first implemented by Shell Oil Company in March 1964 at the Person gas plant near Karnes City, Texas. The sulfinol process purifies natural gas by removing H2S, CO2, COS and mercaptans from natural gas with a mixture of alkanolamine and sulfolane.

Chemical Properties

colourless crystals

Chemical Properties

Sulfolane is a colorless oily liquid

Uses

Selective solvent for liquid-vapor extractions.

Uses

Process solvent for extractions of aromatics and for purification of acid gases.

Uses

Sulfolane is used in lithium-ion batteries.

Definition

ChEBI: Sulfolane is a member of the class of tetrahydrothiophenes that is tetrahydrothiophene in which the sulfur has been oxidised to give the corresponding sulfone. A colourless, high-boiling (285℃) liquid that is miscible with both water and hydrocarbons, it is used as an industrial solvent, particularly for the purification of hydrocarbon mixtures by liquid-vapour extraction. It has a role as a polar aprotic solvent. It is a sulfone and a member of tetrahydrothiophenes. It derives from a hydride of a tetrahydrothiophene.

Synthesis Reference(s)

Journal of the American Chemical Society, 63, p. 2939, 1941 DOI: 10.1021/ja01856a021

General Description

Colorless oily liquid with a weak oily odor. Solidifies (freezing point is 79°) and sinks on first contact with water, then mixes with water. F.

Air & Water Reactions

Water soluble.

Reactivity Profile

Mixing Sulfolane in equal molar portions with any of the following substances in a closed container caused the temperature and pressure to increase: chlorosulfonic acid and oleum [NFPA 1991]. With nitrating agents (nitronium tetrafluoroborate in Sulfolane) very highly exothermic reactions are known to occur, [J. Org. Chem., 1978, 43, 4677].

Hazard

Combustible. Toxic by ingestion.

Health Hazard

Very mildly irritating to the eyes.

Fire Hazard

Special Hazards of Combustion Products: Toxic, irritating gases may be generated in fires.

Industrial uses

Sulfolane is the most common commercially available sulfone solvent. The solvent, also known as tetrahydrothiophene-1,1-dioxide, is a colorless, highly polar liquid consisting of a fully hydrogenated five-member sulfur-carbon heterocyclic thiophene ring. The solvent is available as both anhydrous sulfolane and as sulfolane containing 3 wt% deionized water. Sulfolane is used as a reaction medium, as a solvent for a wide variety of organic chemicals and polymers, and as an extraction solvent.
Sulfolane is a very high boiling point, colorless liquid with a very high viscosity (10.3 centipoises) and medium surface tension value (35.5 dynes/cm).Sulfolane is miscible with water and many organic solvents.
Sulfolane is used to separate aromatic hydrocarbons from aliphatic hydrocarbons. The extraction process first developed by Shell Oil in 1959 and which is referred to as the "Sulfolane" process is used worldwide. The solvency of sulfolane for certain fatty acids and fatty acid esters is the basis for upgrading animal and vegetable fatty acids used in food products, paints, plastics, resins, and soaps.
Sulfolane is used to remove acidic components like hydrogen sulfide and carbon dioxide from gas feed stocks. Sulfolane is used as a polymerization solvent for the production of polysulfones, polysiloxanes, polyphenylene ethers, and other polymers. Sulfolane is said to increase the reaction rates, afford easier polymer purification, and improved thermal stability. Sulfolane is a solvent for dissolving a variety of polymers for use in the fiberspinning process.Cellulose and cellulose ester polymers can be plasticized with sulfolane to give improved flexibility and other physical property improvements. Other application areas that have used sulfolane include electronic and electrical uses, textile dye uses, curing of polysulfide sealant, and as a catalyst in certain synthetic reactions.

Potential Exposure

Sulfolane is used primarily as a process solvent for extraction of aromatics and for purification of acid gases. Used as a curing agent for epoxy resins, in medicine ash an antibacterial; fractionation of wood tars, tall oil, and other fatty acids; a component of hydraulic fluid; in textile finishing.

Carcinogenicity

Sulfolane was not mutagenic in bacterial assays with or without metabolic activation.

Shipping

UN3334 Aviation regulated liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material. Technical Name Required.

Purification Methods

prepared commercially by a Diels-Alder reaction of between 1,3-butadiene and sulfur dioxide, followed by Raney nickel hydrogenation. The principal impurities are water, 3-sulfolene, 2-sulfolene and 2-isopropyl sulfolanyl ether. It is dried by passage through a column of molecular sieves. Distil it under reduced pressure through a column packed with stainless steel helices. Again dry it with molecular sieves and distil. [Cram et al. J Am Chem Soc 83 3678 1961, Coetzee Pure Appl Chem 49 211 1977.] Alternatively, it is stirred at 50o, and small portions of solid KMnO4 are added until the colour persists during 1hour. Dropwise addition of MeOH then destroys the excess KMnO4; the solution is filtered, freed from potassium ions by passage through an ion-exchange column and dried under vacuum. It has also been distilled in a vacuum from KOH pellets. It is hygroscopic. [See Sacco et al. J Phys Chem 80 749 1976, J Chem Soc, Faraday Trans 1 73 1936 1977, 74 2070 1978, Trans Faraday Soc 62 2738 1966.] Coetzee has reviewed the methods of purification of sulfolane, and also the removal of impurities. [Coetzee in Recommended Methods of Purification of Solvents and Tests for Impurities, Coetzee Ed. Pergamon Press, 1982, Beilstein 17 I 5, 17 III/IV 37, 17/1 V 39.]

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Contact with nitronium tetrafluoroborate(1-) is potentially explosive.

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