Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 6498Generated: October 23, 2026

3-Sulfolene

BUTADIENE SULFONE · SULFOLENE · 2,5-DIHYDROTHIOPHENE-1,1-DIOXIDE · Sulfol-3-ene · beta-Sulfolene · NCI-C04557 · 3-Sulfolene · 3-SULPHOLENE

https://huagongshe.com/en/chemical/6498

3-Sulfolene molecular structure

Identifiers & Physical Properties

CAS No.20966-34-1
Molecular formulaC4H6O2S
Average molar mass118.16 g/mol
Monoisotopic mass118.00885043 g/mol
SMILESO=S1(=O)CC=CC1
InChIKeyMBDNRNMVTZADMQ-UHFFFAOYSA-N
PubChem CID6498
ChEMBLCHEMBL3182104
ChEBICHEBI:194619
EC No.201-059-7
DTXSIDDTXSID6021294

Chemical & Physical Properties

XLogP-0.2
Topological polar surface area42.5
Hydrogen bond donors0
Hydrogen bond acceptors2
Rotatable bonds0
Heavy atoms7
Formal charge0
Complexity156
Chemical classesOther Classes -> Sulfur Compounds
SpringerMaterials PropertiesCoriolis coupling
LogP (partition coefficient)log Kow= -1.448
Density1.3 at 59 °F (NTP, 1992) - Denser than waterwill sink
Color/FormCRYSTALS
Solubility50 to 100 mg/mL at 61 °F (NTP, 1992)SOL IN WATER, ORGANIC SOLVENTSPARTIALLY SOL IN ACETONE & TOLUENE130g/lSoluble in water, ethanol, benzene, ether.
Flash point235 °F (NTP, 1992)113 °C>230 °F
Boiling pointDecomposes (NTP, 1992)190.71°C (rough estimate)
Melting point147 to 149 °F (NTP, 1992)64-65.5 °C65-66 °C(lit.)
Vapor pressure0.34 [mmHg]
Physical Description3-sulfolene appears as white crystals with a pungent odor. Melting point 64-65.5 °C.Large CrystalsWhite solid with pungent odor[CAMEO] Off-white crystalline solid[Alfa Aesar MSDS]
Bulk density840kg/m3
Refractive index1.4765 (estimate)
Storage conditionsStore below +30°C.
Physical statePowder
ColorYellow to orange or light brown
Merck14,8956
BRN107004
Henry's law constant2.3×100 mol/(m3Pa) at 25℃, HSDB (2015)
StabilityStable, but decomposes above the melting point. Combustible. Incompatible with strong oxidizing agents.
InChI1S/C4H6O2S/c5-7(6)3-1-2-4-7/h1-2H,3-4H2
InChIKeyMBDNRNMVTZADMQ-UHFFFAOYSA-N
SMILESO=S1(=O)CC=CC1
Toxicology and CarcinogenesisBioassay of 3-Sulfolene for Possible Carcinogenicity (CASRN 77-79-2)
CAS DataBase Reference77-79-2(CAS DataBase Reference)
EWG's Food Scores1
FDA UNIIZ6003L44MN
EPA Substance Registry System3-Sulfolene (77-79-2)
UNSPSC Code12352119
NACRESNA.22
GHS pictogramGHS07
Signal wordWarning
GHS hazard statementsH319
GHS precautionary statementsP264-P280-P305+P351+P338-P337+P313
Personal protective equipment (PPE)dust mask type N95 (US), Eyeshields, Gloves
Hazard symbolsXi
Risk statements (R)41
Safety statements (S)26-37/39
UN transport numberUN 3335
Water hazard class (WGK)1
RTECS numberXM9100000
TSCA inventory statusTSCA listed
Customs code2934 99 90
Storage class11 - Combustible Solids
Hazard classEye Irrit. 2
Hazardous substances data77-79-2(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 2547 mg/kg LD50 dermal Rabbit > 5000 mg/kg

Safety & Regulations

GHS classificationDangerH318 (55.3%): Causes serious eye damage [Danger Serious eye damage/eye irritation]P264+P265, P280, P305+P351+P338, P305+P354+P338, P317, and P337+P317 (click each P-code to see the statement)Aggregated GHS information provided per 76 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.H318 (100%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
Regulatory informationThiophene, 2,5-dihydro-, 1,1-dioxide is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Thiophene, 2,5-dihydro-, 1,1-dioxide are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Thiophene, 2,5-dihydro-, 1,1-dioxide: Does not have an individual approval but may be used under an appropriate group standard
Fire hazardsThis chemical is combustible. (NTP, 1992)
Health hazardsSYMPTOMS: Symptoms of exposure to this compound include headache, nausea, tiredness, gastrointestinal upset, tremors and convulsions. It is irritating to the eyes and prolonged exposure may cause skin irritation.
Hazards summaryNot mutagenic to four strains of Salmonella typhimuriumNo evidence of carcinogenicity in mice or rats[HSDB] A severe eye irritant[CAMEO] Not irritating to rabbit skinIrritating to rabbit eyesNot sensitizing in guinea pig maximization test[EPA HPVIS] Causes somnolence, tremor, convulsions, and damage to esophagus and salivary glands in oral lethal-dose studies of rats and mice[RTECS] An irritantMay cause serious eye injury[Alfa Aesar MSDS]
Reactive groupHydrocarbons, Aliphatic Unsaturated
Special ReportsDHEW/NCIBioassay of 3-Sulfolene for Possible Carcinogenicity (1978) Technical Rpt Series No. 102 DHEW Pub No. (NIH) 78-1352
TSCA requirementsPursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Sulfolene is included on this list.Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, use, and exposure to EPA as cited in the preamble of the 51 FR 41329.
Reactivity Profile3-SULFOLENE is a sulfone. May be sensitive to elevated temperatures. May react with strong reducing agents to generate toxic and flammable hydrogen sulfide.
Air and Water ReactionsWater soluble.
Hazard Classes and CategoriesEye Dam. 1 (55.3%)Eye Dam. 1 (100%)
Fire fightingFires involving this compound can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. A water spray may also be used. (NTP, 1992)
First aidEYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
Nonfire spill responseSMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
Personal Protective Equipment (PPE)RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)
Environmental fateTERRESTRIAL FATE: An estimated Koc value of 4(1) for 2,5-dihydrothiophene 1,1-dioxide indicates high mobility in soil(2) and leaching may occur. No data were located which suggest biodegradation is an important terrestrial fate process of 2,5-dihydrothiophene 1,1-dioxide(SRC).AQUATIC FATE: Based on an estimated Koc value of 4 and an estimated BCF value of 4.7(1), 2,5-dihydrothiophene 1,1-dioxide is not expected to adsorb to sediment or bioconcentrate in aquatic organisms. A volatilization half-life of 225 days has been estimated for a model river (one meter deep) suggesting slow volatilization from shallow rivers(1,SRC). No data were located which suggest biodegradation is an important environmental fate process of 2,5-dihydrothiophene 1,1-dioxide in aquatic systems(SRC).ATMOSPHERIC FATE: Vapor phase 2,5-dihydrothiophene 1,1-dioxide is degraded in the ambient atmosphere by reaction with photochemically formed hydroxyl radicalsthe half-life for this reaction in air can be estimated to be about 6.7 hrs(1,SRC). Vapor phase 2,5-dihydrothiophene 1,1-dioxide is also rapidly degraded by reaction with ozone in the tropospherethe half-life for this reaction in air can be estimated to be about 1.4 hrs(1,SRC).
Adverse effectsNeurotoxin - Other CNS neurotoxin
Ongoing Test StatusThe following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=77-79-2]
Soil Adsorption/MobilityBased on an estimated log Kow of -1.448(2) the Koc for 2,5-dihydrothiophene 1,1-dioxide can be estimated to be about 4 using a recommended regression derived equation(1,SRC). This Koc value suggests that 2,5-dihydrothiophene 1,1-dioxide will have very high mobility in soil and will leach(3).
Artificial Pollution Sources2,5-Dihydrothiophene 1,1-dioxide is used as a specialty solvent in petroleum refining and during the manufacture of sulfolane which is also a solvent in petroleum refining(1)it may be released to the environment in waste streams from its production and use(SRC).
Carcinogen Classification3-SulfoleneTR-102: Bioassay of 3-Sulfolene for Possible Carcinogenicity (CASRN 77-79-2) (1978 )03/06/78No Evidence
Environmental BioconcentrationBased on an estimated log Kow of -1.448(2) the BCF for 2,5-dihydrothiophene 1,1-dioxide can be estimated to be 4.7 using a recommended regression derived equation(1,SRC). This BCF value suggests that 2,5-dihydrothiophene 1,1-dioxide would not bioconcentrate in aquatic organisms(SRC).
Volatilization from Water/SoilThe Henry's Law constant for 2,5-dihydrothiophene 1,1-dioxide can be estimated to be 4.3X10-6 atm-cu m/mole at 25 °C using a chemical structure estimation method(1). This value of Henry's Law constant suggests that 2,5-dihydrothiophene 1,1-dioxide may slowly volatilize from water(2). Based on this Henry's Law constant value, the volatilization half-life of 2,5-dihydrothiophene 1,1-dioxide from a model river 1 m deep flowing 1 m/sec with a wind velocity of 3 m/sec has been estimated to be approximately 225 days(2,SRC).
Non-Human Toxicity Excerpts3-Sulfolene was tested for mutagenicity in the Salmonella/microsome preincubation assay using a protocol approved by the National Toxicology Program. 3-Sulfolene was tested over a wide range of doses (0, 100, 333, 1000, 3333, and 10,000 ug/plate) in four Salmonella typhimurium strains (TA98, TA100, TA1535, and TA1537) in the presence and absence of Aroclor-induced rat or hamster liver S9. 3-Sulfolene was negative in these tests and the highest ineffective dose level tested in any Salmonella tester strain was 10,000 ug/plate.
Environmental Abiotic DegradationThe rate constant for the vapor-phase reaction of 2,5-dihydrothiophene 1,1-dioxide with photochemically produced hydroxyl radicals can be estimated to be 5.74X10-11 cu cm/molecule-sec at 25 °C which corresponds to an atmospheric half-life of about 6.7 hrs at an atmospheric concn of 5X10+5 hydroxyl radicals per cu cm(1). The rate constant for the vapor-phase reaction of 2,5-dihydrothiophene 1,1-dioxide with ozone in the troposphere can be estimated to be 2X10-16 cu cm/molecule-sec at 25 °C which corresponds to a half-life of about 1.4 hrs at an atmospheric concn of 7X10+11 molecules per cu cm(1-2,SRC).
Probable Routes of Human Exposure2,5-Dihydrothiophene 1,1-dioxide is used as a specialty solvent in petroleum refining and during the manufacture of sulfolane which is also a solvent in petroleum refining(1). In occupational settings, workers may be exposed to 2,5-dihydrothiophene 1,1-dioxide by inhalation of vapors and through eye and skin contact(SRC).
Environmental Fate/Exposure Summary2,5-Dihydrothiophene 1,1-dioxide may be released to the environment in waste streams from oil refineries during its production and use. If released to soil, 2,5-dihydrothiophene 1,1-dioxide is expected to leach (estimated Koc of 4). No data were located which suggest biodegradation is an important fate process of 2,5-dihydrothiophene 1,1-dioxide in soil or water. If released to water, adsorption to sediment and bioconcentration in aquatic organisms are not expected to be environmentally important removal processes of 2,5-dihydrothiophene 1,1-dioxide. A volatilization half-life of 225 days has been estimated for a model river (one meter deep). If released to the atmosphere, vapor-phase 2,5-dihydrothiophene 1,1-dioxide is expected to degrade by reaction with photochemically produced hydroxyl radicals (estimated half-life of 6.7 hrs). Vapor phase 2,5-dihydrothiophene 1,1-dioxide may also be rapidly degraded by reaction with ozone in the tropospherethe half-life for this reaction in air can be estimated to be about 1.4 hrs. In occupational settings, exposure to 2,5-dihydrothiophene 1,1-dioxide may occur through inhalation of vapors and through eye and skin contact. (SRC)
Personal protective equipment (PPE)dust mask type N95 (US), Eyeshields, Gloves
Water hazard class (WGK)1
TSCA inventory statusTSCA listed
RTECS numberXM9100000
UN transport numberUN 3335
Customs code2934 99 90
ToxicityLD50 orally in Rabbit: 2547 mg/kg LD50 dermal Rabbit > 5000 mg/kg
Risk statements (R)41
Signal wordWarning
GHS pictogramGHS07
Hazard symbolsXi
Safety statements (S)26-37/39
Storage class11 - Combustible Solids
GHS hazard statementsH319
Hazard classEye Irrit. 2
GHS precautionary statementsP264-P280-P305+P351+P338-P337+P313
Hazardous substances data77-79-2(Hazardous Substances Data)

Applications & Uses

Uses

3-SULFOLENE was used in the isomerization of isoprene rubber. Sulfolene is also an analytical reagent used in the investigation of role of adducts in protein supercharging with sulfolane.

Uses

It is a source of cisoid butadiene for Diels-Alder reactions. This chemical is also a convenient source of sulfur dioxide. It is a solvent used in the petrochemical industry for the extraction of aromatics from hydrocarbon streams.