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Tetramethylene sulfone

CAS 126-33-0C4H8O2SMW 120.17

Tetramethylene sulfone (CAS 126-33-0) — formula C4H8O2S, molecular weight 120.17; category organic chemicals.

Product Overview

CAS Number126-33-0
Molecular FormulaC4H8O2S
Molecular Weight120.17
Melting Point79 °F (USCG, 1999)
Boiling Point545 °F at 760 mmHg (USCG, 1999)
LogP-0.8
ApplicationsUses: Used as a solvent (aromatics extraction and polymerization), plasticizer, curing agent (epoxy resins) and therapeutic (antibacterial, convulsant, and radiation-protective agent), Also used for acid gas purification, fractionation (wood tars, tall oil, and other fatty acids), and textile finishing, [HSDB] Used in electronic applications, pharmaceutical manufacturing (solvent), jet printing inks (solvent), and medicines (believed to exist only in patent literature), [SIDS UNEP], Semiconductor Manufacturing [Category: Industry], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], Selective solvent for liquid-vapor extractions., Solvent for aromatics extraction, for acid gas purification., Extraction of aromatic hydrocarbons from oil refinery streams, polymerization solvent, plasticizer., Fractionation of wood tars, and other fatty acids, component of hydraulic fluid, textile finishing., For more Uses (Complete) data for SULFOLANE (6 total), please visit the HSDB record page., Industry Uses: Other, Solvent, Processing aids, specific to petroleum production, Intermediate, Cleaning agent, Consumer Uses: Solvent, Methods of Manufacturing: Prepared by catalytic hydrogenation of sulfolene oxides: Mahan, Fauske, US 2578565 (1951 to Phillips Petroleum)., ... From butadiene and sulfur dioxide ... Evans, Morris, US 2360859 (1944 to Shell)., Sulfolane ... is made by reacting sulfur dioxide and butadiene to form sulfolene, which is then hydrogenated to give sulfolane, Formulations, Preparations: Commercially available as anhydrous sulfolane and as sulfolane containing 3% wt deionized water, Grade: Technical, Sulfolane-W (97% 1, 1-tetrahydrothiophenedioxide and 3% water), U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 10, 000 - <50, 2021: 10, 2020: 10, Thiophene, tetrahydro-, 1, 1-dioxide is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., (1986) >1 million - 10 million pounds, (1990) >1 million - 10 million pounds, (1994) >1 million - 10 million pounds, For more U.S. Production (Complete) data for SULFOLANE (7 total), U.S. Imports: (1972) NEGLIGIBLE, U.S. Exports: (1972) NEGLIGIBLE, General Manufacturing Information: Petrochemical Manufacturing, All Other Basic Organic Chemical Manufacturing, All other Petroleum and Coal Products Manufacturing, Petroleum Refineries, Adhesive Manufacturing, Computer and Electronic Product Manufacturing, Pharmaceutical and Medicine Manufacturing, All Other Basic Inorganic Chemical Manufacturing, 1-dioxide: ACTIVE
CategoryOrganic Chemicals

Applications

Documented applications: Uses: Used as a solvent (aromatics extraction and polymerization), plasticizer, curing agent (epoxy resins) and therapeutic (antibacterial, convulsant, and radiation-protective agent), Also used for acid gas purification, fractionation (wood tars, tall oil, and other fatty acids), and textile finishing, [HSDB] Used in electronic applications, pharmaceutical manufacturing (solvent), jet printing inks (solvent), and medicines (believed to exist only in patent literature), [SIDS UNEP], Semiconductor Manufacturing [Category: Industry], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], Selective solvent for liquid-vapor extractions., Solvent for aromatics extraction, for acid gas purification., Extraction of aromatic hydrocarbons from oil refinery streams, polymerization solvent, plasticizer., Fractionation of wood tars, and other fatty acids, component of hydraulic fluid, textile finishing., For more Uses (Complete) data for SULFOLANE (6 total), please visit the HSDB record page., Industry Uses: Other, Solvent, Processing aids, specific to petroleum production, Intermediate, Cleaning agent, Consumer Uses: Solvent, Methods of Manufacturing: Prepared by catalytic hydrogenation of sulfolene oxides: Mahan, Fauske, US 2578565 (1951 to Phillips Petroleum)., ... From butadiene and sulfur dioxide ... Evans, Morris, US 2360859 (1944 to Shell)., Sulfolane ... is made by reacting sulfur dioxide and butadiene to form sulfolene, which is then hydrogenated to give sulfolane, Formulations, Preparations: Commercially available as anhydrous sulfolane and as sulfolane containing 3% wt deionized water, Grade: Technical, Sulfolane-W (97% 1, 1-tetrahydrothiophenedioxide and 3% water), U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 10, 000 - <50, 2021: 10, 2020: 10, Thiophene, tetrahydro-, 1, 1-dioxide is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., (1986) >1 million - 10 million pounds, (1990) >1 million - 10 million pounds, (1994) >1 million - 10 million pounds, For more U.S. Production (Complete) data for SULFOLANE (7 total), U.S. Imports: (1972) NEGLIGIBLE, U.S. Exports: (1972) NEGLIGIBLE, General Manufacturing Information: Petrochemical Manufacturing, All Other Basic Organic Chemical Manufacturing, All other Petroleum and Coal Products Manufacturing, Petroleum Refineries, Adhesive Manufacturing, Computer and Electronic Product Manufacturing, Pharmaceutical and Medicine Manufacturing, All Other Basic Inorganic Chemical Manufacturing, 1-dioxide: ACTIVE.

Technical Profile

What this product is

Tetramethylene sulfone is a carbon-based organic compound with CAS registry number 126-33-0 and molecular formula C4H8O2S (molecular weight 120.17), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 126-33-0

Its molecular formula C4H8O2S comprises 4 C, 8 H, 2 O, 1 S atoms.

Also known as: Tetramethylene sulfone · Sulfolane

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Tetramethylene sulfone?

The CAS registry number of Tetramethylene sulfone is 126-33-0.

What is the molecular formula and molecular weight of Tetramethylene sulfone?

Molecular formula C4H8O2S, molecular weight 120.17.

What other names is Tetramethylene sulfone known by?

It is also registered under: Tetramethylene sulfone, Sulfolane.

What are the documented applications of Tetramethylene sulfone?

Recorded applications: Uses: Used as a solvent (aromatics extraction and polymerization), plasticizer, curing agent (epoxy resins) and therapeutic (antibacterial, convulsant, and radiation-protective agent), Also used for acid gas purification, fractionation (wood tars, tall oil, and other fatty acids), and textile finishing, [HSDB] Used in electronic applications, pharmaceutical manufacturing (solvent), jet printing inks (solvent), and medicines (believed to exist only in patent literature), [SIDS UNEP], Semiconductor Manufacturing [Category: Industry], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], Selective solvent for liquid-vapor extractions., Solvent for aromatics extraction, for acid gas purification., Extraction of aromatic hydrocarbons from oil refinery streams, polymerization solvent, plasticizer., Fractionation of wood tars, and other fatty acids, component of hydraulic fluid, textile finishing., For more Uses (Complete) data for SULFOLANE (6 total), please visit the HSDB record page., Industry Uses: Other, Solvent, Processing aids, specific to petroleum production, Intermediate, Cleaning agent, Consumer Uses: Solvent, Methods of Manufacturing: Prepared by catalytic hydrogenation of sulfolene oxides: Mahan, Fauske, US 2578565 (1951 to Phillips Petroleum)., ... From butadiene and sulfur dioxide ... Evans, Morris, US 2360859 (1944 to Shell)., Sulfolane ... is made by reacting sulfur dioxide and butadiene to form sulfolene, which is then hydrogenated to give sulfolane, Formulations, Preparations: Commercially available as anhydrous sulfolane and as sulfolane containing 3% wt deionized water, Grade: Technical, Sulfolane-W (97% 1, 1-tetrahydrothiophenedioxide and 3% water), U.S. Production: 2023: 1, 000, 000 - <5, 000 lb, 2022: 10, 000 - <50, 2021: 10, 2020: 10, Thiophene, tetrahydro-, 1, 1-dioxide is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., (1986) >1 million - 10 million pounds, (1990) >1 million - 10 million pounds, (1994) >1 million - 10 million pounds, For more U.S. Production (Complete) data for SULFOLANE (7 total), U.S. Imports: (1972) NEGLIGIBLE, U.S. Exports: (1972) NEGLIGIBLE, General Manufacturing Information: Petrochemical Manufacturing, All Other Basic Organic Chemical Manufacturing, All other Petroleum and Coal Products Manufacturing, Petroleum Refineries, Adhesive Manufacturing, Computer and Electronic Product Manufacturing, Pharmaceutical and Medicine Manufacturing, All Other Basic Inorganic Chemical Manufacturing, 1-dioxide: ACTIVE.

Which category does Tetramethylene sulfone belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for Tetramethylene sulfone (CAS 126-33-0), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number126-33-0
PubChem CID31347
Molecular formulaC4H8O2S
IUPAC namethiolane 1,1-dioxide
UNII (FDA)Y5L06AH4G5

Computed descriptors

Molecular Weight120.17
XLogP3-0.8
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass120.02450067
Monoisotopic Mass120.02450067
Topological Polar Surface Area42.5
Heavy Atom Count7

Physicochemical values on record

Boiling Point545 °F at 760 mmHg (USCG, 1999)
Boiling Point285 °C
Boiling Point285 °C @760 [mm Hg]
Melting Point79 °F (USCG, 1999)
Melting Point27.4-27.8 °C
Flash Point330 °F (USCG, 1999)
Flash Point177 °C (350 °F) (OPEN CUP)
Density1.2606 at 30 °C/4 °C
Density1.261 @25 °C
Vapor Pressure0.0062 [mmHg]

Documented uses on record

    Used as a solvent (aromatics extraction and polymerization), plasticizer, curing agent (epoxy resins) and therapeutic (antibacterial, convulsant, and radiation-protective agent); Also used for acid gas purification, fractionation (wood tars, tall oil, and other fatty acids), and textile finishing; [HSDB] Used in electronic applications, pharmaceutical manufacturing (solvent), jet printing inks (solvent), and medicines (believed to exist only in patent literature); [SIDS UNEP]Semiconductor Manufacturing [Category: Industry]

    Synonyms and trade names

    SULFOLANE; 126-33-0; Tetrahydrothiophene 1,1-dioxide; Tetramethylene sulfone; Sulfolan; 1,1-Dioxothiolan; Sulpholane; Thiophene, tetrahydro-, 1,1-dioxide; thiolane 1,1-dioxide; Sulfalone; Sulphoxaline; Dioxothiolan; Thiophan sulfone; Bondelane A; Bondolane A; Thiophane dioxide

    GHS hazard classification

    Reported hazard statementsH302, H360 (22.7%), H320, H361

    H302: Harmful if swallowed [Warning Acute toxicity, oral]

    P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)

    What the public record says

    Tetramethylene sulfone · CAS 126-33-0 · C4H8O2S. UNII Y5L06AH4G5. Boiling Point: 545 °F at 760 mmHg (USCG, 1999); Boiling Point: 285 °C; Boiling Point: 285 °C @760 [mm Hg].

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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