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Details

Stereochemistry ACHIRAL
Molecular Formula C4H8O2S
Molecular Weight 120.17
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFOLANE

SMILES

O=S1(=O)CCCC1

InChI

InChIKey=HXJUTPCZVOIRIF-UHFFFAOYSA-N
InChI=1S/C4H8O2S/c5-7(6)3-1-2-4-7/h1-4H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Graphene fluoride: a stable stoichiometric graphene derivative and its chemical conversion to graphene.
2010-12-20
Physicochemical properties and activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-decyl-3-methylimidazolium tetracyanoborate.
2010-12-16
Ion mobility-mass spectrometry of phosphorylase B ions generated with supercharging reagents but in charge-reducing buffer.
2010-11-07
Effects of supercharging reagents on noncovalent complex structure in electrospray ionization from aqueous solutions.
2010-10
New reagents for enhanced liquid chromatographic separation and charging of intact protein ions for electrospray ionization mass spectrometry.
2010-09-01
Effects of electrochemical reduction reactions on the biodegradation of recalcitrant organic compounds (ROCs) and bacterial community diversity.
2010-08
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 1-(3-hydroxypropyl)pyridinium trifluorotris(perfluoroethyl)phosphate.
2010-05-27
Liquid-phase synthesis of cyanuric acid from urea.
2010-03-16
New reagents for increasing ESI multiple charging of proteins and protein complexes.
2010-01
Acid-, water- and high-temperature-stable ruthenium complexes for the total catalytic deoxygenation of glycerol to propane.
2009-10-05
Ionic liquids as superior solvents for headspace gas chromatography of residual solvents with very low vapor pressure, relevant for pharmaceutical final dosage forms.
2009-08-07
Synthesis of ruthenium carbonyl complexes with phosphine or substituted Cp ligands, and their activity in the catalytic deoxygenation of 1,2-propanediol.
2009-07-20
[Purification of sulfolene and its UV-Vis and FTIR spectral analysis].
2009-02
Chemical hydrophobicity and uptake by plant roots.
2009-01-15
Ring inversion, structural stability and vibrational assignments of sulfolane c-C4H8SO2 and 3-sulfolene c-C4H6SO2.
2008-10
Conformation and hydrogen bonding for the bicyclic compound 3-thiabicyclo[3.2.0]heptane-6,7-dicarboxylic acid 3,3-dioxide.
2008-09
Tandem Friedel-Crafts annulation to novel perylene analogues.
2008-08-15
Limiting conductances of electrolytes and the walden product in mixed solvents in a phenomenological approach.
2008-06-12
Inhibition of acid-catalyzed depolymerization of cellulose with boric acid in non-aqueous acidic media.
2008-02-04
Semi-quantitative immunohistochemical analysis of male rat-specific alpha2u-globulin accumulation for chemical toxicity evaluation.
2006-02
Preparation of a fludarabine intermediate via selective alkylation of 2-fluoroadenine.
2006
Sulfolane attenuation by surface and subsurface soil matrices.
2006
Recovery of acetic acid from waste streams by extractive distillation.
2003
A review of analytical methods for the determination of sulfolane and alkanolamines in environmental studies.
2002-03-07
Structure of N,4-dinitroaniline and its complex with sulfolane at 85 K; on the proton donor-acceptor affinity of the primary nitramine (HNNO2) group.
2002-02
The enhancement of PCR amplification by low molecular-weight sulfones.
2001-08-22
Ion solvation and association in LiClO4/sulfolane solution: a vibrational spectroscopic and molecular orbital study.
2001-07
Nutrient stimulation of sulfolane biodegradation in a contaminated soil from a sour natural gas plant and in a pristine soil.
2001-06
Phenylene ethynylene diazonium salts as potential self-assembling molecular devices.
2001-04-05
Infrared matrix-assisted laser desorption/ionization of polycyclic aromatic hydrocarbons with a sulfolane matrix.
2001
Patents
Name Type Language
NSC-46443
Preferred Name English
SULFOLANE
HSDB   MI  
Systematic Name English
TETRAMETHYLENE SULFONE
Systematic Name English
SULFOLANE [HSDB]
Common Name English
SULFOLANE [MI]
Common Name English
SULFOLANE [USP-RS]
Common Name English
THIOPHENE, TETRAHYDRO-, 1,1-DIOXIDE
Systematic Name English
TETRAHYDROTHIOPHENE 1,1-DIOXIDE
Systematic Name English
SULFOLAN
Common Name English
Code System Code Type Description
FDA UNII
Y5L06AH4G5
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
PUBCHEM
31347
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
MESH
C013693
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID3027037
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
SMS_ID
300000053584
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
NSC
46443
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
MERCK INDEX
m10355
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY Merck Index
CAS
126-33-0
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
CHEBI
74794
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
HSDB
122
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-783-1
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
RS_ITEM_NUM
1601769
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY
WIKIPEDIA
SULFOLANE
Created by admin on Mon Mar 31 17:46:17 GMT 2025 , Edited by admin on Mon Mar 31 17:46:17 GMT 2025
PRIMARY