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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
Molecular Formula C4H8O2S
Molecular Weight 120.17
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Infrared matrix-assisted laser desorption/ionization of polycyclic aromatic hydrocarbons with a sulfolane matrix.
2001
Phenylene ethynylene diazonium salts as potential self-assembling molecular devices.
2001 Apr 5
Ion solvation and association in LiClO4/sulfolane solution: a vibrational spectroscopic and molecular orbital study.
2001 Jul
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 Feb
A review of analytical methods for the determination of sulfolane and alkanolamines in environmental studies.
2002 Jan-Feb
Recovery of acetic acid from waste streams by extractive distillation.
2003
Preparation of a fludarabine intermediate via selective alkylation of 2-fluoroadenine.
2006
Sulfolane attenuation by surface and subsurface soil matrices.
2006
Semi-quantitative immunohistochemical analysis of male rat-specific alpha2u-globulin accumulation for chemical toxicity evaluation.
2006 Feb
Ring inversion, structural stability and vibrational assignments of sulfolane c-C4H8SO2 and 3-sulfolene c-C4H6SO2.
2008 Oct
Conformation and hydrogen bonding for the bicyclic compound 3-thiabicyclo[3.2.0]heptane-6,7-dicarboxylic acid 3,3-dioxide.
2008 Sep
Ionic liquids as superior solvents for headspace gas chromatography of residual solvents with very low vapor pressure, relevant for pharmaceutical final dosage forms.
2009 Aug 7
Physicochemical properties and activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-decyl-3-methylimidazolium tetracyanoborate.
2010 Dec 16
Graphene fluoride: a stable stoichiometric graphene derivative and its chemical conversion to graphene.
2010 Dec 20
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 1-(3-hydroxypropyl)pyridinium trifluorotris(perfluoroethyl)phosphate.
2010 May 27
Ion mobility-mass spectrometry of phosphorylase B ions generated with supercharging reagents but in charge-reducing buffer.
2010 Nov 7
Effects of supercharging reagents on noncovalent complex structure in electrospray ionization from aqueous solutions.
2010 Oct
New reagents for enhanced liquid chromatographic separation and charging of intact protein ions for electrospray ionization mass spectrometry.
2010 Sep 1
Patents

Patents

04167568
1
04167570
1
04213993
1
04409228
1
04438141
2
04473701
1
04555370
1
04572912
1
04590271
1
04645863
1
04816591
1
04873236
2
04960905
1
04973772
1
05227531
1
05380729
4
05436257
1
05486610
1
05616537
1
05637706
2
05700820
1
05763718
3
05998627
1
06441201
1
06514992
1
07169924
1
07238699
4
07582626
1
08217056
1
08268843
1
08273926
1
08278442
1
08415469
3
08685991
2
08742132
1
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:05:47 GMT 2023
Edited
by admin
on Fri Dec 15 15:05:47 GMT 2023
Record UNII
Y5L06AH4G5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFOLANE
HSDB   MI  
Systematic Name English
TETRAMETHYLENE SULFONE
Systematic Name English
NSC-46443
Code 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 Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
PUBCHEM
31347
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
MESH
C013693
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
EPA CompTox
DTXSID3027037
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
NSC
46443
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
MERCK INDEX
m10355
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY Merck Index
CAS
126-33-0
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
CHEBI
74794
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
HSDB
122
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-783-1
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
RS_ITEM_NUM
1601769
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
WIKIPEDIA
SULFOLANE
Created by admin on Fri Dec 15 15:05:47 GMT 2023 , Edited by admin on Fri Dec 15 15:05:47 GMT 2023
PRIMARY
NIH
NCATS
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