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Details

Stereochemistry ACHIRAL
Molecular Formula C4H10S2
Molecular Weight 122.252
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIETHYL DISULFIDE

SMILES

CCSSCC

InChI

InChIKey=CETBSQOFQKLHHZ-UHFFFAOYSA-N
InChI=1S/C4H10S2/c1-3-5-6-4-2/h3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C4H10S2
Molecular Weight 122.252
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Copper coated silica nanoparticles for odor removal.
2010-10-19
Variation of some fermentative sulfur compounds in Italian "millesime" classic sparkling wines during aging and storage on lees.
2010-09-08
Characterization of the kringle fold and identification of a ubiquitous new class of disulfide rotamers.
2009-11
Thermodynamic role of glutathione oxidation by peroxide and peroxybicarbonate in the prevention of Alzheimer's disease and cancer.
2009-08-13
Alternative reagents for chemical noise reduction in liquid chromatography-mass spectrometry using selective ion-molecule reactions.
2009-01
Treatment of waste gas containing diethyldisulphide (DEDS) in a bench scale biofilter.
2009-01
Aging effects and grape variety dependence on the content of sulfur volatiles in wine.
2007-12-26
Comparison of three lychee cultivar odor profiles using gas chromatography-olfactometry and gas chromatography-sulfur detection.
2007-03-07
Aquasonolysis of thioethers.
2006-05
Transferable potentials for phase equilibria. 8. United-atom description for thiols, sulfides, disulfides, and thiophene.
2005-12-22
Sensitive quantification of sulfur compounds in wine by headspace solid-phase microextraction technique.
2005-07-08
Ultrasonic cleavage of thioethers.
2005-04-28
Comparative haemolytic activity of bis(phenylmethyl) disulphide, bis(phenylethyl) disulphide and bis(phenylpropyl) disulphide in rats.
2003-11
A novel pathway for mineralization of the thiocarbamate herbicide molinate by a defined bacterial mixed culture.
2003-10
Photocatalytic oxidation of gaseous 2-chloroethyl ethyl sulfide over TiO2.
2003-08-01
Catalytic oxidation of gaseous reduced sulfur compounds using coal fly ash.
2002-11-11
Synthesis and stable isotope dilution assay of ethanethiol and diethyl disulfide in wine using solid phase microextraction. Effect of aging on their levels in wine.
2002-11-06
Self-assembled monolayers of globotriaosylceramide (Gb3) mimics: surface-specific affinity with shiga toxins.
2002-11-01
Artifact formation due to ethyl thio-incorporation into silylated steroid structures as determined in doping analysis.
2002-04-19
Kinetics of oxidation of odorous sulfur compounds in aqueous alkaline solution with H2O2.
2001-10
Electroanalytical applications of cationic self-assembled monolayers: square-wave voltammetric determination of dopamine and ascorbate.
2001-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:42:29 GMT 2025
Edited
by admin
on Mon Mar 31 19:42:29 GMT 2025
Record UNII
X2SFL51MH0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 4093
Preferred Name English
DIETHYL DISULFIDE
FHFI  
Systematic Name English
DIETHYL DISULPHIDE
Systematic Name English
ETHYLDITHIOETHANE
Systematic Name English
3,4-DITHIAHEXANE
Systematic Name English
DIETHYL DISULFIDE [FHFI]
Common Name English
NSC-8839
Code English
ETHYL DISULFIDE
Systematic Name English
DISULFIDE, DIETHYL
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION DIETHYL DISULFIDE
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
Code System Code Type Description
CAS
110-81-6
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
PRIMARY
PUBCHEM
8077
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-805-7
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
PRIMARY
NSC
8839
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
PRIMARY
JECFA MONOGRAPH
1686
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
PRIMARY
FDA UNII
X2SFL51MH0
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID3051464
Created by admin on Mon Mar 31 19:42:29 GMT 2025 , Edited by admin on Mon Mar 31 19:42:29 GMT 2025
PRIMARY