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Details

Stereochemistry ACHIRAL
Molecular Formula C4H10S
Molecular Weight 90.187
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIETHYL SULFIDE

SMILES

CCSCC

InChI

InChIKey=LJSQFQKUNVCTIA-UHFFFAOYSA-N
InChI=1S/C4H10S/c1-3-5-4-2/h3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C4H10S
Molecular Weight 90.187
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Diethyl sulfide, a food flavor ingredient, possesses garlic-like odor. It is used as a solvent and to make other chemicals. Diethyl sulfide can irritate the skin and eyes, breathing of this compound can irritate the nose and throat.

Approval Year

PubMed

PubMed

TitleDatePubMed
Variation of some fermentative sulfur compounds in Italian "millesime" classic sparkling wines during aging and storage on lees.
2010-09-08
Electron transfer-oxygen transfer oxygenation of sulfides catalyzed by the H5PV2Mo10O40 polyoxometalate.
2010-08-25
O-H...O versus O-H...S hydrogen bonding. 3. IR-UV double resonance study of hydrogen bonded complexes of p-cresol with diethyl ether and its sulfur analog.
2010-05-20
Pathways and substrate specificity of DMSP catabolism in marine bacteria of the Roseobacter clade.
2010-02-15
"Lantern-Shaped" Platinum(III) Complexes with Axially Bound 9-Ethylguanine or 1-Methylcytosine (L) of General Formula [Pt(2){HN=C(Bu)O}(4)L(2)](NO(3))(2).
2010
Molybdenum(VI) dioxo complexes with tridentate phenolate ligands.
2009-11-02
Selective preconcentration of volatile mercaptans in small SPE cartridges: quantitative determination of trace odor-active polyfunctional mercaptans in wine.
2009-11
Calculation of the aqueous thermodynamic properties of citric acid cycle intermediates and precursors and the estimation of high temperature and pressure equation of state parameters.
2009-06-22
Sulfur versus oxygen reactivity of organic molecules at the Ge(100)-2 x 1 surface.
2009-05-27
Desensitization of beta-adrenergic receptors in lung injury induced by 2-chloroethyl ethyl sulfide, a mustard analog.
2009-02-10
Et2SBrSbCl5Br: an effective reagent for direct bromonium-induced polyene cyclizations.
2009
Sulfur-containing malodorant vapors enhance responsiveness to the sensory irritant capsaicin.
2008-07
Aging effects and grape variety dependence on the content of sulfur volatiles in wine.
2007-12-26
CNDOL: A fast and reliable method for the calculation of electronic properties of very large systems. Applications to retinal binding pocket in rhodopsin and gas phase porphine.
2007-10-14
Experimental and theoretical studies of the reaction of the OH radical with alkyl sulfides: 2. Kinetics and mechanism of the OH initiated oxidation of methylethyl and diethyl sulfides; observations of a two channel oxidation mechanism.
2007-08-21
Quantitative determination of wine highly volatile sulfur compounds by using automated headspace solid-phase microextraction and gas chromatography-pulsed flame photometric detection. Critical study and optimization of a new procedure.
2007-03-02
Breakthrough behavior of diethyl sulphide vapor on active carbon systems.
2007-01-02
Efficacy of a novel biofilter in hatchery sanitation: II. Removal of odorogenous pollutants.
2007
Aquasonolysis of thioethers.
2006-05
Performances and microbial features of an aerobic packed-bed biofilm reactor developed to post-treat an olive mill effluent from an anaerobic GAC reactor.
2006-04-05
Characteristics of sulfur response in a micro-flame photometric detector.
2006-02-10
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
Photosensitized oxygenation of sulfides within an amphiphilic dendrimer containing a benzophenone core.
2005-05-12
Atropisomerization, C-H activation, and dissociative substitution at some biphenyl platinum(II) complexes.
2004-05-26
[Study on odors treatment by the combination of bacteria and fungi].
2004-03
Synthesis of beta-substituted alpha-amino acids with use of iridium-catalyzed asymmetric allylic substitution.
2003-08-08
Oxidative degradation of dimethyl sulfoxide by Cryptococcus humicolus WU-2, a newly isolated yeast.
2003
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
Trace determination of volatile sulfur compounds by solid-phase microextraction and GC-MS.
2002-08
Determination of volatile alkyl sulfides in wastewater by headspace solid-phase microextraction followed by gas chromatography-mass spectrometry.
2002-07-19
Molecular metal sulfide cluster model for substrate binding to oil-refinery hydrodesulfurization catalysts.
2002-03-25
Coordination and oxidative addition at a low-coordinate rhodium(I) beta-diiminate centre.
2002-03-15
Regular and inverse secondary kinetic enthalpy effects (KHE) for the rate of inversion of thioether and 1,1'-biisoquinoline complexes of ruthenium and osmium.
2001-12-17
Investigation of the storage stability of selected volatile sulfur compounds in different sampling containers.
2001-05-11
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:50 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:50 GMT 2025
Record UNII
9191Y76OTC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYL SULFIDE
MI  
Preferred Name English
DIETHYL SULFIDE
FHFI   HSDB  
Systematic Name English
DIETHYL SULFIDE [FHFI]
Common Name English
DIETHYL SULFIDE [HSDB]
Common Name English
FEMA NO. 3825
Code English
NSC-75157
Code English
ETHYL SULFIDE [MI]
Common Name English
DIETHYL THIOETHER
Systematic Name English
1,1'-THIOBISETHANE
Systematic Name English
THIOBISETHANE, 1,1'-
Systematic Name English
ETHANE, 1,1'-THIOBIS-
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION DIETHYL SULFIDE
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
Code System Code Type Description
MESH
C051751
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
MERCK INDEX
m5175
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY Merck Index
HSDB
5563
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-526-9
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
PUBCHEM
9609
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
CAS
352-93-2
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
NSC
75157
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
WIKIPEDIA
DIETHYL SULFIDE
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
CHEBI
27710
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID5027146
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
JECFA MONOGRAPH
534
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
FDA UNII
9191Y76OTC
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY