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Details

Stereochemistry ACHIRAL
Molecular Formula C3H6OS2
Molecular Weight 122.209
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYLXANTHATE

SMILES

CCOC(S)=S

InChI

InChIKey=ZOOODBUHSVUZEM-UHFFFAOYSA-N
InChI=1S/C3H6OS2/c1-2-4-3(5)6/h2H2,1H3,(H,5,6)

HIDE SMILES / InChI

Molecular Formula C3H6OS2
Molecular Weight 122.209
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Flow injection analysis of ethyl xanthate by gas diffusion and UV detection as CS2 for process monitoring of sulfide ore flotation.
2010-07-15
Inhibition of protein kinase C-driven nuclear factor-kappaB activation: synthesis, structure-activity relationship, and pharmacological profiling of pathway specific benzimidazole probe molecules.
2010-06-24
Cancer cell death induced by phosphine gold(I) compounds targeting thioredoxin reductase.
2010-01-15
Uptake of hydrophobic metal complexes by three freshwater algae: unexpected influence of pH.
2009-05-01
[Stabilization of heavy metals in municipal solid waste incineration fly ash with the thiol collectors].
2007-08
Flow injection analysis of ethyl xanthate by in-line dialysis and UV spectrophotometric detection.
2007-05-15
Application of pneumatic flow injection-tandem spectrometer system for chromium speciation.
2007
Water soluble polymeric nanogels by xanthate-mediated radical crosslinking copolymerisation.
2006-05-14
New aspects of the electroadsorption of ethyl xanthate on copper electrodes.
2005-12-08
Acetaminophen decreases intracellular glutathione levels and modulates cytokine production in human alveolar macrophages and type II pneumocytes in vitro.
2005-08
Synthesis, characterization, and luminescent properties of dinuclear gold(I) xanthate complexes: X-ray structure of [Au2(nBu-xanthate)2].
2004-06-28
Preconcentrative separation of chromium(VI) species from chromium(III) by coprecipitation of its ethyl xanthate complex onto naphthalene.
2004-06-17
Use of 13C as an indirect tag in 15N specifically labeled nucleosides. Syntheses of [8-13C-1,7,NH2-15N3]adenosine, -guanosine, and their deoxy analogues.
2003-10-31
Interpretation of colloidal dyeing of polyester fabrics pretreated with ethyl xanthogenate in terms of zeta potential and surface free energy balance.
2003-09-15
Derivatives of xanthic acid are novel antioxidants: application to synaptosomes.
2003-04
Integrated copper-containing wastewater treatment using xanthate process.
2002-09-02
Pyridazine derivatives and related compounds, part 9. tetrazolo[1,5-b]pyridazine-8-carbohydrazide: synthesis and some reactions.
2002-07-24
The removal of heavy metals from contaminated soil by a combination of sulfidisation and flotation.
2002-05-06
Determination of low concentrations of the flotation reagent ethyl xanthate by sampled DC polarography and flow injection with amperometric detection.
2001-04-12
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:58:20 GMT 2025
Edited
by admin
on Mon Mar 31 19:58:20 GMT 2025
Record UNII
B7B55M6MK1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYLXANTHATE
HSDB  
Systematic Name English
CARBONIC ACID, DITHIO-, O-ETHYL ESTER
Preferred Name English
CARBONODITHIOIC ACID, O-ETHYL ESTER
Common Name English
ETHYL XANTHOGENATE
Common Name English
O-ETHYL DITHIOCARBAMATE
Common Name English
XANTHIC ACID, ETHYL-
Systematic Name English
ETHYLXANTHIC ACID
Systematic Name English
ETHYLXANTHOGENIC ACID
Common Name English
XANTHOGENIC ACID
Common Name English
O-ETHYL DITHIOCARBONATE
Systematic Name English
ETHOXYDITHIOFORMIC ACID
Systematic Name English
O-ETHYL HYDROGEN DITHIOCARBONATE
Systematic Name English
XANTHATE
Common Name English
ETHYLXANTHATE [HSDB]
Common Name English
XANTHOGENIC ACID, ETHYL-
Systematic Name English
Code System Code Type Description
FDA UNII
B7B55M6MK1
Created by admin on Mon Mar 31 19:58:20 GMT 2025 , Edited by admin on Mon Mar 31 19:58:20 GMT 2025
PRIMARY
PUBCHEM
8823
Created by admin on Mon Mar 31 19:58:20 GMT 2025 , Edited by admin on Mon Mar 31 19:58:20 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-780-8
Created by admin on Mon Mar 31 19:58:20 GMT 2025 , Edited by admin on Mon Mar 31 19:58:20 GMT 2025
PRIMARY
EPA CompTox
DTXSID3045063
Created by admin on Mon Mar 31 19:58:20 GMT 2025 , Edited by admin on Mon Mar 31 19:58:20 GMT 2025
PRIMARY
HSDB
5652
Created by admin on Mon Mar 31 19:58:20 GMT 2025 , Edited by admin on Mon Mar 31 19:58:20 GMT 2025
PRIMARY
CAS
151-01-9
Created by admin on Mon Mar 31 19:58:20 GMT 2025 , Edited by admin on Mon Mar 31 19:58:20 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT