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254770

Sigma-Aldrich

Potassium ethyl xanthogenate

96%

Synonym(s):

O-Ethylxanthic acid potassium salt, KEX, Potassium O-ethyl dithiocarbonate, Potassium xanthogenate

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About This Item

Linear Formula:
C2H5OCSSK
CAS Number:
140-89-6
Molecular Weight:
160.30
Beilstein:
3596974
EC Number:
205-439-3
MDL number:
MFCD00004931
UNSPSC Code:
12352100
PubChem Substance ID:
24855406
NACRES:
NA.22

Quality Level

100

Assay

96%

form

powder

mp

210 °C (dec.) (lit.)

solubility

alcohol: soluble(lit.)
water: very soluble(lit.)

SMILES string

[K+].CCOC([S-])=S

InChI

1S/C3H6OS2.K/c1-2-4-3(5)6;/h2H2,1H3,(H,5,6);/q;+1/p-1

InChI key

JCBJVAJGLKENNC-UHFFFAOYSA-M

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Application

Potassium ethyl xanthogenate (ethyl potassium xanthogenate) has been used:
  • in synthesis of unsymmetrical sulfides via cross-coupling reaction, using recyclable CuO nanoparticles under ligand-free conditions
  • as surfactant to investigate the adsorption of colloidal dye Disperse Blue 3 onto pretreated polyester fabric
  • in determination of microgram amounts of cadmium in water samples by substoichiometric radiochemical method

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

EUH018

Storage Class Code

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 3

Flash Point(F)

204.8 °F

Flash Point(C)

96 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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M C De Ungria et al.
Helicobacter, 3(4), 269-277 (1998-12-09)
Plasmids are extra-chromosomal DNA that may encode products that aid in virulence, pathogenesis, and the spread of antibiotic resistance among a wide spectrum of bacteria. Plasmids have been detected in Helicobacter pylori, H. felis, H. fennelliae, and H. cinaedi. However
H Tjälve et al.
The Science of the total environment, 148(2-3), 217-242 (1994-06-06)
Dithiocarbamates, thiuram sulphides, xanthates, pyridinethiones and halogenated 8-hydroxyquinolines are groups of compounds which can form lipophilic complexes with Ni2+. These compounds are widely used as drugs and pesticides, and in industry. We have exposed rodents (mice, rats) and fish (brown
Anthony J Shallop et al.
The Journal of organic chemistry, 68(22), 8657-8661 (2003-10-25)
We have previously reported the use of a 13C tag at the C2 of 15N-multilabeled purine nucleosides to distinguish the adjacent-labeled 15N atoms from those in an untagged nucleoside. We now introduce the use of an indirect tag at the
Amiel Boullemant et al.
Environmental science & technology, 43(9), 3308-3314 (2009-06-19)
Cadmium forms neutral, lipophilic Cd(L)2(0) complexes with diethyldithiocarbamate (DDC) and with ethylxanthate (XANT). Uptake of these complexes bythree unicellularfreshwater green algae (Chlamydomonas reinhardtii, Chlorella fusca, and Pseudokirchneriella subcapitata) was determined at two pH values (7.0 and 5.5) and compared to
J Gottofrey et al.
Pharmacology & toxicology, 63(1), 46-51 (1988-07-01)
Brown trouts, Salmo trutta, were exposed to water containing 0.1 or 10 micrograms/l of 63Ni2+, alone or with potassium ethylxanthate or sodium diethyldithiocarbamate. After one and three weeks the accumulation and disposition of the 63Ni2+ in the fish were examined
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