O-Ethylhydrogendithiocarbonat
Ethyl xanthate
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Grundinformationen
- CAS
151-01-9- Standard-SMILES
CCOC(=S)S- InChIKey
ZOOODBUHSVUZEM-UHFFFAOYSA-N- Summenformel
- C3H6OS2
- Durchschnittliche Molmasse
- 122,21 g/mol
- Monoisotopische Masse
- 121,98600681
Überblick
structure in first source
Namen und Bezeichner
- Bevorzugter Name
- Ethyl xanthate
- IUPAC
- ethoxymethanedithioic acid
- Lokaler Name
- O-Ethylhydrogendithiocarbonat
- Englischer Name
- O-ethyl hydrogen dithiocarbonate
- Summenformel
- C3H6OS2
- Molmasse
- 122.21
Namen und Synonyme
ETHYLXANTHATEEthyl xanthogenateEthyl xanthateEthylxanthic acid151-01-9Ethoxydithioformic acidEthylxanthogenic acidXanthic acid, ethyl-O-Ethyl dithiocarbamateO-Ethyl dithiocarbonateXanthogenic acid, ethyl-Carbonic acid, dithio-, O-ethyl ester
Weitere Namen anzeigen
ETHYLXANTHOGENATEBrn 1740597Einecs 205-780-8ethyl dithiocarbonateCarbonodithioic acid O-ethyl
B7B55M6MK1RefChem:596809205-780-8XanthateXanthogenic acidO-Ethyl hydrogen dithiocarbonateethoxymethanedithioic acidCarbonodithioic acid, O-ethyl ester
Datenbank-Bezeichner
- CAS
151-01-9- PubChem CID
- 8823
- DTXSID
DTXSID3045063- ChEMBL
CHEMBL3039661- UNII
- B7B55M6MK1
- EC Number
- 205-780-8
- Nikkaji
- J5.860B
Eigenschaften
Berechnete StruktureigenschaftenWird ergänzt
- XLogP
- 1,7
- Polarare Oberfläche (TPSA)
- 42,3 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 6
- Formalladung
- 0
- Komplexität
- 52,8
Experimentelle und physikochemische Eigenschaften
Chemical ClassesOther Classes -> Sulfur Compounds
Color/FormLIQUID
SolubilitySLIGHTLY SOL IN WATER
Melting PointFREEZING POINT -53 °C
Physical DescriptionLiquid; [HSDB]
Stability/Shelf LifeUNSTABLE
Other Experimental PropertiesDECOMPOSES @ 25 °C
Physikochemische Eigenschaften
- Schmelzpunkt
- 140 °C · 140 °C
- Siedepunkt
- 197.67 °C · 197.67°C (rough estimate)
- Dichte
- 1.194 · 1.194 (estimate)
- Brechungsindex
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Gefahrenhinweise
Hazards SummaryMay react with water or moisture producing carbon disulfide; [CAMEO] See Carbon disulfide.
Sicherheit und Schutzausrüstung
Cleanup MethodsXANTHATE REMOVAL BY OXIDATION ON POROUS CARBON GRAPHITE ANODES.
Toxikologische Informationen
Interactions
THE EFFECT OF POTASSIUM ETHYLXANTHOGENATE ON THE PENTOBARBITAL (40 MG/KG, BODY WT IV) SLEEPING TIME, PHARMACOKINETICS, AND METABOLISM WERE STUDIED IN COMPARATIVE EXPERIMENTS ON MALE ALBINO MICE. POTASSIUM ETHYLXANTHOGENATE CAUSED AN ALMOST TWO-FOLD DECR IN ELIMINATION RATE CONSTANT OF PLASMA PENTOBARBITAL. POTENTIATING EFFECT OF POTASSIUM ETHYLXANTHOGENATE ON PENTOBARBITAL SLEEPING TIME IS MAINLY DUE TO INHIBITION OF PENTOBARBITAL LIVER METABOLISM.
GAMMA-AMINOBUTYRIC ACID CONTAINING PREPN NOT ONLY RESTORE THE ETHYL XANTHATE-CAUSED PHYSIOLOGICAL AND BIOCHEMICAL METABOLIC CHANGES OF SOME BIOGENIC AMINES AND AMINO ACIDS BUT TO A DEFINITE DEGREE PREVENTED THE DEVELOPMENT OF THESE CHANGES IN ANIMALS.
INFLUENCE ON THE DRUG METABOLISM POTASSIUM ETHYLXANTHOGENATE ON THE ANILINE TOXICITY, METHEMOGLOBIN FORMATION AND ANILINE-HYDROXYLASE ACTIVITY INCR ANILINE TOXICITY IN WHITE MALE RATS AND INHIBITED ANILINE-HYDROXYLASE ACTIVITY.
Non-Human Toxicity Excerpts
WHITE RATS CHRONICALLY EXPOSED BY INHALATION TO ETHYL XANTHATE REVEALED HIGHER FREQUENCY OF CHROMOSOMAL REARRANGEMENTS IN LYMPHOCYTES OF PERIPHERAL BLOOD THAN CONTROLS.
THE OBJECTIVE OF THIS STUDY WAS TO ESTABLISH THE 96 HR MEDIAN LETHAL CONCN OF ETHYLXANTHATE IN RAINBOW TROUT.
Sicherheitsdaten
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological ClassificationSubstances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection.
Verwendung und Herstellung
General Manufacturing Information
Carbonodithioic acid, O-ethyl ester: INACTIVE
XANTHIC ACID: A SUBSTITUTED DITHIOCARBONIC ACID OF THE TYPE ROC(S)SH, IN WHICH R IS ORDINARILY AN ALKYL RADICAL. UNLESS OTHERWISE DESIGNATED, XANTHIC ACID IS UNDERSTOOD TO BE THE ETHYL DERIV, ALSO CALLED ETHYLXANTHIC ACID.
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