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HCID 75552Erstellt: 4. November 2026

Diallyltetrasulfid

diallyl tetrasulfide · ICD-1585 · Fema no. 3533 · Einecs 219-485-7 · diallyl tetrasulphide · Diallyl pertetrasulfide · Bis(allylthio) persulfide · Tetrasulfide, di-2-propenyl

https://huagongshe.com/de/chemical/75552

Molekülstruktur von Diallyltetrasulfid

Identifikatoren & physikalische Daten

CAS No.2444-49-7
SummenformelC6H10S4
Durchschnittliche Molmasse210,4 g/mol
Monoisotopische Masse209,96653501 g/mol
SMILESC=CCSSSSCC=C
InChIKeyRMKCQUWJDRTEHE-UHFFFAOYSA-N
PubChem CID75552
ChEMBLCHEMBL1947232
ChEBICHEBI:177763
EC No.219-485-7
DTXSIDDTXSID70179196
Lokaler NameDiallyltetrasulfid

Chemische & physikalische Eigenschaften

XLogP3,1
Polarare Oberfläche (TPSA)101
H-Brücken-Donoren0
H-Brücken-Akzeptoren4
Frei drehbare Bindungen7
Schwere Atome10
Formalladung0
Komplexität79,7
Siedepunkt279.00 to 280.00 °C. @ 760.00 mm Hg>45 °C(Press: 0.001 Torr)
Dichte1.211±0.06 g/cm3(Predicted)
LagerbedingungenStore at -20°C
LöslichkeitDMF: 30 mg/mlDMSO: 30 mg/mlDMSO:PBS (pH 7.2) (1:1): 0.5mg/mlEthanol: 30 mg/ml
AggregatzustandAn oil
Geruchat 0.01 % in propylene glycol. strong garlic onion
Geruchsartsulfurous
LogP (Verteilungskoeffizient)5.62

Sicherheit & Vorschriften

GHS-EinstufungWarningH302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Regulatorische InformationenTetrasulfide, di-2-propenyl: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Hazard Classes and CategoriesAcute Tox. 4 (100%)
AlarmwortWarnung
GefahrenhinweiseCode Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code H302

Anwendungen & Verwendung

Verwenden

Diallyl Tetrasulfide is a mitotic inhibitor and apoptosis inducers. An anti-carcinogenic agent.Also, it is derived from Allyl Bromide (A549655), which is used as a reagent in the synthesis of Resveratrol derivatives. Resveratrol (R150000) is a minor constitutent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression.