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CAS No.: | 352-93-2 |
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Name: | 1,1'-Thiobisethane |
Article Data: | 164 |
Molecular Structure: | |
Formula: | C4H10S |
Molecular Weight: | 90.1894 |
Synonyms: | Ethyl sulfide(8CI);1,1'-Thiobisethane;3-Thiapentane;Diethyl sulfide;Diethylthioether;Ethyl monosulfide;Ethyl thioether;Ethylthioethane;NSC 75157;Thioethyl ether; |
EINECS: | 206-526-9 |
Density: | 0.831 g/cm3 |
Melting Point: | -100 °C(lit.) |
Boiling Point: | 94.4 °C at 760 mmHg |
Flash Point: | 15°F |
Solubility: | Miscible with alcohol, ethanol and ether. Slightly miscible with carbon tetrachloride. Immiscible with water. |
Appearance: | Colourless liquid |
Hazard Symbols: | F; Xi |
Risk Codes: | 11-38 |
Safety: | 9-16-26-33-36 |
Transport Information: | UN 2375 3/PG 2 |
PSA: | 25.30000 |
LogP: | 1.75940 |
Reported in EPA TSCA Inventory.
DOT Classification: 3; Label: Flammable Liquid
The Ethyl sulfide with CAS registry number of 352-93-2 is also known as Diethyl sulfide. The IUPAC name is Ethylsulfanylethane. It belongs to product categories of Sulfide Flavor. Its EINECS registry number is 206-526-9. In addition, the formula is C4H10S and the molecular weight is 90.19. This chemical is a colourless liquid and should be sealed in cool place.
Physical properties about Ethyl sulfide are: (1)ACD/LogP: 1.95; (2)ACD/LogD (pH 5.5): 1.95; (3)ACD/LogD (pH 7.4): 1.95; (4)ACD/BCF (pH 5.5): 17.86; (5)ACD/BCF (pH 7.4): 17.86; (6)ACD/KOC (pH 5.5): 274.03; (7)ACD/KOC (pH 7.4): 274.03; (8)Index of Refraction: 1.439; (9)Molar Refractivity: 28.57 cm3; (10)Molar Volume: 108.5 cm3; (11)Surface Tension: 24.6 dyne/cm; (12)Density: 0.831 g/cm3; (13)Enthalpy of Vaporization: 31.77 kJ/mol; (14)Boiling Point: 94.4 °C at 760 mmHg; (15)Vapour Pressure: 54.2 mmHg at 25 °C.
Preparation of Ethyl sulfide: it is prepared by reaction of crude ethylsulfide. Firstly, mercury chloride is added to ethanol, then crude ethylsulfide is put into the mixture. Secondly, generated complex is refined by recrystallization and added to hydrochloric acid. At last, product is obtained by heating, washing and drying.
Uses of Ethyl sulfide: it is used to produce triethylsulfoniuim ethylsulfate by reaction with sulfuric acid diethyl ester. The reaction occurs with solvent acetonitrile and other condition of heating for 2.5 hours. The yield is about 85%. Besides, it is also used as a solvent for anhydrous minerals and in plating baths for gold and silver.
When you are using this chemical, please be cautious about it. As a chemical, it is irritating to skin and highly flammable. During using it, wear suitable protective clothing. After using it, keep container in a well-ventilated place away from sources of ignition. If contact with eyes accidently, rinse immediately with plenty of water and seek medical advice. Take precautionary measures against static discharges.
You can still convert the following datas into molecular structure:
1. Canonical SMILES: CCSCC
2. InChI: InChI=1S/C4H10S/c1-3-5-4-2/h3-4H2,1-2H3
3. InChIKey: LJSQFQKUNVCTIA-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LC | inhalation | > 1850mg/m3/10 (1850mg/m3) | National Defense Research Committee, Office of Scientific Research and Development, Progress Report.Vol. NDCrc-132, Pg. Nov, 1942. |