| Weight | 146.299 g/mol |
|---|---|
| Formula | C8H18S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
Dibutyl sulfide (544-40-1)
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- Electron Transfer and Singlet Oxygen Mechanisms in the Photooxygenation of Dibutyl Sulfide and Thioanisole in MeCN Sensitized by N-Methylquinolinium Tetrafluoborate and 9,10-Dicyanoanthracene. The Probable Involvement of a Thiadioxirane Intermediate in Electron Transfer Photooxygenations (Journal of the American Chemical Society, 2003)
- Adsorption, Assembly, and Dynamics of Dibutyl Sulfide on Au{111} (Journal of Physical Chemistry C, 2010)
- Adsorption, interaction, and manipulation of dibutyl sulfide on cu{111}. (ACS Nano, 2007)
- Separation of Boron Isotopes. VIII. BF3 Addition Compounds of Dimethyl Ether, Dimethyl Sulfide, Dimethyl Selenide, Dimethyl Telluride, Dibutyl Ether, and Ethyl Formate (Journal of Chemical Physics, 1967)
- Neutron activation determination of gold in rocks using dibutyl sulfide extraction for gold separation (Journal of Radioanalytical and Nuclear Chemistry, 1971)
- Photosensitized anaerobic oxidation of dibutyl sulfide (Journal of Organic Chemistry, 1979)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCSCCCC
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InChIKeyHTIRHQRTDBPHNZ-UHFFFAOYSA-N
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Dibutyl sulfide
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