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Ethane-1,2-dithiol, also known as EDT, [1] is a colorless liquid with the formula C 2 H 4 2. It has a very characteristic odor which is compared by many people to rotten cabbage . It is a common building block in organic synthesis and an excellent ligand for metal ions.
Thiol with a blue highlighted sulfhydryl group.. In organic chemistry, a thiol (/ ˈ θ aɪ ɒ l /; [1] from Ancient Greek θεῖον (theion) 'sulfur' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent.
A common 1,4-dithiol is dithiothreitol (DTT), HSCH 2 CH(OH)CH(OH)CH 2 SH, sometimes called Cleland's reagent, for to reduce protein disulfide bonds. Oxidation of DTT results a stable six-membered heterocyclic ring with an internal disulfide bond. Reduction of a typical disulfide bond by DTT via two sequential thiol-disulfide exchange reactions.
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1,2-Ethanedithiol, compound commonly used for cleavage during peptide synthesis; EDT (Digital), text editor for PDP-11 and VAX/VMS computer systems EDT (Univac), text editor for UNIVAC Series 90 and Fujitsu BS2000 computer systems
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The molecular formula C 2 H 6 S 2 (molar mass: 94.20 g/mol, exact mass: 93.99109 u) may refer to: Dimethyl disulfide (DMDS) 1,1-Ethanedithiol; 1,2-Ethanedithiol (EDT)
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