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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.
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)
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.
Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...
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1,2-Propanedithiol, sometimes called 1,2-dimercaptopropane, is a thiol with the formula HSCH 2 CH(SH)CH 3. This colorless, intensely odorous liquid is the simplest chiral dithiol. Related dithiols include 1,2-ethanedithiol , 2,3-dimercapto-1-propanesulfonic acid , and 1,3-propanedithiol .
New York City's spectacularly unpopular congestion pricing scheme is on death row as the Trump administration announced Wednesday it is pulling its approval of the toll in a major blow to Gov ...
Flavouring uses of ethane-1,1-dithiol may include drinks, oil, gravy, soup, meat, fruit, seasonings, and snacks. Maximum concentrations in use that are generally recognised as safe (GRAS) is five parts per million (ppm) but typical uses are around 0.2 ppm. [1] It is supplied as a 1% solution in ethanol, due to its strong offensive smell. [2]
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