Talk:Dithiothreitol
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DTT should be moved from the catalyst section, since it is not actually a catalyst, but a stoichometric reagent
- Go ahead and move it then. Alison Chaiken 05:11, 2 May 2006 (UTC)
done
DTT is not actually a reducing reagent. The oxidation numbers of the sulfer atoms involved in the disulfide exchange remain constant at -1. It should be more properly stated that it attacks disulfide bonds as a nucleophile.
- The vast majority of the chemistry world disagrees with you. In a disulfide, you have 4 lone electron pairs on the two sulfurs, plus the 1 pair in the bond, for a total of 10 electrons (ignoring bonding to the rest of the molecule). In the two free thiols case, you still have the 4 lone pairs, plus 2 pairs in each of the bonds to hydrogen, for a total of 12 electrons. (The hydrogens come in as H+ ions, and don't bring electrons with them.) Change in electron number absolutely implies redox chemistry. As "reduction describes the gain of an electron by a molecule, atom or ion", and since the disulfide gained electrons, it has been reduced by the action of DTT. Thus DTT is a "reducing agent", by definition. -- Tmhand 19:29, 6 July 2006 (UTC)
On the image, the DTT is 2R-3R at the beginning and at the final, it is 2S-3R, please change the image!
Talk about L-DTT and D-DTT. Usually DTT is a DL-DTT racemic mixture, but it is important to do the difference.