Chemical Formula: C4H10O2S2

Chemical Formula C4H10O2S2

Found 16 metabolite its formula value is C4H10O2S2

1,4-Dithiothreitol

DL-Threo-1,4-dimercapto-2,3-butanediol

C4H10O2S2 (154.01222)


Dithiothreitol (DTT) is the common name for a small-molecule redox reagent known as Clelands reagent. DTTs formula is C4H10O2S2 and the molecular structure of its reduced form is shown at the right; its oxidized form is a disulfide-bonded 6-membered ring (shown below). Its name derives from the four-carbon sugar, threose. DTT has an epimeric (sister) compound, dithioerythritol. A common use of DTT is as a reducing or "deprotecting" agent for thiolated DNA. The terminal sulfur atoms of thiolated DNA have a tendency to form dimers in solution, especially in the presence of oxygen. Dimerization greatly lowers the efficiency of subsequent coupling reactions such as DNA immobilization on gold in biosensors. Typically DTT is mixed with a DNA solution and allowed to react, and then is removed by filtration (for the solid catalyst) or by chromatography (for the liquid form). The DTT removal procedure is often called "desalting.". DTT is frequently used to reduce the disulfide bonds of proteins and, more generally, to prevent intramolecular and intermolecular disulfide bonds from forming between cysteine residues of proteins. However, even DTT cannot reduce buried (solvent-inaccessible) disulfide bonds, so reduction of disulfide bonds is sometimes carried out under denaturing conditions (e.g., at high temperatures, or in the presence of a strong denaturant such as 6 M guanidinium hydrochloride, 8 M urea, or 1\\% sodium dodecylsulfate). Conversely, the solvent exposure of different disulfide bonds can be assayed by their rate of reduction in the presence of DTT. DTT can also be used as an oxidizing agent. Its principal advantage is that effectively no mixed-disulfide species are populated, in contrast to other agents such as glutathione. In very rare cases, a DTT adduct may be formed, i.e., the two sulfur atoms of DTT may form disulfide bonds to different sulfur atoms; in such cases, DTT cannot cyclize since it has no remaining free thiols. Due to air oxidation, DTT is a relatively unstable compound whose useful life can be extended by refrigeration and handling in an inert atmosphere. Since protonated sulfurs have lowered nucleophilicities, DTT becomes less potent as the pH lowers. Tris(2-carboxyethyl)phosphine HCl (TCEP hydrochloride) is an alternative which is more stable and works even at low pH. Dithiothreitol (DTT) is the common name for a small-molecule redox reagent known as Clelands reagent. DTT has an epimeric compound, dithioerythritol. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Dithioerythritol

erythro-1,4-Dimercapto-2,3-butanediol

C4H10O2S2 (154.01222)


D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D013439 - Sulfhydryl Reagents

   

(2R,3S)-3,4-DImercaptobutane-1,2-diol

(2R,3S)-3,4-DImercaptobutane-1,2-diol

C4H10O2S2 (154.01222)


   

2-Hydroxyethyl disulfide

2-[(2-hydroxyethyl)disulfanyl]ethan-1-ol

C4H10O2S2 (154.01222)


   

Dithioerythritol

DL-Threo-1,4-dimercapto-2,3-butanediol

C4H10O2S2 (154.01222)


   

2,2-DITHIODIETHANOL

2-Hydroxyethyl disulfide

C4H10O2S2 (154.01222)


   

Methyl propanethiosulfonate

Methyl propanethiosulfonate

C4H10O2S2 (154.01222)


   

1,4-Dithioerythritol

1,4-Dithioerythritol

C4H10O2S2 (154.01222)


   

Hydroxyethyl cellulose

Hydroxyethyl cellulose

C4H10O2S2 (154.01222)


   

S-Ethyl ethanethiosulfonate

S-Ethyl ethanethiosulfonate

C4H10O2S2 (154.01222)


   

DL-Dithiothreitol

(2S,3S)-1,4-Dimercaptobutane-2,3-diol

C4H10O2S2 (154.01222)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

1,2-Butanediol, 3,4-dimercapto-

1,2-Butanediol, 3,4-dimercapto-

C4H10O2S2 (154.01222)


   

1,4-Dithiothreitol

1,4-Dithiothreitol

C4H10O2S2 (154.01222)


The threo-diastereomer of 1,4-dimercaptobutane-2,3-diol.

   

Dithiothreitol

D-1,4-dithiothreitol

C4H10O2S2 (154.01222)


   

L-1,4-dithiothreitol

L-1,4-dithiothreitol

C4H10O2S2 (154.01222)


   

D-1,4-dithiothreitol

D-1,4-dithiothreitol

C4H10O2S2 (154.01222)