Dithioerythritol

Dithioerythritol

Names
Preferred IUPAC name (2R,3S)-1,4-Bis(sulfanyl)butane-2,3-diol
Other names (2R,3S)-1,4-Dimercaptobutane-2,3-diol (no longer recommended) 2,3-Dihydroxybutane-1,4-dithiol Erythro-2,3-dihydroxy-1,4-butanedithiol Erythro-1,4-dimercapto-2,3-butanediol Cleland's reagent (also used for DTT)
Identifiers
CAS Number	6892-68-8 Y
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:17456 Y
ChemSpider	388475 Y
ECHA InfoCard	100.027.271
PubChem CID	439352
InChI InChI=1S/C4H10O2S2/c5-3(1-7)4(6)2-8/h3-8H,1-2H2/t3-,4+ Y Key: VHJLVAABSRFDPM-ZXZARUISSA-N Y InChI=1/C4H10O2S2/c5-3(1-7)4(6)2-8/h3-8H,1-2H2/t3-,4+ Key: VHJLVAABSRFDPM-ZXZARUISBS
SMILES C([C@@H]([C@@H](CS)O)O)S SC[C@@H](O)[C@@H](O)CS
Properties
Chemical formula	C4H10O2S2
Molar mass	154.253 g/mol
Melting point	82 to 84 °C (180 to 183 °F; 355 to 357 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y  (what is YN ?)
Infobox references

Dithioerythritol (DTE) is a sulfur containing sugar derived from the corresponding 4-carbon monosaccharide erythrose. It is an epimer of dithiothreitol (DTT). The molecular formula for DTE is C₄H₁₀O₂S₂.

Like DTT, DTE makes an excellent reducing agent, although its standard reduction potential is not quite as negative, i.e., DTE is slightly less effective at reducing than DTT, presumably because the lesser steric repulsion of its OH groups makes the cyclic disulfide-bonded form of DTE less stable compared to that of DTT. In DTT, these hydroxyl groups are cis to each other, whereas they are trans to each other in DTE.