Ethane dimethanesulfonate

Ethane dimethanesulfonate
Names
	Preferred IUPAC name Ethane-1,2-diyl di(methanesulfonate)
	Other names Ethane 1,2-dimethane sulfonate; Ethane dimethanesulphonate
Identifiers
CAS Number	4672-49-5;
3D model (JSmol)	Interactive image;
Abbreviations	EDS
ChEMBL	ChEMBL170630;
ChemSpider	19574;
PubChem CID	20796;
UNII	EW8V7BJ66Q;
CompTox Dashboard (EPA)	DTXSID40196931 ;
	InChI InChI=1S/C4H10O6S2/c1-11(5,6)9-3-4-10-12(2,7)8/h3-4H2,1-2H3 Key: QSQFARNGNIZGAW-UHFFFAOYSA-N; InChI=1S/C4H10O6S2/c1-11(5,6)9-3-4-10-12(2,7)8/h3-4H2,1-2H3 Key: QSQFARNGNIZGAW-UHFFFAOYSA-N;
	SMILES CS(=O)(=O)OCCOS(=O)(=O)C;
Properties
Chemical formula	C4H10O6S2
Molar mass	218.24 g·mol−1
Density	1.65 g/cm3
Melting point	35–36 °C (95–97 °F; 308–309 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Ethane dimethanesulfonate (EDS) is an organic compound with formula (CH₂OSO₂CH₃)₂. It can be regarded as the esterification product of one glycol and two Methanesulfonic acids. EDS can eliminate all adult Leydig cells in testis of adult male rats, after which Leydig cells will regenerate from stem cells.^[1]

References

^ Risbridger, GP; Davies, A (June 1994). "Isolation of rat Leydig cells and precursor forms after administration of ethane dimethane sulfonate". The American Journal of Physiology. 266 (6 Pt 1): E975-9. doi:10.1152/ajpendo.1994.266.6.E975. PMID 8023929.

[1] Risbridger, GP; Davies, A (June 1994). "Isolation of rat Leydig cells and precursor forms after administration of ethane dimethane sulfonate". The American Journal of Physiology. 266 (6 Pt 1): E975-9. doi:10.1152/ajpendo.1994.266.6.E975. PMID 8023929.

[1]

See also

References