D3514

Sigma

 

4,4′-Diisothiocyanatostilbene-2,2′-disulfonic acid disodium salt hydrate

≥80% (elemental analysis), powder

Synonym:DIDS, Disodium 4,4′-diisothiocyanatostilbene-2,2′-disulfonate
CAS Number:207233-90-7
Linear Formula:C16H8N2Na2O6S4 · xH2O
Molecular Weight:498.48 (anhydrous basis)
Beilstein Registry Number:8179433
MDL number:MFCD00009638
PubChem Substance ID:24893761

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Description

ApplicationA negatively charged homobifunctional cross-linking reagent. The isothiocyanate groups react with primary amines at pH 9.0-10.0.
Biochem/physiol ActionsA specific inhibitor of cellular anion permeability used in cell transport studies.

Properties

assay≥80% (elemental analysis)
formpowder
color yellow
solubility0.1 M potassium bicarbonate: 50 mg/mL
storage temp.2-8°C

Safety

Personal Protective Equipmentdust mask type N95 (US), Eyeshields, Faceshields, Gloves
Hazard CodesXn
Risk Statements36/37/38-42
Safety Statements22-26
WGK Germany3

References

referenceOkada, Y., et al., Volume-sensitive chloride channels involved in apoptotic volume decrease and cell death. J. Membr. Biol. 209, 21-29, (2006)
 Pusch, M., et al., Channel or transporter? The CLC saga continues. Exp. Physiol. 91, 149-152, (2006)
 Alper, S.L., Molecular physiology of SLC4 anion exchangers. Exp. Physiol. 91, 153-161, (2006)
 Hua, S., and Inesi, G., Lys515-Lys492 cross-linking by DIDS interferes with substrate utilization by the sarcoplasmic reticulum ATPase. Biophys. J. 73, 2149-2155, (1997)
 Kavanaugh, M.P., et al., Affinity labeling of hemoglobin with 4,4'-diisothiocyanostilbene-2,2'-disulfonate: covalent cross-linking in the 2,3-diphosphoglycerate binding site. Biochemistry 27, 1804-1808, (1988)