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Sulpho NONOate

Cayman Chemical Item Number 83300

(CAS 61142-90-3)

Sulpho NONOate (CAS 61142-90-3)

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Description

Sulpho NONOate produces nitrous oxide but no NO at physiological pH. Therefore, this compound may be used as a negative control in experiments using other NO donors of the NONOate class.1,2

1 Maragos, C.M., Morley, D., Wink, D.A., et al. Complexes of ·NO with nucleophiles as agents for the controlled biological release of nitric oxide. Vasorelaxant effects. J Med Chem 34 3242-3247 (1991).

2 Keefer, L.K., Nims, R.W., Davies, K.M., et al. “NONOates” (1-substituted diazen-1-ium-1,2-diolates) as nitric oxide donors: Convenient nitric oxide dosage forms. Methods Enzymol 268 281-293 (1996).

Formal Name disodium (E)-​1-​sulfonatodiazen-​1-​ium-​1,​2-​diolate
CAS Number 61142-90-3
Molecular Formula N2O5S · 2Na
Formula Weight 186.1
Formulation A crystalline solid
Purity >90%
λmax 259 nm
ε 7
Stability 1 year
Storage -80°C
Shipping Dry ice in continental US; may vary elsewhere
SMILES
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O=NN(O)​S(=O)​(=O)​O

Background Reading

Maragos, C.M., Morley, D., Wink, D.A., et al. Complexes of ·NO with nucleophiles as agents for the controlled biological release of nitric oxide. Vasorelaxant effects. J Med Chem 34 3242-3247 (1991).

Maragos, C.M., Wang, J.M., Hrabie, J.A., et al. Nitric oxide/nucleophile complexes inhibit the in vitro proliferation of A375 melanoma cells via nitric oxide release. Cancer Res 53 564-568 (1993).

Switkes, E.G., Dasch, G.A., and Ackermann, M.N. Kinetics of boric acid catalyzed decomposition of the N-nitrosohydroxylamine-N-sulfonate ion. Inorg Chem 12 1120-1123 (1973).

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