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146625

Sigma-Aldrich

Bathocuproinedisulfonic acid disodium salt hydrate

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About This Item

Fórmula empírica (notación de Hill):
C26H18N2Na2O6S2 · xH2O
Número de CAS:
1257642-74-2
Peso molecular:
564.54 (anhydrous basis)
Número MDL:
MFCD00149974
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
24848788
NACRES:
NA.22

formulario

powder

mp

300 °C (lit.)

grupo funcional

phenyl
sulfonic acid

cadena SMILES

O.[Na+].[Na+].Cc1nc2c(ccc3c(-c4ccccc4)c(c(C)nc23)S([O-])(=O)=O)c(-c5ccccc5)c1S([O-])(=O)=O

InChI

1S/C26H20N2O6S2.2Na.H2O/c1-15-25(35(29,30)31)21(17-9-5-3-6-10-17)19-13-14-20-22(18-11-7-4-8-12-18)26(36(32,33)34)16(2)28-24(20)23(19)27-15;;;/h3-14H,1-2H3,(H,29,30,31)(H,32,33,34);;;1H2/q;2*+1;/p-2

Clave InChI

ZAGWMJUGRCMNGX-UHFFFAOYSA-L

Descripción general

Bathocuproine disulfonic acid (BCDS) is a stable Cu+ chelator and BCDS-Cu+ inhibits the HIV-1 wild type protease as well as a mutant HIV-1 protease lacking cysteine. It is an extracellular copper chelator.

Aplicación

Bathocuproinedisulfonic acid disodium salt hydrate was used as chelator in electron spin resonance spin trapping technique to study free radical generation in rats with acute sodium formate poisoning. It was used as reagent for determination of Cu and Cu-protein complexes.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
BCCG3838
BCCF6028
BCCC8928
BCCB7321
BCCB4873

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Proceedings of the National Academy of Sciences of the United States of America, 98(24), 13549-13553 (2001-11-22)
Electron spin resonance spectroscopy has been used to study free radical generation in rats with acute sodium formate poisoning. The in vivo spin-trapping technique was used with alpha-(4-pyridyl-1-oxide)-N-t-butylnitrone (POBN), which reacts with free radical metabolites to form radical adducts, which
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A method of protein determination has been developed which combines the biuret reaction and the copper(I)-bathocuproine chelate reaction. Protein in the specimen forms a Cu(2+)-protein chelate complex (biuret reaction) during the first step. Excess Cu2+ is reduced to Cu+ by
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