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Merck

199648

Sigma-Aldrich

Phenosafranin

Dye content 80 %

Sinónimos:

3,7-Diamino-5-phenylphenazinium chloride

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About This Item

Fórmula empírica (notación de Hill):
C18H15ClN4
Número de CAS:
Peso molecular:
322.79
Número de índice de color:
50200
Beilstein:
3642082
Número CE:
Número MDL:
Código UNSPSC:
12171500
ID de la sustancia en PubChem:
NACRES:
NA.47

formulario

powder

composición

Dye content, 80%

técnicas

titration: suitable

mp

>300 °C (lit.)

λmáx.

519 nm

aplicaciones

diagnostic assay manufacturing
hematology
histology

temp. de almacenamiento

room temp

cadena SMILES

[Cl-].Nc1ccc2nc3ccc(N)cc3[n+](-c4ccccc4)c2c1

InChI

1S/C18H14N4.ClH/c19-12-6-8-15-17(10-12)22(14-4-2-1-3-5-14)18-11-13(20)7-9-16(18)21-15;/h1-11H,(H3,19,20);1H

Clave InChI

SOUHUMACVWVDME-UHFFFAOYSA-N

Aplicación

Phenosafranin has been used for nuclear staining.

Acciones bioquímicas o fisiológicas

Phenosafranin (PSF) is a red dye released from cells with intact plasma membrane. PSF at lower concentration is used to stain mitochondria supravitally.

Pictogramas

Exclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órganos de actuación

Respiratory system

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

dust mask type N95 (US), Eyeshields, Gloves


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Singlet molecular oxygen was generated by illumination of phenosafranin in phosphate buffer at pH 7.5. Relative efficiencies of various imidazole compounds to form endoperoxides were assayed by following at 25 degrees C the rate of light- and imidazole-dependent bleaching of
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The electrochemical regeneration of NADH/NAD(+) redox couple has been studied using poly(phenosafranin) (PPS)-modified carbon electrodes to evaluate the formal potential and catalytic rate constant for the oxidation of NADH. The PPS-modified electrodes were prepared by electropolymerization of phenosafranin onto different

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