Merck
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P9625

Sigma-Aldrich

Phenazine methosulfate

≥90% (UV)

Synonym(s):
5-Methylphenazinium methyl sulfate, N-Methylphenazonium methyl sulfate, PMS
Linear Formula:
C13H11N2 · CH3SO4
CAS Number:
Molecular Weight:
306.34
Beilstein:
3898869
Número de EC:
Número MDL:
ID de la sustancia en PubChem:
NACRES:
NA.77

Nivel de calidad

200

ensayo

≥90% (UV)

formulario

powder

mp

158-160 °C (dec.) (lit.)

λ

0.01 g/L in H2O, 1 cm path

Absorción UV

λ: 387.5 nm Amax: ≥90%

espectro de actividad antibiótica

fungi

Modo de acción

DNA synthesis | interferes
cell membrane | interferes

temp. de almacenamiento

−20°C

SMILES string

COS([O-])(=O)=O.C[n+]1c2ccccc2nc3ccccc13

InChI

1S/C13H11N2.CH4O4S/c1-15-12-8-4-2-6-10(12)14-11-7-3-5-9-13(11)15;1-5-6(2,3)4/h2-9H,1H3;1H3,(H,2,3,4)/q+1;/p-1

InChI key

RXGJTUSBYWCRBK-UHFFFAOYSA-M

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Descripción general

Phenazines are heterocyclic compounds produced as secondary metabolites by bacteria.

Aplicación

Phenazine methosulfate is used with ascorbic acid to determine nitric oxide reductase activity.
Phenazine methosulfate has been used:
  • as a component of succinate dehydrogenase enzyme substrate solution
  • to induce superoxide radical generation in red blood cell suspensions and to study its influence on RBC deformability
  • as a component of complex II histochemistry media

Envase

500 mg in glass bottle
1, 5, 10, 25 g in glass bottle

Acciones bioquímicas o fisiológicas

Phenazine m ethosulfate (PMS) acts as a good electron acceptor. PMS is reduced non-enzymatically by (nicotinamide adenine dinucleotide) NADH and (nicotinamide adenine dinucleotide phosphate) NADPH.

Código de clase de almacenamiento

11 - Combustible Solids

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

Certificate of Analysis

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Certificate of Origin

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