P9625
Phenazine methosulfate
powder, electron acceptor
Sinónimos:
5-Methylphenazinium methyl sulfate, N-Methylphenazonium methyl sulfate, PMS
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Fórmula lineal:
C13H11N2 · CH3SO4
Número CAS:
Peso molecular:
306.34
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
206-072-1
MDL number:
Beilstein/REAXYS Number:
3898869
Form:
powder
Quality level:
Servicio técnico
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Permítanos ayudarleNombre del producto
Phenazine methosulfate,
form
powder
Quality Level
λ
0.01 g/L in H2O, 1 cm path
UV absorption
λ: 387.5 nm Amax
antibiotic activity spectrum
fungi
mode of action
DNA synthesis | interferes, cell membrane | interferes
storage temp.
−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
General description
Phenazines are heterocyclic compounds produced as secondary metabolites by bacteria.
Application
Phenazine methosulfate is used with ascorbic acid to determine nitric oxide reductase activity.
Phenazine methosulfate has been used:
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
Biochem/physiol Actions
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.
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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