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Phenazine methosulfate

SIGMA/P9625

Synonym: 5-Methylphenazinium methyl sulfate; N-Methylphenazonium methyl sulfate; PMS

CAS Number: 299-11-6
Empirical Formula (Hill Notation): C14H14N2O4S
Molecular Weight: 306.34
EC Number: 206-072-1
MDL Number: MFCD00011923
Linear Formula: C13H11N2 · CH3SO4
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-P9625-500MG 500 mg
 $35.70
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45-P9625-1G 1 g
 $61.30
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45-P9625-5G 5 g
 $247.00
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45-P9625-10G 10 g
 $366.00
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45-P9625-25G 25 g
 $686.00
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λ 0.01 g/L in H2O, 1 cm path
antibiotic activity spectrum fungi
form powder
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
mode of action cell membrane | interferes
  DNA synthesis | interferes
Quality Level 200 
SMILES string COS([O-])(=O)=O.C[n+]1c2ccccc2nc3ccccc13
storage temp. −20°C
UV absorption λ: 387.5 nm Amax
Application: 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
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.
General description: Phenazines are heterocyclic compounds produced as secondary metabolites by bacteria.
Packaging: 1, 5, 10, 25 g in glass bottle
Packaging: 500 mg in glass bottle
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Storage Temp. −20°C
UNSPSC 12352200

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