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M8640

Sigma-Aldrich

1-Methoxy-5-methylphenazinium methyl sulfate

≥95% purity , powder

Synonym(s):

1-Methoxyphenazine methosulfate

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About This Item

Empirical Formula (Hill Notation):
C15H16N2O5S
CAS Number:
Molecular Weight:
336.36
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

product name

1-Methoxy-5-methylphenazinium methyl sulfate, ≥95%

Quality Level

Assay

≥95%

form

powder

composition

Nitrogen: ≥ 7.9%

color

red to brown

solubility

H2O: 1 mg/mL, clear, red

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

COS([O-])(=O)=O.COc1cccc2[n+](C)c3ccccc3nc12

InChI

1S/C14H13N2O.CH4O4S/c1-16-11-7-4-3-6-10(11)15-14-12(16)8-5-9-13(14)17-2;1-5-6(2,3)4/h3-9H,1-2H3;1H3,(H,2,3,4)/q+1;/p-1

InChI key

MASUWVVNWALEEM-UHFFFAOYSA-M

General description

1-Methoxy-5-methylphenazinium methyl sulfate (MPMS) is a photochemically stable electron-transport mediator between NAD(P)H and tetrazolium dyes. The reduced form of MPMS converts tetrazolium salt to purple precipitate formazan.It is a very stable and non-enzymic electron carrier that mediates electron transfer by dehydrogenases in vitro to various electron acceptors such as tetrazolium dyes or the electrode of an enzymic electric cell.

Application

1-Methoxy-5-methylphenazinium methyl sulfate has been used as a component of buffers or solutions for the assay of lactate dehydrogenase and muscle succinate dehydrogenase.

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 2

Target Organs

Nervous system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Patries M Herst et al.
Biochimica et biophysica acta, 1767(2), 170-177 (2007-02-03)
Oxygen consumption for bioenergetic purposes has long been thought to be the prerogative of mitochondria. Nevertheless, mitochondrial gene knockout (rho(0)) cells that are defective in mitochondrial respiration require oxygen for growth and consume oxygen at the cell surface via trans-plasma
An optimized lactate dehydrogenase release assay for screening of drug candidates in neuroscience.
Kaja S, et. al.
Journal of Pharmacological and Toxicological Methods, 73, 1-1 (2015)
Early life exposure to chronic intermittent hypoxia causes upper airway dilator muscle weakness, which persists into young adulthood.
McDonald FB, et. al.
Experimental Physiology, 100, 947-947 (2015)
Kuniyo Inouye et al.
Journal of biochemistry, 131(1), 97-105 (2002-01-05)
A synchronous enzyme-reaction system using water-soluble formazan and a non-enzymatic electron mediator was developed and applied to an enzyme immunoassay (EIA). The reaction system consists of four steps: (I) dephosphorylation of NADP(+) to produce NAD(+) by alkaline phosphatase (ALP), (II)
Maxim Bychkov et al.
PloS one, 14(5), e0217339-e0217339 (2019-06-01)
Lynx1 is the first three-finger prototoxin found in the mammalian central nervous system. It is a GPI-anchored protein modulating nicotinic acetylcholine receptors (nAChRs) in the brain. Besides the brain, the Lynx1 protein was found in the lung and kidney. Endogenous

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