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P4544

Sigma-Aldrich

Phenazine ethosulfate

≥95% purity, powder

Synonym(s):

N-Ethyldibenzopyrazine ethyl sulfate salt

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About This Item

Linear Formula:
C16H18N2SO4
CAS Number:
Molecular Weight:
334.39
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

product name

Phenazine ethosulfate, ≥95%

Quality Level

Assay

≥95%

form

powder

solubility

ethanol: 50 mg/mL, clear

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

−20°C

SMILES string

CCOS([O-])(=O)=O.CC[n+]1c2ccccc2nc3ccccc13

InChI

1S/C14H13N2.C2H6O4S/c1-2-16-13-9-5-3-7-11(13)15-12-8-4-6-10-14(12)16;1-2-6-7(3,4)5/h3-10H,2H2,1H3;2H2,1H3,(H,3,4,5)/q+1;/p-1

InChI key

VDJKJPMLWJWQIH-UHFFFAOYSA-M

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General description

Phenazine ethosulfate is a cationic dye and a chemical electron acceptor. It is used in dye-linked enzyme assays. At a high pH, the dye produces free radicals, which may be the actual electron acceptors.

Application

Phenazine ethosulfate has been used:
  • in the spectrophotometric assessment of Plasmodium falciparum lactate dehydrogenase activity
  • to study the use of the dye during culture of embryos on fetal and postnatal calf development
  • to test and validate a fluorescence approach to quantify lipid content of individual bovine oocytes and blastocysts

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Emanuele Zonaro et al.
Microbial cell factories, 16(1), 215-215 (2017-12-01)
Bacteria have developed different mechanisms for the transformation of metalloid oxyanions to non-toxic chemical forms. A number of bacterial isolates so far obtained in axenic culture has shown the ability to bioreduce selenite and tellurite to the elemental state in
Cross-validation of techniques for measuring lipid content of
bovine oocytes and blastocysts
M. Barcelo
Theriogenology (2011)
High-Throughput Screening in Drug Discovery (2006)
Victor Davidson
Principles and Applications of Quinoproteins (1992)
Gianfranco Fontana et al.
Bioorganic chemistry, 90, 103054-103054 (2019-06-19)
Oleanolic and ursolic acids are two ubiquitous isomeric triterpene phytochemicals known for their anticancer activity. A set of derivatives of the two compounds with a modified oxidation state and lipophylicity at C-3 and C-28 positions, were prepared and tested as

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