N-[4-[[4-(Dimethylamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidenen]-N-methyl-methanaminium, ethanedioate (1:1)

CAS: 13425-25-7

Ref. 3D-FD07808

Produktinformation

• Name: N-[4-[[4-(Dimethylamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidenen]-N-methyl-methanaminium, ethanedioate (1:1)
• Synonyme: 2-Hydroxy-2-Oxo-Acetate, 219-441-7, Ethanedioic acid, ion(1-), N-[4-[[4-(dimethylamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-N-methylmethanaminium, Methanaminium, N-[4-[[4-(dimethylamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-N-methyl-, ethanedioate (1:1), N-[4-[[4-(Dimethylamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-N-methylmethanaminium ethanedioate (1:1), Oxalic Acid, [4-[(4-Dimethylaminophenyl)-Phenyl-Methylene]-1-Cyclohexa-2,5-Dienylidene]-Dimethyl-Ammonium
• CAS: 13425-25-7

Beschreibung

N-[4-[[4-(Dimethylamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidenen]-N-methyl-methanaminium, ethanedioate (1:1) (EMC) is a surface methodology that employs a model system to study the kinetics of various reactions. It is used in the analysis of blood samples stained with cresyl violet acetate and tetrazolium chloride. The histology and electrochemical impedance spectroscopy are also used to examine EMC's morphology and conductivity, respectively. EMC is an analytical method that has been shown to give kinetic data for the reaction between activated sludge and phenol.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 418.49 g/mol
• Formel: C₂₃H₂₅N₂·C₂HO₄
• Reinheit: Min. 95%