5464-91-5

Usage

General Description

10-methyl-9-phenylacridinium is a chemical compound with the molecular formula C20H16N+. It is a cationic dye with a bright green fluorescence, making it useful in various applications such as industrial and biological staining, fluorescence microscopy, and flow cytometry. 10-methyl-9-phenylacridinium is commonly used as a fluorescent label for nucleic acids, proteins, and lipid membranes due to its high quantum yield and photostability. Additionally, it can also be utilized as a fluorescent probe for detecting DNA, RNA, and protein in biological samples. Furthermore, 10-methyl-9-phenylacridinium has been studied for its potential use in photodynamic therapy owing to its photosensitizing properties, showing promise in cancer treatment. Overall, this chemical compound is significant in various fields due to its fluorescent properties and potential applications in research and medical diagnostics.

Upstream product

• 602-56-2 9-phenylacridine 
• 74-88-4 methyl iodide 
• 7647-01-0 hydrogenchloride 
• 64-17-5 ethanol 
• 56875-26-4 10-methyl-9-phenyl-9,10-dihydroacridine 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 2989-45-9 1-benzylidene-2-methyl-2-phenylhydrazine 
• 13466-29-0 1-benzylidene-2-methylhydrazine 
• 36648-32-5 (2-(dimethylamino)phenyl)(phenyl)methanone 
• 100-52-7 benzaldehyde 
• 618-40-6 1-Methyl-1-phenylhydrazine 
• 1075-70-3 benzaldehyde N,N-dimethylhydrazone 
• 1338830-00-4 N,N-dimethyl-2-[imino(phenyl)methyl]aniline 
• 56733-21-2 N-methyl-9-phenylacridinium iodide 

Downstream Products

• 99682-60-7 9-methoxy-10-methyl-9-phenyl-9,10-dihydroacridine 
• 56875-26-4 10-methyl-9-phenyl-9,10-dihydroacridine 
• 5096-13-9 1-benzylnicotinamide chloride 
• 15519-25-2 3-(aminocarbonyl)-1-(phenylmethyl)pyridinium perchlorate 
• 100667-92-3 9-phenyl-10-methylacridinyl radical 
• 99354-51-5 9-Deuterio-10-methyl-9-phenylacridan 
• 13089-53-7 C₁₃H₁₂⁽²⁾HN₂O⁽¹⁺⁾*Cl^(1-) 
• 96003-36-0 10-methyl-9-phenyl-9-phenylsulfanyl-9,10-dihydro-acridine 

Relevant academic research and scientific papers

Thermal and Photochemical Reactions of 10-Mehtyl-9-phenylacridinium Chloride in Alcohols

The photoreduction of 10-methyl-9-phenylacridinium chloride in methanol containing K2CO3 involves the nucleophilic addition of methanol to the 9-position of the acridinium cation, the photoinduced heterolysis of the methanol adduct, and the hydride transf

Synthesis of o -(dimethylamino)aryl ketones, acridones, acridinium salts, and 1 H -indazoles by the reaction of hydrazones and arynes

A novel, efficient route to biologically and pharmaceutically important o-(dimethylamino)aryl ketones, acridones, acridinium salts, and 1H-indazoles has been developed starting from readily available hydrazones of aldehydes and o-(trimethylsilyl)aryl triflates. The reaction proceeds through arynes under mild conditions, tolerates a wide range of functional groups, and provides the final products in good to excellent yields.

Electrochemistry of the 9-phenyl-10-methyl-acridan/acridinium redox system; a high-potential NADH/NAD+ analogue

Cyclic voltammetry and preparative controlled potential electrolysis show that the 9-phenyl-10-methyl-acridinium/acridan (AcPh+/AcPhH) redox couple can be cycled electrochemically between the oxidized (AcPh+) and reduced states (AcPhH) without any apparent side-reaction.The 9-phenyl-10-methyl-acridanyl radical (AcPh*) was identified as a first intermediate in the electrochemical reduction of AcPh+ by cyclic voltammetry as well as by electronic absorption and ESR spectroscopy.In contrast to other acridanyl and related dihydropyridyl radicals, AcPh* shows no tendency to undergo dimerization.In aprotic media, AcPh. is shown to undergo a second reversible one-electron reduction to yield AcPh-, which is, even in these media readily protonated to give AcPhH.The stability of these intermediates seems to be the major factor responsible for the clean electrochemical interconversion of the AcPh+/AcPhH redox couple.The implementation of this redox couple as part of photo-electrochemical energy conversion systems is discussed.