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9-amino-10-methylacridinium chloride is a chemical compound with the molecular formula C14H14ClN2. It is an organic compound derived from the acridine family, characterized by its tricyclic structure with a methyl group at the 10th position and an amino group at the 9th position. 9-amino-10-methylacridinium chloride is known for its potential applications in various fields, including pharmaceuticals and as a chemical intermediate. It is typically synthesized through a series of chemical reactions and is used in the preparation of certain dyes and pigments. Due to its specific structure, it may also have implications in the development of new materials with unique properties.

5776-38-5

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5776-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5776-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5776-38:
(6*5)+(5*7)+(4*7)+(3*6)+(2*3)+(1*8)=125
125 % 10 = 5
So 5776-38-5 is a valid CAS Registry Number.

5776-38-5Downstream Products

5776-38-5Relevant academic research and scientific papers

Fluorescence Quenching of 9-Aminoacridines by Purine Mononucleotides

Kubota, Yukio,Motoda, Yuko

, p. 2855 - 2861 (1980)

The kinetics of fluorescence quenching of 9-aminoacridine (9AA) and 9-amino-10-methylacridinium (10Me-9AA) by purine mononucleotides (adenosine 5'-monophosphate (AMP) and guanosine 5'-monophosphate (GMP)) has been studied over the temperature range of 25-46 deg C in 0.1 M phosphate buffer (pH 7.0).A set of quenching parameters has been obtained on the basis of the kinetic scheme which takes into account complex formation in the ground state as well as in the excited singlet state. Both steady-state and transient fluorescence measurements have been carried out in order to determine rate constants.The rate constant for the complex formation is found to be 3.5E9 - 7E9 M-1 s-1, indicating that the reaction is a diffusion-controlled one, while the rate constant for the complex dissociation is found to be much smaller than that for the complex formation.The dye-GMP complex is shown to relax nonradiatively, whereas the dye-AMP complerr is accompanied by weak fluorescence and its decay kinetics obeys a double-exponential decay law.It is found that the quenching behavior for the mutagenic dye 9AA is very similar to that for the nonmutagenic dye 10Me-9AA.Thermodynamic properties for the complex formation are also discussed.

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