Identification | Back Directory | [Name]
TOTO 3 | [CAS]
166196-17-4 | [Synonyms]
TOTO 3 Chebi:52299 Toto 3 Iodide 1,1'-[4,8-Bis(dimethyliminio)undecane-1,11-diyl]bis{4-[3-(3-methyl-1,3-benzothiazol-2(3H)-ylidene)prop-1-en-1-yl]quinolinium} tetraiodide 1,1'-(1,3-Propanediylbis((dimethyliminio)-3,1-propanediyl))bis(4-(3-(3-methyl-2(3H)-benzothiazolylidene)-1-propenyl)quinolinium) tetraiodide QUINOLINIUM, 1,1'-[1,3-PROPANEDIYLBIS[(DIMETHYLIMINIO)-3,1-PROPANEDIYL]]BIS[4-[3-(3-METHYL-2(3H)-BENZOTHIAZOLYLIDENE)-1-PROPENYL]-, TETRAIODIDE Quinolinium, 1,1
0
-[1,3-propanediylbis
[(dimethyliminio)-3,1-propanediyl]]bis[4-[3-(3-methyl-2
(3h)-benzothiazolylidene)-1-propenyl]-, Tetraiodide 2,2'-{[4,8-Bis(dimethyliminio)undecane-1,11-diyl]bis[quinolin-1-yl-4-ylideneprop-1-en-1-yl-3-ylidene]}bis(3-methyl-1,3-benzothiazol-3-ium) tetraiodide 2-((E)-3-[1-(3-[(3-[DIMETHYL(3-(4-[(Z,2E)-3-(3-METHYL-1,3-BENZOTHIAZOL-3-IUM-2-YL)-2-PROPENYLIDENE]-1-QUINOLINYL)PROPYL)AMMONIO]PROPYL)(DIMETHYL)AMMONIO]PROPYL)-4(1H)-QUINOLINYLIDENE]-1-PROPENYL)-3-METHYL-1,3-BENZOTHIAZOL-3-IUM TETRAIODIDE | [Molecular Formula]
C53H62IN6S2+3 | [MDL Number]
MFCD07433937 | [MOL File]
166196-17-4.mol | [Molecular Weight]
974.14 |
Chemical Properties | Back Directory | [solubility ]
Soluble in dimethyl sulfoxide | [form ]
powder | [color ]
Red | [λmax]
642nm (H2O/DNA) | [Biological Applications]
Nucleic acid hybridization; detecting nucleic acids,cells,human papilloma virus (HPV),pathogens; counting embryoblasts; determining nuclease activity; retinal toxicity screening methods; studying cellular uptake of gene transfer complexes | [Major Application]
Semiconductor devices |
Hazard Information | Back Directory | [Uses]
TOTO-3 (TOTO 3) is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells. | [References]
[1] Sultana M, et al. A review on experimental chemically modified activated carbon to enhance dye and heavy metals adsorption[J]. Cleaner engineering and technology, 2022, 6: 100382. |
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