![]() Sodium 9,10-Dimethoxyanthracene-2-sulfonate [Fluorimetric Ion-Pair Reagent for Amines] structure
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Common Name | Sodium 9,10-Dimethoxyanthracene-2-sulfonate [Fluorimetric Ion-Pair Reagent for Amines] | ||
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CAS Number | 67580-39-6 | Molecular Weight | 340.32600 | |
Density | 1.393g/cm3 | Boiling Point | N/A | |
Molecular Formula | C16H13NaO5S | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Tuning the photodriven electron transport within the columnar perylenediimide stacks by changing the π-extent of the electron donors.
Phys. Chem. Chem. Phys. 15(7) , 2539-46, (2013) Photodriven electron-transport properties of the self-assemblies of N,N'-di(2-(trimethylammoniumiodide)ethylene)perylenediimide stacks (TAIPDI)(n) with three electron donors, disodium 4,4'-bis(2-sulfonatostyryl)biphenyl (BSSBP, stilbene-420), sodium 9,10-dime... |
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D. Westerland, K.O. Borg
Anal. Chim. Acta 67 , 89, (1973)
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J.C. Gfeller et al.
J. Chromatogr. A. 172 , 141, (1979)
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J.M. Huen, J.P. Thevenin, J. High
Resolut. Chromatogr. Commun. 3 , 154, (1979)
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[Studies on the fluorometric ion pair method for the determination of several tertiary amines].
Yao Xue Xue Bao 20(10) , 752-8, (1985)
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Analysis of benzalkonium chloride in the effluent from European hospitals by solid-phase extraction and high-performance liquid chromatography with post-column ion-pairing and fluorescence detection.
J. Chromatogr. A. 774(1-2) , 281-6, (1997) A highly reproducible and specific method for the analysis of the quaternary ammonium compound, benzalkonium chloride, in effluents from European hospitals is presented. Benzalkonium chloride was extracted with end-capped RP-18 solid-phase cartridges and was ... |
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Spectrofluorometric determination of some beta-blockers in tablets and human plasma using 9,10-dimethoxyanthracene-2-sodium sulfonate.
Pharmazie 60(4) , 265-8, (2005) A simple and sensitive spectrofluorometric method was developed for the quantitative determination of some beta-blockers, namely arotinolol, atenolol and labetalol as hydrochloride salts. The method is based on the reaction of these drugs as n-electron donors... |