6059-62-7

Usage

Uses

Used in Research and Development:
Dansyl-diMethylaMine is used as a fluorescent labeling agent for the detection and analysis of specific molecules in biological and chemical research. Its fluorescent properties enable researchers to track and visualize the behavior of molecules in various experimental setups.
Used in Pharmaceutical Industry:
Dansyl-diMethylaMine is used as a reagent in the synthesis of pharmaceutical compounds. Its ability to form fluorescent derivatives aids in the development of new drugs and the optimization of existing ones by providing a means to monitor their interactions with biological targets.
Used in Environmental Monitoring:
Dansyl-diMethylaMine is used as a tracer in environmental studies to monitor the presence and distribution of specific compounds in various ecosystems. Its fluorescent properties make it easier to detect and quantify target substances, providing valuable insights into their impact on the environment.
Used in Analytical Chemistry:
Dansyl-diMethylaMine is used as a derivatization agent in analytical chemistry to enhance the detection and quantification of certain compounds. By converting analytes into fluorescent derivatives, it improves the sensitivity and selectivity of analytical techniques, such as high-performance liquid chromatography (HPLC) and mass spectrometry (MS).

Upstream product

• 605-65-2 5-(dimethylamino)naphth-1-ylsulfonyl chloride 
• 124-40-3 dimethyl amine 

Downstream Products

• 112681-04-6 N-<5-<(dimethylamino)sulfonyl>naphth-1-yl>-N,N-dimethyl-N-(p-cyanobenzyl)ammonium trifluoromethanesulfonate 

Relevant academic research and scientific papers

Novel Water-Soluble β-Cyclodextrin-Calix[4]arene Couples as Fluorescent Sensor Molecules for the Detection of Neutral Analytes

The synthesis and the host-guest chemistry of two novel fluorescent β-cyclodextrin-calix[4]arene couples 1 and 2 is described. The compounds were prepared by coupling a β-cyclodextrin linked with an aminoxylyl spacer with two different calix[4]arene building blocks each bearing a fluorophore. The fluorophores attached to 1 and 2 are the 2-naphthylamine and the dansyl moiety, respectively. The unsymmetric calix[4]arene functionalization was achieved by monoprotection of the 1,3-diformylcalix[4]arene. The host molecules 1 and 2 were used as fluorescent probes for several organic analytes in aqueous solution. 1 shows sensitivity for a series of neutral organic guest species, such as steroids, terpenes, and other natural products. In contrast, compound 2 does not show sensitivity for organic analytes in aqueous solution. The different behavior of the two fluorescent probes 1 and 2 is explained by the different strength of self-inclusion of each fluorphoric group into the β-cyclodextrin cavity.

Photochemistry of Some Group V Onium Salts. Effect of Magnetic Nuclei on In-Cage Radical Coupling Reactions

A series of group V arylammonium, arylphosphonium, and arylarsonium salts have been synthesized and their photochemical behaviour investigated.Direct irradiation of the onium salts in acetonitrile provided photoproducts that were dependent on the magnitude of the nuclear hyperfine coupling constant of the heteroatom rather than spin-orbit coupling.The ammonium and phosphonium salts provided only out-of-cage coupling products while the arsonium salt provided both in-cage and out-of-cage coupling products.