Chloride substituents modify the physical properties of organic compounds in several ways. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Related Products of 104-86-9.
Huang, Yan;Shen, Yinjing;Li, Sichen;Zheng, Ruijie;Zhang, Chengjian;Li, Benxia;Zhang, Kun research published ã?Dual-emission samarium macrocycle as a lab-on-a-molecule enables high-throughput discrimination of anionic sulfonate surfactantsã? the research content is summarized as follows. Nowadays, it is still a huge challenge to efficiently discriminate of analogus anionic sulfonate surfactants, which are noxious xenobiotics related to many safety concerns of environment and life. Recently, great advances in orthogonal detection have shown the great advantages of principal component anal. (PCA) to construct a comprehensive statistical method for sensing signals in recognizing more analytes with similar structures. Inspired by sensor arrays, we propose a new â²one-element-two-channelâ?protocol upon a dual-emission samarium macrocycle Sm-2o as the lab-on-a-mol., containing two isolated emissions of macrocycle (443 nm) and Sm(III) (643 nm) emitters as two fluorescence channels. Herein, these targeted surfactants instruct original fluorescences of Sm-2o to generate diverse sensing signals which can finally convert into unique fingerprint patterns and distinguish four anionic surfactants (SDS, SDSO, SCI and AOS) from other ten ones, even their proportional concentrations Significantly, this high-throughput discrimination is realized by different receptor-analyte interactions and the structure transformation of Sm-2o in diverse microenvironments formed in various types of surfactants. Furthermore, these sensing systems also show satisfactory discrimination and semiquantitation performances for mixtures of anionic surfactants, especially the SDS and SDBS, in real water sample, revealing the practicability of our lab-on-a-mol. probe. On the basis of the PCA method, this work provides a vital reference for the design and application of multianalyte chemosensors.
Related Products of 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics