Tetrachloro-m-xylene (tetrachlorometaxylene, or TCMX) is the organochlorine compound with the formula C6Cl4(CH3)2. It is the chlorinated derivative of m-xylene in which the four aromatic hydrogen atoms are replaced by chlorine. It is prepared by ferric chloride-catalyzed reaction of the xylene with chlorine.[1]
^Riegger, Paul; Steffen, Klaus Dieter (1979). "Chlorination of xylenes and secondary Products. I. Chlorination of the nucleus and Side Chains of Xylenes". Chemiker-Zeitung. 103: 1-7.
tetrachloro, xylene, tetrachlorometaxylene, tcmx, organochlorine, compound, with, formula, c6cl4, chlorinated, derivative, xylene, which, four, aromatic, hydrogen, atoms, replaced, chlorine, prepared, ferric, chloride, catalyzed, reaction, xylene, with, chlori. Tetrachloro m xylene tetrachlorometaxylene or TCMX is the organochlorine compound with the formula C6Cl4 CH3 2 It is the chlorinated derivative of m xylene in which the four aromatic hydrogen atoms are replaced by chlorine It is prepared by ferric chloride catalyzed reaction of the xylene with chlorine 1 Tetrachloro m xylene NamesPreferred IUPAC name 1 2 3 5 Tetrachloro 4 6 dimethylbenzeneOther names Tetrachlorometaxylene2 4 5 6 TetrachlorometaxyleneIdentifiersCAS Number 877 09 8 Y3D model JSmol Interactive imageAbbreviations TCMXChemSpider 63327 YECHA InfoCard 100 011 715EC Number 212 886 8PubChem CID 70139UNII O8XMK3B4S9 YCompTox Dashboard EPA DTXSID6075433InChI InChI 1S C8H6Cl4 c1 3 5 9 4 2 7 11 8 12 6 3 10 h1 2H3 YKey NTUBJKOTTSFEEV UHFFFAOYSA N YInChI 1 C8H6Cl4 c1 3 5 9 4 2 7 11 8 12 6 3 10 h1 2H3Key NTUBJKOTTSFEEV UHFFFAOYANSMILES Clc1c c Cl c c Cl c1Cl C CPropertiesChemical formula C 8H 6Cl 4Molar mass 243 94524Appearance colorless or white solidMelting point 223 C 433 F 496 K Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox references TCMX is used as an internal standard in the analysis of organochlorides particularly organochloride pesticides 2 3 References Edit Riegger Paul Steffen Klaus Dieter 1979 Chlorination of xylenes and secondary Products I Chlorination of the nucleus and Side Chains of Xylenes Chemiker Zeitung 103 1 7 Organochlorine Pesticides by GCxGC ECD Wang Wentao Meng Bingjun Lu Xiaoxia Liu Yu Tao Shu 2007 Extraction of polycyclic aromatic hydrocarbons and organochlorine pesticides from soils A comparison between Soxhlet extraction microwave assisted extraction and accelerated solvent extraction techniques Analytica Chimica Acta 602 2 211 222 doi 10 1016 j aca 2007 09 023 This article about an organic halide is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Tetrachloro m xylene amp oldid 1092565108, wikipedia, wiki, book, books, library,
