Tetrachloro-m-xylene
(Redirected from Tetrachlorometaxylene)
<templatestyles src="Chembox/styles.css"/>
Template:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox HazardsTemplate:Chembox Datapage checkTemplate:Yesno| Template:Chembox image sbs cell | |
| Template:Longitem | Template:Unbulleted list |
| Abbreviations | TCMX |
| ChEBI | Template:Unbulleted list |
| ChemSpider | Template:Unbulleted list |
| DrugBank | Template:Unbulleted list |
| EC Number | Template:Unbulleted list |
| KEGG | Template:Unbulleted list |
| Template:Longitem | Template:Unbulleted list |
| RTECS number | Template:Unbulleted list |
| Script error: No such module "collapsible list". | |
| Script error: No such module "collapsible list". | |
| Template:Longitem | Template:Chembox Elements/molecular formula |
| Molar mass | 243.94524 |
| Appearance | colorless or white solid |
| Melting point | Template:Chembox CalcTemperatures |
Template:Chembox Footer/tracking container onlyScript error: No such module "TemplatePar".Template:Short description
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]
TCMX is used as an internal standard in the analysis of organochlorides, particularly organochloride pesticides.[2][3]
References
<templatestyles src="Reflist/styles.css" />
- ↑ Script error: No such module "Citation/CS1".
- ↑ Organochlorine Pesticides by GCxGC-ECDScript error: No such module "Unsubst".
- ↑ Script error: No such module "Citation/CS1".
Script error: No such module "Check for unknown parameters".