1,4-Bis(trichloromethyl)benzene
Chemical compound
From Wikipedia, the free encyclopedia
1,4-Bis(trichloromethyl)benzene is an organic compound with the formula C6H4(CCl3)2. A white solid, it is prepared industrially by chlorination of para-xylene. It reacts with terephthalic acid to give terephthaloyl chloride, a precursor to Kevlar.[1] It also reacts with sulfur dioxide to give the same acid chloride and thionyl chloride.[2] It reacts with hydrogen fluoride in 1,2-dichloroethane to form 1,4-bis(chlorodifluoromethyl)benzene in a yield of 79%.[3]
| Names | |
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| Preferred IUPAC name
1,4-Bis(trichloromethyl)benzene | |
| Other names
hexachloroxylene; hexachloroparaxylene; Chloxil; Chloxyl | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.624 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| Appearance | white solid |
| Density | 1.778 g/cm3 |
| Melting point | 108â110 °C (226â230 °F; 381â383 K) |
| Boiling point | 213 °C (415 °F; 486 K) |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H301, H311, H314, H331 | |
| P260, P264, P270, P271, P280, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P311, P312, P321, P322, P330, P361, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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