1,1,1-Trichloroethane
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| Names | |||
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| Preferred IUPAC name
1,1,1-Trichloroethane | |||
| Other names
1,1,1-TCA, Methyl chloroform, Chlorothene, Solvent 111, R-140a, Genklene, monochlorethylidene chloride (archaic) | |||
| Identifiers | |||
3D model (JSmol) |
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| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.000.688 | ||
| EC Number |
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| 82076 | |||
| KEGG | |||
PubChem CID |
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| RTECS number |
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| UNII | |||
| UN number | 2831 | ||
CompTox Dashboard (EPA) |
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| Properties | |||
| C2H3Cl3 or CH3CCl3 | |||
| Molar mass | 133.40 g/mol | ||
| Appearance | Colourless liquid | ||
| Odor | mild, chloroform-like | ||
| Density | 1.32 g/cm3 | ||
| Melting point | −33 °C (−27 °F; 240 K) | ||
| Boiling point | 74 °C (165 °F; 347 K) | ||
| 0.4% (20 °C) 0.480 g/litre at 20 °C | |||
| Vapor pressure | 100 mmHg (20°C) | ||
Refractive index (nD) |
1.437 | ||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards |
Ozone layer impact. Irritant to the upper respiratory tract. Causes severe irritation and swelling to eyes. | ||
| GHS labelling: | |||
| Warning | |||
| H332, H420 | |||
| P261, P271, P304+P312, P304+P340, P312, P502 | |||
| NFPA 704 (fire diamond) | |||
| Explosive limits | 7.5–12.5% | ||
| Lethal dose or concentration (LD, LC): | |||
LD50 (median dose) |
9600 mg/kg (oral, rat) 6000 mg/kg (oral, mouse) 5660 mg/kg (oral, rabbit) | ||
LC50 (median concentration) |
3911 ppm (mouse, 2 hr) 18000 ppm (rat, 4 hr) | ||
| NIOSH (US health exposure limits): | |||
PEL (Permissible) |
TWA 350 ppm (1900 mg/m3) | ||
REL (Recommended) |
C 350 ppm (1900 mg/m3) [15-minute] | ||
IDLH (Immediate danger) |
700 ppm | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
1,1,1-Trichloroethane, also known as methyl chloroform and chlorothene, is a chloroalkane with the chemical formula CH3CCl3. It is an isomer of 1,1,2-trichloroethane. A colourless and sweet-smelling liquid, it was once produced industrially in large quantities for use as a solvent. It is regulated by the Montreal Protocol as an ozone-depleting substance and as such use has declined since 1996. Trichloroethane should not be confused with the similar-sounding trichloroethene which is also commonly used as a solvent.