1,1,1-Trichloroethane
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| Names | |||
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| Preferred IUPAC name
1,1,1-Trichloroethane | |||
Other names
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| 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−1 | ||
| Appearance | Colourless liquid | ||
| Odor | mild, chloroform-like | ||
| Density |
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| Melting point | −33 °C (−27 °F; 240 K) | ||
| Boiling point | 74–76 °C (165–169 °F; 347–349 K) | ||
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| log P | 2.49 (20 °C (68 °F; 293 K)) | ||
| Vapor pressure | 100 mmHg (13 kPa) (20 °C (68 °F; 293 K)) | ||
Refractive index (nD)
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1.437 D | ||
| Viscosity | 0.86 cP (20 °C (68 °F; 293 K)) | ||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H332, H350, H402, H420 | |||
| P201, P202, P261, P271, P273, P280, P304+P340+P312, P308+P313, P405, P501, P502 | |||
| NFPA 704 (fire diamond) | |||
| 537 °C; 998 °F; 810 K | |||
| Explosive limits | 7.5%–15% | ||
Threshold limit value (TLV)
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350 ppm (1,4-dioxane: 20 ppm, danger of cutaneous absorption) (TWA), 450 ppm (STEL), 350 ppm (1900 mg/m3) (C) | ||
| Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
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LC50 (median concentration)
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| NIOSH (US health exposure limits): | |||
PEL (Permissible)
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REL (Recommended)
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IDLH (Immediate danger)
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700 ppm | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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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.