Deuterated chloroform
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| Names | |||
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| IUPAC name
trichloro(deuterio)methane | |||
| Preferred IUPAC name
trichloro(²H)methane | |||
| Other names
Chloroform-d Deuterochloroform | |||
| Identifiers | |||
3D model (JSmol) |
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| 1697633 | |||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.011.585 | ||
| EC Number |
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PubChem CID |
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| UNII | |||
| UN number | 1888 | ||
CompTox Dashboard (EPA) |
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| Properties | |||
| CDCl3 | |||
| Molar mass | 120.384 g/mol | ||
| Appearance | Colorless liquid | ||
| Odor | chloroform-like | ||
| Density | 1.500 g/cm3 | ||
| Melting point | −64 °C (−83 °F; 209 K) | ||
| Boiling point | 61 °C (142 °F; 334 K) | ||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H302, H315, H319, H331, H336, H351, H361, H372, H373 | |||
| P201, P202, P260, P261, P264, P270, P271, P280, P281, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P313, P311, P312, P314, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |||
| NFPA 704 (fire diamond) | |||
| Related compounds | |||
Related compounds |
Chloroform | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Deuterated chloroform, also known as chloroform-d, is the organic compound with the formula CDCl3. Deuterated chloroform is a common solvent used in NMR spectroscopy. The properties of CDCl3 and ordinary CHCl3 (chloroform) are virtually identical.
Deuterochloroform was first made in 1935 during the years of research on deuterium.