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| Names | |||
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IUPAC name
1,3-Dibromopropane
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Other names
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| Identifiers | |||
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109-64-8 |
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| 3D model (Jmol) | Interactive image | ||
| 635662 | |||
| ChemSpider |
7710 |
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| ECHA InfoCard | 100.003.356 | ||
| EC Number | 203-690-3 | ||
| MeSH | 1,3-dibromopropane | ||
| PubChem | 8001 | ||
| RTECS number | TX8575000 | ||
| UNII |
YQR3048IX9 |
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| UN number | 1993 | ||
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| Properties | |||
| C3H6Br2 | |||
| Molar mass | 201.89 g·mol−1 | ||
| Appearance | Colorless liquid | ||
| Density | 1.989 g mL−1 | ||
| Melting point | −34.20 °C; −29.56 °F; 238.95 K | ||
| Boiling point | 167 °C; 332 °F; 440 K | ||
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Henry's law
constant (kH) |
11 μmol Pa−1 kg−1 | ||
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Refractive index (nD)
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1.524 | ||
| Thermochemistry | |||
| 163.7 J K mol−1 | |||
| Hazards | |||
| GHS pictograms |
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| GHS signal word | WARNING | ||
| H226, H302, H315, H411 | |||
| P273 | |||
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EU classification (DSD)
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| R-phrases | R10, R22, R38, R51/53 | ||
| S-phrases | S16, S26, S36 | ||
| Flash point | 56 °C (133 °F; 329 K) | ||
| Lethal dose or concentration (LD, LC): | |||
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LD50 (median dose)
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315 mg kg−1(oral, rat) | ||
| Related compounds | |||
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Related alkanes
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Related compounds
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Mitobronitol | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |||
1,3-Dibromopropane is a halogenated hydrocarbon. When at room temperature, it is a colorless to light-brown liquid. Synthetically, it is very useful to form C3-bridged compounds such as through C-N coupling reactions.
1,3-Dibromopropane was used in the first cyclopropane synthesis in 1881, known as the Freund reaction.
1,3-Dibromopropane can be prepared via the free radical addition between allyl bromide and hydrogen bromide.