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| Names | |||
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IUPAC name
Butanenitrile
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Other names
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| Identifiers | |||
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3D model (Jmol)
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| 1361452 | |||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.003.365 | ||
| EC Number | 203-700-6 | ||
| MeSH | N-butyronitrile | ||
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PubChem CID
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| RTECS number | ET8750000 | ||
| UN number | 2411 | ||
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| Properties | |||
| C4H7N | |||
| Molar mass | 69.11 g·mol−1 | ||
| Appearance | Colorless | ||
| Odor | Sharp and suffocating | ||
| Density | 794 mg mL−1 | ||
| Melting point | −111.90 °C; −169.42 °F; 161.25 K | ||
| Boiling point | 117.6 °C; 243.6 °F; 390.7 K | ||
| 0.033 g/100 mL | |||
| Solubility | soluble in benzene miscible in alcohol, ether, dimethylformamide |
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| Vapor pressure | 3.1 Pa | ||
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Henry's law
constant (kH) |
190 μmol Pa−1 kg−1 | ||
| -49.4·10−6 cm3/mol | |||
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Refractive index (nD)
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1.38385 | ||
| 3.5 | |||
| Thermochemistry | |||
| 134.2 J K−1 mol−1 | |||
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Std enthalpy of
formation (ΔfH |
−6.8–−4.8 kJ mol−1 | ||
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Std enthalpy of
combustion (ΔcH |
−2.579 MJ mol−1 | ||
| Hazards | |||
| GHS pictograms |
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| GHS signal word | DANGER | ||
| H225, H301, H311, H331 | |||
| P210, P261, P280, P301+310, P311 | |||
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EU classification (DSD)
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| R-phrases | R11, R23/24/25 | ||
| S-phrases | (S1/2), S16, S36/37, S45, S63 | ||
| NFPA 704 | |||
| Flash point | 18 °C (64 °F; 291 K) | ||
| 488 °C (910 °F; 761 K) | |||
| Explosive limits | 1.65%–? | ||
| Lethal dose or concentration (LD, LC): | |||
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LD50 (median dose)
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50 mg kg−1(oral, rat) | ||
| US health exposure limits (NIOSH): | |||
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PEL (Permissible)
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none | ||
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REL (Recommended)
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TWA 8 ppm (22 mg/m3) | ||
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IDLH (Immediate danger)
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N.D. | ||
| Related compounds | |||
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Related alkanenitriles
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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 | |||
Butyronitrile or butanenitrile or propyl cyanide, is a nitrile with the formula C3H7CN. This colorless liquid is miscible with most polar organic solvents.
Butyronitrile is mainly used as a precursor to the poultry drug amprolium.
Butyronitrile is prepared industrially by the ammoxidation of n-butanol:
Butyronitrile has been detected in the Large Molecule Heimat.