sec-Butylamine
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Template:Chembox image cellTemplate:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox SolubilityInWaterTemplate:Chembox headerbarTemplate:Chembox HazardsTemplate:Chembox headerbarTemplate:Chembox Datapage checkTemplate:Yesno| Template:Longitem | Template:Unbulleted list |
| Abbreviations | 2-AB |
| Template:Longitem | 1361345, 1718761 (R), 1718760 (S) |
| ChEBI | Template:Unbulleted list |
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| DrugBank | Template:Unbulleted list |
| EC Number | Template:Unbulleted list |
| KEGG | Template:Unbulleted list |
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| RTECS number | Template:Unbulleted list |
| UN number | 2733 |
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| Template:Longitem | Template:Chembox Elements/molecular formula |
| Molar mass | Template:Chem molar mass |
| Appearance | Colorless liquid |
| Odor | Fishy, ammoniacal |
| Density | 0.724 g cm−3 |
| Melting point | Template:Chembox CalcTemperatures |
| Boiling point | Template:Chembox CalcTemperatures |
| Template:Longitem | 1.3928 |
| Viscosity | 500 μPa s (at 20 °C) |
| Template:Longitem | −138.5 to −136.5 kJ mol−1 |
| Template:Longitem | −3.0095 to −3.0077 MJ mol−1 |
| Template:Longitem | Template:Unbulleted list |
| Template:Longitem | 2-Methyl-2-nitrosopropane |
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sec-Butylamine is an organic chemical compound (specifically, an amine) with the formula CH3CH2CH(NH2)CH3. It is a colorless liquid. sec-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, tert-butylamine, and isobutylamine. sec-Butylamine is chiral and therefore can exist in either of two enantiomeric forms.
sec-Butylamine is used in the production of some pesticides.[2]
File:Bromacil skeletal.svg Bromacil, a commercial herbicide, is produced from sec-butylamine.[3]
Safety
The LD50 (rat) for primary alkylamines is 100 – 1 mg/kg.[2]
References
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- ↑ a b Template:Ullmann
- ↑ United States Environmental Protection Agency. "Bromacil". 1996, pp. 1–11. Accessed 9 October 2012
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