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*sec*-Butylamine
Names

Preferred IUPAC name Butan-2-amine
Other names 2-Aminobutane 2-Butanamine (±)-sec-Butylamine DL-sec-Butylamine 1-Methylpropylamine Mono-sec-butylamine
Identifiers
CAS Number	13952-84-6^Y 13250-12-9 (R)^Y 513-49-5 (S)^Y
3D model (JSmol)	Interactive image
Abbreviations	2-AB
Beilstein Reference	1361345, 1718761 (R), 1718760 (S)
ChEBI	CHEBI:74526^N
ChemSpider	23255^Y 2006669 (R)^N 5145745 (S)^N
ECHA InfoCard	100.034.288
EC Number	237-732-7
KEGG	C18706^Y
PubChem CID	24874 2724537 (R) 6713753 (S)
RTECS number	EO3325000
UNII	QAZ452YGSG^Y 29HC5ICB6K (R)^Y Z192XWH21O (S)^Y
UN number	2733
CompTox Dashboard (EPA)	DTXSID4022284
InChI InChI=1S/C4H11N/c1-3-4(2)5/h4H,3,5H2,1-2H3^Y Key: BHRZNVHARXXAHW-UHFFFAOYSA-N^Y
SMILES CCC(C)N
Properties
Chemical formula	C₄H₁₁N
Molar mass	73.139 g·mol⁻¹
Appearance	Colorless liquid
Odor	Fishy, ammoniacal
Density	0.724 g cm⁻³
Melting point	−104.50 °C; −156.10 °F; 168.65 K
Boiling point	63 °C; 145 °F; 336 K
Solubility in water	Miscible^[1]
Refractive index (n_D)	1.3928
Viscosity	500 μPa s (at 20 °C)
Thermochemistry
Std enthalpy of formation (Δ_fH^⦵₂₉₈)	−138.5 to −136.5 kJ mol⁻¹
Std enthalpy of combustion (Δ_cH^⦵₂₉₈)	−3.0095 to −3.0077 MJ mol⁻¹
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H225, H302, H314, H332, H400
Precautionary statements	P210, P273, P280, P305+P351+P338, P310
NFPA 704 (fire diamond)	3 3 0
Flash point	19 °C (66 °F; 292 K)
Lethal dose or concentration (LD, LC):
LD₅₀ (median dose)	152 mg kg⁻¹ (oral, rat) 2.5 g kg⁻¹ (dermal, rabbit)
Related compounds
Related alkanamines	Propylamine Isopropylamine Isobutylamine tert-Butylamine n-Butylamine
Related compounds	2-Methyl-2-nitrosopropane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references

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]

Safety

The LD50 (rat) for primary alkylamines is 100 – 1 mg/kg.^[2]

References

^ "ICSC 0401 - sec-BUTYLAMINE".
^ ^a ^b Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2005). "Amines, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_001. ISBN 978-3527306732.
^ United States Environmental Protection Agency. "Bromacil". 1996, pp. 1–11. Accessed 9 October 2012

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