I14150
Isobutylamine
99%
Synonym(s):
1-Amino-2-methylpropane
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About This Item
Linear Formula:
(CH3)2CHCH2NH2
CAS Number:
Molecular Weight:
73.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-145-4
Beilstein/REAXYS Number:
385626
MDL number:
Assay:
99%
Form:
liquid
Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.397 (lit.)
bp
64-71 °C (lit.)
mp
−85 °C (lit.)
density
0.736 g/mL at 25 °C (lit.)
SMILES string
CC(C)CN
InChI
1S/C4H11N/c1-4(2)3-5/h4H,3,5H2,1-2H3
InChI key
KDSNLYIMUZNERS-UHFFFAOYSA-N
Application
Isobutylamine may be used in the synthesis of N-i-butyl-9(Z),12(Z),15(Z)-octadecatrienamide by reacting with trilinolenin. It can also react with tropolone to form a hydrogen-bonded complex, isobutylammonium 7-oxocyclohepta-1,3,5-trien-1-olate. Fullerene (C60) can undergo oxyamination with isobutylamine to form polyamines.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Flam. Liq. 2 - Skin Corr. 1A
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
15.8 °F - closed cup
flash_point_c
-9 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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The tropolone?isobutylamine complex: a hydrogen-bonded troponoid without dominant ??? interactions.
Vealey ZN
Acta Crystallographica Section C, Structural Chemistry, 72(10), 730-737 (2016)
A new window on fullerene chemistry: An electrospray mass spectrometric study of the amination of C60.
Wilson SR
Journal of Mass Spectrometry : Jms, 29(4), 186-191 (1994)
Synthesis of a fatty tetrahydroxyamide using peroxygenase from oat seeds.
Piazza GJ
Journal of the American Oil Chemists' Society, 81(10), 933-937 (2004)