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Merck
CN

I14150

Isobutylamine

99%

Synonym(s):

1-Amino-2-methylpropane

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About This Item

Linear Formula:
(CH3)2CHCH2NH2
CAS Number:
78-81-9
Molecular Weight:
73.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24895931
EC Number:
201-145-4
Beilstein/REAXYS Number:
385626
MDL number:
MFCD00008146
Assay:
99%
Form:
liquid

Key Documents

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Product Name

Isobutylamine, 99%

InChI key

KDSNLYIMUZNERS-UHFFFAOYSA-N

InChI

1S/C4H11N/c1-4(2)3-5/h4H,3,5H2,1-2H3

SMILES string

CC(C)CN

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.)

Quality Level

200

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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.

signalword

Danger

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SDBB7020
SDBB4029
SDBB0466
STBL2091
STBL1740

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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)
The tropolone?isobutylamine complex: a hydrogen-bonded troponoid without dominant ??? interactions.
Vealey ZN
Acta Crystallographica Section C, Structural Chemistry, 72(10), 730-737 (2016)
Synthesis of a fatty tetrahydroxyamide using peroxygenase from oat seeds.
Piazza GJ
Journal of the American Oil Chemists' Society, 81(10), 933-937 (2004)
L Wang et al.
Journal of immunology (Baltimore, Md. : 1950), 167(11), 6195-6201 (2001-11-21)
Whereas cytokine production in alphabeta T cells is rapidly regulated by exposure to peptide Ag, the mechanisms regulating cytokine production by gammadelta T cells are unknown. In this study, we demonstrate that human Vgamma2Vdelta2 T cells produce IFN-gamma and TNF-alpha
Chun-Zhao Liu et al.
Journal of agricultural and food chemistry, 54(22), 8456-8460 (2006-10-26)
Inoculation of leaf explants of Echinacea purpurea (Moench) with Agrobacterium rhizogenes induced hairy roots with the capacity to produce biologically active caffeic acid derivatives (CADs), especially cichoric acid. The kinetics of growth, the uptake of macronutrients, and the accumulation of
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