Skip to Content
Merck
All Photos(1)

Key Documents

Safety Information

I14150

Sigma-Aldrich

Isobutylamine

99%

Synonym(s):

1-Amino-2-methylpropane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)2CHCH2NH2
CAS Number:
Molecular Weight:
73.14
Beilstein:
385626
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

Looking for similar products? Visit Product Comparison Guide

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.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Flam. Liq. 2 - Skin Corr. 1A

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

15.8 °F - closed cup

Flash Point(C)

-9 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water soluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

I14150-5ML:
I14150-1L:
I14150-250ML:
I14150-BULK:
I14150-500ML:
I14150-100ML:
I14150-2.5L:
I14150-VAR:


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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)
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
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service