Skip to Content
Merck
All Photos(2)

Documents

135186

Sigma-Aldrich

Diisobutylamine

99%

Synonym(s):

2-Methyl-N-(2-methylpropyl)-1-propanamine, N,N-Bis(2-methylpropyl)amine

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(CH3)2CHCH2NHCH2CH(CH3)2
CAS Number:
110-96-3
Molecular Weight:
129.24
Beilstein:
1209251
EC Number:
203-819-3
MDL number:
MFCD00008930
UNSPSC Code:
12352100
PubChem Substance ID:
24848204
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.4081 (lit.)

bp

137-139 °C (lit.)

mp

−77 °C (lit.)

density

0.74 g/mL at 25 °C (lit.)

SMILES string

CC(C)CNCC(C)C

InChI

1S/C8H19N/c1-7(2)5-9-6-8(3)4/h7-9H,5-6H2,1-4H3

InChI key

NJBCRXCAPCODGX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Diisobutylamine forms crystalline adducts with zinc and copper(II)-dithiocarbamate complexes.

Application

Diisobutylamine was used to study the effect of achiral amine on hydrogenation of ethyl pyruvate over cinchonidine-Pt/Al2O3 catalyst system.

Signal Word

Danger

Hazard Statements

H226,H301,H314,H412

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

86.0 °F - closed cup

Flash Point(C)

30 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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

Slide 1 of 3

1 of 3

Dicyclohexylamine 99%

Sigma-Aldrich

185841

Dicyclohexylamine

Dibenzylamine 97%

Sigma-Aldrich

D34108

Dibenzylamine

Diethylamine ≥99.5%

Sigma-Aldrich

471216

Diethylamine

Influence of achiral amine additives on the Orito's reaction.
Talas E, et al.
J. Mol. Catal. A: Chem., 357, 87-94 (2012)
Adducts of zinc and copper (II) dialkyldithiocarbamate complexes with dibutyl-and diisobutylamines: Synthesis, structures, EPR and solid-state natural abundance 13C and 15N CP/MAS NMR spectra.
Ivanov AV, et al.
Russian Journal of Coordination Chemistry, 33(4), 233-243 (2007)
Sarah Otto et al.
Carbohydrate polymers, 254, 117280-117280 (2020-12-29)
Polysaccharides have been used widely in many industries, from food technology and mining to cosmetics and biomedical applications. Over recent years there has been growing interest in the development of responsive polysaccharides with unique and switchable properties, particularly systems that

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