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135186

Sigma-Aldrich

Diisobutylamine

99%

Synonym(s):

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

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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
Pricing and availability is not currently available.

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.)

functional group

amine

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

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General description

Diisobutylamine forms crystalline adducts with zinc and copper(II)-dithiocarbamate complexes[1].

Application

Diisobutylamine was used to study the effect of achiral amine on hydrogenation of ethyl pyruvate over cinchonidine-Pt/Al2O3 catalyst system[2].

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX1377
MKCS9790
MKCM3274
MKCF2050
MKBZ1089V

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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

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