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Merck
CN

135186

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848204
EC Number:
203-819-3
Beilstein/REAXYS Number:
1209251
MDL number:
MFCD00008930

Key Documents

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Product Name

Diisobutylamine, 99%

InChI key

NJBCRXCAPCODGX-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)CNCC(C)C

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

Quality Level

200

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Application

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

General description

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

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

86.0 °F - closed cup

flash_point_c

30 °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
MKCX1377
MKCS9790
MKCM3274
MKCF2050
MKBZ1089V

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Influence of achiral amine additives on the Orito's reaction.
Talas E, et al.
J. Mol. Catal. A: Chem., 357, 87-94 (2012)
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
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)

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