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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/REAXYS Number:
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

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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.

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_germany

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

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’.

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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)
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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