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About This Item
Linear Formula:
[(CH3)2CH]2NC2H5
CAS Number:
Molecular Weight:
129.24
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-392-0
MDL number:
Assay:
99.5%
Form:
liquid
Product Name
N,N-Diisopropylethylamine, purified by redistillation, 99.5%
vapor pressure
31 mmHg ( 37.7 °C)
Quality Level
assay
99.5%
form
liquid
purified by
redistillation
refractive index
n20/D 1.414 (lit.)
bp
127 °C (lit.)
mp
<−50 °C (lit.)
solubility
water: soluble 4.01 g/L at 20 °C
density
0.742 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CCN(C(C)C)C(C)C
InChI
1S/C8H19N/c1-6-9(7(2)3)8(4)5/h7-8H,6H2,1-5H3
InChI key
JGFZNNIVVJXRND-UHFFFAOYSA-N
General description
N,N-diisopropylethylamine is an aliphatic sterically hindered amine.
Application
N,N-diisopropylethylamine may be used in the following processes:
- As an organic base in the synthesis of indenopyrones.
- As an activator for chiral iridium N, P ligand complexes which can be utilized in the hydrogenation of α,β-unsaturated nitriles.
- As a non-nucleophilic base for substitution reaction.
- As a starting material in the preparation of bis[1,2]dithiolo[1,4]thiazines and bis[1,2]dithiolopyrroles.
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signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
49.1 °F
flash_point_c
9.5 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Enantioselective N-heterocyclic carbene-catalyzed synthesis of indenopyrones.
Chen KQ, et al.
Organic & Biomolecular Chemistry (2015)
Selective Syntheses of Bis [1, 2] dithiolo [1, 4] thiazines and Bis [1, 2] dithiolopyrroles from Hunig's Base.
Rees CW, et al.
The Journal of Organic Chemistry, 63(7), 2189-2196 (1998)
Sequential Michael Addition and Enamine-Promoted Inverse Electron Demanding Diels-Alder Reaction upon 3-Vinyl-1,2,4-triazine Platforms.
Lorion M, et al.
Organic Letters (2015)



