Skip to Content
Merck
All Photos(1)

Key Documents

03440

Sigma-Aldrich

N-Ethyldiisopropylamine

BASF quality, ≥98.0%

Synonym(s):

N,N-Diisopropylethylamine, Hünigs base

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH2N[CH(CH3)2]2
CAS Number:
Molecular Weight:
129.24
Beilstein:
605301
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

BASF quality

Quality Level

Assay

≥98.0%

form

liquid

impurities

≤0.5% water

refractive index

n20/D 1.414

bp

126-128 °C (lit.)

density

0.755 g/mL at 20 °C (lit.)
0.755 g/mL at 20 °C
0.757 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

Looking for similar products? Visit Product Comparison Guide

General description

N,N-Diisopropylethylamine (DIPEA), also known as Hunig′s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed in substitution reactions, alkylations, and amide couplings, etc. DIPEA is also used as a base in the Pd catalyzed cross-coupling reactions, which include Heck coupling and Sonagashira coupling reactions.

Application


  • Catalytic activity in dioxygen reduction: A study utilized Mn complexes with pendent proton donor relays and added base, including N-Ethyldiisopropylamine, to control product selectivity during dioxygen reduction, providing insights into catalytic mechanisms and potential industrial applications (Cook et al., 2024).

  • Three-dimensional imaging in medical applications: N-Ethyldiisopropylamine was mentioned in the context of its role in improving the resolution of three-dimensional imaging techniques based on computed tomography angiography (CTA), crucial for preoperative perforator selection in reconstructive surgery (Su et al., 2024).

  • Synthesis of Spirocyclopropane-Containing Compounds: Research demonstrated the application of N-Ethyldiisopropylamine in the synthesis of spirocyclopropane-containing 4H-pyrazolo[1,5-a]indoles through alkylative dearomatization and intramolecular N-imination, highlighting its utility in complex organic synthesis (Huang et al., 2023).

Signal Word

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 Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

49.1 °F

Flash Point(C)

9.5 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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

Palladium-Catalyzed Carbon- Sulfur Cross-Coupling Reactions with Indium Tri (organothiolate) and Its Application to Sequential One-Pot Processes
Lee J-Y and Lee PH
The Journal of Organic Chemistry, 73(18), 7413-7416 (2008)
Palladium-catalysed cross-coupling reactions in supercritical carbon dioxide
Early TR, et al.
Chemical Communications (Cambridge, England), 73(19), 1966-1967 (2001)
Probing the structural properties of DNA/RNA grooves with sterically restricted phosphonium dyes: screening of dye cytotoxicity and uptake
Crnolatac I, et al.
ChemMedChem, 8(7), 1093-1103 (2013)
An easy and fast ultrasonic selective S-alkylation of hetaryl thiols at room temperature
Deligeorgiev T, et al.
Ultrasonics Sonochemistry, 17(5), 783-788 (2010)
B J Poorthuis et al.
Clinica chimica acta; international journal of clinical chemistry, 216(1-2), 53-61 (1993-07-16)
A high-performance liquid chromatographic method is presented for the determination of urinary acylcarnitines. After solid phase extraction on silica columns the acylcarnitines are converted to 4'-bromophenacyl esters with 4'-bromophenacylbromide in the presence of N,N-diisopropylethylamine. Complete derivatization was achieved at 37

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