Skip to Content
Merck
All Photos(1)

Key Documents

03439

Sigma-Aldrich

N-Ethyldiisopropylamine solution

suitable for peptide synthesis, ~2 M in 1-methyl-2-pyrrolidinone

Synonym(s):

N,N-Diisopropylethylamine, DIPEA, Hünig’s base

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H19N
CAS Number:
Molecular Weight:
129.24
Beilstein:
4124745
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

form

liquid

Quality Level

concentration

~2 M in 1-methyl-2-pyrrolidinone

impurities

≤0.2% water (KFT)

refractive index

n20/D 1.454

application(s)

peptide synthesis

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-Ethyldiisopropylamine (EDIA) reacts with monoactivated Michael acceptors to afford symmetrical sulfones.

Application

N,N-Diisopropylethylamine (DIPEA), also known as Hünig′s base, is a sterically hindered amine. It is commonly employed as a base in peptide synthesis. Additionally, DIPEA is also used in the Pd-catalyzed cross-coupling reactions, which include Heck coupling and Sonagashira coupling reactions.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Repr. 1B - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

73.4 °F

Flash Point(C)

23 °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

Eugene F, et al.
The Journal of Organic Chemistry, 59(9), 2599-2603 (1994)
J-N Volle et al.
Biosensors & bioelectronics, 19(5), 457-464 (2003-11-19)
We present a silicon chip-based approach for the enhanced sensitivity detection of surface-immobilized fluorescent molecules. Green fluorescent protein (GFP) is bound to the silicon substrate by a disuccinimidyl terephtalate-aminosilane immobilization procedure. The immobilized organic layers are characterized by surface analysis
Tristan Doussineau et al.
Journal of colloid and interface science, 339(1), 266-270 (2009-08-15)
This paper describes the preparation of two-dye-doped silica nanoparticles for ratiometric pH measurements in the biologically relevant pH-range. While a rhodamine derivative is embedded in a silica core and used as the reference, a pH-sensitive naphthalimide dye is immobilized on
H U Shetty et al.
Journal of the American Society for Mass Spectrometry, 2(2), 168-173 (1991-04-01)
An automatic reaction control chemical ionization technique in an ion trap detector (lTD) was used to quantitate the levels of the cholinergic drug, arecoline, in plasma of treated patients with Alzheimer's disease. The chemical ionization reaction was carried out with
Stéphane Bach et al.
The Journal of biological chemistry, 280(35), 31208-31219 (2005-06-25)
(R)-Roscovitine (CYC202) is often referred to as a "selective inhibitor of cyclin-dependent kinases." Besides its use as a biological tool in cell cycle, neuronal functions, and apoptosis studies, it is currently evaluated as a potential drug to treat cancers, neurodegenerative

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