MilliporeSigma
All Photos(1)

03440

Sigma-Aldrich

N-Ethyldiisopropylamine

BASF quality, ≥98.0%

Synonym(s):
N,N-Diisopropylethylamine, Hünigs base
Linear Formula:
CH3CH2N[CH(CH3)2]2
CAS Number:
Molecular Weight:
129.24
Beilstein:
605301
EC Number:
MDL number:
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.)

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

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
3876494962198.45017
assay

≥98.0%

assay

99.5%

assay

99.5%

assay

≥99.5% (GC)

form

liquid

form

liquid

form

liquid

form

liquid

impurities

≤0.5% water

impurities

-

impurities

<0.050% water

impurities

-

refractive index

n20/D 1.414

refractive index

n20/D 1.414 (lit.)

refractive index

n20/D 1.414 (lit.)

refractive index

-

bp

126-128 °C (lit.)

bp

127 °C (lit.)

bp

127 °C (lit.)

bp

127 °C/1013 hPa

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.

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

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’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (Example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Customers Also Viewed

Slide 1 of 3

1 of 3

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