Skip to Content
Merck
CN

67994

Sigma-Aldrich

N-Ethyldiisopropylamine

produced by BASF, ≥98.0% (GC)

Synonym(s):

N,N-Diisopropylethylamine, Hünigs base

Sign Into View Organizational & Contract Pricing

Select a Size

About This Item

Linear Formula:
CH3CH2N[CH(CH3)2]2
CAS Number:
7087-68-5
Molecular Weight:
129.24
Beilstein:
605301
EC Number:
230-392-0
MDL number:
MFCD00008868
UNSPSC Code:
12352116
PubChem Substance ID:
57652117

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Assay

≥98.0% (GC)

bp

126-128 °C (lit.)

density

0.755 g/mL at 20 °C (lit.)
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

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

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBK5634V
BCBH0401V
1351839
BCBD8020V
BCBB7819V

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.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Zhouen Zhang et al.
Organic & biomolecular chemistry, 3(4), 592-596 (2005-02-11)
A new family of antitumor prodrugs (1-3) of 5-fluorouracil (5-FU) possessing photolabile 2-nitrobenzyl chromophores have been designed and synthesized to investigate the efficiency and mechanism of photoactivated 5-FU release upon UV-irradiation at lambda(ex)= 365 nm. The photoactivated prodrug 3 derived
Matthew D Disney et al.
Journal of the American Chemical Society, 126(41), 13343-13346 (2004-10-14)
Many pathogens that infect humans use cell surface carbohydrates as receptors to facilitate cell-cell adhesion. The hallmark of these interactions is their multivalency, or the simultaneous occurrence of multiple interactions. We have used a carbohydrate-functionalized fluorescent polymer, which displays many
Jonathan F Lovell et al.
Biomacromolecules, 12(9), 3115-3118 (2011-07-23)
We demonstrate that porphyrins can be used as efficient cross-linkers to generate a new class of hydrogels with enabling optical properties. Tetracarboxylic acid porphyrins reacted with PEG diamines to form a condensation polyamide in a range of appropriate conditions, with
Junfeng Shi et al.
Biomacromolecules, 15(10), 3559-3568 (2014-09-18)
Peptides made of D-amino acids, as the enantiomer of corresponding L-peptides, are able to resist proteolysis. It is, however, unclear or much less explored whether or how D-amino acids affect the cellular response of supramolecular nanofibers formed by enzyme-triggered self-assembly
Massimo Varisco et al.
ChemMedChem, 9(6), 1221-1230 (2014-05-07)
Materials foreign to the body are used ever more frequently, as increasing numbers of patients require implants. As a consequence, the numbers of implant-related infections have grown as well, and with increasing resistance. Treatments often fail; thus, new antibacterial coating
View All Related Papers

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