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Merck
CN

67994

N-Ethyldiisopropylamine

produced by BASF, ≥98.0% (GC)

Synonym(s):

N,N-Diisopropylethylamine, Hünigs base

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About This Item

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



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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

Regulatory Information

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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
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
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