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Details

Stereochemistry ACHIRAL
Molecular Formula C8H19N
Molecular Weight 129.2432
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Diisopropylethylamine

SMILES

CCN(C(C)C)C(C)C

InChI

InChIKey=JGFZNNIVVJXRND-UHFFFAOYSA-N
InChI=1S/C8H19N/c1-6-9(7(2)3)8(4)5/h7-8H,6H2,1-5H3

HIDE SMILES / InChI
Molecular Formula C8H19N
Molecular Weight 129.2432
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Dansylation of unactivated alcohols for improved mass spectral sensitivity and application to analysis of cytochrome P450 oxidation products in tissue extracts.
2010-09-15
HIV-1 gp41 and TCRalpha trans-membrane domains share a motif exploited by the HIV virus to modulate T-cell proliferation.
2010-09-02
4-Methyl-N-[(S)-1-phenyl-eth-yl]benzene-sulfonamide.
2010-08-21
Formation of a leuco spirolactone from 4-(2-carboxyphenyl)-7-diethylamino-4'-dimethylamino-1-benzopyrylium: design of a phase-change thermochromic system based on a flavylium dye.
2010-07-12
Extension of the PNA world by functionalized PNA monomers eligible candidates for inverse Diels Alder Click Chemistry.
2010-06-27
Optimization of solvent bar microextraction combined with gas chromatography for the analysis of aliphatic amines in water samples.
2010-06-15
Stimuli of sensory-motor nerves terminate arterial contractile effects of endothelin-1 by CGRP and dissociation of ET-1/ET(A)-receptor complexes.
2010-06-01
tert-Butyl N-[6-(N,N-dipropyl-carbamo-yl)-1,3-benzothia-zol-2-yl]carbamate.
2010-04-30
N-octanoyl dopamine, a non-hemodyanic dopamine derivative, for cell protection during hypothermic organ preservation.
2010-03-16
A second-generation ionic liquid matrix-assisted laser desorption/ionization matrix for effective mass spectrometric analysis of biodegradable polymers.
2009-11
Synergistic antibacterial and anti-inflammatory activity of temporin A and modified temporin B in vivo.
2009-09-28
A catalytic, Brønsted base strategy for intermolecular allylic C-H amination.
2009-08-26
Chemical tools selectively target components of the PKA system.
2009-02-12
Synthesis and spectral properties of novel fluorescent poly(oxyethylene phosphate) tris(beta-diketonate) europium (III) complexes.
2009-01
Surfaces for immobilization of N-terminal cysteine derivatives via native chemical ligation.
2008-12-16
Signal transduction of hyaluronic acid-peptide conjugate for formyl peptide receptor like 1 receptor.
2008-12
Trans-stereoselectivity in the reaction between homophthalic anhydride and imines.
2008-11-06
Selenium derivatization of nucleic acids for phase and structure determination in nucleic acid X-ray crystallography.
2008-03
Alpha-methylprednisolone conjugated cyclodextrin polymer-based nanoparticles for rheumatoid arthritis therapy.
2008
Synthesis of novel phytosphingosine derivatives and their preliminary biological evaluation for enhancing radiation therapy.
2007-12-01
RGD targeted poly(L-glutamic acid)-cystamine-(Gd-DO3A) conjugate for detecting angiogenesis biomarker alpha(v) beta3 integrin with MRT, mapping.
2007
Novel glycosylation reactions using glycosyl thioimidates of N-acetylneuraminic acid as sialyl donors.
2006-05-15
Monolithic silica-based capillary column with strong chiral cation-exchange type surface modification for enantioselective non-aqueous capillary electrochromatography.
2006-02-17
Synthesis of stable dodecaalkoxy derivatives of hypercloso-B12H12.
2005-12-28
Inhibition of HIV derived lentiviral production by TAR RNA binding domain of TAT protein.
2005-11-17
C2-symmetric macrocyclic carbohydrate/amino acid hybrids through copper(I)-catalyzed formation of 1,2,3-triazoles.
2005-06-10
Affinity enhancement bivalent morpholino for pretargeting: initial evidence by surface plasmon resonance.
2005-03-17
Synthesis and photochemical properties of photoactivated antitumor prodrugs releasing 5-fluorouracil.
2005-02-21
Detection of bacteria with carbohydrate-functionalized fluorescent polymers.
2004-10-20
Synthesis and characterization of human alpha-defensins 4-6.
2004-09
Solid-phase synthesis and spectral properties of 2-alkylthio-6H-pyrano[2,3-f]benzimidazole-6-ones: a combinatorial approach for 2-alkylthioimidazocoumarins.
2004-07-13
Design and application of an alpha-helix-mimetic scaffold based on an oligoamide-foldamer strategy: antagonism of the Bak BH3/Bcl-xL complex.
2003-02-03
Peptide-bond modification for metal coordination: peptides containing two hydroxamate groups.
2003
Practical protocols for stepwise solid-phase synthesis of cysteine-containing peptides.
2002-11
Use of phenyl 2-alpha-selenoglycosides of N-acetylneuraminic acid as a glycosyl donor for the glycosylation reactions.
2002-09-02
Synthesis of a membrane protein with two transmembrane regions.
2002-04
Sterically hindered C(alpha, alpha)-disubstituted alpha-amino acids: synthesis from alpha-nitroacetate and incorporation into peptides.
2001-10-19
Solid phase extraction purification of carboxylic acid products from 96-well format solution phase synthesis with DOWEX 1x8-400 formate anion exchange resin.
2001-04-13
Patents

Patents

03984248
2
04010166
3
04094989
2
04179510
6
JP2000053655A
2
JP2001089425A
2
JP2007523906A
3
JP2007529520A
3
JP2007532693A
2
JP2011509916A
2
JP4733129B2
6
JPH04149176A
2
JPH0641075A
2
JPH0656878A
2
JPH0673049A
2
JPH072763A
2
JPH0797397A
2
JPH08157417A
2
JPH09136870A
2
JPH09151331A
2
JPH10130270A
2
JPS5592732A
2
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:13:26 GMT 2025
Edited
by admin
on Mon Mar 31 21:13:26 GMT 2025
Record UNII
5SIQ15721L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Diisopropylethylamine
Systematic Name English
NSC-147491
Preferred Name English
N-Ethyl-N-(1-methylethyl)-2-propanamine
Systematic Name English
iPr2NEt
Common Name English
DIEA
Common Name English
N,N-Diisopropylethylamine
Systematic Name English
N-Ethyldiisopropylamine
Systematic Name English
Huenig's base
Common Name English
Hünig's base
Common Name English
DIPEA
Common Name English
Hunig's base
Common Name English
Diisopropylethylamine [MI]
Common Name English
Ethyldiisopropylamine
Systematic Name English
1,1'-Dimethyltriethylamine
Common Name English
Code System Code Type Description
NSC
147491
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY
MERCK INDEX
m4489
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY Merck Index
FDA UNII
5SIQ15721L
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID8064561
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY
CAS
7087-68-5
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
230-392-0
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY
WIKIPEDIA
N,N-DIISOPROPYLETHYLAMINE
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY
PUBCHEM
81531
Created by admin on Mon Mar 31 21:13:26 GMT 2025 , Edited by admin on Mon Mar 31 21:13:26 GMT 2025
PRIMARY
Related Record Type Details
Structure of Ethyldiisopropylamine hydrochloride
SALT/SOLVATE -> PARENT
NIH
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