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126942

Sigma-Aldrich

N,N′-Diethylethylenediamine

95%

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About This Item

Linear Formula:
CH3CH2NHCH2CH2NHCH2CH3
CAS Number:
111-74-0
Molecular Weight:
116.20
EC Number:
203-902-4
MDL number:
MFCD00009033
UNSPSC Code:
12352100
PubChem Substance ID:
24847751
NACRES:
NA.22

Assay

95%

form

liquid

refractive index

n20/D 1.4326 (lit.)

bp

152-154 °C (lit.)

density

0.811 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCNCCNCC

InChI

1S/C6H16N2/c1-3-7-5-6-8-4-2/h7-8H,3-6H2,1-2H3

InChI key

CJKRXEBLWJVYJD-UHFFFAOYSA-N

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Application

N,N′-Diethylethylenediamine has been used as an internal standard in selective liquid chromatographic method developed for the assay of ethambutol in serum samples. It has also been used for the solvation of lithium hexamethyldisilazide.

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

91.4 °F - closed cup

Flash Point(C)

33 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000260393
0000232017
0000241334
0000266595
0000246220

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Yukitaka Nakano et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 20(3), 489-493 (2004-04-08)
A selective liquid chromatographic method has been developed for the assay of ethambutol in serum samples. The assay involves intramolecular excimer-forming derivatization with 4-(1-pyrene)butanoyl chloride (PBC) and isocratic reversed-phase chromatography with fluorescence detection. After acetonitrile-deproteinization of the serum sample, the
Lucht BL and Collum DB.
Journal of the American Chemical Society, 118(14), 3529-3530 (1996)
V H Nissinen et al.
Dalton transactions (Cambridge, England : 2003), 46(13), 4452-4460 (2017-03-18)
In this study, crystalline magnesium chloride-electron donor complexes were prepared by recrystallization of δ-MgCl
Francisco Martínez-Peña et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(64), 16231-16241 (2017-07-25)
The potential use of organoruthenium complexes as anticancer drugs is well known. Herein, a family of activatable tethered ruthenium(II) arene complexes of general formula [Ru{η

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