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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.)

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

signalword

Danger

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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’.

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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.
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In this study, crystalline magnesium chloride-electron donor complexes were prepared by recrystallization of δ-MgCl
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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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