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308145

Sigma-Aldrich

N-Propylethylenediamine

≥97%

Synonym(s):

2-Propylaminoethylamine

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About This Item

Linear Formula:
CH3CH2CH2NHCH2CH2NH2
CAS Number:
Molecular Weight:
102.18
Beilstein/REAXYS Number:
1697232
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥97%

form

liquid

refractive index

n20/D 1.441 (lit.)

bp

147-150 °C (lit.)

density

0.829 g/mL at 25 °C (lit.)

SMILES string

CCCNCCN

InChI

1S/C5H14N2/c1-2-4-7-5-3-6/h7H,2-6H2,1H3

InChI key

CFNHVUGPXZUTRR-UHFFFAOYSA-N

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General description

N-Propylethylenediamine columns help in quantitatively removing Cu(2+) from buffered solutions at pH 6.

Application

N-Propylethylenediamine was used in the synthesis of N-acetyl-N′-propylethylenediamine.

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

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


Certificates of Analysis (COA)

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D K Ryan et al.
Talanta, 32(9), 859-863 (1985-09-01)
Three types of chelating agents immobilized on glass were compared with Chelex 100 for removing and preconcentrating trace Cu(2+) from laboratory-prepared solutions. Columns of immobilized N-propylethylenediamine (diamine), its bis(dithiocarbamate) (DTC) and immobilized 8-hydroxyquinoline (8-HQ) quantitatively remove Cu(2+) (10-200 mug l.
Murakami Y, et al.
Tetrahedron Letters, 38(21), 3751-3754 (1997)
Shengmiao Liu et al.
Biosensors, 11(2) (2021-03-07)
This research reports a portable immunochip, based on quartz crystal microbalance (QCM) for label-free, low-cost qualitative detection of zearalenone (ZEN) in food samples. The experimental parameters in the functionalization and working process were evaluated in detail, in order to achieve
Liang Li et al.
Talanta, 202, 494-506 (2019-06-07)
A new 3,5-dichlorophenylcarbamated cellulose-bonded silica gel stationary phase (CELCSP) was prepared by a "thiol-ene" addition reaction. The alkenyl group was first introduced onto the cellulose, and then the cellulose was completely isocyanated with 3,5-dichlorophenyl isocyanate. Finally, the alkenyl group was

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