308145
N-Propylethylenediamine
≥97%
Synonym(s):
2-Propylaminoethylamine
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About This Item
Linear Formula:
CH3CH2CH2NHCH2CH2NH2
CAS Number:
Molecular Weight:
102.18
Beilstein:
1697232
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
113.0 °F - closed cup
Flash Point(C)
45 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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