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Merck
CN

A55357

1-(2-Aminoethyl)pyrrolidine

98%

Synonym(s):

2-Pyrrolidinoethylamine

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About This Item

Empirical Formula (Hill Notation):
C6H14N2
CAS Number:
Molecular Weight:
114.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-509-5
Beilstein/REAXYS Number:
102978
MDL number:
Assay:
98%
Form:
liquid
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InChI key

WRXNJTBODVGDRY-UHFFFAOYSA-N

InChI

1S/C6H14N2/c7-3-6-8-4-1-2-5-8/h1-7H2

SMILES string

NCCN1CCCC1

assay

98%

form

liquid

bp

66-70 °C/23 mmHg (lit.)

density

0.901 g/mL at 25 °C (lit.)

General description

1-(2-Aminoethyl)pyrrolidine is a heterocyclic building block. Nickel(II) salts of 1-(2-aminoethyl)pyrrolidine have been synthesized and thermal studies have been reported. The isomeric complexes trans-[NiL2(NCS)2] (violet) and cis-[NiL2(NCS)2] (blue) [L=1-(2-aminoethyl)pyrrolidine] have been synthesized and their X-ray crystal structure have been studied.

Application

1-(2-Aminoethyl)pyrrolidine may be used in the preparation of one-dimensional coordination polymer of nickel(II), [(μN,S-NCS)2{Ni(ampy)}]n (ampy=1-(2-aminoethyl)pyrrolidine).

pictograms

FlameCorrosion

signalword

Danger

hcodes

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

116.6 °F - closed cup

flash_point_c

47 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Syntheses, characterisation and solid state thermal studies of 1-(2-aminoethyl) piperidine (L), 1-(2-aminoethyl) pyrrolidine (L') and 4-(2-aminoethyl) morpholine (L ?) complexes of nickel (II):
Laskar IR, et al.
Polyhedron, 20(15), 2073-2082 (2001)
A 1D thiocyanato bridge nickel (II) system: crystal structure and magnetic property.
Maji TK, et al.
Polyhedron, 20(7), 651-655 (2001)
Synthesis and characterization of cis and trans isomers of [NiL 2 (NCS) 2][L= 1-(2-aminoethyl) pyrrolidine]: X-ray single-crystal structures.
Laskar IR, et al.
Polyhedron, 19(15), 1803-1807 (2000)
Krzysztof Sztandera et al.
International journal of molecular sciences, 21(12) (2020-06-27)
Photodynamic therapy (PDT) is a skin cancer treatment alternative to chemotherapy and radiotherapy. This method exploits three elements: a phototoxic compound (photosensitizer), light source and oxygen. Upon irradiation by light of a specific wavelength, the photosensitizer generates reactive oxygen species
Jinlong Ma et al.
ACS applied materials & interfaces, 9(20), 16767-16777 (2017-05-11)
A reversible programmed targeting strategy could achieve high tumor accumulation due to its long blood circulation time and high cellular internalization. Here, targeting ligand-modified poly(ethylene glycol) (PEG-ligand), dibutylamines (Bu), and pyrrolidinamines (Py) were introduced on the surface of gold nanoparticles

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