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127159

Sigma-Aldrich

N-(2-Aminoethyl)-1,3-propandiamin

97%

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About This Item

Lineare Formel:
H2N(CH2)3NHCH2CH2NH2
CAS-Nummer:
13531-52-7
Molekulargewicht:
117.19
EG-Nummer:
236-882-0
MDL-Nummer:
MFCD00008211
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847766
NACRES:
NA.22

Assay

97%

Form

liquid

Brechungsindex

n20/D 1.4815 (lit.)

Dichte

0.928 g/mL at 25 °C (lit.)

Funktionelle Gruppe

amine

SMILES String

NCCCNCCN

InChI

1S/C5H15N3/c6-2-1-4-8-5-3-7/h8H,1-7H2

InChIKey

DTSDBGVDESRKKD-UHFFFAOYSA-N

Anwendung

N-(2-Aminoethyl)-1,3-propanediamine has been used as a templating agent in the synthesis of a new open framework iron(III) phosphite {(C5H18N3)[Fe3(HPO3)6].3H2O}. It has also been used in the preparation of dinitrocobalt(III) compound: (11-amino-4-methyl-5,8-diazaundeca-2,4-dien-2-olato-kappa4N(5,8,11),O)-dinitrocobalt(III), [Co(C10H20N3O)(NO2)2].

Piktogramme

Skull and crossbonesCorrosion
GHS06,GHS05

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - Skin Sens. 1

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flammpunkt (°F)

206.6 °F - closed cup

Flammpunkt (°C)

97 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BGBC3069V
MKBH8779V
MKBF1249V
MKBD1249
09807DJ

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Sigma-Aldrich

447706

5-Chlorsalicylaldehyd

N-Ethylethylendiamin 98%

Sigma-Aldrich

127000

N-Ethylethylendiamin

2-Hydroxy-1-Naphthaldehyd technical grade

Sigma-Aldrich

H45353

2-Hydroxy-1-Naphthaldehyd

H Chun et al.
Acta crystallographica. Section C, Crystal structure communications, 57(Pt 1), 33-35 (2001-02-15)
The reaction of Co(acac)3 with N-(2-aminoethyl)-1,3-propanediamine in the presence of NaNO2 results in the preparation of an unexpected dinitrocobalt(III) compound, (11-amino-4-methyl-5,8-diazaundeca-2,4-dien-2-olato-kappa4N(5,8,11),O)-dinitrocobalt(III), [Co(C10H20N3O)(NO2)2], containing the tetradentate anion of 11-amino-4-methyl-5,8-diazaundeca-2,4-dien-2-ol. Two isomers of the compound were obtained by recrystallization of the crude
U-Chan Chung et al.
Inorganic chemistry, 45(22), 8965-8972 (2006-10-24)
A new open framework iron(III) phosphite with formula (C5H18N3)[Fe3(HPO3)6].3H2O has been prepared by hydrothermal synthesis with N-(2-aminoethyl)-1,3-propanediamine as a templating agent. The crystal structure was solved from single-crystal X-ray diffraction data in the trigonal space group R. The unit cell
Naciye Esma Tirtom et al.
Physical chemistry chemical physics : PCCP, 22(21), 11928-11935 (2020-05-21)
Polyamines are naturally occurring cationic molecules in cells. In addition to their roles in modulating gene expression and cell proliferation, they have been shown to stimulate DNA recombination. The molecular mechanism for stimulation is not clear. We utilized single-molecule tethered
Lucas Vu et al.
Theranostics, 2(12), 1160-1173 (2013-02-06)
A focused library of twenty-one cationic poly(amino ethers) was synthesized following ring-opening polymerization of two diglycidyl ethers by different oligoamines. The polymers were screened in parallel for plasmid DNA (pDNA) delivery, and transgene expression efficacies of individual polymers were compared

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