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127159

Sigma-Aldrich

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

97%

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About This Item

Fórmula linear:
H2N(CH2)3NHCH2CH2NH2
Número CAS:
13531-52-7
Peso molecular:
117.19
Número CE:
236-882-0
Número MDL:
MFCD00008211
Código UNSPSC:
12352100
ID de substância PubChem:
24847766
NACRES:
NA.22

Ensaio

97%

Formulário

liquid

índice de refração

n20/D 1.4815 (lit.)

densidade

0.928 g/mL at 25 °C (lit.)

grupo funcional

amine

cadeia de caracteres SMILES

NCCCNCCN

InChI

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

chave InChI

DTSDBGVDESRKKD-UHFFFAOYSA-N

Aplicação

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}[1]. 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][2].

Pictogramas

Skull and crossbonesCorrosion
GHS06,GHS05

Palavra indicadora

Danger

Frases de perigo

H302,H310,H314,H317

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

206.6 °F - closed cup

Ponto de fulgor (°C)

97 °C - closed cup

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
0000139771
0000130133
0000129204
0000111615
0000101274

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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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