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D23807

Sigma-Aldrich

1,3-Diaminopropane dihydrochloride

98%

Synonym(s):

1,3-Propanediamine, 1,3-Propanediamine dihydrochloride

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About This Item

Linear Formula:
H2N(CH2)3NH2·2HCl
CAS Number:
10517-44-9
Molecular Weight:
147.05
MDL number:
MFCD00012525
UNSPSC Code:
12352100
PubChem Substance ID:
24893680
NACRES:
NA.22

assay

98%

form

powder

mp

246-250 °C (lit.)

SMILES string

Cl[H].Cl[H].NCCCN

InChI

1S/C3H10N2.2ClH/c4-2-1-3-5;;/h1-5H2;2*1H

InChI key

HYOCSVGEQMCOGE-UHFFFAOYSA-N

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Application

  • Tetradentate bis-phosphine ligands (P(2)N(2) and P(2)S(2)) and their Rh(III), Ni(II) and (105)Rh complexes: X-ray crystal structures of trans-[RhCl(2)(L2)]PF(6), [Ni(L2)](PF(6))(2) and μ-O(2)SO(2)-[Ni(L5)](2)(PF(6))(2).: This study explores the synthesis and characterization of tetradentate bis-phosphine ligands and their complexes, demonstrating significant advancements in ligand design and potential applications in catalysis and medicinal chemistry (Cagnolini et al., 2011).

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 22(5), 655-657 (2006-06-14)
Pyrene-appended alpha-cyclodextrin (3) in which a trimethylenediamine linker connected the pyrene residue to the alpha-cyclodextrin moiety showed pH-dependent fluorescence intensity changes. The fluorescence intensity was almost linearly changed within the pH range of 5 - 10. The unique fluorescence response
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European journal of medicinal chemistry, 43(7), 1530-1535 (2007-11-06)
The synthesis of novel 1,3-diaryl propenone derivatives and their antimalarial activity in vitro against asexual blood stages of human malaria parasite, Plasmodium falciparum, are described. Chalcone derivatives were prepared via Claisen-Schmidt condensation of substituted aldehydes with substituted methyl ketones. Antiplasmodial
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