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Merck
CN

D23807

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

Key Documents

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Quality Level

200

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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Related Categories

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

Signal Word

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 Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000472341
0000472341
0000420367
0000420367
0000336944

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Rolando Barbucci et al.
Acta biomaterialia, 8(12), 4244-4252 (2012-09-18)
Hybrid magnetic hydrogels are of interest for applications in biomedical science as controlled drug-delivery systems. We have developed a strategy to obtain novel hybrid hydrogels with magnetic nanoparticles (NPs) of CoFe(2)O(3) and Fe(3)O(4) as crosslinker agents of carboxymethylcellulose (CMC) or
Iwao Suzuki et al.
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
Nidhi Mishra et al.
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
Roland Meier et al.
Chemical communications (Cambridge, England), (38)(38), 3960-3962 (2007-09-27)
The equilibrium between the twist-boat (tb) and half-chair (hc) conformers of the central diamine chelate ring of [Fe(III)(tmdta)]- in solids and aqueous solution has been studied by Raman spectroscopy, supported by calculated Raman spectra using Density Functional Theory.
Jorge Martín et al.
Applied and environmental microbiology, 77(16), 5688-5696 (2011-07-05)
Filamentous fungi produce an impressive variety of secondary metabolites; many of them have important biological activities. The biosynthesis of these secondary metabolites is frequently induced by plant-derived external elicitors and appears to also be regulated by internal inducers, which may
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