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D23807

Sigma-Aldrich

1,3-Diaminopropane dihydrochloride

98%

Synonyme(s) :

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

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About This Item

Formule linéaire :
H2N(CH2)3NH2·2HCl
Numéro CAS:
10517-44-9
Poids moléculaire :
147.05
Numéro MDL:
MFCD00012525
Code UNSPSC :
12352100
ID de substance PubChem :
24893680
Nomenclature NACRES :
NA.22

Pureté

98%

Forme

powder

Pf

246-250 °C (lit.)

Chaîne SMILES 

Cl[H].Cl[H].NCCCN

InChI

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

Clé InChI

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).

Pictogrammes

Skull and crossbones
GHS06

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
BGBC3015V
BGBB8413
MKAA3288V
1421414
1421553

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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
Adeeb El-Dahshan et al.
Organic letters, 9(6), 949-952 (2007-02-20)
C-Acylations of polymer-supported 2-phosphoranylidene acetates ("linker reagents") with protected amino acids yielded 2-acyl-2-phosphoranylidene acetates as flexible intermediates for the C-terminal variation of carboxylic acids: peptidyl-2,3-diketoesters, peptidyl vinyl ketones, peptidyl-2-ketoaldehydes, and 1,3-diamino-2-hydroxy-propanes were obtained as products. [reaction: see text]
Nicholas T Nolan et al.
Journal of hazardous materials, 211-212, 88-94 (2011-10-04)
In order to study the visible light photocatalytic activity of nitrogen doped titanium dioxide, the interaction between nitrogen dopant sources and titania precursors during sol-gel synthesis is investigated. N-TiO(2) was synthesised using the sol-gel method using 1,3-diaminopropane as a nitrogen
Katrien Vandamme et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 74(2), 202-208 (2009-10-13)
Two synthesis methods of poly(methyl vinyl ether-co-maleic anhydride) (Gantrez AN 119) nanoparticles (NP) (used for oral vaccination) were compared. Wheat germ agglutinin (WGA) was used as ligand to enhance the bioadhesive properties of NP and beta-galactosidase as antigen. The first
Krista Weikkolainen et al.
Glycoconjugate journal, 24(2-3), 157-165 (2007-02-03)
Carbohydrates present on cell surfaces participate in numerous biological recognition phenomena including cell-cell interactions, cancer metastasis and pathogen invasion. Therefore, synthetic carbohydrates have a potential to act as pharmaceutical substances for treatment of various pathological phenomena by inhibiting specifically the
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