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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
0000336944
0000247226
0000246777
0000241869
0000265773

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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
L D Kagliwal et al.
Bioresource technology, 100(9), 2600-2606 (2009-01-22)
In this study, Nocardia lactamdurans NRRL 3802 was explored for the first time for production of cephamycin C by using solid-state fermentation. The effects of various substrates, moisture content, inoculum size, initial pH of culture medium, additional nitrogen source and
Romualda Bregier-Jarzebowska et al.
Journal of inorganic biochemistry, 103(9), 1228-1235 (2009-08-04)
Interactions of aspartic acid between 1,3-diaminopropane (tn) and 1,4-diaminobutane (Put) in metal-free systems as well as in the systems including copper(II) ions were studied. The composition and overall stability constants of the complexes formed were determined by the potentiometric method.
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.
Nirmala Devi Kanika et al.
American journal of physiology. Cell physiology, 297(4), C916-C927 (2009-08-07)
Intracorporal injection of plasmids encoding opiorphins into retired breeder rats can result in animals developing a priapic-like condition. Microarray analysis demonstrated that following intracorporal gene transfer of plasmids expressing opiorphins the most significantly upregulated gene in corporal tissue was the
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