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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
NACRES:
NA.22
PubChem Substance ID:
24893680
UNSPSC Code:
12352100
MDL number:
MFCD00012525
Assay:
98%
Form:
powder

Key Documents

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Product Name

1,3-Diaminopropane dihydrochloride, 98%

InChI key

HYOCSVGEQMCOGE-UHFFFAOYSA-N

SMILES string

Cl[H].Cl[H].NCCCN

InChI

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

assay

98%

form

powder

mp

246-250 °C (lit.)

Quality Level

200

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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

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000525129
0000525129
0000472341
0000472341
0000420367

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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.
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
Evelyn Skiebe et al.
International journal of medical microbiology : IJMM, 302(3), 117-128 (2012-05-09)
While flagella-independent motility has long been described in representatives of the genus Acinetobacter, the mechanism of motility remains ambiguous. Acinetobacter baumannii, a nosocomial pathogen appearing increasingly multidrug-resistant, may profit from motility during infection or while persisting in the hospital environment.
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