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Spermidine

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Identification
Molecular formula
C7H19N3
CAS number
124-20-9
IUPAC name
N'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine
State
State

At room temperature, Spermidine is a liquid that solidifies upon cooling.

Melting point (Celsius)
23.50
Melting point (Kelvin)
296.65
Boiling point (Celsius)
248.00
Boiling point (Kelvin)
521.15
General information
Molecular weight
145.25g/mol
Molar mass
145.2530g/mol
Density
0.9256g/cm3
Appearence

Spermidine is typically a white crystalline solid.

Comment on solubility

Solubility of N'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine (C7H19N3)

N'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine, also known as a polyamine, displays interesting solubility characteristics. Its solubility is influenced by several factors:

  • Polarity: The presence of multiple amine groups contributes to its polar nature, which typically enhances solubility in polar solvents, particularly water.
  • Hydrogen Bonding: The amine functional groups can form hydrogen bonds with water molecules, facilitating dissolution.
  • Concentration: At higher concentrations, solubility may be affected due to intermolecular interactions between dissolved molecules.
  • pH Dependence: The solubility of amines like this compound can vary significantly with pH; they tend to be more soluble in acidic conditions due to protonation of the amine groups.

In summary, the solubility of C7H19N3 is characterized by its ability to readily dissolve in polar solvents like water, especially under acidic conditions. As with many amine compounds, understanding the influence of environmental conditions on solubility is crucial for practical applications.

Interesting facts

Interesting Facts about N'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine

N'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine is a fascinating organic compound that showcases the intricate interplay between genetics and biochemistry. Here are some intriguing points that highlight its significance:

  • Biological Importance: This compound is often studied in relation to its role as a *potential pharmaceutical agent*, particularly in the development of drugs that target various biological pathways.
  • Structure and Function: The unique structural features of this compound, which includes an *alkyl and amine functional groups*, make it a key candidate for studies in *enzyme inhibition* and *receptor binding*. Its branched structure enhances its ability to interact with biological systems.
  • Potential Applications: Researchers are exploring its utility in the field of *drug design*, particularly for its potential in treating conditions related to neurotransmitter imbalances. The amine groups provide excellent *binding sites* for modifications, leading to enhanced efficacy.
  • Research Significance: The compound is a part of ongoing studies in medicinal chemistry, as scientists investigate its interactions with various cellular targets. Its complexity offers *challenges and opportunities* in optimization for therapeutic purposes.
  • Environmental Impact: Like many organic compounds, studying the environmental implications of this compound is crucial. Understanding its degradation and bioaccumulation in ecosystems contributes to *sustainable practices* in synthetic chemistry.

In summary, N'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine is more than just a chemical; it is a compound that bridges the gaps between various scientific domains, sparking curiosity and innovation in the fields of chemistry, biology, and medicine.

Synonyms
10563-26-5
N,N'-Bis(3-aminopropyl)ethylenediamine
1,5,8,12-Tetraazadodecane
1,3-Propanediamine, N,N''-1,2-ethanediylbis-
N,N'-Bis(3-aminopropyl)-1,2-diaminoethane
N,N'-Bis(gamma-aminopropyl)diaminoethane
N,N'-Di(3-aminopropyl)-1,2-ethylenediamine
1,3-Propanediamine, N,N''-ethylenebis-
EINECS 234-147-9
NSC 180823
0EXW8894XX
N4 AMINE
NSC-180823
DTXSID2065127
4,7-diazadecane-1,10-diamine
EC 234-147-9
1,3-Propanediamine, N1,N1'-1,2-ethanediylbis-
3,2,3-TET
BIS(3-AMINOPROPYL)ETHYLENEDIAMINE, N,N'-
N,N'-BIS(.GAMMA.-AMINOPROPYL)DIAMINOETHANE
N-(2-(3-AMINOPROPYLAMINO)ETHYL)-1,3-PROPANEDIAMINE
1,5,8,12Tetraazadodecane
N,N'Diaminopropylethylenediamine
DTXCID3032969
N,N'Bis(3aminopropyl)diaminoethane
1,3Propanediamine, N,N''ethylenebis
N,N'Bis(gammaaminopropyl)diaminoethane
N,N'Bis(3aminopropyl)1,2diaminoethane
N,N'Di(3aminopropyl)1,2ethylenediamine
1,3Propanediamine, N,N''1,2ethanediylbis
1,3Propanediamine, N1,N1'1,2ethanediylbis
N1,N1'1,2Ethanediylbis(1,3propanediamine)
N(2(3Aminopropylamino)ethyl)1,3propanediamine
234-147-9
N1,N1'-(Ethane-1,2-diyl)bis(propane-1,3-diamine)
1,2-Bis(3-aminopropylamino)ethane
3,2,3-tetramine
N'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine
NSC180823
CHEMBL259148
N,N'-Bis(3-aminopropyl)-1,2-ethanediamine
CHEBI:39476
N,N''-ethylenebis-1,3-propanediamine
N,N''-1,2-ethanediylbis-1,3-propanediamine
N(1'),N(3)-ethane-1,2-diyldipropane-1,3-diamine
(3-aminopropyl)({2-[(3-aminopropyl)amino]ethyl})amine
1,2-Bis(3-aminopropylamino)ethane, 96%
MFCD00008210
UNII-0EXW8894XX
N,N'-Bis(3-aminopropyl)-1,2-ethylenediamine
1,8,12-Tetraazadodecane
1, N,N''-ethylenebis-
SCHEMBL20976
BIDD:GT0255
1,5,8, 12-Tetraazadodecane
SCHEMBL10874825
1,10-diamino-4,7-diazadecane
3,3'-Ethylenediiminodipropylamine
1, N,N''-1,2-ethanediylbis-
KAA56326
BDBM50376458
AKOS015894471
CS-W017488
N, N'-Bis(3-aminopropyl)ethylenediamine
LS-13569
DB-040641
B1952
NS00019760
E83024
EN300-157336
N,N'-Di(3-aminopropyl)-1, 2-ethylenediamine
1, 3-Propanediamine, N,N''-1,2-ethanediylbis-
Q27120355
1,2-Bis(3-aminopropylamino)ethane, technical grade, 94%
N~1~-(2-((3-Aminopropyl)amino)ethyl)-1,3-propanediamine