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Spermidine

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Identification
Molecular formula
C7H19N3
CAS number
124-20-9
IUPAC name
N'-(4-aminobutyl)butane-1,4-diamine
State
State

At room temperature, spermidine is a liquid.

Melting point (Celsius)
-23.50
Melting point (Kelvin)
249.65
Boiling point (Celsius)
128.00
Boiling point (Kelvin)
401.15
General information
Molecular weight
145.25g/mol
Molar mass
145.2510g/mol
Density
0.9254g/cm3
Appearence

Spermidine appears as a colorless to pale yellow liquid. It is hygroscopic and tends to absorb water from the air, resulting in a slightly oily appearance.

Comment on solubility

Solubility of N'-(4-aminobutyl)butane-1,4-diamine

N'-(4-aminobutyl)butane-1,4-diamine, with the chemical formula C7H19N3, exhibits a distinctive solubility profile owing to its molecular structure. This compound is characterized by its multiple amine groups, which significantly influence its interactions with solvents. Here are some key points regarding its solubility:

  • Polar Characteristics: Due to the presence of amino groups (–NH2), the compound is likely to be polar, enhancing its solubility in polar solvents such as water.
  • Induced Solubility: Its solubility may be increased in situations where hydrogen bonding occurs, facilitating better interaction with the solvent.
  • Solvent Dependence: The solubility of N'-(4-aminobutyl)butane-1,4-diamine can be expected to vary depending on the choice of solvent, showing higher solubility in aqueous solutions compared to nonpolar solvents.

While the specific solubility data for this compound in various solvents may vary, it is reasonable to conclude that its amine groups play a crucial role in enhancing solubility in polar environments. Researchers should consider the solvent characteristics and molecular interactions when evaluating the solubility of this intriguing compound.

Interesting facts

Interesting Facts about N'-(4-aminobutyl)butane-1,4-diamine

N'-(4-aminobutyl)butane-1,4-diamine, often referred to in a shortened form as "ABDA," is a fascinating compound with a variety of interesting properties and applications in the field of chemistry.

Key Characteristics

  • Versatile Building Block: This compound is utilized in the synthesis of various polymers and materials. Its amine functional groups make it ideal for creating cross-linked networks in plastics.
  • Biological Applications: Research has indicated potential uses in biomedical fields, particularly in drug delivery systems. Its ability to interact with biological molecules can lead to advancements in targeted therapies.
  • Polymeric Applications: N'-(4-aminobutyl)butane-1,4-diamine can be a precursor for polyamides, which are known for their strength and thermal stability.

Unique Properties

One of the most striking features of ABDA is its capability to form hydrogen bonds due to its amino groups. This allows for a range of intermolecular interactions, important in:

  • Stabilizing structures in complex systems
  • Facilitating adhesion between different materials

Chemical Behavior

As a diamine, N'-(4-aminobutyl)butane-1,4-diamine can act both as a nucleophile and an electrophile, presenting opportunities for reactions such as:

  • Condensation reactions with carbonyl compounds
  • Amination processes, further extending its functional capabilities

Conclusion

The study of N'-(4-aminobutyl)butane-1,4-diamine not only enriches our understanding of chemical compounds but also expands our capabilities in both industrial and medical applications. As stated by renowned chemists, "The future of material innovation lies in the molecules we create." This compound is a perfect example of that principle in action.

Synonyms
sym-homospermidine
4427-76-3
bis(4-aminobutyl)amine
Homospermidine
1,4-Butanediamine, N-(4-aminobutyl)-
1,6,11-triazaundecane
N-(4-aminobutyl)-1,4-butanediamine
N1-(4-aminobutyl)butane-1,4-diamine
N-(4-aminobutyl)butane-1,4-diamine
N'-(4-aminobutyl)butane-1,4-diamine
0IJ25X1H4R
CHEBI:16554
4,4'-Diaminodibutylamine
1,9-diamino-5-azanonane
CHEMBL36119
DTXSID00196098
4,4'-IMINOBIS(BUTYLAMINE)
n-(4-aminobutyl)-1,4-diaminobutane
DIBUTYLAMINE, 4,4'-DIAMINO-
1,4-BUTANEDIAMINE, N1-(4-AMINOBUTYL)-
UNII-0IJ25X1H4R
SCHEMBL138047
DTXCID10118589
BDBM50032505
AKOS015855215
N-(4-Aminobutyl)-1,4-butanediamine, 9CI
C06366
G66120
EN300-7434636
Q3882311
890-697-5