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N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine

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Identification
Molecular formula
C12H22N2
CAS number
139979-20-5
IUPAC name
N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine
State
State

This diamine is in a liquid state at room temperature, featuring an aromatic smell typical of amines. Its volatility is moderate, making it less prone to rapid evaporation under ambient conditions.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
194.32g/mol
Molar mass
194.3200g/mol
Density
0.8700g/cm3
Appearence

The compound N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine is typically a colorless liquid, though slight coloration may occur depending on purity. It can be characterized by its relatively lower viscosity compared to other diamines, given its alkyl and butadiene substituents.

Comment on solubility

Solubility of N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine

N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine, with the chemical formula C12H22N2, presents interesting solubility characteristics.

This compound is a non-polar organic compound, largely due to its hydrophobic alkyl side chains. The solubility behavior can be summarized as follows:

  • Solubility in Organic Solvents: N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine is expected to be soluble in non-polar solvents such as hexane, toluene, and chloroform. This is attributed to the compatibility of non-polar molecules with similar non-polar solvents.
  • Water Solubility: This compound is likely to exhibit low solubility in water. The inability to form significant hydrogen bonds with water molecules is a key factor in its limited solubility.
  • Temperature Dependence: The solubility of such compounds can also vary with temperature, where increased temperatures might enhance solubility to some extent in organic solvents.

In summary, the solubility profile of N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine emphasizes its affinity for organic solvents over polar solvents like water. Understanding this characteristic is crucial for its applications in various chemical processes and formulations.

Interesting facts

Introduction to N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine

N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine, commonly referred to by its more informal names, is an interesting organic compound that occupies a unique space in the world of chemical research. Recognized for its application in various synthetic processes, it showcases fascinating properties due to its molecular structure.

Key Properties and Uses

  • Versatile Building Block: This compound serves as a crucial building block in organic synthesis, particularly for creating polymers and other advanced materials.
  • Potential Applications: Due to its dual amine functional groups, it can be utilized in the development of specialty coatings, adhesives, and possibly in biomedical applications.
  • Research Interest: Scientists are investigating its reactivity characteristics, particularly in the context of click chemistry, where its conjugated diene units can participate in Diels-Alder reactions.

Chemical Structure Insights

The structure of N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine is particularly notable:

  • Conjugated Dienes: The presence of conjugated diene systems provides the compound with unique electronic properties that can influence reactivity.
  • Amine Groups: The butane-1,4-diamine backbone allows for multiple derivatization opportunities, enhancing its utility in various chemical reactions.

Research and Development

Researchers are continuing to explore the potential of this compound in creating sustainable chemicals and materials. With ongoing efforts in green chemistry, compounds like N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine are being studied for their low toxicity and biodegradability.

Conclusion

In conclusion, the advancement of chemistry is significantly supported by compounds like N,N’-bis(buta-2,3-dien-1-yl)butane-1,4-diamine. Whether it's used in academic research, industrial applications, or innovative product development, its multifaceted nature makes it an intriguing subject of study within the scientific community.

Synonyms
99207-33-7
MDL-72527 free base
N1,N4-Di(buta-2,3-dienyl)butane-1,4-diamine
MDL72527
N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diamine
1,4-Butanediamine, N1,N4-di-2,3-butadien-1-yl-
CHEMBL417844
G28L05X0YB
1,4-Butanediamine, N,N'-di-2,3-butadienyl-
N1,N4-Bis(2,3-butadienyl)-1,4-butanediamine
(buta-2,3-dien-1-yl)({4-[(buta-2,3-dien-1-yl)amino]butyl})amine
UNII-G28L05X0YB
(buta-2,3-dien-1-yl)((4-((buta-2,3-dien-1-yl)amino)butyl))amine
MDL 72527 (free base)
SCHEMBL3505002
DTXSID901259716
GLXC-26096
BDBM50015358
AKOS015998856
DB04188
GS-3754
CS-0764511
NS00069523
N,N''-Di-buta-2,3-dienyl-butane-1,4-diamine
N,N'-dibuta-2,3-dien-1-ylbutane-1,4-diamine
N, N1-bis-(buta-2,3-dienyl)-1,4-diaminobutane
N1,N4-Di-2,3-butadien-1-yl-1,4-butanediamine
Q27095016
N,N''-BIS(2,3-BUTADIENYL)-1,4-BUTANE-DIAMINE