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Santénine

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Identification
Molecular formula
C10H20Cl2N2
CAS number
186-74-1
IUPAC name
N,N'-bis(2-chloroethyl)hexane-1,6-diamine
State
State

At room temperature, N,N'-bis(2-chloroethyl)hexane-1,6-diamine is in a liquid state.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
282.70
Boiling point (Kelvin)
555.90
General information
Molecular weight
239.18g/mol
Molar mass
239.2040g/mol
Density
1.0960g/cm3
Appearence

N,N'-bis(2-chloroethyl)hexane-1,6-diamine typically appears as a colorless to pale yellow liquid.

Comment on solubility

Solubility of N,N'-bis(2-chloroethyl)hexane-1,6-diamine

N,N'-bis(2-chloroethyl)hexane-1,6-diamine is a specialized organic compound that exhibits unique solubility characteristics due to its chemical structure. Understanding solubility behavior is crucial for its applications in various chemical processes. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar Solubility: This compound possesses both polar (due to the amine groups) and nonpolar characteristics (due to the hexane backbone), making it soluble in a variety of solvents.
  • Solvent Preference:
    • Water: It is expected to have limited solubility in water due to the hydrophobic nature of the hexane chain.
    • Organic Solvents: It is more likely to be soluble in organic solvents like ethanol or acetone, which can engage with both the polar and nonpolar regions of the molecule.
  • Temperature Impact: The solubility may increase with temperature, which often enhances the solvation process, particularly in organic solvents.
  • Applications: Its solubility qualities are important for its use in fields such as materials science and pharmaceuticals, where optimal dissolubility facilitates better reactivity and interaction.

In conclusion, while the solubility of N,N'-bis(2-chloroethyl)hexane-1,6-diamine can vary based on the solvent and temperature, it holds potential for diverse applications thanks to its fascinating solubility profile.

Interesting facts

Interesting Facts about N,N'-bis(2-chloroethyl)hexane-1,6-diamine

N,N'-bis(2-chloroethyl)hexane-1,6-diamine is a fascinating compound with a range of intriguing properties and applications. Here are some engaging aspects to consider:

  • Structure and Functionality: This compound features two chloroethyl groups attached to a hexane-1,6-diamine backbone. The presence of multiple functional groups enhances its reactivity, making it a valuable building block in organic synthesis.
  • Pharmaceutical Applications: Compounds with similar structures are often investigated for potential pharmaceutical applications. The ability of this compound to participate in various chemical reactions makes it a candidate for developing novel therapeutic agents.
  • Potential Uses as a Crosslinking Agent: Due to its amine functional groups, N,N'-bis(2-chloroethyl)hexane-1,6-diamine can serve as a crosslinking agent in polymers or resins. This ability can lead to improved material properties such as enhanced strength or thermal stability.
  • Safety Considerations: The presence of chloroethyl groups introduces considerations for handling and safety. Compounds that contain chlorine can be hazardous, so appropriate safety measures are essential when working with this compound.
  • Research Interest: Ongoing research explores the synthesis and application of N,N'-bis(2-chloroethyl)hexane-1,6-diamine in various fields of chemistry. Scientists are particularly interested in its role in developing materials with unique properties.

In summary, N,N'-bis(2-chloroethyl)hexane-1,6-diamine presents a unique combination of structural features and reactivity that makes it a subject of interest in both academic and industrial research. As with many compounds in the realm of organic chemistry, its full potential is likely yet to be realized, encouraging ongoing investigation and study.

Synonyms
SCHEMBL11080594