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Hexyl 3-(aziridin-1-yl)propanoate

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Identification
Molecular formula
C11H21NO2
CAS number
.
IUPAC name
hexyl 3-(aziridin-1-yl)propanoate
State
State

At room temperature, hexyl 3-(aziridin-1-yl)propanoate is a liquid.

Melting point (Celsius)
0.00
Melting point (Kelvin)
273.15
Boiling point (Celsius)
272.00
Boiling point (Kelvin)
545.15
General information
Molecular weight
213.32g/mol
Molar mass
213.3150g/mol
Density
0.9601g/cm3
Appearence

Hexyl 3-(aziridin-1-yl)propanoate appears as a clear, colorless liquid with a slight amine-like odor.

Comment on solubility

Solubility Characteristics of Hexyl 3-(aziridin-1-yl)propanoate

Hexyl 3-(aziridin-1-yl)propanoate, a compound with the molecular formula C11H19N1O2, exhibits unique solubility properties that are worth exploring. The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of the aziridine ring can alter the polarity of the compound. Generally, compounds with polar functional groups tend to have increased solubility in polar solvents.
  • Hydrophobic Chain: The hexyl group contributes a hydrophobic character, making the compound more soluble in nonpolar organic solvents while potentially limiting solubility in water.
  • Temperature: Solubility can vary with temperature, often increasing as temperatures rise, particularly for organic compounds like this one.
  • pH Levels: The solubility may also depend on the pH of the solution, given the potential for ionization of various functional groups in the compound.

In summary, one may expect hexyl 3-(aziridin-1-yl)propanoate to display moderate solubility in organic solvents, while exhibiting limited solubility in water due to its hydrophobic hexyl chain. As noted, the combination of structural features plays a significant role in influencing the overall solubility characteristics, making this a compound of interest for solubility studies.

Interesting facts

Interesting Facts about Hexyl 3-(aziridin-1-yl)propanoate

Hexyl 3-(aziridin-1-yl)propanoate is a fascinating compound with numerous potential applications in chemical science and technology. Here are some interesting aspects related to this compound:

  • Structure and Functionality: The presence of the aziridine ring in its structure adds unique reactivity, making this compound suitable for various synthetic applications, particularly in the pharmaceutical industry.
  • Reactiveness: Aziridines are known for their strained three-membered ring, which can undergo ring-opening reactions under various conditions, making them useful intermediates in the synthesis of larger molecules.
  • Biological Relevance: There is growing interest in aziridine derivatives for their potential biological activities, including antimicrobial and anticancer properties, which makes this compound a subject of increasing research.
  • Applications: This compound can be utilized in the development of drug delivery systems due to its ability to modify the solubility and permeability of pharmaceutical formulations.
  • Environmental Considerations: Understanding the synthesis and degradation of hexyl 3-(aziridin-1-yl)propanoate is crucial for assessing its environmental impact, particularly as researchers seek to develop greener chemistry methods.

Overall, hexyl 3-(aziridin-1-yl)propanoate exemplifies the complex interplay of structure and reactivity in organic compounds, highlighting its importance in both academic research and practical applications.

Synonyms
1-AZIRIDINEPROPIONIC ACID, HEXYL ESTER
1-Aziridinepropanoic acid, hexyl ester
10526-03-1
DTXSID50147035
DTXCID7069526