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1-Butylaziridine

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Identification
Molecular formula
C7H15N
CAS number
694-84-8
IUPAC name
1-butylaziridine
State
State

At room temperature, 1-butylaziridine exists as a liquid.

Melting point (Celsius)
-75.00
Melting point (Kelvin)
198.15
Boiling point (Celsius)
129.00
Boiling point (Kelvin)
402.15
General information
Molecular weight
113.21g/mol
Molar mass
113.2110g/mol
Density
0.8103g/cm3
Appearence

1-Butylaziridine is a clear, colorless liquid. It often has a faint fishy or amine-like odor typical of many organic nitrogen compounds.

Comment on solubility

Solubility of 1-butylaziridine

1-butylaziridine, a cyclic amine, displays notable solubility characteristics that are influenced by its chemical structure. As a nitrogen-containing compound, it exhibits the following solubility properties:

  • Water Solubility: 1-butylaziridine is partially soluble in water due to its polar amine group. However, the long butyl chain reduces overall solubility compared to smaller amines.
  • Organic Solvents: It is more soluble in organic solvents such as ethanol, diethyl ether, and dichloromethane. This is largely due to its hydrophobic butyl group.
  • Temperature Effect: As with many organic compounds, solubility may increase with temperature, allowing for enhanced interactions with solvent molecules.

In summary, the solubility of 1-butylaziridine can be described as limited in water but favorable in organic solvents, making it suitable for various chemical applications where a non-polar environment is preferred. Understanding these solubility dynamics is essential for its practical use in chemical synthesis and reaction formulation.

Interesting facts

Interesting Facts about 1-Butylaziridine

1-Butylaziridine is an intriguing compound that belongs to the family of aziridines, which are cyclic amines known for their unique structural properties. Here are some captivating details about this compound:

  • Structure & Reactivity: 1-Butylaziridine features a three-membered aziridine ring, which contributes to its distinctive reactivity. The strain inherent in the ring makes it a valuable intermediate in organic synthesis.
  • Synthetic Applications: This compound is often used in the synthesis of various biologically active molecules. Its ability to easily undergo ring-opening reactions allows for the introduction of diverse functional groups, making it a common choice in pharmaceutical chemistry.
  • Biological Relevance: Though specific biological functions of 1-butylaziridine are still being studied, compounds within the aziridine family have been known to exhibit anti-cancer, anti-bacterial, and anti-inflammatory properties, which opens pathways for future research.
  • Laboratory Importance: Chemists often appreciate 1-butylaziridine for its role in developing new materials and applications in polymer chemistry. The unique properties of aziridines can lead to innovative uses and formulations.
  • Historical Context: Aziridines have garnered attention since their first isolation; however, 1-butylaziridine emphasizes the ongoing exploration of nitrogen-containing heterocycles in modern chemistry.

In summary, 1-butylaziridine exemplifies the complexity and potential of small organic molecules, showcasing the interplay between structure, reactivity, and application in various scientific fields. The future of research surrounding this compound is promising, and its potential breakthroughs may significantly impact various industrial and medical sectors.

Synonyms
Aziridine, 1-butyl-
1-BUTYLAZIRIDINE
N-Butylaziridine
N-Butylethylenimine
BRN 0102491
AI3-50668
DTXSID30149810
5-20-01-00008 (Beilstein Handbook Reference)
DTXCID5072301
xiejptdttyfcjm-uhfffaoysa-n
1120-85-0
1-butyl-aziridine
Butylaziridine, N-
aziridine, N-n-butyl-
DXT3E73857
AKOS015907371