Skip to main content

Oxetacaine

ADVERTISEMENT
Identification
Molecular formula
C18H33N3O5
CAS number
32444-24-9
IUPAC name
[3-(diethylcarbamoyloxymethyl)oxetan-3-yl]methyl N,N-diethylcarbamate
State
State

At room temperature, oxetacaine is typically in a solid state. It maintains its crystalline form in ambient conditions, making it suitable for various applications where solid-state formulations are preferred.

Melting point (Celsius)
49.00
Melting point (Kelvin)
322.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
340.45g/mol
Molar mass
340.4530g/mol
Density
1.0481g/cm3
Appearence

Oxetacaine appears as a crystalline solid. It is typically colorless to pale yellow depending on its purity. The crystalline structure is evident when viewed under a microscope, and it tends to dissolve in certain solvents designed for pharmaceutical formulations.

Comment on solubility

Solubility of [3-(diethylcarbamoyloxymethyl)oxetan-3-yl]methyl N,N-diethylcarbamate

The solubility of [3-(diethylcarbamoyloxymethyl)oxetan-3-yl]methyl N,N-diethylcarbamate can be influenced by several factors, making it a compound of interest in various chemical contexts. Understanding its solubility properties is essential for applications in pharmaceuticals, agrochemicals, and materials science.

Factors Affecting Solubility:

  • Polarity: The presence of the diethylcarbamoyl group may contribute to a moderate polarity, enhancing solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds greatly affects the compound's interaction with solvents, potentially increasing solubility in polar environments.
  • Molecular Structure: The oxetane ring introduces unique steric and electronic effects, which may either promote or hinder solubility based on the arrangement within the compound.

Generally, compounds with similar functional groups tend to exhibit certain trends in solubility:

  1. Amides and carbamates typically show enhanced solubility in polar solvents.
  2. Long aliphatic chains, like those in diethyl groups, could increase solubility in less polar solvents.

Overall, while the solubility of [3-(diethylcarbamoyloxymethyl)oxetan-3-yl]methyl N,N-diethylcarbamate can exhibit diversity depending on the solvent's nature, its unique structural features suggest that it may favorably dissolve in a range of polar solutions.

Interesting facts

Interesting Facts about [3-(diethylcarbamoyloxymethyl)oxetan-3-yl]methyl N,N-diethylcarbamate

This compound is a fascinating example of organic synthesis, particularly within the realm of carbamates, which are esters of carbamic acid. Here are some noteworthy aspects:

  • Functional Group Diversity: The presence of both diethylcarbamate and oxetane moieties demonstrates a rich structural complexity, paving the way for diverse chemical reactivity and potential applications.
  • Potential Applications: Due to its unique structure, this compound may serve as an intermediate in drug development, particularly for pharmaceuticals designed to interact with specific biological targets.
  • Stability and Reactivity: Compounds like this often exhibit interesting stability profiles, making them suitable candidates for various chemical transformations. Their reactivity can lead to the creation of new compounds with enhanced properties.
  • Synthetic Utility: Chemists appreciate such structures for their potential use in synthesis, as the diethylcarbamate moiety can act as a protective group or a leaving group in organic reactions.

As one researcher aptly put it, "Understanding the relationships between molecular structure and reactivity is key to paving the way for innovative chemical solutions." The exploration of compounds like [3-(diethylcarbamoyloxymethyl)oxetan-3-yl]methyl N,N-diethylcarbamate not only enriches our chemical knowledge but also highlights the endless possibilities in the field of synthetic chemistry.

Synonyms
BRN 1654277
CARBAMIC ACID, DIETHYL-, 3-OXETANYLIDENEDIMETHYLENE ESTER
Diethylcarbamic acid 3-oxetanylidenedimethylene ester
6722-92-5
DTXSID00217535
DTXCID50140026
5-17-05-00036 (beilstein handbook reference)