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Ethyl N-isobutylcarbamate

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Identification
Molecular formula
C8H17NO2
CAS number
16350-96-6
IUPAC name
ethyl N-isobutylcarbamate
State
State

At room temperature, Ethyl N-isobutylcarbamate is a liquid.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
235.30
Boiling point (Kelvin)
508.45
General information
Molecular weight
159.22g/mol
Molar mass
159.2200g/mol
Density
0.9670g/cm3
Appearence

Ethyl N-isobutylcarbamate typically appears as a colorless to pale yellow liquid. It is important to store it properly to maintain its colorless state.

Comment on solubility

Solubility of Ethyl N-isobutylcarbamate

Ethyl N-isobutylcarbamate, with its unique structure, presents interesting solubility characteristics. Understanding its solubility is crucial for various applications in chemical processes and formulations. Here are some key points about its solubility:

  • Polar and Non-Polar Interaction: Ethyl N-isobutylcarbamate features both polar and non-polar elements in its structure, allowing it to interact favorably with a range of solvents.
  • Solubility in Organic Solvents: This compound is generally soluble in organic solvents such as ethanol and chloroform, thanks to its ethyl and isobutyl groups.
  • Poor Solubility in Water: However, its solubility in water is limited. This can be attributed to the hydrophobic nature of the isobutyl group, which tends to repel water molecules.

In summary, while ethyl N-isobutylcarbamate shows good solubility in organic solvents, it exhibits limited solubility in water, making it more suitable for non-aqueous environments. This balance of solubility properties plays a significant role in its applications within various chemical contexts.

Interesting facts

Ethyl N-isobutylcarbamate: A Unique Compound

Ethyl N-isobutylcarbamate is an intriguing compound that has gained attention in various fields of study, particularly in organic chemistry and agricultural sciences. Here's what makes this compound noteworthy:

  • Formation of Carbamates: Ethyl N-isobutylcarbamate belongs to the family of carbamates, which are derived from carbamic acid. Carbamates are significant due to their roles as intermediates in organic synthesis and their applications in pharmaceuticals and agrochemicals.
  • Pesticide Usage: This compound has been explored as a potential pesticide. Carbamates often exhibit insecticidal and herbicidal properties, making them valuable in the agricultural industry for pest control.
  • Biological Activity: Research indicates that ethyl N-isobutylcarbamate may possess interesting biological activities, including potential antitumor effects. This opens avenues for further investigation in medicinal chemistry.
  • Environmental Considerations: Due to the widespread use of carbamate-based pesticides, it is crucial for scientists to evaluate their environmental impact. Understanding the degradation processes and ecological effects of compounds like ethyl N-isobutylcarbamate is fundamental for sustainable agricultural practices.
  • Versatility in Synthesis: Ethyl N-isobutylcarbamate is often utilized as a building block in organic synthesis, which can lead to a variety of derivatives with diverse functionalities. Chemists value such compounds for their potential to yield new materials and compounds.

In conclusion, ethyl N-isobutylcarbamate shines as a compound of interest not only for its chemical properties but also for its potential impacts in agriculture and medicine. Further research may reveal even greater significance, highlighting the ever-evolving frontier of chemical science.

Synonyms
ISOBUTYL URETHANE
539-89-9
ethyl isobutylcarbamate
UNII-D67W14T992
D67W14T992
ISOBUTYL URETHANE, N-
AI3-16186
ISOBUTYL URETHANE [MI]
N-(2-Methylpropyl)carbamic acid ethyl ester
DTXSID90202172
ISOBUTYLCARBAMIC ACID ETHYL ESTER
Carbamic acid, (2-methylpropyl)-, ethyl ester
DTXCID90124663
ethyl N-(2-methylpropyl)carbamate
Isobutylurethan
SCHEMBL8917423
isobutyl-carbamic acid ethyl ester
AKOS003860665
N-(2-methyl-propyl)-carbamic acid ethyl ester
Q27276161