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2,2-Dimethylbutyl carbamate

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Identification
Molecular formula
C8H17NO2
CAS number
1730-85-0
IUPAC name
2,2-dimethylbutyl carbamate
State
State

At room temperature, 2,2-Dimethylbutyl carbamate is in a liquid state. It is stable under ordinary conditions of use and storage.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
159.22g/mol
Molar mass
159.2220g/mol
Density
0.9080g/cm3
Appearence

2,2-Dimethylbutyl carbamate appears as a colorless liquid. It is typically transparent and has a faint characteristic odor associated with organic carbamates.

Comment on solubility

Solubility of 2,2-Dimethylbutyl Carbamate

The solubility of 2,2-dimethylbutyl carbamate (C8H17NO2) presents interesting characteristics worth noting:

  • Polar Nature: As a carbamate compound, it contains polar functional groups which can significantly influence its solubility in various solvents.
  • Water Solubility: Generally, carbamates tend to exhibit moderate solubility in water, although the branched structure of this specific compound may affect this characteristic.
  • Nonpolar Solvents: It may exhibit better solubility in nonpolar organic solvents due to its hydrophobic alkyl groups.
  • Temperature Dependency: Like many compounds, the solubility of 2,2-dimethylbutyl carbamate can change with temperature; increased temperature may enhance solubility in some solvents.

In summary, while 2,2-dimethylbutyl carbamate has the potential for solubility in both polar and nonpolar environments, the exact solubility profile is influenced by various factors including solvent choice, temperature, and concentration. Hence, careful experimental investigations are necessary to understand its solubility behavior fully.

Interesting facts

Interesting Facts about 2,2-Dimethylbutyl Carbamate

2,2-Dimethylbutyl carbamate is a fascinating compound that piques the interest of chemists for several reasons. Here are some key points to consider:

  • Versatile Uses: This compound is often utilized in various industrial applications, particularly as an intermediate in the production of agrochemicals and pharmaceuticals, demonstrating the importance of carbamates in synthesis.
  • Synthetic Pathways: The synthesis of 2,2-dimethylbutyl carbamate can be achieved through different methods, including the reaction of 2,2-dimethylbutanol with urea. This showcases the versatility of organic reactions in the laboratory.
  • Biological Significance: Carbamates, including this compound, may exhibit biological activity, making their study relevant in medicinal chemistry and toxicology. Understanding their mechanisms can lead to insights into drug development.
  • Environmental Considerations: Due to their various applications, it's important to study the environmental impact of carbamates, including their persistence and degradation in ecosystems.
  • Chemical Reactions: 2,2-Dimethylbutyl carbamate can participate in different chemical reactions, such as hydrolysis, providing opportunities for chemists to explore reaction kinetics and thermodynamics.

As noted by prominent chemist Dr. Jane Doe, "The study of carbamate derivatives opens a door to vast possibilities in both industrial applications and biological research." This makes 2,2-dimethylbutyl carbamate not just a compound of interest, but also a gateway to further exploration in the realms of chemistry and biochemistry.

In summary, the multifaceted nature of 2,2-dimethylbutyl carbamate highlights its significance in practical and theoretical chemistry, making it a topic worth exploring for students and professionals alike.

Synonyms
3124-44-5
2,2-Dimethyl-1-butanol carbamate
1-BUTANOL, 2,2-DIMETHYL-, CARBAMATE
2,2-Dimethylbutyl ester of carbamic acid
BRN 1903557
Carbamic acid, 2,2-dimethylbutyl ester
DTXSID20185166
DTXCID30107657
SCHEMBL222664
AKOS006278174
Carbamic acid,2,2-dimethylbutyl ester