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2-(benzotriazol-1-yl)ethyl carbamate

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Identification
Molecular formula
C9H11N3O2
CAS number
2527-58-4
IUPAC name
2-(benzotriazol-1-yl)ethyl carbamate
State
State

At room temperature, 2-(benzotriazol-1-yl)ethyl carbamate is a solid. It is stable under normal conditions and does not readily undergo phase changes without the application of heat.

Melting point (Celsius)
63.00
Melting point (Kelvin)
336.00
Boiling point (Celsius)
298.50
Boiling point (Kelvin)
571.70
General information
Molecular weight
220.20g/mol
Molar mass
220.2250g/mol
Density
1.3002g/cm3
Appearence

The compound 2-(benzotriazol-1-yl)ethyl carbamate typically appears as a white to off-white crystalline solid. It may exist in a powdery form and is known for its relatively stable nature under ambient conditions.

Comment on solubility

Solubility of 2-(benzotriazol-1-yl)ethyl carbamate

2-(benzotriazol-1-yl)ethyl carbamate is a unique compound with intriguing solubility properties. Its behavior in various solvents is significant for both practical applications and chemical behavior. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound exhibits varying solubility in polar and non-polar solvents.
  • Polar Solvents: It generally shows good solubility in methanol and ethanol, indicating that the carbamate functional group contributes positively to its interaction with polar solvents.
  • Non-Polar Solvents: Conversely, in non-polar solvents such as hexane, solubility is quite limited. This suggests that the structure of the compound may not favor hydrophobic interactions.
  • pH Influence: The solubility of 2-(benzotriazol-1-yl)ethyl carbamate can also be influenced by the pH of the solution, potentially leading to increased solubility in alkaline environments where the carbamate group can exist in a more soluble ionic form.

In summary, understanding the solubility of 2-(benzotriazol-1-yl)ethyl carbamate is crucial for its application in various fields, including pharmaceuticals and agricultural chemistry. The solubility is characterized by:

  1. Varied performance in polar versus non-polar solvents.
  2. Potential enhanced solubility in alkaline conditions.

“Solubility is the key to unlocking the potential of compounds in diverse applications.”
This statement resonates strongly with 2-(benzotriazol-1-yl)ethyl carbamate, as its solubility properties can dictate its effectiveness in target applications.

Interesting facts

Exploring 2-(Benzotriazol-1-yl)ethyl Carbamate

2-(Benzotriazol-1-yl)ethyl carbamate is an intriguing compound that combines the structural features of a carbamate with the protective properties of benzotriazole. This fusion creates a compound that has garnered interest in both academic and industrial circles for several reasons:

  • Corrosion Inhibition: One of the primary applications of 2-(benzotriazol-1-yl)ethyl carbamate lies in its ability to inhibit corrosion, particularly in metal surfaces. This makes it a valuable component in coatings and treatments designed to protect metals from degradation.
  • UV Protection: The presence of the benzotriazole moiety provides excellent UV absorption properties. This not only helps in protecting materials from UV radiation but also enhances the stability and lifespan of products such as plastics and paints.
  • Biological Applications: Research indicates potential biological activity, with studies suggesting that this compound may play a role in certain therapeutic applications. Its dual functionality in both chemical protection and biological efficacy positions it as a candidate for further exploration in pharmaceuticals.
  • Sustainability Aspects: As the demand for environmentally friendly chemicals rises, the development of compounds like 2-(benzotriazol-1-yl)ethyl carbamate reflects the industry's shift toward more sustainable and effective solutions for corrosion prevention and material stabilizations.

As with many chemical compounds, understanding the unique characteristics of 2-(benzotriazol-1-yl)ethyl carbamate opens doors to innovative applications and further research. The ongoing exploration of its properties highlights the importance of interdisciplinary approaches in chemistry and material science.

This compound truly exemplifies the intersection of practicality and innovation in the field of chemicals.

Synonyms
1-(2-CARBAMYLOXYETHYL)BENZOTRIAZOLE
13260-62-3
1H-Benzotriazole-1-ethanol, 1-carbamate
09L17842T9
1H-Benzotriazole-1-ethanol, carbamate (ester)
UNII-09L17842T9