4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

Identification

Molecular formula

C₁₃H₂₀Cl₃N₅

CAS number

4008-43-1

IUPAC name

4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

State

At room temperature, this compound is typically in a solid state.

Melting point (Celsius)

182.00

Melting point (Kelvin)

455.15

Boiling point (Celsius)

424.00

Boiling point (Kelvin)

697.15

General information

Molecular weight

308.64g/mol

Molar mass

308.6430g/mol

Density

1.3520g/cm³

Appearence

The compound appears as a colorless to pale yellow solid. It may exhibit a crystalline structure depending on its specific polymorphic form and purity level.

Comment on solubility

Solubility of 4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

The solubility of 4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine can be particularly intriguing due to its unique chemical structure and substituents. Here are some key points regarding its solubility:

Polar vs. Nonpolar: The presence of the trichloromethyl group introduces a polar character to the molecule, potentially influencing its solubility in polar solvents.
Solvent Interaction: It may exhibit solubility in organic solvents such as dichloromethane and chloroform, where similar triazine derivatives have been observed to dissolve effectively.
Temperature Dependence: Like many organic compounds, solubility may increase with temperature, suggesting enhanced dissolution kinetics at elevated temperatures.
Hydrophobic Influence: The pentyl and propyl groups contribute to hydrophobic interactions, which may reduce solubility in aqueous environments.

In summary, while the solubility profile of 4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine is influenced by both polar and nonpolar characteristics, understanding its full solubility behavior requires careful consideration of the interplay between its structural features and the solvent environment. As with many compounds of this nature, experimentation will provide the most reliable data in determining its exact solubility limits in various conditions.

Interesting facts

Interesting Facts about 4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine, commonly referred to as a triazine derivative, is a compound that showcases the fascinating interplay between organic chemistry and agricultural applications. Here are some noteworthy points about this intriguing molecule:

Herbicidal Properties: This compound is primarily known for its efficacy as a herbicide. Its unique structure contributes to its ability to inhibit the growth of certain unwanted plants, making it valuable in agricultural practices.
Structure-Activity Relationship: The incorporation of the trichloromethyl group is significant as it enhances the biological activity of the compound. The presence of multiple functional groups such as the pentyl and propyl chains also influences its solubility and interactions with target sites.
Sustainability Focus: Researchers are continuously exploring variations of triazine derivatives to improve their environmental compatibility. This involves modifying the compound to reduce toxicity while maintaining its herbicidal effectiveness.
Mode of Action: This compound disrupts key metabolic pathways in plants, providing an effective means of controlling weed populations. Understanding its mode of action can help chemists design better, more targeted herbicides.
Global Importance: As a widely studied herbicide, the implications of its use extend beyond local farming. It plays a role in food production and impacts global agriculture by helping to enhance crop yields.

In summary, 4-pentyl-N-propyl-6-(trichloromethyl)-1,3,5-triazin-2-amine is not just a simple chemical compound; it reflects the advances in agricultural science, emphasizing the ongoing quest for more efficient and sustainable methods for weed management. As chemists continue to unravel its complexities, there's potential for fostering innovations that balance productivity with environmental stewardship.