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N-ethyl-4-heptadecyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

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Identification
Molecular formula
C23H41Cl3N4
CAS number
79529-94-1
IUPAC name
N-ethyl-4-heptadecyl-6-(trichloromethyl)-1,3,5-triazin-2-amine
State
State

The compound is a solid at room temperature, with a crystalline structure aiding its stable form. It transitions from solid to liquid when heated above its melting point, which is characteristic of organic compounds with long alkyl chains.

Melting point (Celsius)
44.00
Melting point (Kelvin)
317.15
Boiling point (Celsius)
294.00
Boiling point (Kelvin)
567.15
General information
Molecular weight
469.88g/mol
Molar mass
469.8800g/mol
Density
1.1350g/cm3
Appearence

The compound, N-ethyl-4-heptadecyl-6-(trichloromethyl)-1,3,5-triazin-2-amine, typically appears as a white crystalline solid. Its structural complexity and chain length contribute to its solid state at room temperature. Although it may be handled in laboratories, it is not commonly encountered in everyday contexts without industrial or research relevance.

Comment on solubility

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

The solubility of N-ethyl-4-heptadecyl-6-(trichloromethyl)-1,3,5-triazin-2-amine can be influenced by various factors related to its molecular structure. In general, compounds with long hydrophobic aliphatic chains, such as the heptadecyl group in this compound, tend to exhibit low solubility in polar solvents, including water. On the other hand, such hydrophobic chains can enhance solubility in nonpolar organic solvents.

Key points to consider regarding the solubility of this compound include:

  • Hydrophobic Effects: The long heptadecyl chain increases the hydrophobic nature of the compound, making it less likely to dissolve in water.
  • Polarity: The presence of the trichloromethyl group could potentially introduce some polar characteristics, affecting overall solubility.
  • Solvent Compatibility: This compound may dissolve more readily in organic solvents such as hexane, benzene, or dichloromethane, due to the nonpolar characteristics of the heptadecyl chain.

As a result, the solubility of N-ethyl-4-heptadecyl-6-(trichloromethyl)-1,3,5-triazin-2-amine will likely be:

  • Low in Water: Limited solubility in aqueous environments.
  • Higher in Organic Solvents: Better compatibility with nonpolar solvents.

In summary, the solubility of this compound underscores the fundamental principles of chemistry, where the interactions between molecular structure and solvent properties dictate the solubility behavior. Understanding these relationships is crucial for practical applications in various fields.

Interesting facts

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

N-ethyl-4-heptadecyl-6-(trichloromethyl)-1,3,5-triazin-2-amine is a fascinating compound that belongs to the class of triazines, which are known for their diverse applications in various fields such as agrochemicals, pharmaceuticals, and materials science. Here are several intriguing aspects of this compound:

  • Unique Structure: The compound features a triazine ring, a six-membered aromatic platform with nitrogen atoms that imparts *notable stability* and *reactivity*, making it ideal for synthetic applications.
  • Biological Activity: Triazine derivatives are known for their potential *biological properties*, such as herbicidal and fungicidal activities. They can interact with enzymes and biological pathways, which is why they are valuable in agricultural chemistry.
  • Environmental Impact: The presence of a trichloromethyl group hints at the compound's potential environmental influence. Chlorinated compounds are often scrutinized for their *persistence* and *toxicity*, which raises important considerations in their use and disposal.
  • Versatile Applications: This compound may be employed in various fields, including:
    • Agriculture: As a *pesticide* or *herbicide*
    • Materials Science: In the development of *coatings* or *polymers*
    • Chemical Synthesis: As a *reagent* in organic chemistry reactions
  • Research Interests: The *exploration of its derivatives* continues in scientific literature, focusing on modifying its structure for enhanced efficacy or reduced environmental impact.

This compound exemplifies the intricate relationship between chemistry and environmental science, highlighting the importance of responsible innovation in the development of new chemical entities. As a colleague once said, *"The beauty of chemistry lies in its ability to harness the elements for betterment but must always be tempered with considerations of safety and sustainability."*

Understanding compounds like N-ethyl-4-heptadecyl-6-(trichloromethyl)-1,3,5-triazin-2-amine not only broadens the horizon of chemical science but also fosters innovation in addressing the challenges we face today.