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DIPTA

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Identification
Molecular formula
C9H18N6
CAS number
71579-71-8
IUPAC name
N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine
State
State

At room temperature, DIPTA is typically in a solid state.

Melting point (Celsius)
96.00
Melting point (Kelvin)
369.15
Boiling point (Celsius)
277.00
Boiling point (Kelvin)
550.15
General information
Molecular weight
196.27g/mol
Molar mass
196.2700g/mol
Density
1.0550g/cm3
Appearence

DIPTA is typically a white to light yellow crystalline powder. Its appearance might vary slightly based on purity and specific formulation.

Comment on solubility

Solubility of N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine

N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine is a compound that exhibits unique solubility characteristics, primarily influenced by its molecular structure and functional groups. Here are some key points regarding its solubility:

  • Solvent Dependency: The solubility of this compound can vary significantly depending on the solvent used. Common solvents include:
    • Polar solvents (e.g., water, methanol)
    • Non-polar solvents (e.g., hexane, toluene)
  • Impacts of Isopropyl Groups: The presence of isopropyl groups is likely to increase hydrophobic interactions, affecting solubility in polar solvents.
  • Temperature Effects: Solubility may also change with temperature, generally increasing in many cases as the temperature rises.
  • pH Sensitivity: The compound may show different solubility behavior based on the pH of the solution due to its amine functionalities.

In summary, the solubility of N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine is complex and can be tailored by adjusting the solvent system, temperature, and pH. This variability underscores the compound's potential applicability in various chemical environments, but also highlights the importance of conducting specific solubility tests for practical uses.

Interesting facts

Interesting Facts about N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine

N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine, commonly referred to as a member of the triazine family, possesses unique structural characteristics that make it of interest in various fields of chemistry, including agricultural and medicinal applications.

Chemical Structure and Significance

This compound is notable for its triazine ring, which is a fused ring structure containing alternating nitrogen and carbon atoms. The significance of the triazine moiety lies in its ability to participate in a range of chemical reactions, making it a useful building block for synthesizing more complex molecules.

Applications

  • Agriculture: It has potential as a herbicide or plant growth regulator, contributing to crop development.
  • Pharmaceuticals: The compound may exhibit biological activity that could lead to the development of new therapeutic agents.
  • Materials Science: Its derivatives are being explored in the development of high-performance materials.

Reactivity and Compatibility

The reactivity of N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine is intriguing due to the presence of amino groups. These functional groups can engage in hydrogen bonding, making them highly interactive with a variety of substrates.

Future Research Directions

Ongoing research is focused on understanding the full potential of this compound. As with many triazine derivatives, scientists are investigating:

  • Strategies for enhancing bioactivity
  • Environmental impact and degradation pathways
  • Synergistic effects when combined with other agricultural chemicals

In conclusion, N2,N4-diisopropyl-1,3,5-triazine-2,4,6-triamine serves as a prime example of how triazine-based compounds can influence diverse areas of research and application. Its structural features, combined with its reactivity, pave the way for exciting developments in chemistry!

Synonyms
16274-44-5
N~2~,N~4~-Di(propan-2-yl)-1,3,5-triazine-2,4,6-triamine
SCHEMBL8059674
DTXSID90274834