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Cyanuric triamide

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Identification
Molecular formula
C9H18N6
CAS number
102-76-3
IUPAC name
N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine
State
State

At room temperature, cyanuric triamide is a solid.

Melting point (Celsius)
92.50
Melting point (Kelvin)
365.65
Boiling point (Celsius)
204.50
Boiling point (Kelvin)
477.65
General information
Molecular weight
201.27g/mol
Molar mass
201.2690g/mol
Density
1.0400g/cm3
Appearence

Cyanuric triamide appears as a white crystalline powder.

Comment on solubility

Solubility of N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine

N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine is a fascinating compound known for its unique structure and potential applications.

When discussing its solubility, several key aspects should be highlighted:

  • Polarity: The presence of ethyl groups contributes to a more non-polar character, which generally implies limited solubility in water.
  • Solvents: This compound may exhibit increased solubility in organic solvents such as:
    • Alcohols
    • Aromatics (e.g., benzene)
    • Ethers
  • Applications: Its solubility properties can influence its use in formulations, particularly in agricultural chemistry and chemical synthesis.

In conclusion, while N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine may not dissolve well in water, it retains considerable solubility in various organic solvents, making it suitable for specific applications. Understanding these solubility characteristics is critical for maximizing its utility in different chemical processes.

Interesting facts

Interesting Facts about N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine

N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine is a fascinating compound that belongs to the family of triazine derivatives. It possesses a unique set of properties and applications that make it stand out in the field of chemistry.

Key Characteristics

  • Versatile Applications: This compound is widely recognized for its role in molecular biology and agriculture as a potential herbicide.
  • Stability: The triazine ring structure contributes to its stability under various conditions, making it a reliable option in chemical formulations.
  • Research Interest: It has gained attention in organic chemistry research due to its ability to form stable complexes with metal ions, which can be utilized in catalysis.

Scientific Significance

Scientists admire N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine for its potential to:

  • Enable the development of new materials with desirable properties.
  • Enhance our understanding of nitrogen-containing compounds and their reactivity.

As chemists delve deeper into the study of this compound, it opens up avenues for innovations in chemical synthesis and applications across various industries.

Anecdote in the Lab

One of the most captivating aspects of working with triazine compounds is the moment one realizes how small changes in the molecular structure can lead to significant differences in behavior and utility: "Chemistry is all about connections, not just atoms." This statement rings particularly true with N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine, serving as a perfect example of how modifications can lead to enhanced performance in applications.

In summary, N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine is much more than just a chemical compound; it is a window into the diverse world of chemistry and its implications in life and technology.

Synonyms
16268-92-1
triethylmelamine
N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triamine
N,N',N''-Triethyl-1,3,5-triazine-2,4,6-triamine
1,3,5-Triazine-2,4,6-triamine, N2,N4,N6-triethyl-
2-N,4-N,6-N-triethyl-1,3,5-triazine-2,4,6-triamine
EINECS 240-372-3
NoName_3757
AI3-60345
SCHEMBL1034033
SCHEMBL9770045
DTXSID50903158
LNCCBHFAHILMCT-UHFFFAOYSA-N
MFCD18430914
AKOS037646317
AS-68119
1,3,5-Triazine, 2,4,6-trisethylamino-
NS00053573
D86727
EN300-844061
1,3,5-Triazine-2,4,6-triamine, N,N',N''-triethyl-, hemihydrate