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Atrazine

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Identification
Molecular formula
C8H14ClN5
CAS number
1912-24-9
IUPAC name
4-chloro-1,3,5-triazin-2-amine
State
State

At room temperature, atrazine is typically found in a solid state. It is relatively stable and not prone to rapid evaporation.

Melting point (Celsius)
172.00
Melting point (Kelvin)
445.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
215.68g/mol
Molar mass
215.6800g/mol
Density
1.1870g/cm3
Appearence

Atrazine appears as a white crystalline solid. It is generally odorless and is often available in granular form. It is known for its stability under normal temperatures and pressures.

Comment on solubility

Solubility of 4-chloro-1,3,5-triazin-2-amine

The solubility profile of 4-chloro-1,3,5-triazin-2-amine can be intriguing due to its chemical structure and functional groups. This compound, containing a triazine ring, may exhibit varying solubility characteristics in different solvents.

Factors influencing solubility:

  • Polarity: The presence of amine functional groups can enhance solubility in polar solvents like water due to the ability to form hydrogen bonds.
  • Temperature: Typically, solubility increases with temperature, making it easier for the compound to dissolve at elevated temperatures.
  • Solvent Characteristics: Organic solvents such as ethanol and acetone may also dissolve this compound effectively, given their suitable polarity and ability to interact with the triazine structure.

As with many organic compounds, the solubility of 4-chloro-1,3,5-triazin-2-amine is often context-dependent. It is worth noting that it might not be freely soluble in all solvents, and limited solubility can impact its practical applications. Therefore, evaluating solubility in potential application environments is essential for optimal use.

Interesting facts

Interesting Facts about 4-Chloro-1,3,5-triazin-2-amine

The compound 4-chloro-1,3,5-triazin-2-amine is a fascinating member of the triazine family, which is notable for its unique ring structure and versatile chemical properties. Here are some intriguing aspects of this compound:

  • Historical Significance: Triazines have played a significant role in agricultural chemistry, particularly as herbicides. The properties of 4-chloro-1,3,5-triazin-2-amine make it relevant in the synthesis of various active herbicidal ingredients.
  • Reactivity: The presence of the chlorine substitution on the triazine ring greatly influences its reactivity, allowing for various chemical modifications. This reactivity is crucial for creating derivatives that can serve specific functions in organic synthesis.
  • Applications: Beyond its potential as an herbicide, this compound could be explored in pharmaceuticals and materials science due to its ability to interact with biological systems and its stability under various conditions.
  • Environmental Considerations: When studying compounds like 4-chloro-1,3,5-triazin-2-amine, scientists must consider their environmental impact, including their degradation pathways and ecological effects, particularly when used in agricultural settings.

As a student of chemistry, delving into the properties and applications of such compounds broadens your understanding of how molecular structure influences behavior and utility. A quote from a leading researcher in the field sums it up well: "Understanding the nuances of compounds like 4-chloro-1,3,5-triazin-2-amine not only enriches our knowledge but also enhances our ability to innovate in chemistry."

This compound exemplifies the intersection of fundamental and applied chemistry, making it an exciting topic of study for anyone interested in the practical applications of organic compounds.

Synonyms
4-Chloro-1,3,5-triazin-2-amine
4-Amino-2-chloro-1,3,5-triazine
1,3,5-Triazin-2-amine, 4-chloro-
2-AMINO-4-CHLORO-S-TRIAZINE
s-Triazine, 2-amino-4-chloro-
DTXSID30227869
DTXCID30150360
823-503-4
7709-13-9
2-amino-4-chloro-1,3,5-triazine
MFCD19203794
C3H3ClN4
2-Amino-4-chloro-s-triazine; 4-Amino-2-chloro-1,3,5-triazine; 4-Chloro-1,3,5-triazin-2-amine
SCHEMBL154798
ULVNIJSKNRGBHX-UHFFFAOYSA-N
HAA70913
AKOS006340660
SB73723
DS-20002
SY044773
DB-331997
CS-0089676
EN300-98634
D71138