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Bromodichloroisocyanuric acid

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Identification
Molecular formula
C4H3Br3N5
CAS number
52480-48-9
IUPAC name
6-(tribromomethyl)-1,3,5-triazine-2,4-diamine
State
State

At room temperature, it is typically found as a solid. It is not volatile.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.00
Boiling point (Celsius)
333.85
Boiling point (Kelvin)
607.00
General information
Molecular weight
328.84g/mol
Molar mass
328.8310g/mol
Density
2.3400g/cm3
Appearence

The compound is a crystalline solid with a pale yellow to white appearance. It might discolor upon exposure to light or moisture.

Comment on solubility

Solubility of 6-(tribromomethyl)-1,3,5-triazine-2,4-diamine

The solubility of 6-(tribromomethyl)-1,3,5-triazine-2,4-diamine presents intriguing aspects that are pivotal to its application and behavior in various media. This compound's solubility is largely influenced by the following factors:

  • Polar Characteristics: The presence of polar functional groups can enhance solubility in polar solvents, such as water, whereas non-polar solvents may exhibit reduced solubility.
  • Hydrophobic Interactions: The tri-bromomethyl group introduces significant hydrophobic characteristics which often leads to diminished solubility in water but improved solubility in organic solvents.
  • Temperature Dependence: Solubility can vary with temperature, generally increasing with heat due to enhanced molecular motion.

As a result, 6-(tribromomethyl)-1,3,5-triazine-2,4-diamine is likely to be more soluble in organic solvents than in water, making it suitable for specific applications in chemical reactions and formulations. It's crucial to evaluate its solubility in various conditions to optimize its use in both laboratory and industrial settings.

Interesting facts

Interesting Facts about 6-(Tribromomethyl)-1,3,5-triazine-2,4-diamine

6-(Tribromomethyl)-1,3,5-triazine-2,4-diamine, commonly known as an intriguing triazine derivative, has several remarkable characteristics that make it a compound of interest in the realm of chemistry. Here are some fascinating aspects:

  • Structure and Stability: This compound features a triazine ring, a three-carbon nitrogen-containing heterocycle, which is renowned for its stability and robustness. The substitution of tribromomethyl groups on the triazine core enhances its chemical stability.
  • Applications in Agriculture: Compounds of this nature often find use as herbicides and fungicides. The tribromomethyl group can enhance biological activity, making it a potent candidate for agricultural applications.
  • Role in Material Science: Research is ongoing into the use of triazines in the development of flame retardants and polymers. The presence of halogen atoms can impart desirable properties such as fire resistance.
  • Environmental Impact: While compounds like 6-(tribromomethyl)-1,3,5-triazine-2,4-diamine serve essential roles, it is crucial to consider their environmental degradation pathways and potential toxicity. Understanding their impact on ecosystems is key to their responsible use.

As with many chemical compounds, the study of 6-(tribromomethyl)-1,3,5-triazine-2,4-diamine showcases the dual nature of such substances—bringing both beneficial applications and environmental considerations to the forefront. Chemists continue to explore the nuances of this compound's reactivity and potential innovations it may inspire in various scientific fields.

Synonyms
6-(tribromomethyl)-1,3,5-triazine-2,4-diamine
16088-72-5
SCHEMBL11146368
DTXSID10274831