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2,4,6-Trichloropyridine

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Identification
Molecular formula
C5HCl3N
CAS number
2402-77-9
IUPAC name
2,4,6-trichloropyridine
State
State

At room temperature, 2,4,6-Trichloropyridine is usually found in a solid state.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.15
Boiling point (Celsius)
224.00
Boiling point (Kelvin)
497.15
General information
Molecular weight
196.45g/mol
Molar mass
196.4520g/mol
Density
1.4960g/cm3
Appearence

2,4,6-Trichloropyridine is a crystalline solid that can also appear as a light yellow powder. This compound exhibits a distinctive aromatic, chemical-like odor.

Comment on solubility

Solubility of 2,4,6-Trichloropyridine

2,4,6-Trichloropyridine, with the chemical formula C5H3Cl3N, is an intriguing compound when it comes to solubility. Its properties can be influenced by various factors:

  • Polar Characteristics: The presence of three chlorine atoms significantly enhances the polarity of the molecule, which typically favors solubility in polar solvents.
  • Solvent Interactions: 2,4,6-Trichloropyridine is known to be soluble in organic solvents such as ethanol, acetone, and dichloromethane, owing to the compatibility of its polar functional groups with these solvents.
  • Water Solubility: Despite its polar nature, its water solubility is relatively low. As a general rule, organic compounds with significant halogen content may exhibit reduced solubility in water due to hydrophobic effects.
  • Concentration Impact: Increased concentrations of 2,4,6-trichloropyridine can lead to saturation in various solvents, thereby limiting solubility at higher levels.

In summary, while 2,4,6-trichloropyridine showcases enhanced solubility in polar organic solvents, its interaction with water is somewhat limited. Thus, understanding the solvent effects is crucial for its practical applications.

Interesting facts

Interesting Facts about 2,4,6-Trichloropyridine

2,4,6-Trichloropyridine is a fascinating compound that has garnered attention in various fields, including agricultural chemistry and pharmaceutical research. Here are some enlightening facts about this intriguing molecule:

  • Structure and Substitution: This compound features a pyridine ring, a six-membered aromatic ring containing one nitrogen atom. The presence of three chlorine atoms at the 2, 4, and 6 positions enhances its reactivity and introduces varying properties distinct from other pyridine derivatives.
  • Applications in Agriculture: 2,4,6-Trichloropyridine is widely used as a building block in the synthesis of herbicides. These herbicides combat invasive plant species and promote agricultural productivity. Its chlorinated structure often improves the compounds' effectiveness against weeds.
  • Pharmaceutical Relevance: Beyond agriculture, this compound also serves as an essential intermediate in the synthesis of pharmaceuticals. The substitution pattern in 2,4,6-trichloropyridine can lead to diverse biological activity, making it a valuable precursor in drug development.
  • Environmental Considerations: Given the persistent nature of chlorinated compounds, studying the environmental impact of 2,4,6-trichloropyridine is vital. Understanding its degradation pathways and potential toxicity helps ensure safe usage in agricultural applications.
  • Research Insights: Chemists continue to explore new synthetic methods for producing 2,4,6-trichloropyridine with improved efficiency and selectivity, reflecting the compound's importance in ongoing research.

As we delve deeper into the characteristics and uses of 2,4,6-trichloropyridine, it becomes evident that its unique chemical properties play a crucial role in enhancing agricultural productivity and advancing medicinal chemistry.

Synonyms
2,4,6-TRICHLOROPYRIDINE
16063-69-7
Pyridine, 2,4,6-trichloro-
BRN 0114335
DTXSID80166951
DTXCID4089442
628-736-3
MFCD00971928
SCHEMBL190461
SCHEMBL2160548
2,4,6-Trichloropyridine, 97%
BBL102394
STL556196
AKOS005259094
AC-1056
CS-W002718
HY-W002718
PB19901
SB21757
AS-16101
SY005839
DB-043462
T3395
EN300-86273