Potassium 4-amino-3,5,6-trichloropyridine-2-carboxylate

Identification

Molecular formula

C₆H₂Cl₃N₂KO₂

CAS number

.not_known

IUPAC name

potassium;4-amino-3,5,6-trichloro-pyridine-2-carboxylate

State

The compound is typically found in a solid state at room temperature, exhibiting a stable crystalline form due to the ionic nature contributed by the potassium salt form.

Melting point (Celsius)

210.00

Melting point (Kelvin)

483.00

Boiling point (Celsius)

350.00

Boiling point (Kelvin)

623.00

General information

Molecular weight

286.44g/mol

Molar mass

286.4380g/mol

Density

2.2400g/cm³

Appearence

This compound typically appears as a crystalline solid due to the presence of multiple chlorine atoms which can influence its crystalline structure. The appearance may vary based on its purity and specific form.

Comment on solubility

Solubility of Potassium 4-Amino-3,5,6-Trichloro-pyridine-2-carboxylate

The solubility of potassium 4-amino-3,5,6-trichloro-pyridine-2-carboxylate can be influenced by several factors, which are essential to understand for its practical applications:

Nature of the Solvent: The compound tends to be more soluble in polar solvents such as water, due to the ionic nature of the potassium salt.
Temperature Effects: Generally, as temperature increases, the solubility of many salts increases. However, this can vary, and specific data is needed for accurate predictions.
pH Influence: The solubility may also change with varying pH levels because the carboxylate group can ionize, enhancing the solubility in more alkaline conditions.

As a general observation, it can be said that salts of organic acids tend to be more soluble than their neutral counterparts. Hence, potassium 4-amino-3,5,6-trichloro-pyridine-2-carboxylate is likely to exhibit decent solubility when properly dissolved. However, empirical testing is always recommended to confirm solubility in specific contexts.

Interesting facts

Interesting Facts About Potassium 4-amino-3,5,6-trichloro-pyridine-2-carboxylate

This fascinating compound, known as potassium 4-amino-3,5,6-trichloro-pyridine-2-carboxylate, serves as a valuable addition to the realm of agrochemicals and pharmaceuticals. Here are some intriguing points to consider:

Complex Structure: The compound is derived from pyridine, a six-membered aromatic ring containing nitrogen. Its chemical complexity arises from the trichlorination and amino substitution at specific carbon atoms.
Herbicidal Properties: This compound exhibits notable herbicidal activity, making it a potential candidate for weed management in various agricultural applications. This characteristic highlights its importance in sustainable agriculture.
Biological Activity: Research indicates that this compound, due to its trichloro-substituents, could have significant interactions with biological systems, potentially influencing many biochemical pathways.
Environmental Impact: As with all agrochemical products, the environmental impact is a critical focus. Investigating its behavior in soil and water systems helps assess its ecological footprint.
Potential for Synthesis: The synthesis of this compound can be explored through various methods in organic chemistry, offering opportunities for students to engage in practical laboratory experiences.

In conclusion, potassium 4-amino-3,5,6-trichloro-pyridine-2-carboxylate is more than just a chemical compound; it represents a blend of chemistry, agricultural science, and environmental considerations. As we continue to research and understand its properties, we unveil its potential contributions to both science and industry.