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Diclofenac hydrochloride

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Identification
Molecular formula
C14H11Cl2NO2
CAS number
15307-79-6
IUPAC name
[N'-[(2,6-dichlorophenyl)methoxy]carbamimidoyl]ammonium;chloride
State
State

At room temperature, diclofenac hydrochloride is in a solid state.

Melting point (Celsius)
165.00
Melting point (Kelvin)
438.00
Boiling point (Celsius)
241.00
Boiling point (Kelvin)
514.00
General information
Molecular weight
318.13g/mol
Molar mass
318.1290g/mol
Density
0.9430g/cm3
Appearence

Diclofenac hydrochloride typically appears as a white or slightly beige crystalline powder. It is odorless.

Comment on solubility

Solubility of N'-[(2,6-dichlorophenyl)methoxy]carbamimidoyl]ammonium;chloride

The solubility of the compound N'-[(2,6-dichlorophenyl)methoxy]carbamimidoyl]ammonium;chloride can be influenced by several factors, reflecting its unique chemical structure. Here are some essential considerations:

  • Ionic Nature: Being a salt, its solubility in water is often dictated by the ionic interactions.
  • Polar vs. Nonpolar: The presence of the chloride anion contributes to increased solubility in polar solvents like water, while the aromatic ring may limit solubility in nonpolar environments.
  • Temperature Dependence: As with many salts, solubility typically increases with temperature. Thus, higher temperatures may facilitate dissolution.
  • pH Sensitivity: The solubility may vary depending on the pH of the solution, with potential alterations in protonation states affecting the compound's overall solubility profile.

In practice, you may observe that solubility plays a critical role in determining the compound's accessibility and functionality in various applications.

In summary, understanding the interactions that dictate solubility is vital when working with N'-[(2,6-dichlorophenyl)methoxy]carbamimidoyl]ammonium;chloride, as it can significantly influence performance in both laboratory and industrial settings.

Interesting facts

Interesting Facts about N'-[(2,6-Dichlorophenyl)methoxy]carbamimidoyl]ammonium Chloride

N'-[(2,6-Dichlorophenyl)methoxy]carbamimidoyl]ammonium chloride is a fascinating compound that plays an interesting role in the realm of chemistry and pharmaceuticals. Here are some engaging aspects to consider:

  • Significance in Research: This compound is often explored in medicinal chemistry for its potential biological activities. Its unique structure may contribute to various pharmacological effects.
  • Diverse Applications: Compounds of this nature typically serve as intermediates in the synthesis of more complex molecules, making them valuable in the development of drugs and agrochemicals.
  • Mechanism of Action: The presence of the carbamimidoyl group in the structure can lead to interesting interactions at the molecular level, which can influence its activity in biochemical pathways. Understanding these interactions could pave the way for new therapeutic agents.
  • Environmental Impact: As a chlorinated compound, the environmental behavior and persistence of this substance warrant investigation, particularly concerning its degradation products and toxicity.
  • Structural Characteristics: The dichlorophenyl group contributes to the compound’s biochemical properties and solubility characteristics, which can be critical during drug formulation.

To summarize, N'-[(2,6-Dichlorophenyl)methoxy]carbamimidoyl]ammonium chloride is not just a simple salt; its intricate structure and potential applications make it a notable subject for study in various fields of chemistry. As scientists delve deeper into its properties, this compound could yield new insights and innovations.