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Ethyl violet

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Identification
Molecular formula
C31H42N3O5
CAS number
2390-59-2
IUPAC name
2-(N-[2-(4-ethoxyphenoxy)acetyl]-3-methoxy-anilino)ethyl-diethyl-ammonium;2,4,6-trinitrophenolate
State
State

At room temperature, ethyl violet is in a solid state, specifically as a crystalline powder. It is not readily soluble in water but can dissolve in organic solvents such as alcohol or acetone.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
405.00
Boiling point (Kelvin)
678.15
General information
Molecular weight
429.58g/mol
Molar mass
429.5800g/mol
Density
0.9800g/cm3
Appearence

Ethyl violet typically appears as a purple to violet crystalline powder. It is often used as a dye and has a distinct and intense coloration.

Comment on solubility

Solubility of 2-(N-[2-(4-ethoxyphenoxy)acetyl]-3-methoxy-anilino)ethyl-diethyl-ammonium; 2,4,6-trinitrophenolate

The solubility of the compound 2-(N-[2-(4-ethoxyphenoxy)acetyl]-3-methoxy-anilino)ethyl-diethyl-ammonium; 2,4,6-trinitrophenolate can be influenced by its complex structure and varied functional groups. Here are some notable aspects regarding its solubility:

  • Polarity: The presence of both polar and non-polar functional groups in the molecule may lead to varying solubility in different solvents.
  • Ammonium Group Solubility: The diethylammonium part of the compound typically exhibits good solubility in water, as quaternary ammonium compounds tend to be hydrophilic.
  • Aromatic Groups: The ethoxy and methoxy substituents connected to the aromatic rings may enhance solubility in organic solvents, while the presence of nitro groups in the 2,4,6-trinitrophenolate can increase the acidic characteristics.
  • Solvent Dependency: This compound may show significant differences in solubility between polar (e.g., water) and non-polar (e.g., hexane) solvents.
  • pH Influence: The solubility of this compound may also be pH-dependent due to the nature of its ionic and non-ionic functionalities.

In summary, while the compound exhibits good solubility characteristics due to its structural components, understanding the exact solubility profile necessitates experimentation across different solvents and conditions to fully appreciate its behavior in various environments.

Interesting facts

Exploring the Intricacies of 2-(N-[2-(4-ethoxyphenoxy)acetyl]-3-methoxy-anilino)ethyl-diethyl-ammonium; 2,4,6-trinitrophenolate

This fascinating compound, often referred to in the field of organic chemistry, combines several intriguing functionalities that make it a subject of interest for researchers and students alike. Here are some key highlights:

  • Dual Role: This compound functions both as a quaternary ammonium compound and as a nitrophenolate, showcasing a blend of properties that can be exploited for various applications.
  • Pharmaceutical Potential: The presence of both ether and amine functionalities contributes to its potential as a pharmaceutical agent, particularly in the design of drug candidates that target specific biological pathways.
  • Structure Activity Relationship: Understanding the structure-activity relationship (SAR) of this compound can provide valuable insights into the mechanisms of action in biological systems. Each structural component can influence its pharmacological properties significantly.
  • Electrochemical Properties: Compounds like this can exhibit unique electrochemical behaviors, making them useful as components in sensors or for targeted delivery systems in medicinal chemistry.

The compound's complex structure features multiple functional groups which allow for intricate interactions in biological systems. As an example, the ethoxy and methoxy groups are known to affect lipophilicity and bioavailability, important factors in drug development.

Moreover, the distinct chemical families present within this compound—including quaternary ammonium, aryl ethers, and nitrophenol—present opportunities for studies in drug design, environmental chemistry, and material science.

In summary, the compound 2-(N-[2-(4-ethoxyphenoxy)acetyl]-3-methoxy-anilino)ethyl-diethyl-ammonium; 2,4,6-trinitrophenolate serves as an impressive example of how combinatorial chemistry can lead to novel compounds with potential applications in diverse scientific domains.

Synonyms
27471-65-4
m-ACETANISIDIDE, N-(2-(DIETHYLAMINO)ETHYL)-2-(p-ETHOXYPHENOXY)-, MONOPICRATE
N-(2-(Diethylamino)ethyl)-2-(p-ethoxyphenoxy)-m-acetanisidide picrate
DTXSID90181897
RefChem:351471
DTXCID30104388
2-(N-[2-(4-ethoxyphenoxy)acetyl]-3-methoxyanilino)ethyl-diethylazanium;2,4,6-trinitrophenolate