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Carvedilol

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Identification
Molecular formula
C24H26N2O4
CAS number
111786-30-5
IUPAC name
2-(dimethylamino)ethanol;2-methyl-4-(4-phenylphenyl)butanoic acid
State
State

At room temperature, Carvedilol is found in a solid crystalline state.

Melting point (Celsius)
114.20
Melting point (Kelvin)
387.40
Boiling point (Celsius)
289.50
Boiling point (Kelvin)
562.60
General information
Molecular weight
406.48g/mol
Molar mass
406.4790g/mol
Density
1.1610g/cm3
Appearence

Carvedilol typically appears as a white to off-white crystalline powder. It is practically insoluble in water but soluble in a mixture of methanol and dichloromethane. This compound may exist in various polymorphic forms.

Comment on solubility

Solubility of 2-(dimethylamino)ethanol

The solubility characteristics of 2-(dimethylamino)ethanol, often referred to in shorthand as DMAE, play a significant role in its applications. This compound is known for its high solubility in a variety of solvents:

  • Water: 2-(dimethylamino)ethanol is readily soluble in water due to its ability to form hydrogen bonds.
  • Alcohols: It is also soluble in common alcohols like methanol and ethanol, further increasing its versatility.
  • Organic solvents: Additionally, this compound shows solubility in organic solvents such as acetone and ether.

In contrast, it is generally insoluble in nonpolar solvents. This solubility profile makes 2-(dimethylamino)ethanol a valuable compound in various chemical processes and formulations.

Solubility of 2-methyl-4-(4-phenylphenyl)butanoic acid

The solubility of 2-methyl-4-(4-phenylphenyl)butanoic acid, commonly referred to as a more complex organic acid, can be quite nuanced:

  • Water solubility: This compound shows limited solubility in water, which is common among large organic acids.
  • Organic solvents: It is more soluble in organic solvents such as dichloromethane or ethyl acetate.
  • Influence of pH: The solubility can also be influenced by the pH of the solution, as deprotonation can enhance solubility in aqueous solutions.

Overall, its solubility behavior highlights the importance of solvent choice in applications involving 2-methyl-4-(4-phenylphenyl)butanoic acid.

Interesting facts

2-(Dimethylamino)ethanol

2-(Dimethylamino)ethanol, often referred to as DMAE, is an intriguing compound known for its applications in both the chemical industry and as a nutritional supplement. Here are some captivating facts about this compound:

  • Versatile Amine: DMAE contains a dimethylamino group, making it a tertiary amine, which contributes to its reactivity and solubility properties.
  • Biological Significance: This compound is recognized for its potential role in cognitive function enhancement and is sometimes included in dietary supplements aimed at improving mental clarity.
  • Synthesis: DMAE can be synthesized from the base-catalyzed alkylation of ethanolamine with dimethyl sulfate or other alkylating agents.
  • Cosmetic Applications: DMAE is prevalent in skincare products due to its purported anti-aging properties, believed to help firm skin and reduce the appearance of wrinkles.

Its versatility and various applications in diverse fields make 2-(dimethylamino)ethanol a compound of significant interest in both scientific research and commercial products.


2-Methyl-4-(4-phenylphenyl)butanoic Acid

2-Methyl-4-(4-phenylphenyl)butanoic acid is a unique acid that has garnered attention for its interesting structural features and potential applications. Consider the following facts:

  • Complex Structure: This compound features a distinct arrangement that includes a branched butanoic acid moiety with phenyl groups that enhance its steric and electronic properties.
  • Organic Chemistry Insights: The presence of multiple phenyl rings in its structure can affect the compound's reactivity and stability, making it a fascinating subject for organic synthesis studies.
  • Potential Applications: Due to its unique characteristics, research is ongoing to explore its applications in various fields, including materials science and pharmaceuticals.
  • Investigative Compound: Being a less common structure, it often serves as a model in studies aimed at understanding the interactions between various substituents in organic compounds.

2-Methyl-4-(4-phenylphenyl)butanoic acid exemplifies the creativity found in organic chemistry and showcases the ability of simple changes in molecular structure to inspire a wide range of research opportunities.

Synonyms
SCHEMBL125407
NS00120048