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Metoprolol

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Identification
Molecular formula
C15H26N2O
CAS number
37350-58-6
IUPAC name
2-(3-methoxyphenoxy)propyl-[2-(m-tolyl)ethanimidoyl]ammonium;4-methylbenzenesulfonate
State
State

At room temperature, metoprolol is typically found in the solid state as a crystalline powder.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
50.00
Boiling point (Kelvin)
323.15
General information
Molecular weight
267.36g/mol
Molar mass
267.3630g/mol
Density
1.0660g/cm3
Appearence

Metoprolol is typically found as a white to off-white, crystalline powder. It is odorless and has a characteristic, bitter taste.

Comment on solubility

Solubility of 2-(3-methoxyphenoxy)propyl-[2-(m-tolyl)ethanimidoyl]ammonium; 4-methylbenzenesulfonate

The solubility of the compound 2-(3-methoxyphenoxy)propyl-[2-(m-tolyl)ethanimidoyl]ammonium; 4-methylbenzenesulfonate is influenced by several key factors, including the nature of its structural components. To understand its solubility characteristics, consider the following points:

  • Polar vs. Nonpolar Characteristics: The presence of ammonium ion in the compound typically enhances solubility in polar solvents, such as water. However, the organic portions of the molecule, arising from the methoxy and tolyl groups, may introduce some hydrophobic characteristics.
  • Solvent Interaction: The solubility is likely to vary significantly depending on the solvent used. For example, in a polar solvent, one can expect higher solubility rates, while in nonpolar solvents, the compound may show limited solubility.
  • Temperature Effects: Solubility is often temperature-dependent; generally, increasing the temperature increases solubility for most solids.

In practical terms, it is important to consult experimental data for precise solubility values, as theoretical predictions can only provide a generalized view:

“Solubility is a compound's first impression in a solvent; it determines the pathways for chemical interactions.”

In summary, while the compound exhibits potential for solubility in polar environments, specific solubility values should always be verified through laboratory investigations for accurate applications.

Interesting facts

Interesting Facts about 2-(3-methoxyphenoxy)propyl-[2-(m-tolyl)ethanimidoyl]ammonium; 4-methylbenzenesulfonate

This compound is a fascinating example of a synthetic ammonium salt that combines complex organic frameworks. Here are some key aspects that highlight its significance:

  • Pharmacological Potential: Compounds like this one are often studied for their potential pharmaceutical applications. The presence of diverse functional groups suggests possible activity in various biological pathways.
  • Structural Diversity: The compound features multiple aromatic rings, which can contribute to its chemical reactivity and interaction with biological systems. The incorporation of a methoxy group suggests enhanced solubility in organic solvents, a crucial property in medicinal chemistry.
  • Development of Selective Agents: The ammonium component indicates potential as a cationic agent. Many such ammonium derivatives serve as drugs or precursors to drug synthesis, particularly in areas like antitumor, anti-inflammatory, and antimicrobial therapies.
  • Scientific Exploration: Chemists are continually exploring the structure-activity relationships (SAR) of similar compounds to optimize their efficacy and reduce toxicity. This process often leads to novel discoveries in drug development.
  • Impact of Sulfonate Groups: The sulfonate part of the compound, particularly the 4-methylbenzenesulfonate, plays a pivotal role in enhancing water solubility and ionic characteristics, making it an ideal candidate for various applications in biological studies.

As we delve deeper into the chemistry of this compound, we can appreciate the intricate balance between structure and function, leading to its potential application in medicinal chemistry. Continual research into compounds like this one not only broadens our understanding of chemical interactions but also expands the frontier of therapeutic options available in modern medicine. One might say, "In the world of chemistry, structure truly dictates function."

Synonyms
Xylamidine tosylate
Xylamidini tosylas
Xylamidini tosilas
Xylamidini tosilas [INN-Latin]
Tosilate de xylamidine
Tosilato de xilamidina
BW 545C64
Tosilate de xylamidine [INN-French]
Tosilato de xilamidina [INN-Spanish]
UNII-4ZF9UZ56C7
N-(2-(3-Methoxyphenoxy)propyl)-2-m-tolylacetamidine p-toluenesulfonate
N-(2-(3-Methoxyphenoxy)propyl)-2-(3-tolyl)acetamidinium-4-tolylsulfonat
Acetamidine, N-(2-(m-methoxyphenoxy)propyl)-2-(m-tolyl)-, mono-p-toluenesulfonate
Xylamidini tosilas (INN-Latin)
Tosilate de xylamidine (INN-French)
Tosilato de xilamidina (INN-Spanish)
6443-40-9
n-(2-(3-methoxyphenoxy)propyl)-m-tolylacetamidine tosylate
n-(2-(m-methoxyphenoxy)propyl)-2-m-tolylacetamidine mono-p-toluenesulfonate
n-(2-(m-methoxyphenoxy)propyl)-2-m-tolylacetamidine mono-p-toluenesulphonate
xylamidine tosylate (usan)
xylamidine tosylate [usan]
xylamidine tosylate anhydrous
xylamidine tosylate hydrate
2-(3-methoxyphenoxy)propyl-[2-(3-methylphenyl)ethanimidoyl]azanium;4-methylbenzenesulfonate
Benzeneethanimidamide, N-(2-(3-methoxyphenoxy)propyl)-3-methyl-, mono(4-methylbenzenesulfonate)
NS00122643
Q27260711