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Desvenlafaxine hydrochloride

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Identification
Molecular formula
C11H16ClNO2
CAS number
386750-22-7
IUPAC name
2-fluoroethyl-[4-(4-methoxy-4-oxo-butyl)phenyl]ammonium;chloride
State
State

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

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.15
Boiling point (Celsius)
305.40
Boiling point (Kelvin)
578.60
General information
Molecular weight
313.87g/mol
Molar mass
313.8700g/mol
Density
0.9998g/cm3
Appearence

Desvenlafaxine hydrochloride appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-fluoroethyl-[4-(4-methoxy-4-oxo-butyl)phenyl]ammonium;chloride

The solubility of 2-fluoroethyl-[4-(4-methoxy-4-oxo-butyl)phenyl]ammonium;chloride can be influenced by several factors due to its complex structure. Here are some key considerations:

  • Polarity: The presence of both polar (ammonium and chloride ions) and non-polar regions in the molecule suggests varying interactions with water and organic solvents.
  • Hydrogen bonding ability: The ammonium group may facilitate solubility in polar solvents through hydrogen bonding.
  • Aromaticity: The phenyl ring can contribute to hydrophobic interactions, potentially leading to decreased solubility in purely aqueous environments.
  • Solvent interactions: This compound may exhibit better solubility in mixed solvents (e.g., polar aprotic solvents) than in water alone.

To summarize, while 2-fluoroethyl-[4-(4-methoxy-4-oxo-butyl)phenyl]ammonium;chloride may be soluble under specific conditions, its actual solubility would ideally be determined through empirical testing in various solvents. Understanding these solubility characteristics is crucial for applications in chemical synthesis and formulation development.

Interesting facts

Exploring 2-Fluoroethyl-[4-(4-methoxy-4-oxo-butyl)phenyl]ammonium Chloride

The compound 2-fluoroethyl-[4-(4-methoxy-4-oxo-butyl)phenyl]ammonium chloride is a fascinating example of quaternary ammonium salts, which are often known for their diverse applications in both industrial and biomedical fields. Here are some intriguing insights about this compound:

  • Antimicrobial Properties: Many quaternary ammonium compounds exhibit antimicrobial activity, making them valuable in healthcare settings as disinfectants and antiseptics. This attribute makes compounds like this one critical in combating healthcare-associated infections.
  • Modifiable Structure: The presence of functional groups such as the methoxy and fluoroethyl moieties illustrates the compound’s versatility. These modifications can influence the biological activity or solubility of the compound, offering pathways for drug design and development.
  • Potential in Drug Design: Compounds containing ammonium functionalities are often explored in medicinal chemistry. The unique configuration of this compound might contribute to its biological interactions, hinting at potential therapeutic roles.
  • Synthetic Pathways: The synthesis of this compound typically involves multi-step reactions that may include nucleophilic substitutions and functional group transformations, illustrating the rich chemistry behind quaternary ammonium derivatization.
  • Research Interest: Ongoing research into compounds like this one is crucial as scientists aim to discover novel agents to tackle drug-resistant microbes and optimize pharmacokinetic properties in drug formulations.

Overall, 2-fluoroethyl-[4-(4-methoxy-4-oxo-butyl)phenyl]ammonium chloride serves as a great example to illustrate the complexities and applications of quaternary ammonium compounds in modern chemistry.

Synonyms
4-(p-((2-Fluoroethyl)amino)phenyl)butyric acid methyl ester hydrochloride
4092-87-9
NSC 85215
BUTYRIC ACID, 4-(p-((2-FLUOROETHYL)AMINO)PHENYL)-, METHYL ESTER, HYDROCHLORIDE