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Diazepam

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Identification
Molecular formula
C16H15ClFN3O
CAS number
439-14-5
IUPAC name
7-chloro-1-[3-(diethylamino)propyl]-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2-one;dihydrochloride
State
State

At room temperature, Diazepam dihydrochloride is found in a solid state as a crystalline compound.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
209.00
Boiling point (Kelvin)
482.15
General information
Molecular weight
321.74g/mol
Molar mass
321.7440g/mol
Density
1.2000g/cm3
Appearence

Diazepam dihydrochloride is typically found in the form of white to slightly yellow crystalline powder. It is often odorless and may appear as small crystals or powder depending on its preparation.

Comment on solubility

Solubility of 7-chloro-1-[3-(diethylamino)propyl]-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2-one; dihydrochloride

The solubility of 7-chloro-1-[3-(diethylamino)propyl]-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2-one; dihydrochloride is influenced by several factors due to its complex molecular structure. Here are key points regarding its solubility:

  • Polarity: The incorporation of both chloro and amino groups increases polarity, thus affecting its solubility in polar solvents.
  • Solvent Type: This compound is typically more soluble in aqueous solutions compared to non-polar solvents given its ionic dihydrochloride form.
  • Temperature Dependency: The solubility may enhance with increasing temperature, making heating a useful method for dissolution.
  • pH Influence: Since it is a hydrochloride salt, solubility can vary significantly with changes in pH levels, making it more soluble in acidic conditions.

In summary, the solubility of this compound is primarily dependent on its inherent chemical structure and the environmental conditions of the solvent. For those looking to work with this benzodiazepine derivative, understanding its solubility characteristics is essential for effective formulation and application.

Interesting facts

Interesting Facts about 7-chloro-1-[3-(diethylamino)propyl]-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2-one; dihydrochloride

This compound, a member of the benzodiazepine family, is known for its notable pharmacological properties. Here are some intriguing points about it:

  • Mechanism of Action: Benzodiazepines, including this compound, primarily function by enhancing the effects of the neurotransmitter gamma-aminobutyric acid (GABA). GABA is a major inhibitory neurotransmitter that plays a crucial role in regulating neuronal excitability across the nervous system.
  • Clinical Applications: Compounds like this are frequently utilized in the treatment of anxiety disorders, insomnia, and muscle spasms. Their ability to induce sedation and relaxation can be invaluable in a clinical setting.
  • Structure-Activity Relationship: The presence of the diethylamino group significantly affects the compound's lipophilicity, enhancing its ability to cross the blood-brain barrier. This structure contributes to its efficacy as a central nervous system depressant.
  • Fluorinated phenyl ring: The incorporation of a fluorine atom in the phenyl ring can enhance the pharmacokinetic properties of the drug. Fluorine is known for its ability to increase metabolic stability, potentially leading to a longer duration of action.

The fascinating interplay between structure and function in benzodiazepines like this compound highlights the intricate world of medicinal chemistry. As noted by several researchers, "an understanding of the molecular structure can lead to the design of safer and more effective therapeutic agents."

Research continues into the potential for this compound in varied therapeutic scenarios, offering promising avenues for future pharmacological advances.

Synonyms
4130-75-0
2H-1,4-Benzodiazepin-2-one, 1,3-dihydro-7-chloro-1-(3-(diethylamino)propyl)-5-(o-fluorophenyl)-, dihydrochloride
DTXSID50194286
DTXCID60116777