Skip to main content

Procaine

ADVERTISEMENT
Identification
Molecular formula
C13H20N2O2
CAS number
59-46-1
IUPAC name
2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate
State
State

Procaine is generally found as a solid at room temperature. It is commonly used in the form of its hydrochloride salt, which also appears as a solid white powder.

Melting point (Celsius)
61.00
Melting point (Kelvin)
334.15
Boiling point (Celsius)
468.70
Boiling point (Kelvin)
741.80
General information
Molecular weight
293.38g/mol
Molar mass
293.3840g/mol
Density
1.1000g/cm3
Appearence

Procaine typically appears as a colorless to white crystalline powder. It is odorless and can be identified by its distinct crystalline nature.

Comment on solubility

Solubility of 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate

The solubility of 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate in various solvents is influenced by its chemical structure, which features both aliphatic and aromatic components.

Factors Affecting Solubility:

  • Polarity: Due to the presence of the diethylamino group, the compound exhibits moderate polarity, which allows it to dissolve in polar solvents like water to some extent, although it is not highly soluble.
  • Hydrophobic Interactions: The aromatic naphthalene moiety contributes to hydrophobic characteristics, which may limit aqueous solubility.
  • Temperature Influence: Solubility may increase with temperature, making it easier to dissolve in solvents at elevated temperatures.
  • pH Dependency: The ionization state of the amine groups can significantly impact solubility; adjusting pH can enhance solubility in aqueous solutions.

In summary, while 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate shows moderate solubility in polar solvents, factors such as polarity, temperature, and pH play crucial roles in determining its solubility profile. Understanding these parameters is essential for applications in various chemical processes.

Interesting facts

Interesting Facts about 2-(Diethylamino)ethyl 4-aminonaphthalene-1-carboxylate

2-(Diethylamino)ethyl 4-aminonaphthalene-1-carboxylate is a fascinating compound that captures the interest of scientists and chemistry enthusiasts alike. Below are some intriguing facts about this compound:

  • Applications in Biology: This compound has shown potential in biological applications, particularly in the field of medicinal chemistry. Its structure suggests that it may act as a useful scaffold for developing novel pharmaceuticals.
  • Dyes and Pigments: Due to the presence of naphthalene in its structure, it can be studied for use in creating dyes and pigments, which are essential in industries ranging from textiles to food.
  • Research in Synthesis: The synthesis of this compound often involves creative and complex organic reactions, making it an interesting subject for students studying organic synthesis techniques.
  • Fluorescent Properties: Many naphthalene derivatives exhibit *fluorescent characteristics*, which may be leveraged in various applications such as sensors and imaging techniques in biological systems.
  • Amine Functionality: The presence of the diethylamino group allows for intriguing interactions with various biological targets and can enhance the compound's solubility in organic solvents.

"Chemistry is the art of transformation;" and in the case of 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate, the transformations it can facilitate make it a valuable compound for various research areas.

Overall, the unique characteristics and potential applications of this compound make it a *rich topic of discussion* for both scientists and students as they explore the boundaries of chemical possibilities.

Synonyms
Naphthocaine
Naphthacaine
UNII-34SP0C39GS
5656-83-7
34SP0C39GS
2-diethylaminoethyl 4-aminonaphthalene-1-carboxylate
1-Naphthoic acid, 4-amino-, 2-(diethylamino)ethyl ester
1-Naphthalenecarboxylic acid, 4-amino-, 2-(diethylamino)ethyl ester
DTXSID60205115
DTXCID60127606
Q27256390