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Chlorpromazine

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Identification
Molecular formula
C8H18ClN
CAS number
281-78-5
IUPAC name
N-(2-chloroethyl)-N-propyl-propan-1-amine
State
State

The compound is a liquid at room temperature.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
174.00
Boiling point (Kelvin)
447.15
General information
Molecular weight
151.65g/mol
Molar mass
151.6520g/mol
Density
0.8964g/cm3
Appearence

N-(2-chloroethyl)-N-propyl-propan-1-amine is a colorless to pale yellow liquid.

Comment on solubility

Solubility of N-(2-chloroethyl)-N-propyl-propan-1-amine

N-(2-chloroethyl)-N-propyl-propan-1-amine, a compound featuring both amine and alkyl functional groups, exhibits unique solubility characteristics that can be influenced by several factors:

  • Polarity: The presence of the amine group suggests that N-(2-chloroethyl)-N-propyl-propan-1-amine is polar, which typically enhances its solubility in polar solvents like w ater.
  • Hydrogen Bonding: The amine group can engage in hydrogen bonding, further promoting solubility in polar media, but limiting solubility in non-polar solvents.
  • Hydrophobic vs. Hydrophilic: The alkyl chains in the molecule present a hydrophobic character which may decrease solubility in highly polar solvents.

As a result, it is likely that N-(2-chloroethyl)-N-propyl-propan-1-amine will demonstrate moderate solubility in water and good solubility in solvent mixtures that can accommodate both its polar and non-polar characteristics. The actual solubility can vary based on temperature and the presence of ions or other solutes in solution.

In conclusion, understanding the balance of hydrophilic and hydrophobic interactions is key to predicting the solubility behavior of N-(2-chloroethyl)-N-propyl-propan-1-amine.

Interesting facts

Interesting Facts about N-(2-Chloroethyl)-N-propyl-propan-1-amine

N-(2-Chloroethyl)-N-propyl-propan-1-amine is a chemical compound that merges intricate organic chemistry with various practical applications. Here are some intriguing insights into this compound:

  • Chemical Classification: This compound belongs to the class of amines, which are organic compounds derived from ammonia by replacing one or more hydrogen atoms with organic groups. Amines have versatile roles in organic synthesis and biological processes.
  • Reactivity: The presence of a chloroethyl group contributes significantly to the compound's reactivity, making it a potential participant in nucleophilic substitution reactions, which are fundamental in organic synthesis.
  • Biological Relevance: Compounds like N-(2-chloroethyl)-N-propyl-propan-1-amine are often examined for their potential use in medicinal chemistry. There is ongoing research into various amine derivatives for their pharmacological effects.
  • Industrial Applications: Because of its structural properties, this compound may be explored for use in producing agrochemicals, pharmaceuticals, and polymers. Its ability to participate in further chemical reactions can help develop essential materials.
  • Historical Background: The development of amine compounds dates back to the early 19th century, where chemists like Alfred von Baeyer analyzed their structures and reactions, paving the way for modern organic chemistry.

In conclusion, N-(2-chloroethyl)-N-propyl-propan-1-amine serves as a fascinating example of how compounds can be pivotal in both academic studies and practical applications. Understanding its properties enables chemists to innovate and discover new materials that can significantly impact various fields.

Synonyms
1-Propanamine, N-(2-chloroethyl)-N-propyl-
2-dipropylaminoethyl chloride
SCHEMBL6739027
2-chlorodi(n-propyl)aminoethane
N,N-Dipropyl aminoethyl-2-chloride
AKOS010539651