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Bis(2-chloroethyl)amine hydrochloride

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Identification
Molecular formula
(C6H7ClN)2Cl2
CAS number
538-07-8
IUPAC name
(2-chlorophenyl)methyl-[2-[(2-chlorophenyl)methylammonio]ethyl]ammonium;dichloride
State
State

The compound is generally solid at room temperature.

Melting point (Celsius)
105.00
Melting point (Kelvin)
378.00
Boiling point (Celsius)
368.00
Boiling point (Kelvin)
641.00
General information
Molecular weight
234.10g/mol
Molar mass
234.1040g/mol
Density
1.3704g/cm3
Appearence

The compound appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of (2-chlorophenyl)methyl-[2-[(2-chlorophenyl)methylammonio]ethyl]ammonium;dichloride

The compound (2-chlorophenyl)methyl-[2-[(2-chlorophenyl)methylammonio]ethyl]ammonium;dichloride exhibits unique solubility characteristics that are influenced by its structural features. As a quaternary ammonium salt, it is known for its distinct solvation behavior in various environments.

Key Points on Solubility:

  • Water Solubility: This compound is generally soluble in water due to the presence of ionic ammonium groups that interact favorably with water molecules.
  • Organic Solvents: It can also dissolve in polar organic solvents such as methanol and ethanol, enhancing its utility in solvent-based applications.
  • Temperature Dependence: Solubility may increase with temperature, as is common with many ionic compounds, allowing for better dissolution at elevated temperatures.
  • pH Influence: The solubility can be affected by changes in pH, as acidic or basic conditions may lead to changes in the protonation state of the ammonium group.

As a general observation, it can be noted that many quaternary ammonium salts have a high degree of solubility in polar solvents, which makes them versatile in both chemical and biological applications. This compound’s solubility suggests potential use in areas such as pharmaceuticals and biochemistry, where solubility profiles are crucial for activity and efficacy.

Interesting facts

Interesting Facts About (2-chlorophenyl)methyl-[2-[(2-chlorophenyl)methylammonio]ethyl]ammonium;dichloride

This compound, with a complex name indicating its multi-functional nature, belongs to a class of chemical compounds known for their biological significance. Here are some intriguing aspects:

  • Biological Activity: Compounds like this have garnered attention for their role in various physiological processes. They may act as antimicrobial agents or possess potential therapeutic applications.
  • Structural Features: The presence of both chloride ions and multiple amine groups contributes to its unique properties. This makes it an interesting subject for studying molecular interactions and binding affinities in biochemical systems.
  • Derivation: The structure features a dichlorobenzene moiety, which is known for its ability to participate in electron transfer reactions, making it relevant in the field of organic electronics.
  • Synthesis Pathways: The synthetic routes leading to the formation of this compound can vary significantly, showcasing the versatility of organic synthesis methodologies. Understanding these pathways sheds light on reaction mechanisms.
  • Research Potential: Ongoing studies are exploring the potential of compounds with similar structures in fields like drug design and material science, particularly in creating novel therapeutic agents or enhancing drug delivery systems.

As a compound with such rich chemistry, it opens avenues for exploration and research, making it a valuable part of chemical science.

Synonyms
N,N'-Bis(o-chlorobenzyl)ethylenediamine dihydrochloride
2056-18-0
N,N'-Ethylenebis(2-chlorobenzylamine) dihydrochloride
Benzylamine, N,N'-ethylenebis(2-chloro-, dihydrochloride
ETHYLENEDIAMINE, N,N'-BIS(o-CHLOROBENZYL)-, DIHYDROCHLORIDE
(2-chlorophenyl)methyl-[2-[(2-chlorophenyl)methylazaniumyl]ethyl]azanium;dichloride