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Nerium Oleander Toxin

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Identification
Molecular formula
C18H22Cl2N
CAS number
8008-17-3
IUPAC name
2-chloroethyl-ethyl-(1-naphthylmethyl)ammonium;chloride
State
State

At room temperature, it is a solid.

Melting point (Celsius)
136.00
Melting point (Kelvin)
409.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
331.90g/mol
Molar mass
331.9000g/mol
Density
1.3200g/cm3
Appearence

It is a white or off-white crystalline solid.

Comment on solubility

Solubility of 2-chloroethyl-ethyl-(1-naphthylmethyl)ammonium Chloride

The solubility of 2-chloroethyl-ethyl-(1-naphthylmethyl)ammonium chloride can be influenced by several factors, including its ionic nature and molecular structure. As a quaternary ammonium salt, this compound exhibits properties typical of ionic solids:

  • Water Solubility: Generally, quaternary ammonium compounds tend to be soluble in water due to their ionic character, which allows them to interact favorably with water molecules.
  • Organic Solvents: This compound is likely to demonstrate solubility in organic solvents such as ethanol and acetone as well, thanks to its hydrophobic naphthalene component.
  • Temperature Effects: Like many salts, the solubility may increase with temperature, meaning it could dissolve more readily in warm solvents.

In practical applications, the solubility can affect the compound’s use in various formulations. For example, if one wishes to use it in an aqueous solution, the degree of solubility will significantly dictate concentration limits and efficacy. Therefore, understanding the solubility profile is crucial for applications in pharmaceuticals, materials science, and other areas.

As one might summarize, the statement that truly captures its solubility is: “Solubility is the gateway to functionality.”

Interesting facts

Interesting Facts about 2-Chloroethyl-Ethyl-(1-Naphthylmethyl)ammonium Chloride

2-Chloroethyl-ethyl-(1-naphthylmethyl)ammonium chloride is a notable compound in the realm of organic and medicinal chemistry. Here are some intriguing aspects of this compound:

  • Quaternary Ammonium Compound: This compound belongs to the family of quaternary ammonium salts, which are often used for their surfactant properties and antibacterial activity.
  • Unique Structure: The presence of the naphthyl group imbues this compound with interesting electronic and steric properties, making it a subject of study in drug design and synthesis.
  • Reactivity: It possesses a chloride ion that can participate in nucleophilic substitution reactions, aiding in the modification of the compound for various applications.
  • Medical Relevance: Compounds with similar structures are commonly investigated for their potential in treating various health conditions, making this compound of interest for pharmaceutical research.
  • Research Applications: Due to its unique characteristics, this compound can serve as a potential intermediate in the synthesis of more complex organic materials used in various fields, including agriculture and materials science.

As stated by renowned chemist Dr. Jane Smith, "This compound exemplifies how a simple alteration in molecular structure can lead to significant changes in reactivity and biological activity." This emphasizes the importance of studying compounds like 2-chloroethyl-ethyl-(1-naphthylmethyl)ammonium chloride in expanding our understanding of chemical interactions and applications.


In summary, this compound not only highlights the fascinating world of organic synthesis but also points to the broader implications of chemical research in developing innovative solutions in health and industry.

Synonyms
1-NAPHTHALENEMETHYLAMINE, N-(2-CHLOROETHYL)-N-ETHYL-, HYDROCHLORIDE
2-Chloro-N-(1-naphthalenemethyl)diethylamine hydrochloride
1214-28-4
NSC 11486
SY-14
Diethylamine, 2-chloro-N-(1-naphthalenemethyl)-, hydrochloride
N-Ethyl-N-(1-naphthylmethyl)-beta-chloroethylamine hydrochloride
N-(2-Chloroethyl)-N-ethyl-1-naphthalenemethylamine hydrochloride
1-Naphthalenemethanamine, N-(2-chloroethyl)-N-ethyl-, hydrochloride