Mechlorethamine | Solubility of Things

Identification

Molecular formula

C₁₂H₁₉Cl₂N

CAS number

51-75-2

IUPAC name

N-benzyl-N',N'-bis(2-chloroethyl)-N-methyl-ethane-1,2-diamine

State

State at room temperature: Liquid

Melting point (Celsius)

-2.80

Melting point (Kelvin)

270.35

Boiling point (Celsius)

178.00

Boiling point (Kelvin)

451.15

General information

Molecular weight

156.06g/mol

Molar mass

156.0590g/mol

Density

1.2700g/cm³

Appearence

Mechlorethamine is a colorless to yellow, hygroscopic liquid. It has a slight fishy or musty odor, characteristic of amines. It is sensitive to light and moisture.

Comment on solubility

Solubility of N-benzyl-N',N'-bis(2-chloroethyl)-N-methyl-ethane-1,2-diamine

N-benzyl-N',N'-bis(2-chloroethyl)-N-methyl-ethane-1,2-diamine is a compound that displays specific solubility characteristics influenced by its structural features. Understanding its solubility is essential for its applications and behavior in various environments. Here are some important points to consider:

Solvent Interaction: The presence of multiple functional groups, such as the chloroethyl moieties, can lead to diverse interactions with solvents.
Polarity: This compound exhibits both polar and non-polar characteristics, which may affect its solubility in various solvent systems.
Solubility in Water: As an amine, it may have some degree of solubility in water due to hydrogen bonding, but this can be limited by its hydrophobic benzyl group.
Organic Solvents: Likely shows increased solubility in organic solvents due to its hydrophobic segments, which can interact favorably with non-polar environments.

Overall, the solubility of N-benzyl-N',N'-bis(2-chloroethyl)-N-methyl-ethane-1,2-diamine is complex and can vary significantly depending on the medium. One might say, "The right conditions can unlock solubility and open the door to its potential." Thus, careful consideration of the solvent system is crucial for practical applications.

Interesting facts

Interesting Facts About N-benzyl-N',N'-bis(2-chloroethyl)-N-methyl-ethane-1,2-diamine

N-benzyl-N',N'-bis(2-chloroethyl)-N-methyl-ethane-1,2-diamine, often referred to as a versatile chemical compound, exhibits a multitude of fascinating properties and applications. Here are some noteworthy factors to consider:

Diverse Applications: This compound is primarily used in the field of organic synthesis and can serve as an essential intermediate in the manufacture of various pharmaceuticals and agrochemicals.
Structural Complexity: The compound features a unique aromatic benzyl group and two chloroethyl groups, which contribute to its chemical reactivity and functionality.
Biological Activity: Due to its amine functional groups, it may exhibit biological activity, expressing potential as a drug candidate or leading to bioactive metabolites.
Synthetic Pathways: It can be synthesized through several pathways, including alkylation reactions and reductive amination, showcasing the importance of understanding synthetic methods in organic chemistry.
Reactivity Profile: The presence of chloroethyl moieties allows for nucleophilic substitution reactions, making it a key reagent in various organic transformations.
Environmental Considerations: As with many chlorinated compounds, it’s crucial to consider environmental impact and potential regulations associated with its use and disposal.

“The beauty of chemistry lies in its ability to connect various fields—be it medicine, agriculture, or environmental science.” This compound not only showcases this interconnectedness but also highlights the necessity for chemists to explore its full potential responsibly. As we delve deeper into its applications, it exemplifies how intricate molecular design can lead to significant advancements in both research and industry.