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1-Methyl-2-(2-phenoxyethyl)hydrazine

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Identification
Molecular formula
C9H14N2O
CAS number
5191-46-8
IUPAC name
1-methyl-2-(2-phenoxyethyl)hydrazine
State
State

At room temperature, 1-methyl-2-(2-phenoxyethyl)hydrazine is in a liquid state. Due to its liquid state at room temperature, it is often stored in tightly sealed containers to prevent evaporation and maintain its stability during handling and storage.

Melting point (Celsius)
-8.00
Melting point (Kelvin)
265.15
Boiling point (Celsius)
303.20
Boiling point (Kelvin)
576.35
General information
Molecular weight
180.23g/mol
Molar mass
180.2330g/mol
Density
1.0830g/cm3
Appearence

1-Methyl-2-(2-phenoxyethyl)hydrazine is typically a liquid compound at room temperature. It does not have a distinctive color and is generally described as clear and colorless or pale yellow. Its clarity and lack of color make it not immediately noticeable in small quantities.

Comment on solubility

Solubility of 1-methyl-2-(2-phenoxyethyl)hydrazine

1-methyl-2-(2-phenoxyethyl)hydrazine is an intriguing compound when it comes to its solubility characteristics. Understanding how this compound interacts with various solvents can provide valuable insights. Here’s a closer look at its solubility:

  • Solvent Interaction: The hydrazine moiety could suggest variable solubility in polar solvents due to the presence of nitrogen atoms, while the phenoxyethyl group may enhance solubility in organic solvents.
  • General Behavior: Compounds with similar structures often display the following trends:
    • Increased solubility in alcohols and ethers.
    • Moderate solubility in water due to hydrogen bonding capabilities.
  • Factors Influencing Solubility: The solubility of 1-methyl-2-(2-phenoxyethyl)hydrazine can be influenced by:
    • Temperature: Higher temperatures may increase solubility.
    • pH levels: Acidic or basic conditions may alter dissolution rates.
    • Concentration: Solutions at varying concentrations will behave differently.

In summary, while the solubility of 1-methyl-2-(2-phenoxyethyl)hydrazine in various media can be quite complex, exploring these factors can help predict how it will behave in different environments. Emphasizing the impact of both the hydrophilic and hydrophobic character of the compound is essential in understanding its comprehensive solubility profile.

Interesting facts

Interesting Facts About 1-methyl-2-(2-phenoxyethyl)hydrazine

1-methyl-2-(2-phenoxyethyl)hydrazine, often abbreviated as MEPH, is a fascinating compound that belongs to the hydrazine class of organic chemicals. This compound captures the attention of chemists for several reasons:

  • Structural Diversity: The molecule showcases a unique structural architecture, featuring a hydrazine backbone combined with a phenoxyethyl group, which adds to its complexity and potential reactivity.
  • Therapeutic Potential: Research has indicated that compounds in the hydrazine family, such as MEPH, may exhibit interesting biological activities, including potential anti-cancer properties.
  • Reactivity: Hydrazines are known for their reactivity, particularly in condensation reactions. This makes 1-methyl-2-(2-phenoxyethyl)hydrazine an important intermediate in organic synthesis.
  • Applications in Research: MEPH and related compounds are researched for their role in medicinal chemistry, particularly in the development of novel pharmaceuticals.
  • Safety Considerations: Like many hydrazines, 1-methyl-2-(2-phenoxyethyl)hydrazine requires careful handling due to its potential toxicity and the presence of hazardous characteristics.

In summary, the study of 1-methyl-2-(2-phenoxyethyl)hydrazine presents exciting opportunities for exploration in medicinal chemistry and organic synthesis. Its structural characteristics and potential applications continue to be a topic of research and discussion in the scientific community. As a student or scientist delving into the world of organic chemistry, understanding such compounds enhances your appreciation for the intricate relationships present in chemical structures.

Synonyms
SCHEMBL8820103