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Methadone Hydrochloride

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Identification
Molecular formula
C21H27NO3Cl
CAS number
1095-90-5
IUPAC name
(1-methylpiperidin-1-ium-2-yl)methyl 2-methoxy-2,2-diphenyl-acetate;chloride
State
State

At room temperature, methadone hydrochloride is usually found in its solid form as a crystalline powder. It can also be dissolved in a solvent to create a solution for medical administration purposes.

Melting point (Celsius)
233.80
Melting point (Kelvin)
506.95
Boiling point (Celsius)
172.90
Boiling point (Kelvin)
446.05
General information
Molecular weight
345.91g/mol
Molar mass
345.9110g/mol
Density
0.9300g/cm3
Appearence

Methadone hydrochloride is typically a white, crystalline powder. It is odorless and is soluble in water and alcohol. The compound can also be administered in a liquid form, where it is typically clear and colorless.

Comment on solubility

Solubility of (1-methylpiperidin-1-ium-2-yl)methyl 2-methoxy-2,2-diphenyl-acetate;chloride

The solubility of the compound (1-methylpiperidin-1-ium-2-yl)methyl 2-methoxy-2,2-diphenyl-acetate;chloride can be influenced by several factors, including its ionic character and molecular structure. Here are some key points to consider:

  • Ionic Nature: As a quaternary ammonium salt, this compound is likely to have good solubility in polar solvents such as water due to its ionic properties.
  • Polar Functional Groups: The presence of the 2-methoxy and acetate groups may enhance its ability to interact with polar solvents.
  • Hydrophobic Contributions: The 2,2-diphenyl moiety introduces a considerable hydrophobic character, which may affect solubility in non-polar solvents.

Overall, the solubility of this compound can be summarized as follows:

  1. Highly soluble in polar solvents.
  2. Moderately soluble in mixed solvent systems.
  3. Lower solubility expected in non-polar solvents.

As a result, the compound would likely be more soluble in aqueous solutions compared to hydrocarbon-based solvents, making it useful for various applications where solubility in polar media is desirable.

Interesting facts

Interesting Facts about (1-methylpiperidin-1-ium-2-yl)methyl 2-methoxy-2,2-diphenyl-acetate; chloride

This unique compound, commonly referred to in abbreviated forms due to its complex structure, presents a fascinating study for both chemists and researchers. Here are some insightful points to consider:

  • Ionization Characteristics: The compound features a quaternary ammonium structure which influences its solubility and potential interactions with biological systems. This makes it interesting for studies related to ionic liquids and their applications.
  • Biological Relevance: With its piperidine framework, this compound could be relevant in medicinal chemistry. The piperidine ring is known for its presence in numerous alkaloids and biologically active molecules.
  • Reaction Pathways: As a precursor or intermediate in synthesizing more complex compounds, it can lead to diverse products. Its reactivity can be explored in the context of organic synthesis and catalysis.
  • Functional Group Diversity: The presence of ester and ether moieties in its structure opens discussion on the behavior of the compound in various donor-acceptor interactions, offering intriguing insights into its potential material applications.
  • Environmentally Friendly Alternatives: Compounds of this nature are often investigated for their environmental impact. Understanding their stability and degradation can aid in developing sustainable chemical practices.

As researchers dive deeper into its properties and applications, this compound could unlock new avenues in both industrial and pharmaceutical chemistry. Overall, the complexity and unique composition of (1-methylpiperidin-1-ium-2-yl)methyl 2-methoxy-2,2-diphenyl-acetate; chloride makes it an exciting subject of study with potential implications in various scientific domains.

Synonyms
Acetic acid, 2,2-diphenyl-2-methoxy-, (1-methyl-2-piperidyl)methyl ester, hydrochloride
2,2-Diphenyl-2-methoxyacetic acid (1-methyl-2-piperidyl)methyl ester hydrochloride