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Dinephetamine

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Identification
Molecular formula
C13H20Cl2N2O
CAS number
465-17-4
IUPAC name
1,2,5-trimethyl-5-piperidin-1-ium-1-yl-piperidin-1-ium-4-one;dichloride
State
State

Dinephetamine is typically in a solid state at room temperature.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
212.00
Boiling point (Kelvin)
485.15
General information
Molecular weight
252.34g/mol
Molar mass
252.3440g/mol
Density
1.2000g/cm3
Appearence

Dinephetamine, or 1,2,5-trimethyl-5-piperidin-1-ium-1-yl-piperidin-1-ium-4-one;dichloride, typically appears as a crystalline solid. The crystals can range from colorless to off-white, depending on the purity and specific form of the compound. The appearance may also vary if the compound is mixed or diluted with other substances.

Comment on solubility

Solubility of 1,2,5-trimethyl-5-piperidin-1-ium-1-yl-piperidin-1-ium-4-one; dichloride

The solubility of 1,2,5-trimethyl-5-piperidin-1-ium-1-yl-piperidin-1-ium-4-one; dichloride is an interesting topic due to its ionic nature. This compound, being a quaternary ammonium salt, often exhibits strong solubility characteristics. Here are some key points regarding its solubility:

  • Polar Solvents: Generally, ionic compounds dissolve well in polar solvents, particularly water. This is due to the ability of the solvent molecules to stabilize the charged ions present in the compound.
  • Hydrophilicity: The presence of the piperidine rings and the quaternary ammonium group contributes to a degree of hydrophilicity, enhancing its solubility in aqueous environments.
  • Salting Out Effects: In highly ionic environments or with the addition of salts, the solubility can change significantly, potentially leading to a decrease in solubility—often referred to as 'salting out.'
  • Temperature Dependence: Solubility may also increase with temperature, which is common for many salts.

In summary, while the specific solubility values can be experimentally determined, the compound is expected to have **significant solubility** in water, primarily due to its ionic structure and interactions with polar solvents. Understanding these properties is critical for applications in chemistry and biochemistry.

Interesting facts

Interesting Facts about 1,2,5-trimethyl-5-piperidin-1-ium-1-yl-piperidin-1-ium-4-one; dichloride

This compound, commonly referred to in scientific circles for its distinctive structure and properties, has caught the attention of chemists and researchers alike for several reasons:

  • Piperidinium Derivative: The presence of the piperidin-1-ium moiety makes this compound part of a class of cyclic amines known for their utility in medicinal chemistry, particularly in the design of drugs targeting neurological disorders.
  • Ion Exchange Properties: As a dichloride salt, this compound exhibits interesting ion exchange properties, making it valuable in various chemical applications, including catalysis and material science.
  • Versatility: The multiple methyl groups attached to the piperidin-1-ium core confer unique steric and electronic properties, enhancing its potential as a building block for more complex architectures in organic synthesis.
  • Research Potential: Due to its structural features, this compound has potential for exploration in areas such as drug delivery systems and as an intermediate in synthesizing pharmaceutical compounds.

Applications and Studies

Beyond its structural significance, ongoing studies are examining:

  • Its role in biological systems as a potential ligand for receptors.
  • How its unique properties can influence interactions in polymer science.
  • The potential toxicity and environmental impact of its degradation products.

In summary, 1,2,5-trimethyl-5-piperidin-5-ium-1-yl-piperidin-1-ium-4-one; dichloride is much more than just a chemical formula; it represents a fascinating area of research in modern chemistry that bridges theoretical concepts with practical applications.

Synonyms
596-99-6
1',3',6'-Trimethyl-1',3'-bipiperidin-4'-one dihydrochloride
1,3'-BIPIPERIDIN-4'-ONE, 1',3',6'-TRIMETHYL-, DIHYDROCHLORIDE