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Nicotine derivative chloride

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Identification
Molecular formula
C7H10ClNO2
CAS number
111983-73-6
IUPAC name
1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride
State
State

At room temperature, this compound exists as a solid. It is a salt, formed from nicotine derivative and chloride, primarily handled in laboratory settings under controlled conditions to prevent unwanted moisture uptake.

Melting point (Celsius)
251.00
Melting point (Kelvin)
524.00
Boiling point (Celsius)
305.80
Boiling point (Kelvin)
578.95
General information
Molecular weight
193.66g/mol
Molar mass
193.6600g/mol
Density
1.2300g/cm3
Appearence

The compound typically appears as a crystalline solid, often colorless or off-white in appearance. It is hygroscopic, meaning it can absorb moisture from the air.

Comment on solubility

Solubility of 1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride

The solubility characteristics of 1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride can be quite intriguing due to its unique structural features. Being a quaternary ammonium salt, this compound typically exhibits a high degree of solubility in polar solvents.

Factors Influencing Solubility

  • Polarity: The presence of ionic and polar functional groups, such as the carboxylic acid and chloride, enhances solubility in water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules contributes significantly to its solvation.
  • Temperature: Solubility generally increases with temperature, making it more effective at elevated temperatures.
  • Concentration: In concentrated solutions, interactions among solute molecules may lower solubility due to saturation limits.

In summary, one can reasonably state that 1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride demonstrates good solubility in aqueous environments, primarily driven by its ionic nature and capability for hydrogen bonding. It frequently finds applications in various fields—including pharmaceuticals and organic synthesis—due to its solubility profile.

Interesting facts

Interesting Facts about 1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride

1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride is a fascinating compound that holds significant interest across various fields of chemistry due to its unique structure and potential applications. Here are some intriguing aspects:

  • Structural Uniqueness: The presence of a tetrahydropyridine ring contributes to its distinct chemical properties. This cyclic structure adds steric hindrance and impacts reactivity.
  • Biological Relevance: Compounds like this one can exhibit pharmacological activities, potentially playing a role in neuroscience as they may affect neurotransmitter systems.
  • Synthetic Pathways: The synthesis of such a compound often involves multi-step organic reactions, showcasing the complexity and creativity involved in modern synthetic organic chemistry.
  • Ion Exchange Properties: As a chloride salt, this compound can participate in ion exchange reactions, which is particularly significant in biochemical applications and systems.
  • Research Potential: The exploration of this compound is ongoing, with researchers investigating its potential therapeutic uses, particularly in the management of neurological disorders.

In summary, 1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride illustrates the intricate interplay of structure and function in chemistry, inspiring both scientific inquiry and innovation. As the saying goes, "Chemistry is not just about substances, but the story they tell," and this compound certainly embodies that narrative.

Synonyms
1-methyl-1,2,3,6-tetrahydropyridin-1-ium-5-carboxylic acid;chloride
AKOS023093304