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Isopropyl nicotinate

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Identification
Molecular formula
C10H13NO2
CAS number
4300-31-4
IUPAC name
isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate
State
State

At room temperature, Isopropyl nicotinate is in a liquid state. It is often used in topical formulations due to its easy spreadability on the skin.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
246.00
Boiling point (Kelvin)
519.15
General information
Molecular weight
171.22g/mol
Molar mass
171.2180g/mol
Density
1.0765g/cm3
Appearence

Isopropyl nicotinate appears as a clear, colorless to slightly yellowish liquid. It has a distinctive ester-like odor that can be quite pungent, often described as fruity or sweet. It is a compound that is oily in texture and can leave a greasy trace upon evaporation.

Comment on solubility

Solubility of Isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate (C10H13NO2)

The solubility of isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate in various solvents can provide important insights into its chemical behavior and potential applications. Generally, the solubility of such compounds can be influenced by several factors, including:

  • Polarity of the solvent: Isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate, being an organic compound, is likely to be more soluble in non-polar to moderately polar organic solvents like ethyl acetate, dichloromethane, or even ethanol.
  • Temperature: Increasing temperature usually enhances the solubility of organic compounds, allowing for greater dissolution in the chosen solvent.
  • Presence of functional groups: The carboxylate functional group may interact favorably with protic solvents, suggesting certain solubility levels in water, although limited.
  • Molecular structure: The presence of both aliphatic and cyclic components in the structure may contribute to its solubility characteristics, allowing the compound to interact diversely with various solvents.

In summary, while isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate may demonstrate some solubility in **polar and non-polar solvents**, it is essential to conduct empirical testing to determine precise solubility values. As a general guideline, "like dissolves like" can serve as a useful rule of thumb when predicting solubility behavior.

Interesting facts

Interesting Facts about Isopropyl 1-Methyl-3,6-Dihydro-2H-Pyridine-5-Carboxylate

Isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate, an intriguing compound belonging to the pyridine family, offers a wealth of insights for both scientists and students. Notably, its unique structure contributes to its fascinating properties and potential applications in various fields.

Key Characteristics

  • Structural Diversity: This compound features a pyridine ring, a cornerstone in organic chemistry known for its stability and reactivity.
  • Versatile Functionalities: The presence of both an isopropyl and a carboxylate group enhances its ability to participate in a variety of chemical reactions, making it a valuable building block in synthetic chemistry.
  • Potential Biological Activity: Many derivatives of pyridine compounds have been studied for their biological properties, suggesting that isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate may possess interesting pharmacological characteristics.

Applications

  • Pharmaceutical Industry: Due to its structural framework, this compound could be explored for the development of new drugs.
  • Agricultural Chemistry: Pyridine derivatives are often investigated for their potential as agrochemicals, providing insight into their role in pest management.

In summary, isopropyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate exemplifies the remarkable potential of nitrogen-containing heterocycles. As researchers continue to explore its properties, this compound could pave the way for innovative solutions in health and agriculture.

Synonyms
BRN 0132010
i-Propyl 1-methyl-1,2,5,6-tetrahydronicotinate
10558-56-2
NICOTINIC ACID, 1,2,5,6-TETRAHYDRO-1-METHYL-, ISOPROPYL ESTER
DTXSID20147204
DTXCID3069695
5-22-01-00323 (beilstein handbook reference)