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Pipradrol

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Identification
Molecular formula
C14H21NO
CAS number
91-83-8
IUPAC name
1-(2-piperidyl)propan-1-ol
State
State

At room temperature, pipradrol exists as a solid.

Melting point (Celsius)
147.00
Melting point (Kelvin)
420.00
Boiling point (Celsius)
266.00
Boiling point (Kelvin)
539.00
General information
Molecular weight
219.32g/mol
Molar mass
209.3200g/mol
Density
1.0037g/cm3
Appearence

Pipradrol typically appears as a white crystalline powder that is odorless.

Comment on solubility

Solubility of 1-(2-piperidyl)propan-1-ol

1-(2-piperidyl)propan-1-ol is a compound that exhibits interesting solubility characteristics, primarily due to its functional groups and molecular structure. When considering the solubility of this compound, several key points come to mind:

  • Polar Nature: The presence of the hydroxyl group (-OH) in its structure contributes to its polar nature, enhancing its solubility in polar solvents, particularly water.
  • Amine Interaction: The piperidine ring within the molecule can engage in hydrogen bonding, further promoting solubility in aqueous environments.
  • Hydrophobic Interactions: Although it is polar, the aliphatic carbon chain can introduce some hydrophobic character, which may affect its solubility in non-polar solvents.

In general, one can expect 1-(2-piperidyl)propan-1-ol to be:

  • Highly soluble in water due to its functional groups.
  • Moderately soluble in organic solvents with some polar characteristics, such as ethanol or methanol.
  • Poorly soluble in non-polar solvents like hexane.

In the realm of chemistry, it often holds true that "like dissolves like," and this compound is no exception. Its solubility profile demonstrates how molecular structure directly influences interactions with various solvents.

Interesting facts

Interesting Facts About 1-(2-Piperidyl)propan-1-ol

1-(2-Piperidyl)propan-1-ol is an intriguing compound that often piques the interest of chemists due to its unique structural characteristics and potential applications. This compound features a piperidine ring, a non-aromatic cyclic structure known for its versatility in organic synthesis.

Unique Structural Features

  • Piperidine Moiety: The presence of the piperidine ring provides the compound with noteworthy pharmacological properties. Piperidine derivatives are often found in many natural and synthetic products.
  • Alcohol Functional Group: The alcohol group contributes to the compound's reactivity, allowing for further modifications that can lead to a variety of derivatives.

Potential Applications

This compound conveys several potential applications in different fields:

  • Pharmaceuticals: Similar piperidine derivatives are studied for their roles in the development of new medications, including neuroactive drugs and antidepressants.
  • Organic Synthesis: Its reactivity can be harnessed in various synthetic pathways, making it valuable for creating complex organic molecules.
  • Material Science: Compounds with multifunctional groups like this one may be used in designing novel polymers or materials with specific properties.

Impact on Chemical Research

The study of 1-(2-Piperidyl)propan-1-ol encourages further exploration in the realm of:

  • Medicinal Chemistry: The quest for targeting specific biological pathways.
  • Asymmetric Synthesis: Exploring methods for producing enantiomerically pure substances.
  • Drug Development: Investigating its potential effects and mechanisms in biological systems.

In summary, 1-(2-piperidyl)propan-1-ol is more than just a simple compound; it embodies a rich tapestry of potential applications and research avenues in chemistry and beyond. Understanding its properties might pave the way for innovations in drug development and organic synthesis.

Synonyms
1-(piperidin-2-yl)propan-1-ol
63401-12-7
DTXSID60871697
DTXCID40819335
831-531-3
1-piperidin-2-ylpropan-1-ol
495-20-5
Conhydrin
SCHEMBL1932043
2-(1-hydroxypropyl)-piperidine
VCCAAURNBULZRR-UHFFFAOYSA-N
AAA49520
NSC172229
AKOS013088470
CCG-357572
NSC-172229
(S)-1-((R)-piperidin-2-yl)propan-1-ol
CS-0259394
EN300-73193
G45048
Z1157652498